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NEWSLETTER
INTERNATIONAL CENTER
FOR AGRICULTURAL
RESEARCH IN THE DRY
AREAS
FAO-ICARDA
INTERNATIONAL
TECHNICAL COOPERATION
NETWORK ON CACTUS
UNIVERSIDAD NACIONAL DE
SANTIAGO DEL ESTERO
ARGENTINA
Table of content
Editorial
Scientific and technical contributions
2
3
18
29
33
Monia Ennouri. Beneficial Effect Of Opuntia Ficus Indica Seeds And Oil
On Animal Health.
36
Saida Ncibi, Dalel Brahim, Amira Akacha, Mohamed Naceur Krifi, Sami
Souid and Lazhar Zourgui. Biochemical and Immunolgical Toxicity of
Chlorpyrifos in Mice.
42
Changping Zou.
Chemoprevention.
47
Cactus
Pear:
Natural
Product
In
Cancer
49
51
57
Network News
New subscribers
61
63
Editorial
Cactus, plant of the desert and flag of the poor, is increasingly attracting scientists and
developers over the entire world. Just few years ago, no one would have imagined that
outstanding advanced research laboratories in Germany, Italy, France, USA, South Korea,
China, Mexico, and others would be investigating the potential uses of cacti as medicinal
plants. In fact, Cactus was largely ignored by the scientific community until the beginning
of 1980, when a multiplication of research and symposia occurred, resulting in a large
number of publications. This renewed interest is to be ascribed in part to the multifunctionality of cactus fruits, pads and flowers.
Also, in recent years a global trend is witnessed toward the use of natural phytochemicals
present in various natural resources, including fruit, vegetables, oilseeds, and herbs, as
antioxidants and functional foods. Natural antioxidants can be used in food industry, and
there is evidence that they may exert their antioxidant properties within the human body.
This issue of Cactusnet newsletter is dedicated to the coverage of medicinal uses of cactus
products. While most of people are familiar with the use of cactus for fruit and fodder
production few are aware of its potential usefulness as medicinal plant. Native Americans
and ancient medicine have realized its anti-diabetic and anti-inflammatory properties, but
Opuntia spp. have hardly been considered for the development of health-promoting food,
most probably due to the little information available.
The main objective of this issue therefore is to fill up this knowledge gap and to keep
scientists, developers, and consumers abreast of recent advances made in the use of cactus
cladodes, fruits and flowers as neutraceutical and medicinal resources.
To confirm the importance given to this new area, a new research group is added to
strengthen the structure of the International Technical Cooperation Network on Cactus
(Cactusnet). Dr Monica Nazareno, Professor of organic chemistry at the University of
Santiago del Estero, Argentina and co-editor of this issue, has been recently appointed to
coordinate this working group.
Created under the initiative of FAO, the cactus network now is fifteen years old, and has
been attracting more and more people with increasing popularity due to the dedication and
continuous support of Dr. Enrique Arias of FAO. The recent Sixth International Congress
held during October 2007 in Brazil, has brought together more than 500 participants, with
34 invited papers and 234 other contributions, which testifies to the success and good
health of the network.
ICARDA serves the non-tropical dry areas where cacti play an important role as a drought
tolerant plant resource for fruit, fodder and land conservation. Therefore, ICARDA is paying
more and more importance to this crop, working closely with FAO to promote cactus in
different parts of the world.
The editors are especially grateful to FAO and ICARDA for their financial and technical
support, and express their thanks and recognition to all partners, with a special mention of
the many authors for their valuable contributions to this issue of Cactusnet newsletter.
The editors
Monica Nazareno and Ali Nefzaoui
Summary
pectins.
1. Introduction
As a CAM plant, Opuntia spp. are
characterized by a high water use efficiency of
410 mmol CO2 per mol H2O compared to
C3- and C4-plants with 1.01.5 mmol and 23
mmol CO2 per mol H2O, respectively. Through
succulence, the ability to store considerable
quantities of water, the plant may survive
despite harsh environmental conditions
(Nobel and De la Barrera, 2003).
Furthermore, and according to the same
author, Opuntia exhibits the highest
production rate of aboveground-growing
plants. Interestingly, the biomass production
was even found to increase upon otherwise
deleterious rise of atmospheric CO2
concentrations (Nobel et al., 2002), thus
counteracting the greenhouse effect.
Cactus was largely ignored by the scientific
world until the beginning of 1980, when there
was a multiplication of research and symposia,
resulting in a large number of publications.
