You are on page 1of 31

585

20

Pharmacology of Marine Macroalgae


Kasım Cemal Güven1, Burak Coban2 and Osman Özdemir3
1
Turkish Marine Research Foundation (TUDAV), PO Box: 11 Beykoz, Istanbul, Turkey
2
Chemistry Department, Bulent Ecevit University, Zonguldak, Turkey
3
Department of Pharmacology, Faculty of Health Sciences, Cyprus International University, Lefkoşa, North Cyprus, Cyprus

20.1 ­Introduction oldest article in the scan is from 1883. When


available active ingredients were written before
Medical use of marine algae goes back to the the name of the alga, otherwise algal extracts
ancient China [1–3] and the use of algae as have been indicated in this review.
food continues today. Alginic acid is the oldest
pharmaceutically active constituent isolated
from brown algae [4]. The antihelmentic
20.2 ­Anti-Bacterial Activity
­properties of Digenea simplex [5] and
20.2.1 Green Algae
Corallina officinalis [6] were also known in
Mediterranean countries. The first alkaloid Extracts of Caulerpa sertularioides, Penicillus
from algae was isolated by Guven et al. [7,8]. capitatus and Aurainvillea rawsoni [5], Entere­
General use of algae was first mentioned by morpha linza [17], lipidic extracts of Clad­
Hoppe et al. [9,10]. Medicinal use of algae was ophora rupestris [18], Ulva reticulate, Caulerpa
first published in 1969 by Baslow [11]. In previ- accidentalis and Cladophora socialis extracts
ous reviews the pharmacology of alkaloids [19], Codium decorticatum [20], Caulerpa rac­
from algae [12,13] and volatile oils of algae [14] emosa var. occidentalis [19], Caulerpa prolifera
were summarized. Subsequent titles were [21], C. protera and C. cupressoides [22], Ulva
summarized according to the chronological lactuca [23,24], Ulva pertussa [25], U. fasciata
order in this chapter. A detailed book [22,26], U. reticulata [19], Ulva rigida [27],
Anticancer Activities of Algae was been pub- Enteremorpha intestinalis [23], E. linza [17],
lished by Kim (2015) [15] and this hot topic is Chlodophora rivularia [28], C. socialis [19],
not included in this chapter. Anticoagulant Chlodophora rupestris [23], Codium bursa
and antilipemic activities of algae have not also [27], C. fragile [24], Scenedesmus quadricauda
been included in this chapter because they [29], Chaetomorpha linum [30], C. antennina
have been prepared for publication elsewhere [26] showed antibacterial effect. Enteromorpha
recently [16]. intestinalis extract proved to be particularly
In this literature review, we took care to put effective against Gram-positive and marine
the earliest studies in the first place and the bacteria [23].

Encyclopedia of Marine Biotechnology: Five Volume Set, First Edition. Edited by Se-Kwon Kim.
© 2020 John Wiley & Sons Ltd. Published 2020 by John Wiley & Sons Ltd.
586 20 Pharmacology of Marine Macroalgae

20.2.2 Brown Algae taxiformis [58], Galaxoura cylindrinea [56],


Gracilaria verrucosa [25], G. dendiroides [19],
The extracts of Laminaria digitata [31],
G. domingensis, G. corticata, Amansia multifida
Desmarestia aculeate and Fucus serratus [32],
[22], Dasya pedicellata and Griffithsia globifera
Sargassum natans [33], S. kjellmanianum [34],
[5], Junia rubens [59], Rhodomela larix [60], R.
S. wightii [35], S. muticum [23], Laminaria
subfusca, Delesseria sanguine extracts [32].
japonica and Kjellmaniella crassifolia [25], L.
Asparagopsis taxiformis also showed activity
ochroleuca, Fucus vesiculosus, Ectocarpus siliqu­
against Leptospira javanica [61]. 3-bromo-
losus, Pelvetia canaliculata and Ascophyllum
4,5-dihydroxybenzaldehyde from Halopytis
nodosum [23], Himanthalia elongata [36],
incurvus [62], cycloeudesmol, a cyclopropane
Padina gymnospora [30,37,38], Colpomenia sin­
containing sesquiterpene from Chondria oppo­
uosa, Scytosiphon lomentaria, Dictyota dicho­
site clada [63], halogenated acyclic monoterpe-
toma var. implex, D. dichotoma and Petolonia
nes from Plocanium cartilagenium [50], simple
fascia [39], P. binghamiae [40], Dictyota indica,
bromophenols isolated from Polysiphonia sp.:
D. divaricata, D. flabella and Padina concresceus,
P. violacea, P. thuyoides, P. urceolata, P. brodiaei,
Fucus serratus [5,24], dictyol F and epidictyol F
P. nigra, P. nigrescens, P. elongata, P. lanosa and
from D. dichotoma [41], phlorotannins from
P. fruticulosa [64], showed antibacterial activi-
Eisenia bicyclis, Ishige okamurae and Pelvetia
ties. A polybrominated 2-heptanone isolated
siliquosa [42], Ecklonia cava [42,43], E. kurome
from Bonnemaisonia hamifera showed anti-
[42,44], E. stolonifera [42,45], lipid extracts of
fouling activity against bacterial colonization
Zanardinia prototypus, Cystoseira barbata and
on the surface of alga [65].
C. jabukae [46] showed antibacterial activities.

20.2.3 Red Algae 20.3 ­Antifungal Activity


Laurencia sp. generally showed antibacterial
20.3.1 Green Algae
effects such as: Methanolic extracts [5,47,48], a
sesquiterpene allolaunterol [49], polyhalogen- Chlamydomonas reinhardtii extract was active
ated terpenes [50], volatile oils and hydrophilic against marine fungi and Caulerpa prolifera
extracts of L. obtusa [51], brominated indols ether extract showed weak effect [23]. Caulerpa
from L. mariannensis, L. majuscula, L. nidifica, rasemosa, C. taxiflora, Halimeda opuntia and
L. cartilaginea, L. concreata [52], pre-pacifenol Udotea flabellum extracts showed weak anti-
from L. filiformis [53], a halogenated C15 ace- fungal activity [66].
togenin from L. mariannensis and a halogen-
ated sesquiterpene from L. majuscula [54],
20.3.2 Brown Algae
chamigran, a sesquiterpene from L. okamurae
[55], ethanolic extracts of L. johnstonii [24], L. Dictyosphaeria favulosa, Dictyota bartayresii, D.
papillosa, [56], L. brongniartii [57], L. pinnati­ divaricata, D. indica and Padina gymnosphora
fida [23], L. ceylonica, L. brandenii [58] showed [66] showed strong antifungal activity.
antibacterial activities. Sargassum muticum, S. filipendula, S. stenophyl­
The other red algae with antibacterial activi- lum, Stypopodium zonale were active against
ties are Chondrus crispus, Ceramium rubrum, marine fungi [23], etanolic extracts of S. muti­
Cryptoleura ramosa, Polysiphinia lanosa [23], cum, Pelvetia canaliculata, Stypopodium zonale,
Dictyopteris justii, D. plagiogramma, Chondria Laurencia dendroidea, Ascophyllum nodosum
littoralis, Falkenbergia hillebrandii, Goniyaulax and Fucus spiralis inhibited Colletotrichum
tamarensis, Wrangelia argus and W. bicuspidata lagenarium but not Aspergillus flavus [67].
extracts [5], Hypnea valentine, Asparagopsis Sesquiterpene cyclodesmol from Ascophyllum
20.5 ­Antiherpetic Activit 587

nodosum and Chondria oppositiclada, meth- of Zanardinia prototypus and Cystoseira


oxybifurcarenone from Cystoseira tamariscifolia ­balerica [92], C. myrica [89,93], C. indica [86]
[68] were active against Candida albicans exhibited antiviral activity. Laminaran from
[23,63]. Turbinaria conoides and Padina gymno­ Laminaria sp. showed inhibitory effect on
spora extracts found active against fungi [69]. virus profileration [94].
Dictyota dichotoma, Dilophus fasciola and D.
spiralis were active but Taonia atomaria was
20.4.3 Red Algae
inactive against dermatophytes [70]. Dictyota
dichotoma [71] and Laminaria ochroleuca, L. Gelidium cartilagineum containing a linear pol-
pinnatifida [23] showed antifungal activity. ysaccharide inhibited the growth of IBV and
mumps virus [95]. Halogenated triterpenes
obtained from Laurencia venusta showed
20.3.3 Red Algae
­antiviral activities [96,97]; sesquiterpenes,
Laurencia papillosa and Wrangelia argus extracts peyssonol-A and peyssonol-B, from Peyssonelia
[66], Odonthalia corymbifera containing bromo- sp. showed HIV-1 and HIV-2-RT activity [98];
phenol [72], Chondrus crispus, Polysiphonia extracts of Constantinea simplex and Farlowia
lanosa and Chryptopleura ramosa extracts [23], mollis [99], lentil, a lectin from Ptilota plumosa
Falkenbergia rufolanosa extract [73], sesquiter- [100] showed antiviral activities. A sulfolipid
pene allolaurinteral from Laurencia obtusa from Gigartina tenella [101] and glycolipids
[49,66], showed antifungal activity. from Osmundaria obtusiva showed inhibitory
effect against HIV-reverse transcriptase (RT)
[102]. Polysaccharides from Schizymenia
pacifica [103], sulfated xylomanan fraction
20.4 ­Antiviral Activity
from Nothogenia fastigiata [104], carrageenans
from Cryptopleura ramose [105], Gigartina
20.4.1 Green Algae
skottsbergii [106,107], G. acicularis and G. pistil­
Cladophora sp. inhibited viral maturation [74]. lata [82], Meristiella gelidium [108], Lau­rencia
Polysaccharides of green algae with antiviral dendroidea [109], polysaccharides from
activity are: Ulvan from Ulva lactuca has anti Grateloupia indica [110], sulfated polysaccha-
influenza A virus (IAV) activity [75] and caul- rides from Aghardhiella tenera and Eucheuma
erpin from Caulerpa sp. had antiviral effects on cottonii [82,111] showed antiviral activities.
bovine viral diarrhea virus (BVDV) [76]. Antivirus activities of carrageenan types have
been studied: Κ-carrageenan [82,107,112–115],
λ-carrageenan [107,113,116–121], ί-carrageenan
20.4.2 Brown Algae
[117,121–125].
Dictiyota acutiba extract inhibits viral matura-
tion [74]. Fucoidan from Fucus vesiculosus [77–
80] and from Undaria pinnatifida [78,81] was
20.5 ­Antiherpetic Activity
found active not only depending on ionic
changes but also sugar rings [81] and potency
20.5.1 Green Algae
increases with the number of sulfate groups
[82]. Galactofucan from Sargassum horneri Caulerpa brachypus, C. okamurai, C. scapell­
[83,84], S. piluliferum [85], S. tenerrimum, S. pat­ iformis, Chaetomorpha crassa, C. spiralis,
ens [86], S. latifolium [83,84,87–89] showed anti- Codium adhaerens, C. fragille, C. latum,
viral activities. Diterpenes from Stoechospermum Enteromorpha compressa and Monostroma niti­
marginatum and Canistrocarpus cervicornis [90], dum extracts showed potent anti-HSV-1 activi-
sulfolipids from Dilophus fasciola [91], extracts ties [126], a rhamnan sulfate from Monostroma
588 20 Pharmacology of Marine Macroalgae

latissimum [127] and Ulva fasciata and Codium Schizymenia binderi [154], Callophyllis varie­
decorticatum extracts were active against HSV-1 gata [155], Cryptopleura ramose [105],
[109], Caulerpa rasemosa extract was active Pterocladia capillacea [156], Gymnogongrus
against HSV-1 and HSV-2 [128]. Torulosus [157], Gymnogongrus griffithsiae and
Cryptonemia crenulata [158], Scinaia hatei
[159], Schizymenia binderi [154], Gigartina
20.5.2 Brown Algae
skottsbergii [106,116], Meristiella gelidium [108].
Sargassum natans [33], S. kjellmanianum [34],
S. muticum [23], S. tenerrimum [69,86], S. ptero­
pleuron [129], S. linum and S. wightii [38], 20.6 ­Antioxidative Activity
S. horneri [84,130], S. patens [131,132], S. latifo­
lium [88], Undaria pinnatifida [78,93,133,134], An antioxidant is a molecule that has a role for
Cystoseira indica [135], Adenocystis utricularis inhibiting oxidation reactions in the human
[136], Stoechospermum marginatum [137], body caused by reactive oxygen species (ROS)
Leathesia difformis [138] containing sulfated and this leads to various disorders. Several
polysaccharides were found to have antiviral compounds such as phlorotannin, carotenoids,
activity against HSV-1 and HSV-2. sulfated polysaccharides, astaxantin, lutein,
The extracts of Cystoseira myrica [89] and C. lycopene have antioxidant activities. Algal pig-
balearica [92], methoxybifurcarenone from C. ments chlorophyll, phaeophytin and porphy-
tamariscifolia [68], a diterpenoid from C. medi­ rin derivatives showed antioxidant activities
terranea [139], crude extracts of S. cymosum, S. [160–164]. Algal extracts possessing antioxi-
polyceratum and Stypopodium zonale [109], dant activities are listed below.
Dilophys fasciola [56], Canistrocarpus cervi­
cornis [90], diterpene derivative from Dictyota
20.6.1 Green Algae
pfaffii and D. menstrualis [140] showed antivi-
ral activities against HSV. Phenolic meso-terpenoids from Halimeda inc­
rassata [165,166], a glycoprotein extracted and
purified from Codium decorticatum [167],
20.5.3 Red Algae
7-hydroxycymopol from Cymopolia barbata
Extracts of Cryptosyphonia woodii and Farlowia [168], methanolic extracts of Halimeda monile
mollis [141], Polysiphonia denudate [142], [169], H. tuna, Caulerpa cupressoides, C. pas­
Asparagopsis armata, Ceramium rubrum, paloides [129], Enteromorpha sp. [170],
Gelidium pulchellum, Gelidium spinulosum, Enteromorpha linza [171], E. compressa [172],
Halopitys incurvus, Hypnea musciformis, E. intestinalis, Monostroma nitidum and Ulva
Plocamium cartilagineum, Boergeseniella thuy­ lactuca [173], Chaetomorpha morphamelagan­
oides, Pterosiphonia complanata and Sphaero­ ium [174], Ulva intestinalis and Cladophora
coccus coronopifolius [143], Symphyocladia vagabunda [175], U. pertusa [176–178], U.
latiuscula [144], bromophenols from Symphyo­ rigida, U. fasciata [179], Codium bursa [27],
cladia latiuscula [144,145] and glycolipids from Codium tomentosum [180], Chaetomorpha
Osmundaria obtusiloba [146] showed antennina and Gayralia nitidum [181] showed
anti-HSV-activities. antioxidant activities.
Algae containing sulfated polysaccharides
having anti-HSV properties are [112], Notho­
20.6.2 Brown Algae
genia fastigiata [104,147], Cryptonemia crenu­
lata [148], Sebdenia polydactyla [149], Bostrychia Carmalol isolated from Ishige okamurae
montagnei [150], Acanthophora spicifera [151], [182], meso terpenoids from Cystoseira crinita
Gracilaria corticata [152], G. salicornia [153], [165,183], phlorotannins from Eisenia bicyclis
20.7 ­Hypoglycemic Activit 589

and Undaria pinnatifida [184,185], E. bicyclis Ahnfeltiopsis concinna, Polysiphonia hovei,


