Professional Documents
Culture Documents
20
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
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 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
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
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
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
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
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.