This renewed interest is to be ascribed in part
to the multi-functionality of cactus fruits, pads
Fibers
The healthy properties of fibres are well
established: control of obesity, diabetes, and
cholesterol (Sloan, 1994). There are two types
of fibres: water soluble and insoluble. Soluble
fibres include mucilage, gums, pectin, and
hemi-celluloses. Soluble fibres are associated
to the reduction of blood glucose and
cholesterol and stabilize intestinal food transit.
Insoluble fibres are composed mainly of
cellulose, lignin, and a large portion of hemicelluloses. They are known for their capacity to
retain water, favour ionic exchange, absorption
of bile acids, minerals, vitamins and other
interaction with microbes (Carmen Saenz,
2006).
Dried cladodes powder contains about 43 %
fibre, 28,5 % of which are insoluble. Some
commercial products based on cladodes
powder are already marketed, as Cactu fibra
and Nutra Sweet in Mexico. These products
are prepared with young cladodes (3-6
months), which have low content of insoluble
fibre.
This powder is also used to prepare several
foods, as biscuits, creams, and other types of
desserts (Saenz et al. 2002). Generally, about
18 % of cladodes powder is incorporated in
such products.
Pigments/dyes
WHO and EC regulations restrain the use of
artificial dyes, favouring therefore the use of
Anti-oxidants
Cactus fruits have a high anti-oxidant activity
conferred by the presence of vitamin C,
betacartenes, falvonides, and betalaines (Kuti,
2004; Galati et al., 2003). Fruits extract have
an antioxidant activity of 4.2-5.3 mol Trolox f1 for white and yellow variety, respectively.
This anti-oxidant activity is twice higher than
pears, apples, tomato, bananas, white grapes,
and similar to red grapes and grape fruit
(Butera, 2002). Significant amounts of ascorbic
acid are present in Opuntia ficus-indica,
ranging from 180 to 300 mg/kg. Cactus fruit is
higher in vitamin C than other common fruits,
such ass apple, pear, grape, and banana.
The most obvious feature of cactus pear fruits
and flowers are the yellow (betaxanthins) and
red
(betacyanins)
betalains,
nitrogencontaining vacuolar pigments that replace
anthocyanins in most plant families of the
Caryophyllales including the Cactaceae (Zryd,
2004). Their identification in cactus pear fruit
has been of renewed interest recently
(Stintizing et al., 2003). In addition to color, the
same pigments have shown antioxidant
properties being higher than for ascorbic acid
(Tesoriere et al., 2005).
Lee et al. (2000) investigate the anti-oxidant
activity of cactus cladodes and conclude that
this anti-oxidant property is due to many
compounds, particularly flavonoids (quercetin,
myricetin), and vitamins.
The presence of phenolics has been detected
in cactus pulp fruit (Tesoriere et al., 2005b;
Butera et al., 2002; Kuti, 2004). Kuti (1992) has
reported an antioxidative effect due to the
major flavonoids encountered in cactus fruits
(quercetin, kaempferol and isorhamnetin).
There is clear evidence that these compounds
are more efficient antioxidants than vitamins,
since phenolic compounds are able to delay
prooxidative effects on proteins, DNA and
lipids by the generation of stable radicals
Lipids
Lipids are present in the peel, pulp, and seeds.
Peel contains an appreciable amount of
polyunsatured fatty acids, mainly linoleic acid,
alpha-tocopherol, sterols, beta-carotene and
vitamin K1 (Ramadan and Morsel, 2003a). The
main sterol is b-sitosterol. Among amino acids
present in the fruit, the highest is the
nutraceutical taurine, with an amount of 572
mg/L (Stintzing et al., 2001).
raw materials.
Interspecific variations of the plant material,
harvest time, and application modes (oral,
intravenous) should be considered.
Some studies have demonstrated the
hypoglycemic activity of the prickly pear cactus
extract on non-diabetics and diabetic-induced
rats or diabetic humans (Enigbokan et al.,
1996). In a study on rats, the combination of
insulin and purified extract of cactus (Opuntia
fuliginosa Griffiths) was found to reduce blood
glucose and glycated hemoglobin levels to
normal (Enigbokan et al., 1996). In this study,
the oral dose of extract (1 mg/kg body weight
per day) necessary to control diabetes contrast
with the high quantities of insulin required for
an equivalent hypoglycemic effect. A recent
study has shown that a supplementation of
rats diets with cactus seed oil (25 mg/kg)
decreases the serum glucose concentration,
which is associated with a glycogen formation
in the liver and skeletal muscle (Laurenz et al.,
2003). These observations were explained by
a potential induction of insulin secretion,
converting glucose to glycogen.