[186], pyropheophytin from Eisenia bicyclis Polysiphonia urceolata, Pterocladia capillacea
[187], polyphenols from Undaria pinnatifida, [205], Polysiphonia morrowii [205,217], Por­
Ecklonia cava, Hizikia fusiforme [178], Ecklonia phyrin derivatives extracted from Porphyra
stolonifera [188], Sargassum siliquastrum haitenensis [218], Plocamium cartilagineum
[189], phenolic meso terpenoids from Cysto­ [180], ethanolic extracts of Porphyra sp. [207],
seira sp. [165], Cystoseira barbata extract [27], porphyra 334 and shinorin from Porphyra
crude polysaccharides from Turbinaria ornata yezoensis [219], floridosides from Laurencia
[190], taondiol, isoepitaondiol, stypodiol, sar- undulata, sesquiterpenes from L. dendroide
gaguinon and sargol from Taonia atomaria [220], phenolic compounds from Gracilaria
[191], Sargassum pallidum [192], fucoxanthin bursa-pastoris [221], Gelidiella acerosa [222],
from Hizikia fusiformis [193,194], sulfated pol- Ceramium diaphanum [27], bromophenols
ysaccharides of Fucus vesicolus [195] and from from Rhodomela confervoides [223], extracts of
Sargassum pallidum [196] and Sargassum ful­ Laurencia intermedia and Porphyra dentata
vellum [197], a lipophilic extract of Laminaria [173] showed antioxidant activity. Chondrus
japonica [198], Petalonia binghamiae [199], ocellatus, Gelidium amansii, Gracilaria verru­
Scytosiphon lomentaria, Papenfussiela kuromo cosa, Grateloupia pradicocytes extracts inhibit
[200], Turbinaria conoides and T. ornata [201], ROS generation [202].
Dictyopteris undulata, Sargassum micracan­
thum [202], extracts of Sargassum ringgoldi­
anum [203], Sargassum siliquastrum [204],
Hydroclathrus clatratus, Sargassum echinocar­ 20.7 ­Hypoglycemic Activity
pum, Colpomenia sinuosa [205,206], Sargassum
horneri, S. siliquastrum, S. macrocarpum, 20.7.1 Green Algae
Eisenia bicyclis [207], Sargassum polycyclum
The extract of Ulva rigida showed anti-hyper-
[208], Ctyopteris undulata, Sargassum hemi­
glycemic effect in experimental diabetes [224].
phyllum [173], methanolic extracts of
Ulva lactuca, Palmaria palmate [225], Codium
Sargassum marginatum, Padina tetrastomatica
tomentosum [226] and Petalonia sp. [227]
and Turbinaria coincides [201], and Sargassum
extracts exerted antidiabetic effect.
pallidum [192] showed antioxidant activities.
The phospholipid fractions of Fucus vesiculo­
sus, F. serratus [209,210] and Ascophyllum
20.7.2 Brown Algae
nodosum showed very low activity [209].
Sargalin from Sargassum confusum was first
isolated compound showed antidiabetic effect
20.6.3 Red Algae
[228]. Fraction II of sargalin had blood reduc-
The extracts of Chondria baileyana, C. atropur­ ing effect, 19% and 23% for sargalin I. Chemical
purea, Heterosiphonia gibbesii, Acanthophora studies of sargalin gave arginine and phenol.
spicifera, Bryothamnian triquetrum, Ceramium Phenolic part showed a remarkable suppres-
nitens, Polysiphonia urceolata, Polysiphonia sive action on diabetes mellitus [229]. Sargas­
morrowii [211], Bryothamnion triquetrum sum vulgare extract fractionated on sephadex
[212], Plocamium cartilagineum [180], G.25 and fraction separated (100–150 mL) had
Euchema kappaphyces, Gracilaria edulis, hypoglycemic activity. Blood sugar lowered by
Acanthophora spicifera [213], Polysiphonia 17% after hydrolysis of this fraction [230].
urceolata [214], Stictosiphonia arbuscula [215], Phyllophora nervosa extract slightly lowered
Grateloupia filicina [198,216], Rhodomela blood sugar level [231]. Cystoseira barbata was
­confervoides [198,200], Laurencia obtuse [208], extracted and fractioned by the same method
590 20 Pharmacology of Marine Macroalgae

and tested on 30 albino rats of Wistar star strain 20.8.1 Brown Algal Sulfated
(against saline and regular insulin references) Polysaccharides
in one week interval, during 1 month. The frac-
Alginic acid and its derivatives were also used
tion II showed antidiabetic activity similar to
for gastrointestinal ulcer [244,245]. Sodium alg-
insulin 60 min after administration blood glu-
inate forms a thick layer of protection over the
cose level decreased 32% [232].
lesion against the hydrochloric acid and it was
Phlorotannins, dieckol, diphloroethohydroxy
used for the treatment of gastrointestinal ulcers
carmalol, 7-phloroeckol isolated from Ecklonia
[246–248]. Alginic acid-antacid also decreased
sp. showed antidiabetic effect in type II diabetic
postprandial reflux in the upright position [249].
mice [233]. Dieckol from E. cava exerted anti-
Fucoidans from Cladosiphon okamuranus,
diabetic effect [234,235]. Methanolic extract of
Fucus evanescens, F. vesiculosus inhibited the
E. cava increased insulin concentration in type
attachment of H. pylori adhesion to the gastric
I diabetes [236]. Fucosterol obtained from
mucosa [250].
Eisenia bicyclis and E. stonolifera [237] and
Petolonia siliquosa [238] have effects on diabe-
tes treatment. Fucus vesiculosus and Himantalia 20.8.2 Red Algal Sulfated
elongata extracts showed significant reduction Polysaccharides
in blood glucose level [226]. Brown algae The therapy of peptic ulcer by carrageenans is a
extracts of Palmaria dulce, Ascophyllum nodo­ controversial topic. Antiulcer activities of
sum and Alaria esculenta showed antidiabetic native, innative and degraded carrageenans
properties [225]. Bromophenol from Grate­ were discussed in various papers, between 1962
loupia elliptica prevent diabetes mellitus [239]. and 1980. Some authors found evidence on
There are many patents on the treatment of ulseration but others did not. Sulfated algal pol-
diabetes by using seaweed consisting red, ysaccharides interfere with proteolysis by reduc-
brown and green algae [240]. ing the proteolytic activity of pepsin by forming
a complex [251]. Carrageenan inhibited the
20.7.3 Red Algae digestion of egg albumin by pepsin [252].
Degraded carrageenan reduced the total acid
A fraction of the extract obtained from
concentration of gastric juice [253]. Degraded
Corallina rubens showed high hypoglycemic
carrageenan prevented the formation of peptic
activity, its effect was very close to insulin
ulcer in guinea pigs when given orally prior to
[241]. A fraction of Pterocladia capillaceae
histamine [254]. Activities of native and
showed the highest activity among other algae
degraded carrageenan were not similar [255].
tested with a sugar reducing effect from 104
Carrageenan was used for digestive diseases in a
mg to 72.7 mg at dose of 20 mg/kg [242].
formulation [256]. There are other formulations
Cystoseira crinata and C. corniculata extract
with therapeutic effects on duodenal ulcers
showed a blood sugar level fall from 130 mg to
[257]. Sulfated polysaccharide fraction of
65 in 120 min [243].
Hypnea musciformis exerts a protective effect
against ethanol induced gastric damage [258].
20.8 ­Gastrointestinal Tract
Diseases 20.9 ­Anti-Inflammatory Activity

The problem of this area is ulceration and Inflammation is a pathological process involved
spasmolysis caused by Helicobacter pylori. in various disorders. The compounds isolated
There are number of algal preparations used to from algae or where they themselves itself show
treat this condition. anti-inflammatory effects are listed below.
20.10 ­Miscellaneou 591

20.9.1 Green Algae from Ecklonia maxima [273] showed inhibitory


effects on acetylcholine esterase activity. These
3-O-beta-D-glucopyranosyl-stigmasta-5,25-dien
compounds maintain memory-enhancing abili-
isolated from Ulva lactuca [259] and Cladophora
ties in mice. Spongomorpha indica, Udotea
fascicularis, phaephytin from Ulva rigida, Codium
indica, Laurencia pedicularioides, Hypnea
bursa, Enteromorpha prolifera [260], lectin from
­valentiae, Padina gymnospora, Ulva reticulate,
Caulerpa cupressoides [261], extracts of Halimeda
Gracilaria edulis showed cholinesterase inhibi-
incrassata [166] and Chaetomorpha melagonium
tory activity [274,275]. Ochtodes secundiramea
[174] showed anti-inflammatory effects.
extract showed 48% inhibitory activity [276].
Farnesylacetone derivatives isolated from Sar­
20.9.2 Brown Algae gassum sagamianum showed moderate activi-
A fucoxantin from Myagropsis myagroides extract ties [277]. Phlorotannins from Eisenia bicyclis
containing 6,6′-bieckol [262], pheophorbide from can be a preventative agent for Alzheimer’s dis-
Saccharina japonica [263], Cystoseira barbata ease, the neurodegenerative disease of human
[27], phenolic mezoterpenoid from Cystoseira sp. brain [278–280]. Brown alga Ishige okamurae
[165] and phlorotannins from Eisenia bicyclis suppresses Alzheimer’s disease [281].
[186], extracts of Dictyopteris undula, Laminaria
japonica [264], Dictyopteris undulata, S. hemi­ 20.10.2 Anti-allergic
phyllum var. chinense [173], S. ringgoldianum
[203], S. siliquastrum [204], S. echinocarpum, In Korean folk medicine Sargassum hemiphy­
Colpomenia sinuusa, Hydroclathrus clatratus lum was used for the treatment of various
[205], S. polycyclum [208], Sargassum sp. [207] allergic diseases [282]. Dioxinodehydroeckol
demonstrated anti-inflammatory effects. (DHE) and phlorofucofuroeckol A (PFF-A)
isolated from Ecklonia stolonifera exerted anti-
20.9.3 Red Algae allergic effect via the inhibition of Fc(epsilon)
RI expression in KU812F cells [283]. The rats
Anti-inflammatory activities have been reported fed with Eisenia arborea became more anti-
for brominated diterpenes isolated from Jania allergic, suggesting that E. arborea might pos-
rubens [265], vidalol A and B from Vidalia obtusa­ sess anti-allergic effects [284]. Ethanol extracts
loba [266], two new C15 acetogenins (12Z)-cis- of brown seaweeds Sargassum tennerimum, S.
maneonene-D and (12E)-cis-maneonene-E cervicorne, S. graminifolium, S. thunbergii, and
from Laurencia obtusa [267], polysaccharides Laminaria japonica have antiallergenic activi-
isolated from Gracilaria caudate [268], from ties [285]. Green alga Enteromorpha compressa
Digenea simplex [269], sulfated galactan from inhibited IgE immune response and may have
Gracilaria fisheri [270], extracts of Ceramium potential in curing various types of allergies
diaphanum [27] and Hypnea musciformis [271] [286]. Phlorotannins, polysaccharides, carote-
and they can be useful as therapeutic agents noids, polyunsaturated fatty acids and phyco-
against inflammatory diseases. cyanin derived from various marine algae were
discussed by Vo et al. (2012) [287].
20.10 ­Miscellaneous
20.10.3 Antiplasmodial Activity
20.10.1 Acetylcholine Esterase
Ethanolic extracts of Caulerpa toxifolia and C.
Activity and Alzheimer’s Disease
peltata showed potential in vitro antiplasmo-
Dieckol and phlorofucofuroeckol, the poly- dial activity against drugs resistant Plasmodium
phonic compounds found in brown algae Eisenia falciparum [288]. Halogenated terpene from
sp. and Ecklonia sp. [272] and phlorotannins South African marine red alga Plocamium
592 20 Pharmacology of Marine Macroalgae

c­ ornutum showed antiplasmodial activity toward 20.10.8 Protective Effect Against


a chloroquine sensitive strain of Plasmodium Radiotherapy Damage
­falciparum [289]. Codium bursa, Caulerpa rase­
Polysaccharides from red algae Ecklonia cava
mosa and Dasya pedicellata extracts showed
[302], Fucus vesiculosus and Laminaria japon­
antiplasmodial activity [290]. P-hydroxy-
ica [303], Ulva pertussa [304], Monostroma
benzaldehyde from Laurencia papillosa showed
angicava [305], Laminaria sp. [306], phenolic
antiplasmodial activity [291]. Bromophycolides
compounds from E. cava and Ishige okamurae
extracted from Callophycus serratus exhibited
[307,308], carotenoids isolated from Sargassum
antiplasmodial activity [292,293].
siliquastrum [309], Dunaliella bardawil [310]
reduced side effects and damage caused by
20.10.4 Anti-Asthmatic Activity
radiotherapy [311].
Ethanolic extract of brown alga, Ecklonia cava
induced a significant inhibition of asthmatic
reactions in a mouse [294,295]. 20.10.9 Vermifuge
Kainic acid and allokainic acid containing
20.10.5 Immune Stimulatory Activity marine algae Digenea simplex has long been
Sulfated galactans isolated from Gracilaria fish­ used in China as a vermifuge [312,313].
eri exhibits immune stimulatory and antiviral
activities against white spot syndrome virus
20.10.10 Antihypertensive and
(WSSV) in shrimp Penaeus monodon [296].
Hypotensive Activity
Polysaccharide immunomodulators biogly-
canes isolated from Laminaria cichorioides Eckol isolated from the brown alga Ecklonia
acted as activators of Fc-gamma-R and C3bR stolonifera, phlorofucofuroeckol A and dieckol
activity, that is the base for control of pathologi- were shown to have marked inhibitory activity
cal processes, related to immune system [297]. against angiotensin-converting enzyme (ACE)
[314–316]. Peptides from Undaria pinnatifida,
20.10.6 Anti-osteoporotic Hizika fusiformis and Porphyira yezoensis
­possess antihypertensive activity [317–319].
Dictyol from Padina pavonica extract increased
Prostaglandins from Gracilaria lichenoides
the uptake and fixation of calcium by osteo-
showed antihypertensive effect [320].
blasts in culture. Sargassum horneri proved
Prostaglandin-like activity was observed from
osteoblastic bone formation properties and
Halopteris filicina [321,322]. Jania rubens eth-
inhibitory effects on bone resorption [298].
anolic and water extracts had a transient
Various brown algae species include Padiva
hypotensive effect [323].
pavonica, Sargassum horneri, Undaria pinnati­
Laminine, a choline-like amino acid, iso-
fida, S. horneri, Eisenia bicyclis, Cryptonemia
lated from Laminaria angustata, Heteroch­
scmitziana, Gelidium amansii, and Ulva per­
ordaria abietina, Chondria armata showed
tusa which showed a preventative effect against
hypotensive effect [324–326]. This activity
osteoporosis [299]. Fucoxantin from Laminaria
was also found in Laminaria species:
japonica, Undaria pinnatifida, Eisenia bicyclis
Laminaria japonica, L. fragilis, L. religiosa,
suppressed osteoclastogenesis [300].
L. angustata, L. cichorioides, L. yessoensis,
L. diabolica, and in small quantities in
20.10.7 Spasmolytic Activity
Kjellmaniella gyrate, K. crassifolia, Costaria
Caulerpine, bis-indole alkaloid isolated from costata, Arthorothammus bifidus, Eisena
Caulerpa genus showed spasmolytic effect on bicyclis, Eckloniopsis radicosa and Ecklonia
guinea pig ileum [301]. cava [325].
20.11 ­Conclusio 593

20.10.11 Antihepatotoxic Effect Gelidium amansii, Gracilaria verrucosa, and


Grateloupia lanceolata extracts significantly pro-
Hot water extract of Ulva reticulate showed
tected against obesity [202].
antihepatotoxic effect against acetaminophen
induced hepatotoxicity in experimental rats
[327]. Laurencia obtusa and Caulerpa prolifera 20.10.14 Hemagglutination Inhibition
extracts are active against aflatoxin B(1) initi-
Lectins from Anadyomene plicata, Avrainvillea
ated hepatotoxicity in rats [328].
erecta, Gracilaria eucheumatoides, G. salicor­
nia, Kappaphycus striatum showed hemagglu-
20.10.12 Hypo-Cholesterolemic Activity tinin effect [347]. The lectin grifithsin from red
alga Griffithsia sp. showed a strong anti-HIV
The green alga Enteromorpha compressa effect [348].
decreased the plasma cholesterol levels of rats
[329]. Ulva pertussa, Enteremorpha prolifera
and Monostroma nitidum showed a positive 20.10.15 Antinociceptive Activity
effect in reducing the plasma cholesterol levels Lectin from Caulerpa cupressoides extract
in rats [330]. Monostroma nitidum extract frac- induced a powerful inhibition of pain sensa-
tions are effective in lowering the plasma cho- tion [349]. Polysaccharides from the red alga
lesterol levels [331–333]. Sterols from brown Digenea simplex possess anti-inflammatory
algae Fucus gardneri and Sargassum muticum and antinociceptive effect [269]. Sulfated
caused a significant diminution in plasma cho- ­polysaccharide carrageenan from Gracilaria
lesterol in Leghorn cockerels [334]. Fucosterols caudate showed an intrinsic peripheral antino-
and other unsaponifiable Sargassum lipids ciceptive action [350]. Corallina officinalis
slightly reduced plasma and liver cholesterol extracts induced analgesic, antipyretic activi-
[335]. Na-alginate demonstrated significant ties [351]. The extract of red alga Laurencia
hypocholesterolemic activity [336,337]. Hetero­ glandulifera containing brominated diterpene
cordaria abietina unsaturated fatty acids exerted analgesic properties in mice [352].
depressed the blood cholesterol levels [337]. Hypnea cervicornis agglutinin, a lectin isolated
The red algal polysaccharide carrageenan from the red marine alga showed important
exhibited hypocholesterolemic activity [336– antinociceptive and anti-inflammatory activity
338]. Porphyra tenera reduced plasma choles- via interaction with the lectin carbohydrate-
terol in rats [330,339]. binding site [353,354].