Wolfram and collaborators (2003) from the
University of Vienna, Austria, suspected a
soluble fibre in lowering cholesterol levels in
both animals and man with hyperlipidemia as
well as being able to slow carbohydrate
absorption and hence reduce the postprandial
rise in blood glucose and serum insulin in
patients with type-II diabetes. The aim of their
work was to investigate the effect of cactus
consumption on glucose and lipid metabolism.
Cactus consumption leads to a decrease of
total cholesterol (12%), low-density lipoproteincholesterol (15%), apolipoprotein B (9%),
triglycerides (12%), fibrinogen (11%), blood
glucose (11%), insulin (11%) and uric acid
(10%), while body weight, high-density
lipoprotein-cholesterol, apolipoprotein A-I, and
lipoprotein(a) remained unchanged. Authors
conclude that the hypocholesterolemic action
of cactus may be partly explained by the fibre
(pectin) content, but the hypoglycaemic actions
(improvement of insulin sensitivity) in the nonobese, non-diabetic need further investigation
to get more insights on the potential advantage
of treating the metabolic syndrome.
An amazing effect of cacti in controlling
appetite has been recently reported in several
media and it may change the life of people
suffering from obesity. It is perceived as a new
miracle diet ingredient. Imagine an organic pill
that kills the appetite and attacks obesity. It
has no known side-effects, and contains a
molecule that fools your brain into believing
10
11
12
13
4. Conclusions
Not only the biofunctional properties but also
the assumed roles of cladode polysaccharides
in the medicinal sector are interesting such as
cholesterol reduction and its preventive action
in diabetes and adipositas therapies. Since the
hydrocolloid fraction is also rich in proteins,
further research should be conducted whether
the alleged positive effects are due to the
pectic substances or rather to the protein
fraction. Furthermore, it should be investigated
whether these proteins are acting as heatshock and anti-freeze proteins [213220] in the
cactus tissue. Whether the same proteins
acting as repair molecules in plants could be
used for pharmaceutical purposes merits
further consideration. Special attention should
also be given to the oligosaccharide fraction
that has not been characterized so far.
Immunomodulatory properties have been
postulated for glucans from roots of Periandra
mediterranea (Vell.) Taub. and glucomannans
from Aloe sp. According to recent publication,
small oligosaccharides with a polymerization
degree of 6 and above with a tendency to form
helical structures are potent immune
modulators.
In summary, the constituents of Opuntia
cladodes are only partly known and often not
quantitatively determined. Investigations were
mostly performed 20 years ago and need to be
validated
with
up-to-date
methods.
Furthermore, data stem from all kinds of
different Opuntia spp. and it is open to
question whether the botanical classification
has properly been assessed in each case.
Beside a sound systematic classification, the
background of cladode physiology needs to be
considered. Based on additional data, a
reliable
nutritional
evaluation
can
be
performed. The technofunctional properties of
the respective extracts can be efficiently
exploited for manifold food, cosmetic and
medicinal applications. Analogies to the
multiple uses of Aloe sp. are obvious. Whether
isolated substances or rather a concerted
action of several components in the complex
plant matrix are responsible for the big variety
of biological activities remains unknown, let
alone the underlying mechanisms of the
traditional curative treatments being still little
under-stood.
From the presented data, it appears that
Opuntia spp. has been subject to intensive
exploitation due to its great compositional
diversity. Nowadays, this hidden knowledge
needs to be discovered and re-evaluated.
Sophisticated analytical approaches and
innovative processing technologies will open
new avenues to further promote the use of
cactus pear stems, fruits and flowers in food,
medicine, cosmetic, and pharmaceutical
industries. An increasing demand would help
encourage farmers to increase their acreage
and thus also help to counterbalance erosion
and increasing atmospheric CO2 levels.
Although much research still needs to be done,
concerted actions of taxonomists, plant
breeders, agriculturists, food technologists,
nutritionists and pharmacologists will help
discover and understand the big potential of
the Opuntia cactus. The exact botanical
classification of the respective Opuntia spp.
under investigation and the growing location
and time of harvest are prerequisites for
analytical and pharmacological studies. The
exact plant parts used in the extraction and
processing conditions need to be accurately
documented to allow proper data evaluation.
5. References
Ahmad A., J. Davies, S. Randall & G.R.B.