20.10.13 Antiobesity Effect 20.10.16 Antiophidic Effect


Fucoxanthin in brown algae Sargassum horneri, Dolastane, diterpene isolated from Canistrocarpus
S. thunbergii, S. fusiforme, U. pinnatifida, Peta­ cervicornis showed antiophidic properties on
lonia binghamiae and Laminaria japonica is an envenomation by Lachesis muta snake venom
effective antiobesity supplement [340–342]. [355].
Fucoidan from brown algae showed antiobesity
effect [343]. Phlorotannins from E. cava may be
effective for antiobesity [340,344,345]. The 20.11 ­Conclusion
antiobesity effect of Ascophyllum nodosum was
reported [346]. Laurencia intermedia, Ecklonia A large number of active substances have been
cava, Sargassum macrocarpum, Polysiphonia isolated from algae. The pharmacological
morrowii, Ishige okamurae, Dictyopteris undu­ properties of algae and these active substances
lata, S. micracanthum, Chondrus ocellatus, have been studied. Some of these are used in
594 20 Pharmacology of Marine Macroalgae

the food, textile and adjunct pharmaceutical cines in various fields in experimental studies,
industries, but not as medicines. The algal because world health organizations require
preparations are not allowed to be used as serious conditions in this area. Extensive
medicines although they are shown as medi- research is needed to overcome this issue.

­References

1 Stuart, G.A., Smith, F.P. (1911). Chinese 11 Baslow, M.H. (1969). The Marine
Materia Medica. Shanghai: American Pharmacology. Baltimore: Williams and
Presbysterian Mission Press. Wilkins Co.
2 Yang, K.M. (1960). Preliminary observations 12 Güven, K.C., Coban, B., Sezik, E.,
on the treatment of five tumors with chinese Erdugan, H., Kaleağasıoğlu, F. (2013).
traditional medicine. Journal of Traditional Alkaloids of marine macroalgae. in
Chinese Medicine, 3, 177–178. Natural Products, Springer Berlin
3 Nikonov, G.K., Leu, T., Chu, C., Ma, L., Heidelberg, pp. 25–37.
Tung, L., Ming, C., Huo, T., Ko, Y. (1961). 13 Kaleağasıoğlu, F., Güven, K.C., Sezik, E.,
Material in the study of drugs from chinese Erdugan, H., Coban, B. (2013).
folk medicine used for the treatment of Pharmacology of macroalgae alkaloids. in
hypertension, nephritis, diabetes and cancer. Natural Products, Springer Berlin
Aptech Delo, 19, 71–83. Heidelberg, pp. 1203–1216.
4 Stanford, E.C.C. (1883). New substance 14 Güven, K.C., Sezik, E., Kaleağasıoğlu, F.,
obtained from some of the commoner Erdugan, H., Coban, B., Karakaş, E. (2013).
species of marine algae; algin. Chem News, Volatile oils from marine macroalgae. in
47, 254–257. Natural Products, Springer, Berlin,
5 Burkholder, P.R., Burkholder, L.M., Heidelberg, pp. 2883–2912.
AlmodÓVar, L.R. (1960). Antibiotic activity 15 Kim, S.-K. (2015). Handbook of anticancer
of some marine algae of Puerto Rico. drugs from marine origin. New York:
Botanica Marina, 2(1-2), 149. Springer International Publishing.
6 Benigni, R., Capra, C., Cattorini, P.E. (1964). 16 Guven, K.C., Coban B. (2017). Anticoagulant
Plante Medicinali. Chimica Farmacologiae and antilipaemic activities of polysaccharides
Therapia Vol. 1. Milan, Italy: Inverni and from seaweeds. in Journal of the Black Sea/
Della-Beffa. Mediterranean Environent 25(2), 232–257.
7 Guven, K.C., Bora, A., Sunam, G. (1969). 17 Sukatar, A., Karabay-Yavaşsoglu, N.U.,
Alkaloid content of marine algae. I. Ozdemir, G., Horzum, Z. (2006).
Hordenine from Phyllophora nervosa. Antimicrobial activity of volatile component
Eczacılık Bulteni, 11, 177–184. and various extracts of Enteromorpha linza
8 Guven, K.C., Bora, A., Sunam, G. (1970). (Linnaeus) J. Agardh from the coast of Izmir,
Hordenine from the alga Phyllophora Turkey. Annals of Microbiology, 56(3),
nervosa. Phytochemistry, 9, 1893. 275–279.
9 Hoppe, H.A. (1977). Drogenkunde Band 2. 18 Stabili, L., Acquaviva, M.I., Biandolino, F.,
Gymnospermen, Krytogamen, Tierishe Drogen Cavallo, R.A., De Pascali, S.A., Fanizzi, F.P.,
8. auslage. Berlin, New York: Walter de Narracci, M., Cecere, E., Petrocelli, A. (2014).
Gruyter. Biotechnological potential of the seaweed
10 Levring, T., Hoppe, H.A., Schimidt, O.J. Cladophora rupestris (Chlorophyta,
(1969). Marine Algae. Hamburg: Cram de Cladophorales) lipidic extract. New
Gruyter and Co. Biotechnology, 31(5), 436–444.
 ­Reference 595

19 Al-Saif, S.S.A.-l., Abdel-Raouf, N., Visakhapatnam Coast, Andhra Pradesh,


El-Wazanani, H.A., Aref, I.A. (2014). India. International Journal of Pharmacy and
Antibacterial substances from marine algae Pharmaceutical Sciences, 3(4), 399–401.
isolated from Jeddah coast of Red Sea, Saudi 27 Frikha, F., Kammoun, M., Hammami, N.,
Arabia. Saudi Journal of Biological Sciences, Lassaad, B., Gargouri, Y., Miled, N., Ben
21(1), 57–64. Rebah, F. (2011). Chemical composition and
20 Sunilson, J.A.J., Suraj, R., Anandarajagopal, some biological activities of marine algae
K., Rejitha, G., Vignesh, M., Promwichit, P. collected in Tunisia. Ciencias Marinas, 37(2),
(2009). Preliminary phytochemical analysis, 113–124.
elemental determination and antibacterial 28 Kamenarska, Z., Stefanov, K., Dimitrova-
screening of Codium decorticatum – A Konaklieva, S., Najdenski, H., Tsvetkova, I.,
marine green algae. International Journal of Popov, S. (2004). Chemical composition and
Biological Chemistry, 3, 84–89. biological activity of the brackish-water
21 Selim, S., Amin, A., Hassan, S., Hagazey, M. green alga Cladophora rivularis (L.) Hoek.
(2015). Antibacterial, cytotoxicity and Botanica Marina, 47, 215–221.
anticoagulant activities from Hypnea esperi 29 Smith, V.J., Desbois, A.P., Dyrynda, E.A.
and Caulerpa prolifera marine algae. (2010). Conventional and unconventional
Pakistan Journal of Pharmaceutical Sciences, antimicrobials from fish, marine
28(2), 525–530. invertebrates and micro-algae. Marine Drugs,
22 Lima-Filho, J.V.M., Carvalho, A.F.F.U., 8(4), 1213–1262.
Freitas, S.M., Melo, V.M.M. (2002). 30 Rosaline, X.D., Sakthivelkumar, S., Chitra, S.,
Antibacterial activity of extracts of six Janarthanan, S. (2017). Antibacterial activity
macroalgae from the northeastern Brazilian of the seaweeds Chaetomorpha linum and
coast. Brazilian Journal of Microbiology, 33, Padina gymnospora on human bacterial
311–314. pathogens. Journal of Environment and
23 Hellio, C., Bremer, G., Pons, A.M., Le Gal, Y., Biotechnology Research, 6(1), 43–52.
Bourgougnon, N. (2000). Inhibition of the 31 Chesters, C.G., Stott, J.A. (1956). The
development of microorganisms (bacteria production of antibiotic substances by
and fungi) by extracts of marine algae from seaweeds. International Seaweed Symposium,
Brittany, France. Applied Microbiology and 2, 49–53.
Biotechnology, 54(4), 543–549. 32 Roos, H. (1957). Unterschungen uber das
24 Aguila-Ramírez, R.N., Arenas-González, A., Vorkommen Ontimikribieller Substanzen in
Hernández-Guerrero, C.J., González-Acosta, Neeresalgen. Kieler Meeresforschungen, 13,
J., Borges-Souza, M., Véron, B., Pope, J., 41–58.
Hellio, C. (2012). Antimicrobial and 33 Ruggieri, G.D. (1976). Drugs from the sea.
antifouling activities achieved by extracts of Science, 194(4264), 491–497.
seaweeds from gulf of California, Mexico. 34 Faulkner, D.J. (1984). Marine natural
Hidrobiologica, 22, 8–15. products: metabolites of marine algae and
25 Kajiwara, T., Matsui, K., Akakabe, Y., herbivorous marine molluscs. Natural
Murakawa, T., Arai, C. (2006). Antimicrobial Product Reports, 1(3), 251–280.
browning-inhibitory effect of flavor 35 Rosaline, X.D., Sakthivelkumar, S.,
compounds in seaweeds. Journal of Applied Rajendran, K., Janarthanan, S. (2016).
Phycology, 18(3), 413–422. Detection of antibacterial activity and its
26 Battu, G.R., Ethadi, S., Prayaga, M.P., characterization from the marine macro-
Praneeth, V.S., Rao, M. (2011). In-vitro algae Sargassum wightii (Greville ex J.
antibacterial activity and preliminary Agardh 1848). Indian Journal of Geo-Marine
phytochemical screening of three algae from Science, 45(10), 1365–1371.
596 20 Pharmacology of Marine Macroalgae

36 Plaza, M., Santoyo, S., Jaime, L., García- 44 Nagayama, K., Iwamura, Y., Shibata, T.,
Blairsy Reina, G., Herrero, M., Señoráns, F.J., Hirayama, I., Nakamura, T. (2002).
Ibáñez, E. (2010). Screening for bioactive Bactericidal activity of phlorotannins from
compounds from algae. Journal of the brown alga Ecklonia kurome. Journal of
Pharmaceutical and Biomedical Analysis, Antimicrobial Chemotherapy, 50(6), 889–893.
51(2), 450–455. 45 Lee, D.S., Kang, M.S., Hwang, H.J., Eom, S.H.,
37 Gomez, E.R., Pena, G., Buttler, M. (2009). Yang, J.Y., Lee, M.S., Lee, W.J., Jeon, Y.J.,
Studying the inhibition properties of brown Choi, J.S., Kim, Y.M. (2008). Synergistic effect
algae Padina gymnospora. Abstracts of Papers between dieckol from Ecklonia stolonifera and
of the American Chemical Society, 237. beta-lactams against methicillin-resistant
38 Rosaline, X.D., Sakthivelkumar, S., Staphylococcus aureus. Biotechnology and
Rajendran, K., Janarthanan, S. (2012). Bioprocess Engineering, 13, 758–764.
Screening of selected marine algae from the 46 Caccamese, S., Toscano, R.M., Furnari, G.,
coastal Tamil Nadu, South India for Cormaci, M. (1985). Antimicrobial activities
antibacterial activity. Asian Pacific Journal of of red and brown algae from Southern Italy
Tropical Biomedicine, 2(1), S140–S146. Coast. Botanica Marina, 8(11), 505–507.
39 Demirel, Z., Yılmaz, F.F., Karabay-Yavasoglu, 47 Caccamese, S., Toscano, R.M., Cerrini, S.,
U.N., Ozdemir, G., Sukatar, A. (2009). Gavuzzo, E. (1982). Laurencianol, a new
Antimicrobial and antioxidant activity of halogenated diterpenoid from the marne
brown algae from the Aegean Sea. Journal of alga Laurencia obtusa. Tetrahedron Letters,
Serbian Chemical Society, 74(6), 619–628. 23(33), 3415–3418.
40 Mizushina, Y., Sugiyama, Y., Yoshida, H., 48 Olesen, P.E., Maretzki, A., Almodovar, L.A.
Hanashima, S., Yamazaki, T., Kamisuki, S., (1964). An investigation of antimicrobial
Ohta, K., Takemura, M., Yamaguchi, T., substance from marine algae. Botanica
Matsukage, A., Yoshida, S., Saneyoshi, M., Marina, 6, 224–232.
Sugawara, F., Sakagauchi, K. (2001). 49 Konig, G.M., Wright, A.D. (1997).
Galactosyldiacylglycerol, a mammalian Sesquiterpene content of the antibacterial
DNA polymerase alpha-specific Inhibitor dichloromethane extract of the marine red
from a sea alga, Petalonia bingbamiae. alga Laurencia obtusa. Planta Medica, 63,
Biological and Pharmaceutical Bulletin, 186–187.
24(9), 982–987. 50 Gonzalez, A.G., Darias, V., Estevez, E. (1982).
41 Enoki, N., Tsuzuki, K., Omura, S., Ishida, R., Chemotherapeutic activity of
Matsumoto, T. (1983). New antibacterial polyhalogenated terpenes from Spanish
diterpenes, dictyol F and epidictyol F from algae. Planta Medica, 44(1), 44–46.
the brown alga Dictyota dichotoma. 51 Demirel, Z., Yilmaz-Koz, F.F., Karabay-
Chemistry Letters, 12(10), 1627–1630. Yavaşoğlu, N.U., Özdemir, G., Sukatar, A.
42 Eom, S.-H., Kim, Y.-M., Kim, S.-K. (2012). (2011). Antimicrobial and antioxidant
Antimicrobial effect of phlorotannins from activities of solvent extracts and the essential
marine brown algae. Food and Chemical oil composition of Laurencia obtusa and
Toxicology, 50(9), 3251–3255. Laurencia obtusa var. pyramidata. Romanian
43 Lee, S.H., Park, M.H., Heo, S.J., Kang, S.M., Biotechnological Letters, 16(1), 5927–5936.
Ko, S.C., Han, J.S., Jeon, Y.J. (2010). Dieckol 52 Guella, G., Mancini, I., Duhet, D., Richer de
isolated from Ecklonia cava inhibits Forges, B., Pietra, F. (1989). Ethyl 6-bromo-3-
alpha-glucosidase and alpha-amylase in vitro indolcarboxylate and 3-hydroxyacetal-6-
and alleviates postprandial hyperglycemia in bromoindole, novel bromoindoles from the
streptozotocin-induced diabetic mice. Food sponge Pleroma menoui of the Coral Sea.
Chemical Toxicology, 48(10), 2633–2637. Zeitschrift für Naturforschung C, 44, 914–916.
 ­Reference 597

53 Sims, J.J., Donnell, M.S., Leary, J.V., Lacy, taxiformis against Leptospira javanica
G.H. (1975). Antimicrobial agents from isolates of rodent reservoirs. Annals of
marine algae. Antimicrobial Agents and Microbiology, 59, 431–437.
Chemotherapy, 7(3), 320–321. 62 Wagner, H., Guven, K.C., Kizil, Z., Vural, S.,
54 Vairappan, C.S., Suzuki, M., Abe, T., Ogutman, R. (1981). A bromo compound in
Masuda, M. (2001). Halogenated metabolites Halopitys incurvus (Huds.) batters. Vie et
with antibacterial activity from the Milieu, 31, 15–16.
Okinawan Laurencia species. 63 Fenical, W., Sims, J.J. (1974). Cycloeudesmol,
Phytochemistry, 58(3), 517–523. an antibiotic cyclopropane containing
55 Li, X.D., Ding, W., Miao, F.P., Ji, N.Y. (2012). sesquiterpene from the marine alga,
Halogenated chamigrane sesquiterpenes Chondria oppositiclada Dawson. Tetrahedron
from Laurencia okamurae. Magnetic Letters, 15(13), 1137–1140.
Resonance in Chemistry, 50(2), 174–177. 64 Glombitza, K.W., Stoffelen, H., Murawski,
56 El Baroty, G.S., El-Baz, F.K., Abd-Elmoein, I., U., Bielaczek, J., Egge, H. (1974). Antibiotica
Abd-ElBaky, H.H., Ali, M.M., Ibrahim, E.A. aus algen. Planta Medica, 25(02), 105–114.
(2011). Evaluation of glycolipids of some 65 Nylund, G.M., Cervin, G., Persson, F.,
Egyptian marine algae as a source of Hermansson, M., Steinberg, P.D., Pavia, H.
bioactive substances. International Research (2008). Seaweed defence against bacteria: a
Journal of Pharmacy, 2(3), 165–174. poly-brominated 2-heptanone from the red
57 Carter, G.T., Rinehart, K.L., Li, L.H., alga Bonnemaisonia hamifera inhibits
Kuentzel, S.L., Connor, J.L. (1978). bacterial colonisation. Marine Ecology
Brominated indoles from Laurencia Progress Series, 369, 39–50.
brongniartii. Tetrahedron Letters, 19(46), 66 Welch, A.M. (1962). Preliminary survey of
4479–4482. fungistatic properties of marine algae.
58 Manilal, A., Sujith, S., Kiran, G.S., Selvin, J., Journal of Bacteriology, 83, 97–99.
Shakir, C., Gandhimathi, R., Lipton, A.P. 67 Peres, J.C.F., Carvalho, L.R.d., Gonçalez, E.,
(2009). Antimicrobial potential and Berian, L.O.S., Felicio, J.D.A. (2012).
seasonality of red algae collected from the Evaluation of antifungal activity of seaweed
Southwest coast of India tested against extracts. Ciência e Agrotecnologia, 36,
shrimp, human and phytopathogens. Annals 294–299.
of Microbiology, 59(2), 207–219. 68 Bennamara, A., Abourriche, A., Berrada, M.,
59 Karabay-Yavasoglu, N.U., Sukatar, A., Charrouf, M., Chaib, N., Boudouma, M.,
Ozdemir, G., Horzum, Z. (2007). Garneau, F.X. (1999).
Antimicrobial activity of volatile Methoxybifurcarenone: an antifungal and
components and various extracts of the red antibacterial meroditerpenoid from the
alga Jania rubens. Phytotherapy Research, brown alga Cystoseira tamariscifolia.
21(2), 153–156. Phytochemistry, 52(1), 37–40.
60 Mautner, H.G., Gardner, G.M., Pratt, R. 69 Manivannan, K., Karthikai devi, G.,
(1953). Antibiotic activity of seaweed Anantharaman, P., Balasubramanian, T.
extracts. II. Rhodomela larix. Journal of the (2011). Antimicrobial potential of selected
American Pharmaceutical Association. brown seaweeds from Vedalai coastal waters,
American Pharmaceutical Association, 42(5), Gulf of Mannar. Asian Pacific Journal of
294–296. Tropical Biomedicine, 1(2), 114–120.
61 Vedhagiri, K., Manilal, A., Valliyammai, T., 70 Moreau, J., Pesando, D., Caram, B. (1984).
Shanmughapriya, S., Sujith, S., Selvin, J., Antifungal and antibacterial screening of
Natarajaseeniva, K. (2009). Antimicrobial Dictyotales from the French Mediterranean
potential of a marine seaweed Asparagopsis coast. Hydrobiologia, 116(1), 521–524.
598 20 Pharmacology of Marine Macroalgae

71 Thirumaran, G., Vijayabaskar, P., 79 Moen, L., Clark, G. (1993). A novel reverse
Anantharaman, P. (2006). Antibacterial and transcriptase inhibitor from Fucus vesiculosus.
antifungal activities of brown marine macro In International Conference AIDS).
alaga (Dictyota dichotoma) from the Gulf of 80 Vo, T.S., Kim, S.K. (2010). Potential anti-HIV
Mannar biosphere reserve. Environmental agents from marine resources: an overview.
Ecology, 24S, 37–40. Marine Drugs, 8(12), 2871–2892.
72 Lee, H.S., Lee, T.H., Lee, J.H., Chae, C.S., 81 Queiroz, K.C., Medeiros, V.P., Queiroz, L.S.,
Chung, S.C., Shin, D.S., Shin, J., Oh, K.B. Abreu, L.R., Rocha, H.A., Ferreira, C.V.,
(2007). Inhibition of the pathogenicity of Juca, M.B., Aoyama, H., Leite, E.L. (2008).
Magnaporthe grisea by bromophenols, Inhibition of reverse transcriptase activity of
isocitrate lyase inhibitors, from the red alga HIV by polysaccharides of brown algae.
Odonthalia corymbifera. Journal of Biomedicine & Pharmacotherapy, 62(5),
Agricultural and Food Chemistry, 55(17), 303–307.
6923–6928. 82 Witvrouw, M., De Clercq, E. (1997). Sulfated
73 Calvo, M.A., Cabañes, F.J., Abarca, L. (1986). polysaccharides extracted from sea algae as
Antifungal activity of some mediterranean potential antiviral drugs. General
algae. Mycopathologia, 93(1), 61–63. Pharmacology, 29(4), 497–511.
74 Starr, T.J., Deig, E.F., Church, K.K., Allen, 83 Hidari, K.I., Takahashi, N., Arihara, M.,
M.B. (1962). Antibacterial and antiviral Nagaoka, M., Morita, K., Suzuki, T. (2008).
activities of algal extracts studied by acridine Structure and anti-dengue virus activity of
orange staining. Texas Reports on Biology and sulfated polysaccharide from a marine alga.
Medicine Journal, 20, 271–278. Biochemical and Biophysical Research
75 Ivanova, V., Rouseva, R., Kolarova, M., Communication, 376(1), 91–95.
Serkedjieva, R., Rachev, R., Manolova, N. 84 Hoshino, T., Hayashi, T., Hayashi, K.,
(1994). Isolation of a polysaccharide with Hamada, J., Lee, J.B., Sankawa, U. (1998). An
antiviraleffect from Ulva lactuca. Preparative antivirally active sulfated polysaccharide
Biochemistry, 24, 83–97. from Sargassum horneri (Turner) C. Agardh.
76 Pinto, A.M.V., Leite, J.P.G., Ferreira, W.J., Biological and Pharmacological Bulletin,
Cavalcanti, D.N., Villaça, R.C., Giongo, V., 21(7), 730–734.
Teixeira, V.L., Paixão, I.C.N.d.P. (2012). 85 Akamatsu, E., Shimanaga, M., Kamei, Y.
Marine natural seaweed products as (2003). Isolation of an anti-influenza virus
potential antiviral drugs against bovine viral substance, MC26 from a marine brown alga,
diarrhea virus. Revista Brasileira de Sargassum piluliferum and its antiviral
Farmacognosia, 22, 813–817. activity against influenza virus. Coastal
77 Beress, A., Wassermann, O., Tahhan, S., Bioenvironment-Saga University, 1, 29–34.
Bruhn, T., Beress, L., Kraiselburd, E.N., 86 Sinha, S., Astani, A., Ghosh, T., Schnitzler,
Gonzalez, L.V., de Motta, G.E., Chavez, P.I. P., Ray, B. (2010). Polysaccharides from
(1993). A new procedure for the isolation of Sargassum tenerrimum: structural features,
anti-HIV compounds (polysaccharides and chemical modification and anti-viral activity.
polyphenols) from the marine alga Fucus Phytochemistry, 71(2-3), 235–242.
vesiculosus. Journal of Natural Products, 87 Zhu, W., Chiu, L.C.M., Ooi, V.E.C., Chan,
56(4), 478–488. P.K.S., Ang, P.O. (2004). Antiviral property
78 Lee, J.-B., Hayashi, K., Hashimoto, M., and mode of action of a sulphated
Nakano, T., Hayashi, T. (2004). Novel polysaccharide from Sargassum patens
antiviral fucoidan from sporophyll of against herpes simplex virus type 2.
Undaria pinnatifida (Mekabu). Chemical and International Journal of Antimicrobial
Pharmaceutical Bulletin, 52(9), 1091–1094. Agents, 24(3), 279–283.
 ­Reference 599

88 Asker, M.M.S., Mohamed, S.F., Ali, F.M., 96 Sakemi, S., Higa, T., Jefford, C.W.,
Sayed, O.H.E. (2007). Chemical structure Bernardinelli, G. (1986). Venustatriol, a
and antiviral activity of water-soluble new anti-viral triterpenes tetracyclic ether
sulfated polysaccharides from Sargassum from Laurencia venusta. Tetrahedron
latifolium. Journal of Applied Science and Letters, 27, 4287–4290.
Research, 3(10), 1178–1185. 97 Higa, T., Sakemi, S., Cross, S.S. (1986). Antiviral
89 Zandi, K., Fouladvand, M., Pakdel, P., organic triterpene composition and derivatives
Sartavi, K. (2007). Evaluation of in vitro and their manufacture from red alga. US. Appl
antiviral activity of a brown alga (Cystoseira 879.092 (826 June 1986) 1938 pp.
myrica) from the Persian Gulf against herpes 98 Loya, S., Bakhanashvili, M., Kashman, Y.,
simplex virus type 1. African Journal of Hizi, A. (1995). Peyssonol-A and Peyssonol
Biotechnology, 6(22), 2511–2514. B, 2 novel inhibitors of the reverse
90 Vallim, M.A., Barbosa, J.E., Cavalcanti, D.N., transcriptases of human immunodeficiency
De-Paula, J.C., da Silva, V.A.G.G., Teixeira, virus type-1 and type-2. Archives in
V.L., Paixão, I.C.N.d.P. (2010). In vitro Biochemistry Biophysics, 316(2), 789–796.
antiviral activity of diterpenes isolated from 99 Richards, J.T., Kern, E.R., Glasgow, L.A.,
the Brazilian brown alga Canistrocarpus Overall, J.C., Deign, E.F., Hatch, M.T.
cervicornis. Journal of Medicinal Plants (1978). Antiviral activity of extracts from
Research, 4(22), 2379–2382. marine algae. Antimicrobial Agents and
91 El Baz, F.K., El Baroty, G.S., Abd El Baky, Chemotherapy, 14(1), 24–30.
H.H., Abd El-Salam, O.I., Ibrahim, E.A. 100 Robinson, W.E., Jr., Montefiori, D.C.,
(2013). Structural characterization and Mitchell, W.M. (1987). Evidence that
biological activity of sulfolipids from selected mannosyl residues are involved in human
marine algae. Grasas y Aceites, 64(5), 561–571. immunodeficiency virus type 1 (HIV-1)
92 Caccamese, S., Azzolina, R., Furnari, G., pathogenesis. AIDS Res Hum Retroviruses,
Cormaci, M., Grasso, S. (1981). 3(3), 265–282.
Antimicrobial and antiviral activities of 101 Ohta, K., Mizushina, Y., Hirata, N.,
some marine algae from Eastern Sicily. Takemura, M., Sugawara, F., Matsukage,
Botanica Marina, 24, 365–367. A., Yoshida, S., Sakaguchi, K. (1998).
93 Hayashi, K., Nakano, T., Hashimoto, M., Sulfoquinovosyldiacylglycerol, KM043, a
Kanekiyo, K., Hayashi, T. (2008). Defensive new potent inhibitor of eukaryotic DNA
effects of a fucoidan from brown alga polymerases and HIV-reverse transcriptase
Undaria pinnatifida against herpes simplex type 1 from a marine red alga, Gigartina
virus infection. International tenella. Chemical and Pharmacological
Immunopharmacology, 8(1), 109–116. Bulletin, 46(4), 684–686.
94 Muto, S., Niimura, K., Oohara, M., Oguchi, 102 de Souza, L.M., Sassaki, G.L., Romanos,
Y., Matsunaga, K., Hirose, K., Kakuchi, J., M.T.V., Barreto-Bergter, E. (2012).
Sugita, N., Furusho, T. Polysaccharides from Structural characterization and anti-HSV-1
marine algae and antiviral drugs containing and HSV-2 activity of glycolipids from the
the same as active ingredients. Eur. Patent marine algae Osmundaria obtusiloba
EP295956, 295921.December.291988. isolated from Southeastern Brazilian Coast.
95 Gerber, P., Dutcher, J.D., Adams, E.V., Marine Drugs, 10(4), 918–931.
Sherman, J.H. (1958). Protective effect of 103 Nakashima, H., Kido, Y., Kobayashi, N.,
seaweed extracts for chicken embryos Motoki, Y., Neushul, M., Yamamoto, N.
infected with influenza B or mumps virus. (1987). Antiretroviral activity in a marine
Proceedings of the Society of Experimental red alga: reverse transcriptase inhibition by
and Biological Medicine, 99, 590–593. an aqueous extract of Schizymenia pacifica.
600 20 Pharmacology of Marine Macroalgae

Journal of Cancer Research and Clinical 111 Witvrouw, M., Este, J.A., Mateu, M.Q.,
Oncology, 113(5), 413–416. Reymen, D., Andrei, G., Snoeck, R., Ikeda,
104 Damonte, E., Neyts, J., Pujol, C.A., Snoeck, S., Pauwels, R., Bianchini, N.V., Desmyter,
R., Andrei, G., Ikeda, S., Witvrouw, M., J., De Clercq, E. (1994). Activity of a
Reymen, D., Haines, H., Matulewicz, M.C., sulfated polysaccharide extracted from the
Cerezo, A., Coto, C.E., De Clerco, E. (1994). red seaweed Aghardhiella Tenera against
Antiviral activity of a sulphated human immunodeficiency virus and other
polysaccharide from the red seaweed enveloped viruses. Antiviral Chemistry and
Nothogenia fastigiata. Biochemical Chemotherapy, 5(5), 297–303.
Pharmacology, 47(12), 2187–2192. 112 Damonte, E.B., Matulewicz, M.C., Cerezo,
105 Carlucci, M.J., Scolaro, L.A., Errea, M.I., A.S. (2004). Sulfated seaweed
Matulewicz, M.C., Damonte, E.B. (1997). polysaccharides as antiviral agents. Current
Antiviral activity of natural sulphated Medicinal Chemistry, 11(18), 2399–2419.
galactans on herpes virus multiplication in 113 Tang, F., Chen, F., Li, F. (2013). Preparation
cell culture. Planta Medica, 63(5), 429–432. and potential in vivo anti-influenza virus
106 Pujol, C.A., Scolaro, L.A., Ciancia, M., activity of low molecular-weight
Matulewicz, M.C., Cerezo, A.S., Damonte, κ-carrageenans and their derivatives. Journal
E.B. (2006). Antiviral activity of a of Applied Polymer Science, 127(3), 2110–2115.
carrageenan from Gigartina skottsbergii 114 Wang, W., Zhang, P., Hao, C., Zhang, X.E.,
against intraperitoneal murine herpes Cui, Z.Q., Guan, H.S. (2011). In vitro
simplex virus infection. Planta Medica, inhibitory effect of carrageenan
72(2), 121–125. oligosaccharide on influenza A H1N1 virus.
107 Carlucci, M.J., Scolaro, L.A., Noseda, D.G., Antiviral Research, 92(2), 237–246.
Cerezo, A.S., Damonte, E.B. (2004). 115 Wang, W., Zhang, P., Yu, G.-L., Li, C.-X.,
Protective effect of a natural carrageenan Hao, C., Qi, X., Zhang, L.-J., Guan, H.-S.
on genital herpes simplex virus infection in (2012). Preparation and anti-influenza A
mice. Antiviral Research, 64, 137–141. virus activity of κ-carrageenan
108 de S.F-Tischer, P.C., Talarico, L.B., Noseda, oligosaccharide and its sulphated
M.D., Pita B. Guimarães, S.M., Damonte, derivatives. Food Chemistry, 133(3), 880–888.
E.B., Duarte, M.E.R. (2006). Chemical 116 Diogo, J.V., Novo, S.G., Gonzalez, M.J.,
structure and antiviral activity of Ciancia, M., Bratanich, A.C. (2015).
carrageenans from Meristiella gelidium Antiviral activity of lambda-carrageenan
against herpes simplex and dengue virus. prepared from red seaweed (Gigartina
Carbohydrate Polymers, 63(4), 459–465. skottsbergii) against BoHV-1 and SuHV-1.
109 Soares, A.R., Robaina, M.C.S., Mendes, G.S., Research in Veterinary Science, 98, 142–144.
Silva, T.S.L., Gestinari, L.M.S., Pamplona, 117 Yamada, T., Ogamo, A., Saito, T., Uchiyama,
O.S., Yoneshigue-Valentin, Y., Kaiser, C.R., H., Nakagawa, Y. (2000). Preparation of
Romanos, M.T.V. (2012). Antiviral activity O-acylated low-molecular-weight
of extracts from Brazilian seaweeds against carrageenans with potent anti-HIV activity
herpes simplex virus. Revista Brasileira de and low anticoagulant effect. Carbohydrate
Farmacognosia, 22, 714–723. Polymers, 41, 115–120.
110 Chattopadhyay, K., Mateu, C.G., Mandal, 118 Yamada, T., Ogamo, A., Saito, T., Watanabe,
P., Pujol, C.A., Damonte, E.B., Ray, B. J., Uchiyama, H., Nakagawa, Y. (1997).
(2007). Galactan sulfate of Grateloupia Preparation and anti-HIV activity of
indica: Isolation, structural features and low-molecular-weight carrageenans and
antiviral activity. Phytochemistry, 68(10), their sulfated derivatives. Carbohydrate
1428–1435. Polymers, 32, 51–55.
 ­Reference 601