Skinner,1996, Antiviral properties of extract
of Opuntia streptacantha. Antiviral Research
30, 75-85.
Aires V., S. Adote, A. Hichami, K. Moutairou, E. S.
E. Boustani & N. A. Khan, 2004. Modulation
of intracellular calcium concentrations and T
cell activation by prickly pear polyphenols.
Mol Cell Biochem 260, 103-110.
Butera D., L. Tesoriere, F. Di Gaudio, A. Bongiorno,
M. Allegra, A.M. Pintaudi, R. Kohen & M.A.
Livrea, 2002. Antioxidant activities of Sicilian
prickly pear (Opuntia ficus indica) fruit
extracts and reducing properties of its
betalains: Betanin and indicaxanthin. J Agric
Food Chem 50, 68956901.
Bwititi, P., Musabayane, C. T., Nhachi, C. F. B.,
2000. Effects of Opuntia megacantha on
blood glucose and kidney function in
streptozotocin
diabetic
rats.
J.
Ethnopharmacol., 69, 247 252.
Bwititi, P., Zamurawo, M., Mabhachi, G., Mashanga,
N., 1997. Toxic and hypericaemic effects of
Opuntia megacantha extract in rats.
Phytother. Res., 11, 389391.
Cancer statistics, 2004. American cancer society
Carbo N., P. Costelli, F.M. Baccino, F.J. LopezSoriano & J.M. Argiles, 1999. Resveratrol, a
natural product present in wine, decreases
tumour growth in a rat tumour model.
Biochem Biophys Res Commun 254, 739
14
743.
Cicero A.F.G., G. Derosa & A. Gaddi, 2004: What
do herbalists suggest to diabetic patients in
order to improve glycemic control?
Evaluation of scientific evidence and
potential risks. Acta Diabetologica 41, 91-98.
Clark W.D. & B.D. Parfitt, 1980. Flower flavonoids of
Opuntia series Opuntiae. Phytochem 19,
1856-1857.
Dok-Go H., K.H. Lee, H.J. Kim, E.H. Lee, J. Lee,
Y.S. Song, Y.-H. Lee, C. Jin, Y.S. Lee & J.
Cho, 2003. Neuroprotective effects of
antioxidative flavonoids, quercetin, (+)dihydroquercetin and quercetin 3-methyl
ether, isolated from Opuntia ficus-indica var.
saboten. Brain Res 965, 130-136.
Dominguez Lopez, A., 1995. Review: use of the
fruits and stems of the prickly pear cactus
(Opuntia spp.) into human food. Food
Science and Technology International, 1, 6574.
Enigbokan, M. A., Felder, T. B., Thompson, J. O.,
Kuti, J. O., Ekpenyong, K. I., 1996.
Hypoglycaemic effects of Opuntia ficus
indica Mill., Opuntia lindheimeri Engelm. and
Opuntia robusta Wendl. in streptozotocininduced diabetic rats. Phytother. Res.,
10,379382.
Ennouri M., E. Bourret, L. Mondolot & H. Attia,
2005. Fatty acid composition and rheological
behaviour of prickly pear seed oils. Food
Chem 93, 431-437.
Fernandez M.L., E.C. Lin, A. Trejo & D.J.
McNamara,1992. Prickly pear (Opuntia sp.)
pectin reverses low density lipoprotein
receptor suppression induced by a
hypercholesterolemic diet in guinea pigs. J
Nutr, 122, 2330 2340.
Fernandez, L.M., Lin, E.C.K., Trejo, A., McNamara,
D.J., 1994. Prockly pear (Opunita sp.) pectin
alters hepatic cholesterol metabolism without
affecting cholesterol absorption in Guinea
pigs fed a hypercholesterolemic diet. J.
Nutrition, 124, 817-824.
Feugang, J.M., Konarski, P., Zou, D., Stintzing,
F.C., and Zou, C. 2006. Nutritional and
medicinal use of cactus (Opuntia spp.)
cladodes and fruits. Frontiers in Bioscience
11, 2574-2589.
Flath, R.A., and J.M. Takahashi, 1978. Volatile
constituents of prickly pear (Opuntia ficus
indica Mill.), de Castilla variety. Journal of
Agriculture and Food Chemistry, 26, 835837.
Frati A., 1992. Medical implication of prickly pear
cactus. In: Proc. 3rd Annual Texas prickly
pear council. Eds: Felkar P, Moss LR, 2425
July, Kingsville, Texas, 29-34.
Galati E. M., M. R. Mondello, E. R. Lauriano, M. F.
Taviano, M. Galluzzo & N. Miceli, 2005.
Opuntia ficus indica (L.) Mill. Fruit Juice
Protects
Liver
from
Carbon
Tetrachlorideinduced Injury. Phytother Res
19, 796800.
Galati E.M., M.M. Tripodo, A. Trovato, A. d'Aquino &
15
16
17
Abstract
Numerous investigations relate free radicals
with the origin of serious diseases. A diet rich
in fruits and vegetables is associated to lower
incidences of cancer and heart illness. Such
beneficial properties of natural foods have
been assigned not only to their vitamin content
but also to the presence of antioxidants,
substances capable to scavenge free radicals.
Cactus fruits have been reported as excellent
sources of antioxidants. Several studies reveal
that the antioxidant capacity is due to its
vitamin C content as well as to the presence of
polyphenols and water-soluble pigments
named betalains. Fruits of cacti present
moderate free radical scavenging ability, and
values are similar to those of other season
fruits. When cactus fruits were minimally
processed or stored under refrigerated
conditions, no important decreases in TEAC
values were found neither significant vitamin
losses were detected. Extracts obtained from
cactus pear fruits where also used as additives
to prevent oxidation of fish oil and its
emulsions showing good thermal stability. In
vivo assays have demonstrated that cactus
fruit consumption improve the oxidative status
of healthy individuals. Betalains present in
cactus pear fruits have been reported to
increase the resistance to human LDL
oxidation. In addition, the regular intake of O.
robusta has been reported to reduce oxidative
injury in patients with hypercholesterolemia.
For these reasons, cactus fruits are excellent
sources of bioactive substances and so, it is
highly recommendable to incorporate them to a
normal diet as fresh fruits. Besides, they are
potentially utilizable in the elaboration of high
added value products such as cosmetics,
nutraceutics or dietary supplements.
Introduction
The
interest
on
natural
antioxidants
is
18
OXIDATIVE STRESS
In vitro measurements
Numerous
methodologies
have
been
developed to determine the antioxidant
capacity of synthetic and natural pure
compounds (Schlesier et al., 2002) extracts
made from fruits, herbs and vegetables as well
as drinks like wine, tea and juices (Pellegrini et
al., 2000). Some of them determine specifically
the free radical scavenging capacity or
antiradical ability of the antioxidants by
measuring radical consumption by effect of the
addition of them. One of the most frequently
chosen techniques by its simplicity is the
evaluation of synthetic radical disappearance
as the 1,1-diphenyl-2-pycrilhydrazyl radical
(DPPH)
or
the
2,2-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) radical cation
or ABTS+.. It measures the ability of pure
substances or crude extracts for trapping free
radicals by donating hydrogen atoms or
electrons producing, as a consequence, the
bleaching of the coloured radical solution and
the formation of less reactive species from the
antioxidant (Brand-Williams et al., 1995). The
reaction
is
monitored
by
UV-Visible
Spectrophotometry measuring the decrease in
19
absorbance
concentration.
associated
to
radical
20
21
1.5
1.3
1.1
1.02
Tradicional fruits
0.85
0.9
0.76
0.72
0.72
0.68
0.7
0.57 0.57
0.54
0.54
0.5
0.27
0.25
0.3
0.46
0.46
peach
tangerine
apricot
grapefruit
orange
pear
O. megacantha (white)
O.f-i (pinkish)
O. anacantha var.utk.
O.f-i (green)
O.spp.
O. megacantha (yellowish)
H. pomanensis
O.crassa
O.f-i (purple)
S. coryne
O.robusta
T. pasacana
C. forbesii
-0.1
O. sulphurea
0.1
0,6
0,5
0,4
Vit C content 0,3
mg/g
0,2
0,1
0
Weeks
Vitamin C
VCEAC
Figure 3. Evolution of Vitamin C content and Antioxidant Activity for refrigerated storage
of cactus pear fruits at 8C
Many cactus species produce edible fruits,
often consumed as fresh fruits as well as dried
food or in processed products as marmalades,
jams, ice-creams, juices or syrup. Antiradical
activity measurements of these fruit derivatives
show that, even after thermal treatments,
marmalades and jams elaborated from cactus
fruits retain this capacity. Opuntia ficus-indica
23
In vivo assays
Although in vitro determinations of the intrinsic
antioxidant activity of food are relevant, is
important to consider that the factors that
influence its efficiency in vivo are complex,
thus, the results obtained in vitro cannot easily
be extrapolated to in vivo systems.