119 Girond, S., Crance, J.M., Van Cuyck- latissimum. Planta Medica, 65(05),
Gandre, H., Renaudet, J., Deloince, R. 439–441.
(1991). Antiviral activity of carrageenan on 128 Ghosh, P., Adhikari, V., Ghosal, P.K., Pujol,
hepatitis A virus replication in cell culture. C.A., Carlucci, M.J., Damonte, E.B., Ray, B.
Research in Virology, 142(4), 261–270. (2004). In vitro anti-herpetic activity of
120 Carlucci, M.J., Scolaro, L.A., Damonte, E.B. sulfated polysaccharide fractions from
(2002). Herpes simplex virus type 1 variants Caulerpa racemosa. Phytochemistry, 65,
arising after selection with an antiviral 3151–3157.
carrageenan: lack of correlation between 129 Zubia, M., Robledo, D., Freile-Pelegrin, Y.
drug susceptibility and syn phenotype. (2007). Antioxidant activities in tropical
Journal of Medicinal Virology, 68(1), 92–98. marine macroalgae from the Yucatan
121 Buck, C.B., Thompson, C.D., Roberts, J.N., Peninsula, Mexico. Journal of Applied
Muller, M., Lowy, D.R., Schiller, J.T. (2006). Phycology, 19(5), 449–458.
Carrageenan is a potent inhibitor of 130 Preeprame, S., Hayashi, K., Lee, J.-B.,
papillomavirus infection. PLoS Pathogens, Sankawa, U., Hayashi, T. (2001). A novel
2(7), e69. antivirally active fucan sulfate derived from
122 Nelson, R.M., Cecconi, O., Roberts, W.G., an edible brown alga, Sargassum horneri.
Aruffo, A., Linhardt, R.J., Bevilacqua, M.P. Chemical and Pharmacological Bulletin,
(1993). Heparin oligosaccharides bind 49(4), 484–489.
L- and P-selectin and inhibit acute 131 Zhu, W., Chiu, L.C., Ooi, V.E., Chan, P.K.,
inflammation. Blood, 82(11), 3253–3258. Ang, P.O., Jr. (2004). Antiviral property and
123 Leibbrandt, A., Meier, C., Konig-Schuster, mode of action of a sulphated
M., Weinmullner, R., Kalthoff, D., polysaccharide from Sargassum patens
Pflugfelder, B., Graf, P., Frank-Gehrke, B., against herpes simplex virus type 2.
Beer, M., Fazekas, T., Unger, H., Prieschl- International Journal of Antimicrobial
Grassauer, E., Grassauer, A. (2010). Agents, 24(3), 279–283.
Iota-carrageenan is a potent inhibitor of 132 Zhu, W., Chiu, L.C., Ooi, V.E., Chan, P.K.,
influenza A virus infection. PLoS One, Ang, P.O., Jr. (2006). Antiviral property and
5(12), 0014320. mechanisms of a sulphated polysaccharide
124 Talarico, L.B., Damonte, E.B. (2007). from the brown alga Sargassum patens
Interference in dengue virus adsorption against Herpes simplex virus type 1.
and uncoating by carrageenans. Virology, Phytomedicine, 13(9-10), 695–701.
363(2), 473–485. 133 Thompson, K.D., Dragar, C. (2004).
125 Talarico, L.B., Noseda, M.D., Ducatti, D.R., Antiviral activity of Undaria pinnatifida
Duarte, M.E., Damonte, E.B. (2011). against herpes simplex virus. Phytotherapy
Differential inhibition of dengue virus Research, 18(7), 551–555.
infection in mammalian and mosquito cells 134 Cooper, R., Dragar, C., Elliot, K., Fitton,
by iota-carrageenan. Journal of General J.H., Godwin, J., Thompson, K. (2002).
Virology, 92(Pt 6), 1332–1342. GFS, a preparation of Tasmanian Undaria
126 Lee, J.B., Hayashi, K., Maeda, M., Hayashi, pinnatifida is associated with healing and
T. (2004). Antiherpetic activities of sulfated inhibition of reactivation of Herpes. BMC
polysaccharides from green algae. Planta Complementary and Alternative Medicine,
Medica, 70(9), 813–817. 2, 11–11.
127 Lee, J.-B., Hayashi, K., Hayashi, T., 135 Mandal, P., Mateu, C.G., Chattopadhyay, K.,
Sankawa, U., Maeda, M. (1999). Antiviral Pujol, C.A., Damonte, E.B., Ray, B. (2007).
activities against HSV-1, HCMV, and HIV-1 Structural features and antiviral activity of
of rhamnan sulfate from Monostroma sulphated fucans from the brown seaweed
602 20 Pharmacology of Marine Macroalgae

Cystoseira indica. Antiviral Chemistry and 144 Park, H.-J., Kurokawa, M., Shiraki, K.,
Chemotherapy, 18(3), 153–162. Nakamura, N., Choi, J.-S., Hattori, M.
136 Ponce, N.M., Pujol, C.A., Damonte, E.B., (2005). Antiviral activity of the marine alga
Flores, M.L., Stortz, C.A. (2003). Fucoidans Symphyocladia latiuscula against Herpes
from the brown seaweed Adenocystis Simplex Virus (HSV-1) in vitro and Its
utricularis: extraction methods, antiviral therapeutic efficacy against HSV-1 infection
activity and structural studies. in mice. Biological and Pharmaceutical
Carbohydrate Research, 338(2), 153–165. Bulletin, 28(12), 2258–2262.
137 Adhikari, U., Mateu, C.G., Chattopadhyay, 145 Xu, X., Yin, L., Gao, J., Gao, L., Song, F.
K., Pujol, C.A., Damonte, E.B., Ray, B. (2014). Antifungal bromophenols from
(2006). Structure and antiviral activity of marine red alga Symphyocladia latiuscula.
sulfated fucans from Stoechospermum Chemical Biodiversity, 11(5), 807–811.
marginatum. Phytochemistry, 67(22), 146 Mattos, B.B., Romanos, M.T.V., Souza,
2474–2482. L.M.d., Sassaki, G., Barreto-Bergter, E.
138 Feldman, S.C., Reynaldi, S., Stortz, C.A., (2011). Glycolipids from macroalgae:
Cerezo, A.S., Damont, E.B. (1999). Antiviral potential biomolecules for marine
properties of fucoidan fractions from biotechnology? Revista Brasileira de
Leathesia difformis. Phytomedicine, 6(5), Farmacognosia, 21, 244–247.
335–340. 147 Pujol, C.A., Coto, C.E., Damonte, E.B.
139 Francisco, C., Banaigs, B., Teste, J., Cave, A. (1995). Determination of the antiviral
(1986). Mediterraneols: a novel biologically activity of a naturally occurring sulfated
active class of rearranged diterpenoid xylomannan under various experimental
metabolites from Cystoseira mediterranea conditions. Revista Argentina de
(Pheophyta). The Journal of Organic Microbiología, 27(2), 91–98.
Chemistry, 51(7), 1115–1120. 148 Talarico, L.B., Duarte, M.E.R., Zibetti,
140 Abrantes, J.L., Barbosa, J., Cavalcanti, D., R.G.M., Noseda, M.D., Damonte, E.B.
Pereira, R.C., Frederico Fontes, C.L., (2007). An algal-derived DL-galactan
Teixeira, V.L., Moreno Souza, T.L., Paixao, hybrid is an efficient preventing agent for
I.C. (2010). The effects of the diterpenes in vitro Dengue Virus Infection. Planta
isolated from the Brazilian brown algae Medica, 73(14), 1464–1468.
Dictyota pfaffii and Dictyota menstrualis 149 Ghosh, T., Pujol, C.A., Damonte, E.B.,
against the herpes simplex type-1 Sinha, S., Ray, B. (2009). Sulfated
replicative cycle. Planta Medica, 76(4), xylomannans from the red seaweed
339–344. Sebdenia polydactyla: structural features,
141 Deig, E.F., Ehresmann, D.W., Hatch, M.T., chemical modification and antiviral
Riedlinger, D.J. (1974). Inhibition of activity. Antiviral Chemistry and
herpesvirus replication by marine algae Chemotherapy, 19(6), 235–242.
extracts. Antimicrobial Agents and 150 Duarte, M.E.R., Noseda, D.G., Noseda,
Chemotherapy, 6, 524–525. M.D., Tulio, S., Pujol, C.A., Damonte, E.B.
142 Serkedjieva, J. (2000). Antiherpes virus (2001). Inhibitory effect of sulfated
effect of the red marine alga Polysiphonia galactans from the marine alga Bostrychia
denudata. Zeitschrift für Naturforschung C, montagnei on herpes simplex virus
55(9-10), 830–835. replication in vitro. Phytomedicine, 8(1),
143 Bouhlal, R., Riadi, H., Bourgougnon, N. 53–58.
(2010). Antiviral activity of the extracts of 151 Duarte, M.E., Cauduro, J.P., Noseda, D.G.,
Rhodophyceae from Morocco. African Noseda, M.D., Goncalves, A.G., Pujol, C.A.,
Journal of Biotechnology, 9(46), 7968–7975. Damonte, E.B., Cerezo, A.S. (2004). The
 ­Reference 603

structure of the agaran sulfate from herpes simplex virus activity of sulfated
Acanthophora spicifera (Rhodomelaceae, galactans from the red seaweeds
Ceramiales) and its antiviral activity. Gymnogongrus griffithsiae and Cryptonemia
Relation between structure and antiviral crenulata. International Journal of
activity in agarans. Carbohydrate Research, Biological Macromolecules, 34(1-2), 63–71.
339(2), 335–347. 159 Mandal, P., Pujol, C.A., Carlucci, M.J.,
152 Mazumder, S., Ghosal, P.K., Pujol, C.A., Chattopadhyay, K., Damonte, E.B., Ray, B.
Carlucci, M.a.J., Damonte, E.B., Ray, B. (2008). Anti-herpetic activity of a sulfated
(2002). Isolation, chemical investigation xylomannan from Scinaia hatei.
and antiviral activity of polysaccharides Phytochemistry, 69(11), 2193–2199.
from Gracilaria corticata (Gracilariaceae, 160 Burton, G., Ingold, K. (1984). beta-
Rhodophyta). International Journal of Carotene: an unusual type of lipid
Biological Macromolecules, 31(1–3), 87–95. antioxidant. Science, 224(4649), 569–573.
153 Zandi, K., Salimi, M., Sartavi, K. (2007). In 161 Cahyana Herry, A., Shuto, Y., Kinoshita, Y.
vitro antiviral activity of the red marine (1993). antioxidative activity of porphyrin
alga from Persian Gulf, Gracilaria derivatives. Bioscience, Biotechnology, and
salicornia, against herpes simplex virus Biochemistry, 57(4), 680–681.
type 2. Journal of Biological Sciences, 7, 162 Endo, Y., Usuki, R., Kaneda, T. (1985).
1274–1277. Antioxidant effects of chlorophyll and
154 Matsuhiro, B., Conte, A.F., Damonte, E.B., pheophytin on the autoxidation of oils in
Kolender, A.A., Matulewicz, M.C., Mejias, the dark. II. The mechanism of
E.G., Pujol, C.A., Zuniga, E.A. (2005). antioxidative action of chlorophyll. Journal
Structural analysis and antiviral activity of of the American Oil Chemists’ Society, 62(9),
a sulfated galactan from the red seaweed 1387–1390.
Schizymenia binderi (Gigartinales, 163 Palozza, P., Krinsky, N.I. (1998). The
Rhodophyta). Carbohydrate Research, antioxidant and biological properties of the
340(15), 2392–2402. carotenoids. Annals of the New York
155 Rodriguez, M.C., Merino, E.R., Pujol, C.A., Academy of Sciences, 854, 443–447.
Damonte, E.B., Cerezo, A.S., Matulewicz, 164 Naguib, Y.M. (2000). Antioxidant activities
M.C. (2005). Galactans from cystocarpic of astaxanthin and related carotenoids.
plants of the red seaweed Callophyllis Journal of Agricultural Food Chemistry,
variegata (Kallymeniaceae, Gigartinales). 48(4), 1150–1154.
Carbohydrate Research, 340(18), 2742–2751. 165 Foti, M., Piattelli, M., Amico, V., Ruberto,
156 Pujol, C.A., Errea, M.I., Matulewicz, M.C., G. (1994). Antioxidant activity of phenolic
Damonte, E.B. (1996). Antiherpetic activity meroditerpenoids from marine algae.
of S1, an algal derived sulphated galactan. Journal of Photochemistry and Photobiology
Phytotherapy Research, 10(5), 410–413. B: Biology, 26(2), 159–164.
157 Pujol, C.A., Estevez, J.M., Carlucci, M.J., 166 Linares, A.F., Loikkanen, J., Jorge, M.-F.,
Ciancia, M., Cerezo, A.S., Damonte, E.B. Soria, R.B., Novoa, A.V. (2004). Antioxidant
(2002). Novel DL-galactan hybrids from the and neuroprotective activity of the extract
red seaweed Gymnogongrus Torulosus are from the seaweed, Halimeda Incrassata
potent inhibitors of herpes simplex virus (Ellis) Lamouroux, against in vitro and in
and dengue virus. Antiviral Chemistry and vivo toxicity induced by methyl-mercury.
Chemotherapy, 13(2), 83–89. Veterinary and Human Toxicology, 46(1), 1–5.
158 Talarico, L.B., Zibetti, R.G., Faria, P.C., 167 Senthilkumar, D., Jayanthi, S. (2015).
Scolaro, L.A., Duarte, M.E., Noseda, M.D., Antioxidant activities of purified
Pujol, C.A., Damonte, E.B. (2004). Anti- glycoprotein extracted from Codium
604 20 Pharmacology of Marine Macroalgae

decorticatum. Journal of Applied algae extracts. Annals of the University


Pharmaceutical Science, 5(12), 101–104. Dunarea de Jos of Galati: Fascicle II, 34(2),
168 Takamatsu, S., Hodges, T.W., Rajbhandari, 313–318.
I., Gerwick, W.H., Hamann, M.T., Nagle, 176 Qi, H., Zhang, Q., Zhao, T., Chen, R.,
D.G. (2003). Marine natural products as Zhang, H., Niu, X., Li, Z. (2005).
novel antioxidant prototypes. Journal of Antioxidant activity of different sulfate
Natural Products, 66(5), 605–608. content derivatives of polysaccharide
169 Mancini-Filho, J., Novoa, A.V., González, extracted from Ulva pertusa (Chlorophyta)
A.E.B., de Andrade-Wartha, E.R.S., de O e in vitro. International Journal of Biological
Silva, A.M., Pinto, J.R., Mancini, D.A.P. Macromolecules, 37(4), 195–199.
(2009). Free phenolic acids from the 177 Qi, H., Zhang, Q., Zhao, T., Hu, R., Zhang,
seaweed Halimeda monile with antioxidant K., Li, Z. (2006). In vitro antioxidant
effect protecting against liver injury. activity of acetylated and benzoylated
Zeitschrift für Naturforschung C, 64(c), derivatives of polysaccharide extracted
657–663. from Ulva pertusa (Chlorophyta).
170 Nishibori, S., Kazuko, N. (1988). Bioorganic Medicinal Chemistry Letters,
Antioxidative substances in the green 16(9), 2441–2445.
fractions of the lipids of Aonori 178 Nagai, T., Yukimoto, T. (2003). Preparation
(Entremorpha sp.). Journal of Home and functional properties of beverages
Economics of Japan, 39(11), 1173–1178. made from sea algae. Food Chemistry, 81(3),
171 Narasimhan, M.K., Pavithra, S.K., 327–332.
Krishnan, V., Chandrasekaran, M. (2013). 179 Vijayavel, K., Martinez, J.A. (2010). In vitro
In vitro analysis of antioxidant, antioxidant and antimicrobial activities of
antimicrobial and antiproliferative activity two Hawaiian marine Limu: Ulva fasciata
of Enteromorpha antenna, Enteromorpha (Chlorophyta) and Gracilaria salicornia
linza and Gracilaria corticata extracts. (Rhodophyta). Journal of Medicinal Food,
Jundishapur Journal of Natural 13(6), 1494–1499.
Pharmaceutical Products, 8(4), 151–159. 180 Valentão, P., Trindade, P., Gomes, D.,
172 Shanab, S.M.M., Shalaby, E.A., El-Fayoumy, Guedes de Pinho, P., Mouga, T., Andrade,
E.A. (2011). Enteromorpha compressa P.B. (2010). Codium tomentosum and
exhibits potent antioxidant activity. Journal Plocamium cartilagineum: Chemistry and
of Biomedicine and Biotechnology, antioxidant potential. Food Chemistry,
2011(Article ID 726405), 11 pages. 119(4), 1359–1368.
doi:10.1155/2011/726405. 181 Heo, S.-J., Hwang, J.-Y., Choi, J.-I., Lee,
173 Lin, H.-C., Tsai, W.-S., Chiu, T.-H. (2012). S.-H., Park, P.-J., Kang, D.-H., Oh, C., Kim,
Antioxidant properties of seven cultivated D.-W., Han, J.-S., Jeon, Y.-J., Kim, H.-J.,
and natural edible seaweed extracts from Choi, I.-W. (2010). Protective effect of
Taiwan. Journal of Aquatic Food Product diphlorethohydroxycarmalol isolated from
Technology, 21(3), 248–264. Ishige okamurae against high glucose-
174 Dummermuth, A.L., Karsten, U., Fisch, induced-oxidative stress in human
K.M., König, G.M., Wiencke, C. (2003). umbilical vein endothelial cells. Food and
Responses of marine macroalgae to Chemical Toxicology, 48(6), 1448–1454.
hydrogen-peroxide stress. Journal of 182 Heo, S.J., Kim, J.P., Jung, W.K., Lee, N.H.,
Experimental Marine Biology and Ecology, Kang, H.S., Jun, E.M., Park, S.H., Kang,
289(1), 103–121. S.M., Lee, Y.J., Park, P.J., Jeon, Y.J. (2008).
175 Horincar, V.B., Parfene, G., Bahrim, G. Identification of chemical structure and
(2011). Antioxidant activity of Romanian free radical scavenging activity of
 ­Reference 605

diphlorethohydroxycarmalol isolated from 191 Nahas, R., Abatis, D., Anagnostopoulou,


a brown alga, Ishige okamurae. Journal of M.A., Kefalas, P., Vagias, C., Roussis, V.
Microbiology and Biotechnology, 18(4), (2007). Radical-scavenging activity of
676–681. Aegean Sea marine algae. Food Chemistry,
183 Fisch, K.M., Bohm, V., Wright, A.D., Konig, 102(3), 577–581.
G.M. (2003). Antioxidative meroterpenoids 192 Ye, H., Zhou, C., Sun, Y., Zhang, X., Liu, J.,
from the brown alga Cystoseira crinita. Hu, Q., Zeng, X. (2009). Antioxidant
Journal of Natural Products, 66(7), 968–975. activities in vitro of ethanol extract from
184 Fujimoto, K., Kaneda, T. (1980). Screening brown seaweed Sargassum pallidum.
test for antioxygenic compounds from European Food Research and Technology,
marine algae and fractionation from 230(1), 101.
Eisenia bicyclis and Undaria pinnatifida. 193 Wu, M., Wu, Y., Qu, M., Li, W., Yan, X.
Bulletin of the Japanese Sociecty for the (2013). Evaluation of antioxidant activities
Science of Fish, 46(9), 1125–1130. of water-soluble polysaccharides from
185 Shin, T., Ahn, M., Hyun, J.W., Kim, S.H., brown alga Hizikia fusiformis. International
Moon, C. (2014). Antioxidant marine algae Journal of Biological Macromolecules, 56,
phlorotannins and radioprotection: A 28–33.
review of experimental evidence. Acta 194 Yan, X., Nagata, T., Fan, X. (1998).
Histochemica, 116(5), 669–674. Antioxidative activities in some common
186 Nakamura, T., Nagayama, K., Uchida, K., seaweeds. Plant Foods for Human Nutrition,
Tanaka, R. (1996). Antioxidant activity of 52(3), 253–262.
phlorotannins isolated from the brown alga 195 Ruperez, P., Ahrazem, O., Leal, J.A. (2002).
Eisenia bicyclis. Fisheries Science, 62(6), Potential antioxidant capacity of sulfated
923–926. polysaccharides from the edible marine
187 Cahyana Herry, A., Shuto, Y., Kinoshita, Y. brown seaweed Fucus vesiculosus. Journal
(1992). Pyropheophytin a as an antioxidative of Agricultural and Food Chemistry, 50(4),
substance from the marine alga, arame 840–845.
(Eisenia bicyclis). Bioscience, Biotechnology, 196 Wang, J., Zhang, Q., Zhang, Z., Li, Z. (2008).
and Biochemistry, 56(10), 1533–1535. Antioxidant activity of sulfated
188 Iwai, K. (2008). Antidiabetic and polysaccharide fractions extracted from
antioxidant effects of polyphenols in brown Laminaria japonica. International Journal of
alga Ecklonia stolonifera in genetically Biological Macromolecules, 42(2), 127–132.
diabetic KK-A(y) mice. Plant Foods for 197 Kim, Y.A., Kong, C.S., Um, Y.R., Lee, J.I.,
Human Nutrition, 63(4), 163–169. Nam, T.J., Seo, Y. (2008). Antioxidant
189 Lim, S.N., Cheung, P.C.K., Ooi, V.E.C., Ang, efficacy of extracts from a variety of
P.O. (2002). Evaluation of antioxidative seaweeds in a cellular system. Ocean
activity of extracts from a brown seaweed, Science Journal, 43(1), 31–37.
Sargassum siliquastrum. Journal of 198 Huang, H.-L., Wang, B.-G. (2004).
Agricultural and Food Chemistry, 50(13), Antioxidant capacity and lipophilic content
3862–3866. of seaweeds collected from the Qingdao
190 Ananthi, S., Raghavendran, H.R., Sunil, Coastline. Journal of Agricultural and Food
A.G., Gayathri, V., Ramakrishnan, G., Chemistry, 52, 4993–4997.
Vasanthi, H.R. (2010). In vitro antioxidant 199 Kuda, T., Hishi, T., Maekawa, S. (2006).
and in vivo anti-inflammatory potential of Antioxidant properties of dried product of
crude polysaccharide from Turbinaria ‘haba-nori’, an edible brown alga, Petalonia
ornata (marine brown alga). Food Chemical binghamiae (J. Agaradh) Vinogradova. Food
Toxicology, 48(1), 187–192. Chemistry, 98(3), 545–550.
606 20 Pharmacology of Marine Macroalgae

200 Kuda, T., Tsunekawa, M., Goto, H., Araki, Quemeneur, F. (1998). Antioxidant and
Y. (2005). Antioxidant properties of four prooxidant activities of the brown algae,
edible algae harvested in the Noto Laminaria digitata, Himanthalia elongata,
Peninsula, Japan. Journal of Food Fucus vesiculosus, Fucus serratus and
Composition and Analysis, 18(7), 625–633. Ascophyllum nodosum. Journal of Applied
201 Chandini, S.K., Ganesan, P., Bhaskar, N. Phycology, 10, 121–129.
(2008). In vitro antioxidant activities of 210 O’Sullivan, A.M., O’Callaghan, Y.C.,
three selected brown seaweeds of India. O’Grady, M.N., Queguineur, B., Hanniffy,
Food Chemistry, 107(2), 707–713. D., Troy, D.J., Kerry, J.P., O’Brien, N.M.
202 Lee, O.H., Yoon, K.Y., Kim, K.J., You, S., Lee, (2011). In vitro and cellular antioxidant
B.Y. (2011). Seaweed extracts as a potential activities of seaweed extracts prepared from
tool for the attenuation of oxidative damage five brown seaweeds harvested in spring
in obesity-related pathologies. Journal of from the west coast of Ireland. Food
Phycology, 47(3), 548–556. Chemistry, 126(3), 1064–1070.
203 Nakai, M., Kageyama, N., Nakahara, K., 211 Fujimoto, K. (1990). Antioxidant activity of
Miki, W. (2006). Phlorotannins as radical algal extracts. in Introduction to Applied
scavengers from the extract of Sargassum Phycology, I. Akatsuka (Ed.), SPB Academic
ringgoldianum. Marine Biotechnology, 8(4), Publishing, The Hague, pp. 199–208.
409–414. 212 Fallarero, A., Loikkanen, J.J., Männistö,
204 Cho, S.H., Kang, S.E., Cho, J.Y., Kim, A.R., P.T., Castañeda, O., Vidal, A. (2003). Effects
Park, S.M., Hong, Y.K., Ahn, D.H. (2007). of aqueous extracts of Halimeda incrassata
The antioxidant properties of brown (Ellis) Lamouroux and Bryothamnion
seaweed (Sargassum siliquastrum) extracts. triquetrum (S.G. Gmelim) Howe on
Journal of Medicinal Food, 10(3), 479–485. hydrogen peroxide and methyl mercury-
205 Kelman, D., Posner, E.K., McDermid, K.J., induced oxidative stress in GT1-7 mouse
Tabandera, N.K., Wright, P.R., Wright, A.D. hypothalamic immortalized cells.
(2012). Antioxidant activity of Hawaiian Phytomedicine, 10(1), 39–47.
marine algae. Marine Drugs, 10(2), 213 Ganesan, P., Kumar, C.S., Bhaskar, N.
403–416. (2008). Antioxidant properties of methanol
206 Heo, S., Park, E., Lee, K., Jeon, Y. (2005). extract and its solvent fractions obtained
Antioxidant activities of enzymatic extracts from selected Indian red seaweeds.
from brown seaweeds. Bioresource Bioresource Technology, 99(8), 2717–2723.
Technology, 96(14), 1613–1623. 214 Duan, X.-J., Zhang, W.-W., Li, X.-M., Wang,
207 Matsukawa, R., Dubinsky, Z., Kishimoto, B.-G. (2006). Evaluation of antioxidant
E., Masaki, K., Masuda, Y., Takeuchi, T., property of extract and fractions obtained
Chihara, M., Yamamoto, Y., Niki, E., from a red alga, Polysiphonia urceolata.
Karube, I. (1997). A comparison of Food Chemistry, 95(1), 37–43.
screening methods for antioxidant activity 215 Burritt, D.J., Larkindale, J., Hurd, C.L. (2002).
in seaweeds. Journal of Applied Phycology, Antioxidant metabolism in the intertidal red
9(1), 29–35. seaweed Stictosiphonia arbuscula following
208 Anggadiredja, J., Andyani, R., Hayati, M. desiccation. Planta, 215(5), 829–838.
(1997). Antioxidant activity of Sargassum 216 Athukorala, Y., Lee, K.-W., Shahidi, F., Heu,
polycystum (Phaeophyta) and Laurencia M.S., Kim, H.-T., Lee, J.-S., Jeon, Y.-J.
obtusa (Rhodophyta) from Seribu Islands. (2003). Antioxidant efficacy of extracts of
Journal of Applied Phycology, 9, 477–479. an edible red alga (Grateloupia filicina) in
209 Le Tutour, B., Benslimane, F., Gouleau, linoleic acid and fish oil. Journal of Food
M.P., Gouygou, J.P., Saadan, B., Lipids, 10(4), 313–327.
 ­Reference 607

217 Je, J.-Y., Ahn, C.-B., Oh, M.-J., Kang, S.Y. potential of Ulva rigida ethanolic extract in
(2009). Antioxidant activity of a red the experimental diabetes mellitus. Food
seaweed Polysiphonia morrowii extract. Chemical Toxicology, 47(8), 1837–1840.
Food Science and Biotechnology, 18(1), 225 Nwosu, F., Morris, J., Lund, V.A., Stewart,
124–129. D., Ross, H.A., McDougall, G.J. (2011).
218 Zhang, Z., Zhang, Q., Wang, J., Shi, X., Anti-proliferative and potential anti-
Song, H., Zhang, J. (2009). In vitro diabetic effects of phenolic-rich extracts
antioxidant activities of acetylated, from edible marine algae. Food Chemistry,
phosphorylated and benzoylated 126(3), 1006–1012.
derivatives of porphyran extracted from 226 Lamela, M., Anca, J., Villar, R., Otero, J.,
Porphyra haitanensis. Carbohydrate Calleja, J.M. (1989). Hypoglycemic activity
Polymers, 78(3), 449–453. op several seaweed extracts. Journal of
219 Tsuge, K., Okabe, M., Yoshimura, T., Sumi, Ethnopharmacology, 27(1), 35–43.
T., Tachibana, H., Yamada, K. (2004). 227 Kang, S.I., Jin, Y.J., Ko, H.C., Choi, S.Y.,
Dietary effects of porphyran from Porphyra Hwang, J.H., Whang, I., Kim, M.H., Shin,
yezoensis on growth and lipid metabolism H.S., Jeong, H.B., Kim, S.J. (2008).
of Sprague-Dawley Rats. Food Science and Petalonia improves glucose homeostasis in
Technology Research, 10(2), 147–151. streptozotocin-induced diabetic mice.
220 Gressler, V., Stein, É.M., Dörr, F., Fujii, Biochemical and Biophysical Research
M.T., Colepicolo, P., Pinto, E. (2011). Communication, 373(2), 265–269.
Sesquiterpenes from the essential oil of 228 Takaoka, M., Saito, K. (1949). A blood sugar
Laurencia dendroidea (Ceramiales, level reducing substance Sargalin. Chemical
Rhodophyta): isolation, biological Industries Japan, 2, 227.
activities and distribution among 229 Saito, K., Nakamura, Y. (1951). Sargalin and
seaweeds. Revista Brasileira de related phenols from maiine algae and theii
Farmacognosia, 21, 248–254. medicinal functions. Journal of Chemical
221 Yildiz, G., Vatan, Ö., Çelikler, S., Dere, Ş. Society Japan, 72, 992–993.
(2011). Determination of the phenolic 230 Guven, K.C., Tekinalp, B. (1971). Short
compounds and antioxidative capacity in communication about Sargassum vulgare
red algae Gracilaria bursa-pastoris. Agardh. Botanica Marina, 14(1), 63–64.
International Journal of Food Properties, 231 Guven, K.C., Bora, A., Aktin, E., Oker, C.,
14(3), 496–502. Hatemi, H., Cetin, E.T. (1972).
222 Suganthy, N., Nisha, S.A., Pandian, S.K., Investigations on Phyllophora nervosa
Devi, K.P. (2013). Evaluation of Gelidiella (D.C.) Grev. Botanica Marina, 15, 46–48.
acerosa, the red algae inhabiting South 232 Guven, K.C., Aktin, E., Koyuncuoglu, H.,
Indian coastal area for antioxidant and Bergisadi, N. (1974). Lipolytic and
metal chelating potential. Biomedicine & hypoglycemic compounds obtained from
Preventive Nutrition, 3(4), 399–406. Cystoseira barbata J. Äg. Arzneimittel-
223 Li, K., Li, X.-M., Gloer, J.B., Wang, B.-G. Forschung. (Drug Research), 24, 144–147.
(2011). Isolation, characterization, and 233 Lee, S.-H., Min, K.-H., Han, J.-S., Lee,
antioxidant activity of bromophenols of the D.-H., Park, D.-B., Jung, W.-K., Park, P.-J.,
marine red alga Rhodomela confervoides. Jeon, B.-T., Kim, S.-K., Jeon, Y.-J. (2012).
Journal of Agricultural and Food Chemistry, Effects of brown alga, Ecklonia cava on
59(18), 9916–9921. glucose and lipid metabolism in C57BL/
224 Celikler, S., Tas, S., Vatan, O., Ziyanok- KsJ-db/db mice, a model of type 2 diabetes
Ayvalik, S., Yildiz, G., Bilaloglu, R. (2009). mellitus. Food and Chemical Toxicology,
Anti-hyperglycemic and antigenotoxic 50(3-4), 575–582.
608 20 Pharmacology of Marine Macroalgae

234 Lee, S.-H., Park, M.-H., Heo, S.-J., Kang, 242 Guven, K.C., Guler, E., Aktin, E.,
S.-M., Ko, S.-C., Han, J.-S., Jeon, Y.-J. Koyuncuoglu, H. (1979). Studies on
(2010). Dieckol isolated from Ecklonia cava Pterocladia capillaceae (Gmel.) Born. et
inhibits α-glucosidase and α-amylase in Thur. Part II Pharmacological, antibacterial
vitro and alleviates postprandial and antifungal investigations. in Marine
hyperglycemia in streptozotocin-induced Algae in Pharmaceutical Science, H.A.
diabetic mice. Food and Chemical Hoppe, T. Levring & Y. Tanaka (Eds.),
Toxicology, 48(10), 2633–2637. Walter de Gruyter, Berlin, pp. 693–710.
235 Lee, S.-H., Yong, L., Karadeniz, F., Kim, 243 Guven, K.C., Guler, E., Ozdemir, O.,
M.-M., Kim, S.-K. (2009). α-Glucosidase Sunam, G., Hakyemez, G. (1980).
and α-amylase inhibitory activities of Pharmacological investigations on the
phloroglucinal derivatives from edible protein fractions of Cystoseira corniculata
marine brown alga, Ecklonia cava. Journal Hauck and Cystoseira crinita Bory. Botanica
of the Science of Food and Agriculture, Marina, 23, 203–204.
89(9), 1552–1558. 244 Beckloff, G.L., Chapman, J.H., Shiverdecker,
236 Kang, C., Jin, Y.B., Lee, H., Cha, M., Sohn, P. (1972). Objective evaluation of an antacid
E.T., Moon, J., Park, C., Chun, S., Jung, with unusual properties. Journal of Clinical
E.S., Hong, J.S., Kim, S.B., Kim, J.S., Kim, Pharmacology, 12, 11–21.
E. (2010). Brown alga Ecklonia cava 245 Sketh, B.B. (1967). Alginat antacids. U.S.
attenuates type 1 diabetes by activating Patent 3,326,755: C.A: 67:84840 (1967).
AMPK and Akt signaling pathways. Food 246 Daigo, K., Wada, Y., Yamada, C., Yamaji,
Chemical Toxicology, 48(2), 509–516. M., Okuda, S., Okada, M., Miyazato, T.
237 Jung, H.A., Islam, M.N., Lee, C.M., Oh, (1981). Pharmacological studies of sodium
S.H., Lee, S., Jung, J.H., Choi, J.S. (2013). alginate. I. Protective effect of sodium
Kinetics and molecular docking studies of alginate on mucous membranes of
an anti-diabetic complication inhibitor upper-gastrointestinal tract. Yakugaku
fucosterol from edible brown algae Eisenia Zasshi, 101(5), 452–457.
bicyclis and Ecklonia stolonifera. Chemico- 247 Daigo, K., Wada, Y., Yamada, C., Yamaji,
Biological Interactions, 206(1), 55–62. M., Okuda, S., Okada, M., Miyazato, T.
238 Lee, Y.S., Shin, K.H., Kim, B.-K., Lee, S. (1981). Pharmacological studies of sodium
(2004). Anti-diabetic activities of fucosterol alginate. II. Hemostatic effect of sodium
from Pelvetia siliquosa. Archives in alginate on gastrointestinal bleeding.
Pharmacological Research, 27(11), Yakugaku Zasshi, 101(5), 458–463.
1120–1122. 248 Daigo, K., Yamaji, C., Yamada, K.,
239 Kim, K.Y., Nam, K.A., Kurihara, H., Kim, Matsutani, M., Yagi, M., Makajima, Y.,
S.M. (2008). Potent alpha-glucosidase Okada, M. (1982). Curative effect of sodium
inhibitors purified from the red alga alginate on experimental hydrochloric acid
Grateloupia elliptica. Phytochemistry, and tetragastrin induced ulcer. Yakuri To
69(16), 2820–2825. Tiryo, 10, 4599–4607.
240 Daniels, B.A. (2004). Seaweed extract 249 Castell, D.O., Dalton, C.B., Becker, D.,
composition for treatment of diabetes and Sinclair, J., Castell, J.A. (1992). Alginic acid
diabetic complications. US Patent Serial decreases postprandial upright
No: 438088. gastroesophageal reflux. Comparison with
241 Güven, K.C., Mutluay, E., Aktin, E., equal-strength antacid. Digestive Diseases
Koyuncuogluc, H. (1975). Chemical and and Sciences, 37(4), 589–593.
pharmacological investigations on Corallina 250 Shibata, H., Iimuro, M., Uchiya, N.,
rubens. Planta Medica, 27(01), 5–13. Kawamori, T., Nagaoka, M., Ueyama, S.,
 ­Reference 609

Hashimoto, S., Yokokura, T., Sugimura, T., derived from edible green alga,
Wakabayashi, K. (2003). Preventive effects Enteromorpha prolifera (Sujiao-nori).
of Cladosiphon fucoidan against International Journal of
Helicobacter pylori infection in Mongolian Immunopharmacology, 19(6), 355–358.
gerbils. Helicobacter, 8(1), 59–65. 261 Vanderlei, E.S.O., Patoilo, K.K.N.R., Lima,
251 Anderson, W. (1961). The antipeptic N.A., Lima, A.P.S., Rodrigues, J.A.G., Silva,
activity of sulphated polysaccharides. L.M.C.M., Lima, M.E.P., Lima, V.,
Journal of Pharmacy and Pharmacology, 13, Benevides, N.M.B. (2010). Antinociceptive
139–147. and anti-inflammatory activities of lectin
252 Hawkins, W.W., Leonard, V.G. (1962). from the marine green alga Caulerpa
Antipeptic and antithrombic properties of cupressoides. International
carrageenin. Journal of Laboratory and Immunopharmacology, 10(9), 1113–1118.
Clinical Medicine, 60, 641–648. 262 Joung, E.-J., Lee, M.-S., Choi, J.-W., Kim,
253 Watt, J., Eagleton, G.B. (1966). Effect of J.-S., Shin, T., Jung, B.-M., Yoon, N.Y., Lim,
degraded carrageenin on gastric secretion C.-W., Kim, J.-I., Kim, H.-R. (2012).
stimulated by histamine and histalog. Anti-inflammatory effect of ethanolic
Nature, 211, 989. extract from Myagropsis myagroides on
254 Anderson, W., Soman, P.D. (1965). murine macrophages and mouse ear
Degraded carrageenan and duodenal edema. BMC Complementary and
ulceration in the guinea pig. Nature, 204, Alternative Medicine, 12(1), 171.
101–102. 263 Islam, M.N., Ishita, I.J., Jin, S.E., Choi, R.J.,
255 Anderson, W., Soman, P.D. (1967). Lee, C.M., Kim, Y.S., Jung, H.A., Choi, J.S.
Degraded and undegraded carrageenans (2013). Anti-inflammatory activity of edible
and experimental gastric and duodenal brown alga Saccharina japonica and its
ulceration. Journal of Pharmacy and constituents pheophorbide a and
Pharmacology, 19, 520–526. pheophytin a in LPS-stimulated RAW 264.7
256 Alf, M. (1966). Medicament for digestive macrophage cells. Food and Chemical
diseases. Fr. Patent M4606; C.A. 69: 5222 Toxicology, 55, 541–548.
(1968). 264 Lee, J.Y., Lee, M.S., Choi, H.J., Choi, J.W.,
257 Hokazono, H. (1982). Oral antiulcer Shin, T., Woo, H.C., Kim, J.I., Kim, H.R.
formulations containing carrageenan. Jap. (2013). Hexane fraction from Laminaria
Kokai Tokkyo Koho JP 82 38,722; C.A. 96: japonica exerts anti-inflammatory effects
223292 (1982). on lipopolysaccharide-stimulated RAW
258 Damasceno, S.R.B., Rodrigues, J.C., Silva, 264.7 macrophages via inhibiting
R.O., Nicolau, L.A.D., Chaves, L.S., Freitas, NF-kappaB pathway. European Journal of
A.L.P., Souza, M.H.L.P., Barbosa, A.L.R., Nutrition, 52(1), 409–421.
Medeiros, J.-V.R. (2013). Role of the NO/ 265 Awad, N.E. (2004). Bioactive brominated
KATP pathway in the protective effect of a diterpenes from the marine red alga Jania
sulfated-polysaccharide fraction from the Rubens (L.) Lamx. Phytotherapy Research,
algae Hypnea musciformis against ethanol- 18(4), 275–279.
induced gastric damage in mice. Revista 266 Wiemer, D.F., Idler, D.D., Fenical, W.
Brasileira de Farmacognosia, 23(2), 320–328. (1991). Vidalols A and B, new anti-
259 Awad, N.E. (2000). Biologically active inflammatory bromophenols from the
steroid from the green alga Ulva lactuca. Caribbean marine red alga Vidalia
Phytotherapy Research, 14(8), 641–643. obtusaloba. Experientia, 47(8), 851–853.
260 Okai, Y., Higashi-Okai, K. (1997). Potent 267 Ayyad, S.-E.N., Al-Footy, K.O., Alarif, W.M.,
anti-inflammatory activity of pheophytin a Sobahi, T.R., Bassaif, S.A., Makki, M.S.,
610 20 Pharmacology of Marine Macroalgae

Asiri, A.M., Al-Halawani, A.Y., Badria, of acetylcholinesterase. Archives in


A.F., Badria, F.A.A.-r. (2011). Bioactive C15 Pharmacological Research, 28(6), 691–698.
acetogenins from the red alga Laurencia 273 Kannan, R.R.R., Aderogba, M.A., Ndhlala,
obtusa. Chemical and Pharmacological A.R., Stirk, W.A., Van Staden, J. (2013).
Bulletin, 59(10), 1294–1298. Acetylcholinesterase inhibitory activity of
268 Chaves, L.d.S., Nicolau, L.A.D., Silva, R.O., phlorotannins isolated from the brown alga,
Barros, F.C.N., Freitas, A.L.P., Aragão, K.S., Ecklonia maxima (Osbeck) Papenfuss. Food
Ribeiro, R.d.A., Souza, M.H.L.P., Barbosa, Research International, 54(1), 1250–1254.
A.L.d.R., Medeiros, J.-V.R. (2013). 274 Suganthy, N., Karutha Pandian, S.,
Antiinflammatory and antinociceptive Pandima Devi, K. (2010). Neuroprotective
effects in mice of a sulfated polysaccharide effect of seaweeds inhabiting South Indian
fraction extracted from the marine red coastal area (Hare Island, Gulf of Mannar
algae Gracilaria caudata. Marine Biosphere Reserve): Cholinesterase
Immunopharmacology and inhibitory effect of Hypnea valentiae and
Immunotoxicology, 35(1), 93–100. Ulva reticulata. Neuroscience Letters, 468(3),
269 Pereira, J.G., Mesquita, J.X., Aragao, K.S., 216–219.
Franco, A.X., Souza, M.H., Brito, T.V., Dias, 275 Gupta, A., Vijayaraghavan, M.R., Gupta, R.
J.M., Silva, R.O., Medeiros, J.V., Oliveira, (1998). The presence of cholinesterase in
J.S., Abreu, C.M., de Paula, R.C., Barbosa, marine algae. Phytochemistry, 49(7),
A.L., Freitas, A.L. (2014). Polysaccharides 1875–1877.
isolated from Digenea simplex inhibit 276 Machado, L.P., Carvalho, L.R., Young,
inflammatory and nociceptive responses. M.C.M., Cardoso-Lopes, E.M., Centeno,
Carbohydrate Polymers, 108, 17–25. D.C., Zambotti-Villela, L., Colepicolo, P.,
270 Wongprasert, K., Rudtanatip, T., Praiboon, Yokoya, N.S. (2015). Evaluation of
J. (2014). Immunostimulatory activity of acetylcholinesterase inhibitory activity of
sulfated galactans isolated from the red Brazilian red macroalgae organic extracts.
seaweed Gracilaria fisheri and development Revista Brasileira de Farmacognosia, 25(6),
of resistance against white spot syndrome 657–662.
virus (WSSV) in shrimp. Fish Shellfish 277 Ryu, G., Park, S.H., Kim, E.S., Choi, B.W.,
Immunology, 36(1), 52–60. Ryu, S.Y., Lee, B.H. (2003). cholinesterase
271 de Brito, T.V., Prudêncio, R.d.S., Sales, A.B., inhibitory activity of two farnesylacetone
Vieira Júnior, F.d.C., Candeira, S.J.N., derivatives from the brown alga Sargassum
Franco, Á.X., Aragão, K.S., Ribeiro, R.d.A., sagamianum. Archives of Pharmacological
Ponte de Souza, M.H.L., Chaves, L.d.S., Research, 26(10), 796–799.
Freitas, A.L.P., Medeiros, J.-V.R., dos Reis 278 Jung, H.A., Oh, S.H., Choi, J.S. (2010).
Barbosa, A.L. (2013). Anti-inflammatory Molecular docking studies of phlorotannins
effect of a sulphated polysaccharide from Eisenia bicyclis with BACE1 inhibitory
fraction extracted from the red algae activity. Bioorganic and Medicinal
Hypnea musciformis via the suppression of Chemistry Letters, 20, 3211–3215.
neutrophil migration by the nitric oxide 279 Ahn, B.R., Moon, H.E., Kim, H.R., Jung,
signalling pathway. Journal of Pharmacy H.A., Choi, J.S. (2012). Neuroprotective
and Pharmacology, 65(5), 724–733. effect of edible brown alga Eisenia bicyclis
272 Myung, C.-S., Shin, H.-C., Bao, H.Y., Yeo, on amyloid beta peptide-induced toxicity in
S.J., Lee, B.H., Kang, J.S. (2005). PC12 cells. Archives of Pharmacological
Improvement of memory by dieckol and Research, 35(11), 1989–1998.
phlorofucofuroeckol in ethanol-treated 280 Choi, J.S., Haulader, S., Karki, S., Jung, H.J.,
mice: possible involvement of the inhibition Kim, H.R., Jung, H.A. (2015). Acetyl- and
 ­Reference 611

butyryl-cholinesterase inhibitory activities 289 Afolayan, A.F., Mann, M.G., Lategan, C.A.,
of the edible brown alga Eisenia bicyclis. Smith, P.J., Bolton, J.J., Beukes, D.R. (2009).
Archives of Pharmacological Research, 38(8), Antiplasmodial halogenated monoterpenes
1477–1487. from the marine red alga Plocamium
281 Yoon, N.Y., Lee, S.-H., Yong, L., Kim, S.-K. cornutum. Phytochemistry, 70(5), 597–600.
(2009). Phlorotannins from Ishige 290 Suzgec-Selcuk, S., Mericli, A.H., Guven,
okamurae and their acetyl- and K.C., Kaiser, M., Casey, R., Hingley-Wilson,
butyrylcholinesterase inhibitory effects. S., Lalvani, A., Tasdemir, D. (2011).
Journal of Functional Foods, 1(4), 331–335. Evaluation of Turkish seaweeds for
282 Na, H.J., Moon, P.D., Ko, S.G., Lee, H.J., antiprotozoal, antimycobacterial and
Jung, H.A., Hong, S.H., Seo, Y., Oh, J.M., cytotoxic activities. Phytotherapy Research,
Lee, B.H., Choi, B.W., Kim, H.M. (2005). 25(5), 778–783.
Sargassum hemiphyllum inhibits atopic 291 Wright, A.D., Konig, G.M., Angerhofer,
allergic reaction via the regulation of C.K., Greenidge, P., Linden, A.,
inflammatory mediators. Journal of Desqueyroux-Fernandez, R. (1996).
Pharmacological Sciences, 97(2), 219–226. Antimalarial activity: the search for marine
283 Shim, S.Y., Choi, J.S., Byun, D.S. (2009). derived natural products with selective
Inhibitory effects of phloroglucinol antimalarial activity. Journal of Natural
derivatives isolated from Ecklonia Products, 59, 710–716.
stolonifera on Fc(epsilon)RI expression. 292 Stout, E.P., Cervantes, S., Prudhomme, J.,
Bioorganic Medicinal Chemistry, 17(13), France, S., La Clair, J.J., Le Roch, K.,
4734–4739. Kubanek, J. (2011). Bromophycolide A
284 Sugiura, Y., Matsuda, K., Okamoto, T., targets heme crystallization in the human
Kakinuma, M., Amano, H. (2008). Anti- malaria parasite Plasmodium falciparum.
allergic effects of the brown alga Eisenia ChemMedChem, 6(9), 1572–1577.
arborea on Brown Norway rats. Fisheries 293 Lane, A.L., Stout, E.P., Lin, A.-S.,
Science, 74(1), 180–186. Prudhomme, J., Roche, K.L., Fairchild,
285 Samee, H., Li, Z.-X., Lin, H., Khalid, J., C.R., Franzblau, S.G., Hay, M.Z.,
Guo, Y.-C. (2009). Anti-allergic effects of Aalberberg, W. (2009). Antimalarial
ethanol extracts from brown seaweeds. bromophycolides from the Fijian red alga
Journal of Zhejiang University. Science. B, Callophycus serratus. Journal of Organic
10(2), 147–153. Chemistry, 74, 2736–2742.
286 Raman, B.V., Rao, D.N., Radhakrishnan, 294 Jung, W.-K., Choi, I., Oh, S., Park, S.-G.,
T.M. (2004). Enteromorpha compressa (L.) Seo, S.-K., Lee, S.-W., Lee, D.-S., Heo, S.-J.,
Greville an edible green alga as a source of Jeon, Y.-J., Je, J.-Y., Ahn, C.-B., Kim, J.S.,
antiallergic principle (S). Indian Journal of Oh, K.S., Kim, Y.-M., Moon, C., Choi, I.-W.
Clinical Biochemistry, 19(1), 105–109. (2009). Anti-asthmatic effect of marine red
287 Vo, T.-S., Ngo, D.-H., Kim, S.-K. (2012). alga (Laurencia undulata) polyphenolic
Marine algae as a potential pharmaceutical extracts in a murine model of asthma.
source for anti-allergic therapeutics. Process Food and Chemical Toxicology, 47(2),
Biochemistry, 47(3), 386–394. 293–297.
288 Ravikumar, S., Inbaneson, S.J., Suganthi, P., 295 Kim, S.K., Lee, D.Y., Jung, W.K., Kim, J.H.,
Gokulakrishnan, R., Venkatesan, M. (2011). Choi, I., Park, S.G., Seo, S.K., Lee, S.W., Lee,
In vitro antiplasmodial activity of ethanolic C.M., Yea, S.S., Choi, Y.H., Choi, I.W.
extracts of seaweed macroalgae against (2008). Effects of Ecklonia cava ethanolic
Plasmodium falciparum. Parasitology extracts on airway hyperresponsiveness and
Research, 108(6), 1411–1416. inflammation in a murine asthma model:
612 20 Pharmacology of Marine Macroalgae

role of suppressor of cytokine signaling. Archives in Pharmacological Research,


Biomedicine & Pharmacotherapy, 62(5), 34(4), 645–651.
289–296. 304 Shi, J., Cheng, C., Zhao, H., Jing, J., Gong,
296 Wongprasert, K., Rudtanatip, T., Praiboon, N., Lu, W. (2013). In vivo anti-radiation
J. (2014). Immunostimulatory activity of activities of the Ulva pertusa
sulfated galactans isolated from the red polysaccharides and polysaccharide-
seaweed Gracilaria fisheri and development iron(III) complex. International Journal of
of resistance against white spot syndrome Biological Macromolecules, 60, 341–346.
virus (WSSV) in shrimp. Fish & Shellfish 305 Mao, W., Li, Y., Wu, L., Wang, H., Zhang, Y.,
Immunology, 36(1), 52–60. Zang, X., Zhang, H. (2005). Chemical
297 Zaporozhets, T.S. (2003). Modulation of characterization and radioprotective effect
Fcgamma and C3b receptor expression by of polysaccharide from Monostroma
marine bioglycans in mouse splenocytes. angicava (Chlorophyta). Journal of Applied
Antibiot Khimioter, 48(3), 17–20. Phycology, 17(4), 349–354.
298 Senthilkumar, K., Venkatesan, J., Kim, S.-K. 306 Kuznetsova, T.A., Krylova, N.V., Besednova,
(2014). Marine derived natural products for N.N., Vasil’eva, V.N., Zviagintseva, T.N.,
osteoporosis. Biomedicine & Preventive Krashevskii, S.V., Eliakova, L.A. (1994).
Nutrition, 4, 1–7. [The effect of translam on the natural
299 Yamaguchi, M. (2013). Marine alga resistance indices of the irradiated
Sargassum Horneri component and bone organism]. Radiatsionnaia Biologiia,
homeostasis: Role in osteoporosis Radioecologiia, 34(2), 236–239.
prevention. International Journal of Food 307 Kang, K.A., Zhang, R., Chae, S., Lee, S.J.,
Science, Nutrition and Dietetics, 2(1), 9–14. Kim, J., Kim, J., Jeong, J., Lee, J., Shin, T.,
300 Das, S.K., Ren, R., Hashimoto, T., Lee, N.H., Hyun, J.W. (2010).
Kanazawa, K. (2010). Fucoxanthin induces Phloroglucinol (1,3,5-trihydroxybenzene)
apoptosis in osteoclast-like cells protects against ionizing radiation-induced
differentiated from RAW264.7 cells. Journal cell damage through inhibition of oxidative
of Agricultural and Food Chemistry, 58(10), stress in vitro and in vivo. Chemico-
6090–6095. Biological Interaction, 185(3), 215–226.
301 Cavalcante-Silva, L.H.A., de Carvalho 308 Ahn, M., Moon, C., Yang, W., Ko, E.J.,
Correia, A.C., Barbosa-Filho, J.M., Araújo Hyun, J.W., Joo, H.G., Jee, Y., Lee, N.H.,
da Silva, B., de Oliveira Santos, B.V., de Park, J.W., Ko, R.K., Kim, G.O., Shin, T.
Lira, D.P., Ferreira Sousa, J.C., de Miranda, (2011). Diphlorethohydroxycarmalol,
G.E.C., de Andrade Cavalcante, F., isolated from the brown algae Ishige
Alexandre-Moreira, M.S. (2013). okamurae, protects against radiation-
Spasmolytic effect of caulerpine involves induced cell damage in mice. Food
blockade of Ca(2+) influx on Guinea Pig Chemical Toxicology, 49(4), 864–870.
ileum. Marine Drugs, 11(5), 1553–1564. 309 Heo, S.-J., Jeon, Y.-J. (2009). Protective
302 Oh, H., Bing, S., Kim, A., Cho, J., Jee, Y. effect of fucoxanthin isolated from
(2013). Radio-protective effect of sulfated Sargassum siliquastrum on UV-B induced
polysaccharide purified from Ecklonia cava cell damage. Journal of Photochemistry and
against small intestinal stem cells of γ-ray Photobiology B: Biology, 95(2), 101–107.
irradiated mice. Journal of Biomedical 310 Ben-Amotz, A., Yatziv, S., Sela, M.,
Research, 14, 220–225. Greenberg, S., Rachmilevich, B.,
303 Rhee, K.H., Lee, K.H. (2011). Protective Shwarzman, M., Weshler, Z. (1998). Effect
effects of fucoidan against gamma- of natural beta-carotene supplementation
radiation-induced damage of blood cells. in children exposed to radiation from the
 ­Reference 613

Chernobyl accident. Radiation and pinnatifida) and their angiotensin-i-


Environmental Biophysics, 37(3), 187–193. converting enzyme inhibitory activity.
311 Oh, J.-Y., Fernando, I.P.S., Jeon, Y.-J. (2016). Annals of Nutrition and Metabolism, 46(6),
Potential applications of radioprotective 259–267.
phytochemicals from marine algae. Algae, 320 Gregson, R.P., Marwood, J.F., Quinn, R.J.
31(4), 403–414. (1979). The occurrence of prostaglandins
312 Husu, C.F. (1934). A chemical study of PGE2 and PGF2α in a plant – the red alga
Hai-jen tsao (Difenea simplex). Science Gracilaria Lichenoides. Tetrahedron Letters,
China, 18, 1418–1437. 20(46), 4505–4506.
313 Nitta, I., Watase, H., Tomiie, Y. (1958). 321 Guven, K.C., Kızıl, Z., Ozdemir, O., Kaya,
Structure of kainic acid and its isomer, G., Ulutin, O.N., Turker, R.K. (1985).
allokainic acid. Nature, 181(4611), 761–762. Prostaglandin-like activity of Halopteris
314 Fukuyama, Y., Miura, I., Kinzyo, Z., filicina (Kutz.) (marine alga) extract. Acta
Nakayama, Y., Takahashi, M., Kido, Y., Pharmaceutica Turcica, 27, 92–95.
Tennen, M. (1983). Anti-plasmine 322 Guven, K.C., Kızıl, Z., Ozdemir, O., Kaya,
inhibitors, polyhydroxydibenzo-P-dioxins G., Ulutin, O.N., Turker, R.K. (2004).
isolated from Ecklonia kurome Okamura. Prostaglandin in algae. Investigation on
Yuki. Kogobutsu Tornokai Koen Yoshishu, Halopteris filicina (Kütz.) extract. Journal of
26, 126–133. the Black Sea and Mediterranean
315 Fukuyama, Y., Kodama, M., Miura, I., Environment, 10(3), 201–208.
Kinzyo, Z., Mori, H., Nakayama, Y., 323 Soliman, F.M., El Tohamy, S.F., Fathy,
Takahashi, M. (1990). Anti-plasmin M.M., Ramadan, A. (1994). Phytochemical
inhibitor. VI. Structure of and biological investigation of Jania rubens
phlorofucofuroeckol A, a novel (L.) Lamx. Amino acids, proteins,
phlorotannin with both dibenzo-1,4-dioxin nitrogenous bases and biological screening.
and dibenzofuran elements, from Ecklonia Journal of Drug Research, 21(1/2), 155–164.
kurome Okamura. Chemical and 324 Takemoto, T., Daigo, K., Takagi, N. (1964).
Pharmacology Bulletin, 38(1), 133–135. Studies on the hypotensive constituents of
316 Jung, H.A., Hyun, S.K., Kim, H.R., Choi, marine algae. Ii. synthesis of laminine and
J.S. (2006). Angiotensin-converting enzyme related compounds. Yakugaku Zasshi, 84,
I inhibitory activity of phlorotannins from 1180–1182.
Ecklonia stolonifera. Fisheries Science, 325 Takemoto, T., Daigo, K., Takagi, N. (1964).
72(6), 1292–1299. Studies on the hypotensive constituents of
317 Suetsuna, K. (1998). Separation and marine algae I. A new basic amino acid
identification of angiotensin i-converting laminine and other basic constituents
enzyme inhibitory peptides from peptic isolated from Laminaria angustata.
digest of Hizikia fusiformis protein. Nippon Yakugaku Zasshi, 84, 1176–1179.
Suisan Gakkaishi, 64(5), 862–866. 326 Girard, J.P., Marion, C., Liutkus, M.,
318 Suetsuna, K. (1998). Purification and Boucard, M., Rechencq, E., Vidal, J.P.,
identification of angiotensin I-converting Rossi, J.C. (1988). Hypotensive constituents
enzyme inhibitors from the red alga of marine algae; 1. Pharmacological studies
Porphyra yezoensis. Journal of Marine of laminine. Planta Medica, 54(3), 193–196.
Biotechnology, 6(3), 163–167. 327 Rao, H.B.R., Sathivel, A., Devaki, T. (2004).
319 Sato, M., Oba, T., Yamaguchi, T., Nakano, Antihepatotoxic nature of Ulva reticulata
T., Kahara, T., Funayama, K., Kobayashi, on acetaminophen induced hepatoxicity in
A., Nakano, T. (2002). Antihypertensive experimental rats. Journal of Medicinal
effects of hydrolysates of wakame (Undaria Food, 7, 495–497.
614 20 Pharmacology of Marine Macroalgae

328 Abdel-Wahhab, M.A., Ahmed, M.A., 338 Murata, K. (1961). Effect of Carrageenin on
Hagazi, M.M. (2006). Prevention of serum lipids and atherosclerosis in rabbits.
aflatoxin B1-initiated hepatotoxicity in rat Nature, 191, 189–190.
by marine algae extracts. Journal of Applied 339 Abe, S., Takeda, F., Kaneda, T. (1967).
Toxicology, 26, 229–238. Studies on the effects of marine products
329 Kaneda, T., Tokuda, S., Arai, K. (1963). om cholesterol metabolism in rats. VII. The
Effect of marine products on cholesterol influence of dried purple lavel on
metabolism. I. the effect of seaweed. cholesterol levels of organs in rats. Bulletin
Nippon Suison Gakkaishi, 29, 1020–1023. of the Japanese Sociecty for the Science of
330 Kaneda, T., Kamasastri, P., Tokuda, S. Fish, 33, 1050–1056.
(1965). Studies on the effects of marine 340 Maeda, H., Hosokawa, M., Sashima, T.,
products om cholesterol metabolism in rats. Miyashita, K. (2007). Dietary combination
V. The effect of edible seaweeds Bulletin of of fucoxanthin and fish oil attenuates the
the Japanese Society for the Science of Fish, weight gain of white adipose tissue and
31, 1026–1029. decreases blood glucose in obese/diabetic
331 Abe, S., Kaneda, T. (1971). The effect of KK-Ay mice. Journal of Agricultural and
edible seaweed on cholesterol metabolism Food Chemistry, 55(19), 7701–7706.
in rats. Proceedings of International 341 Terasaki, M., Hirose, A., Narayan, B., Baba,
Seaweed Symposium, 7(562-565). Y., Kawagoe, C., Yasui, H., Saga, N.,
332 Abe, S., Kaneda, T. (1973). Effet of marine Hosokawa, M., Miyashita, K. (2009).
products on cholesterol metabolism in rats. Evaluation of recoverable functional lipid
VIII. Isolation of the hypocholesterolemic components of several brown seaweeds
substance from green algae Nippon Suisan (Phaeophyta) from Japan with special
Gakkaishi, 39, 383–389. reference to fucoxanthin and fucosterol
333 Kaneda, T., Abe, S. (1984). contents. Journal of Phycology, 45(4),
Hypocholesterolemic effect of seaweeds on 974–980.
rats. Hydrobiologia, 116/117, 149–152. 342 Mori, K., Ooi, T., Hiraoka, M., Oka, N.,
334 Reiner, E., Topliff, I., Wood, J.D. (1962). Hamada, H., Tamura, M., Kusumi, T.
Hypocholesterolemic agents derived from (2004). Fucoxanthin and its metabolites in
sterols of marine algae. Canadian Journal edible brown algae cultivated in deep
of Biochemistry and Physiology, 40, seawater. Marine Drugs, 2(2), 63–72.
1401–1406. 343 Kim, M.J., Chang, U.J., Lee, J.S. (2009).
335 Kaneda, T., Arai, K. (1964). Studies on the Inhibitory effects of fucoidan in 3T3-L1
effects of marine products om cholesterol adipocyte differentiation. Marine
metabolism in rats. III. The effect of lipid Biotechnology, 11(5), 557–562.
isolated from Sargassum ringoldianum 344 Kim, S.K., Kong, C.S. (2010). Anti-adipogenic
seaweeds. Bulletin of the Japanese Sociecty effect of dioxinodehydroeckol via AMPK
for the Science of Fish, 30, 589–593. activation in 3T3-L1 adipocytes. Chemico-
336 Ito, K., Tsuchiya, Y. (1972). The effect of Biological Interaction, 186(1), 24–29.
algal polysaccharides on the depressing of 345 Kong, C.-S., Kim, J.-A., Ahn, B.-N., Vo, T.S.,
plasma cholesterol levels in rats. Yoon, N.-Y., Kim, S.-K. (2010).
International Symposium on Seaweed 1-(3′,5′-dihydroxyphenoxy)-7-(2″,4″,6-
Research, Sapporo, 7, 558–561. trihydroxyphenoxy)-2,4,9-
337 Tsuchiya, Y. (1969). Comparative trihydroxydibenzo-1,4-dioxin inhibits
hypocholesterolemic activityes of marine adipocyte differentiation of 3T3-L1
algae. Proceedings of International Seaweed fibroblasts. Marine Biotechnology, 12(3),
Symposium, 6, 746–757. 299–307.
 ­Reference 615

346 He, M.L., Wang, Y., You, J.S., Mir, P.S., 351 Awad, N.E., Selim, M.A., Saleh, M.M.,
McAllister, T.A. (2009). Effect of a seaweed Matloub, A.A. (2003). Seasonal variation of
extract on fatty acid accumulation and the lipoidal matters and hypolipidaemic
glycerol-3-phosphate dehydrogenase activity of the red alga Corallina officinalis
activity in 3T3-L1 adipocytes. Lipids, 44(2), L. Phytotherapy Research, 17(1), 19–25.
125–132. 352 Chatter, R., Cenac, N., Roussis, V., Kharrat,
347 Dinh, H.L., Hori, K., Quang, N.H. (2008). R., Vergnolle, N. (2012). Inhibition of
Screening and preliminary sensory afferents activation and visceral
characterization of hemagglutinins in pain by a brominated algal diterpene.
Vietnamese marine algae. Journal of Neurogastroenterology & Motility, 24(7),
Applied Phycology, 21(1), 89. e336–e343.
348 Mori, T., O’Keefe, B.R., Sowder, R.C., 2nd, 353 Figueiredo, J.G., Bitencourt, F.S., Cunha,
Bringans, S., Gardella, R., Berg, S., T.M., Luz, P.B., Nascimento, K.S., Mota,
Cochran, P., Turpin, J.A., Buckheit, R.W., M.R.L., Sampaio, A.H., Cavada, B.S.,
Jr., McMahon, J.B., Boyd, M.R. (2005). Cunha, F.Q., Alencar, N.M.N. (2010).
Isolation and characterization of griffithsin, Agglutinin isolated from the red marine
a novel HIV-inactivating protein, from the alga Hypnea cervicornis J. Agardh reduces
red alga Griffithsia sp. Journal of Biological inflammatory hypernociception:
Chemistry, 280(10), 9345–9353. Involvement of nitric oxide. Pharmacology
349 Vanderlei, E.S., Patoilo, K.K., Lima, N.A., Biochemistry and Behavior, 96(4), 371–377.
Lima, A.P., Rodrigues, J.A., Silva, L.M., 354 Bitencourt, F.d.S., Figueiredo, J.G., Mota,
Lima, M.E., Lima, V., Benevides, N.M. M.R.L., Bezerra, C.C.R., Silvestre, P.P., Vale,
(2010). Antinociceptive and anti- M.R., Nascimento, K.S., Sampaio, A.H.,
inflammatory activities of lectin from the Nagano, C.S., Saker-Sampaio, S., Farias,
marine green alga Caulerpa cupressoides. W.R.L., Cavada, B.S., Assreuy, A.M.S., de
International Immunopharmacology, 10(9), Alencar, N.M.N. (2008). Antinociceptive
1113–1118. and anti-inflammatory effects of a mucin-
350 das Chagas Vieira Júnior, F., Sales, A.B., binding agglutinin isolated from the red
Barros, F.C.N., Chaves, L.d.S., Freitas, marine alga Hypnea cervicornis. Naunyn-
A.L.P., Vale, M.L., Ribeiro, R. d.A., Souza, Schmiedeberg’s Archives of Pharmacology,
M.H.L.P., Medeiros, J.-V.R., Barbosa, 377(2), 139.
A.L.d.R. (2012). Involvement of the NO/ 355 Moura, L.D.A., Sanchez, E.F., Bianco, É.M.,
cGMP/PKG/KATP pathway and Pereira, R.C., Teixeira, V.L., Fuly, A.L.
endogenous opioids in the antinociceptive (2010). Antiophidian properties of a
effect of a sulphated-polysaccharide dolastane diterpene isolated from the
fraction extracted from the red algae, marine brown alga Canistrocarpus
Gracilaria caudata. Biomedicine & cervicornis. Biomedicine & Preventive
Preventive Nutrition, 2(4), 303–309. Nutrition, 1(1), 61–66.

You might also like