The effectiveness of an antioxidant depends
on diverse factors as its bioavailability, the
action site, the type of reactive species with
which it will react and the possible synergistic
effects with other compounds present in the
food matrix. Among factors previously
mentioned, one of most important is the
bioavailability which mainly depends on the
antioxidant releasing from the food matrix, its
24
Description
Ref.
(Roberts and
Morrow, 2000;
Tesoriere et al.,
2004; Budinsky
et al., 2001)
Malondialdehyde
(MDA) in plasma
or serum
(Cadenas, 2001;
Halliwell and
Grootveld, 1987;
Janero, 1990)
Glutation redox
status in red bood
cells
(Martnez
Sarrasague et al.,
2006).
F2-isoprostanes
(8-epi-PGF2)
in plasma or urine
Low Density
Lipoprotein (LDL)
analysis in plasma
(Cadenas, 2001;
Tesoriere et al.,
2004).
the
original
molecule
undergoes
an
isomerization process probably due to body
high temperature (Kanner et al., 2001).
Betalains have also been detected in blood
after 3 h of ingestion of 500 g of fresh cactus
pulps. After this period, pigment concentration
was decreasing along time and almost
disappeared in 8 h (Tesoriere et al., 2005).
Betalain levels were also measured in human
body fluids showed after intake of cactus pear
fruits. Urine recovery after 12 hours was about
76 % for indicaxanthin and 3.7 % for betanin.
Pigment peak concentrations were reached in
plasma in 3 hours after ingestion for both of
them and completely disappeared in12 h after
ingestion (Tesoriere et al., 2004).
Betalains have been reported to increase the
resistance to human LDL oxidation (Tesoriere
et al., 2003; Zakharova and Petrova, 1998).
They are able to bind to low density
lipoproteins (LDL) and this union prevent their
oxidation. After fruit consumption, LDL
extracted from plasma in this conditions
indicated that 3 h after intake, indicaxanthin
was incorporated in 98 pmol/mg of protein
diminishing in 5 h and it complete disappeared
in 8 h. Betanin was detected only 3 h after fruit
consumption and lag time of LDL oxidation
25
Conclusions
Protective effects towards oxidation processes
exerted by fruits, juices and their processed
products have been widely demonstrated in
Acknowledgements
Authors are especially grateful to Prof.
Judith Ochoa and her team work from
INDEAS for fruit and plant material supply,
technical support and valuable discussions.
This work was supported by CONICET,
ANPCYT and CICYT-UNSE.
References
Ames, B. M.; Shigena, M. K.; Hagen, T. M., 1993,
Oxidants, antioxidants and the degenerative
diseases of aging. Proc. Natl. Acad. Sci.
USA 90, 7915-7922.
Aruoma, O. I., 2003, Methodological considerations
for characterizing potential antioxidant
actions of bioactive components in plant
foods. Mutation Research, 9, 523524.
Bazzano, L.A.; He, J.; Ogden, L.G.; Loria, C.M.;
Vupputuri; S., Myers, L.; Whelton, P.K. 2002,
Fruit and vegetable intake and risk of
cardiovascular disease in US adults: the first
national health and nutrition examination
survey epidemiologic follow-up study. Am. J.
Clin. Nutr. 76, 93-99.
Brand-Williams, W.; Cuvelier, M.E.; Berset, C.,
1995, Use of a free radical method to
evaluate antioxidant activity. Lebensm.-Wiss.
U.-Technol. 28, 25-30.
Budinsky, A.; Wolfram, R.; Oguogho, A.; Elthimiou,
Y.; Stamatopoulos, Y.; Sinzinger, H., 2001,
Regular ingestion of Opuntia robusta lowers
oxidation injury. Protaglandins, leucotrienes
and essential fatty acids. 55, 45-50.
Butera, D.; Tesoriere, L.; Di Gaudio, F.; Bongiorno,
A.; Allegra, M.; Pintaudi, A. M.; Kohen, R.;
Livrea, M. A., 2002, Antioxidant activities of
Sicilian prickly pear (Opuntia ficus-indica)
fruit extracts and reducing properties of its
betalains: betanin and indicaxanthin J. Agric.
Food Chem. 50, 6895-6901.
Cadenas, E.; Packer, L. 2001, Handbook of
Antioxidants. Marcel Dekker Inc. ISBN
0824705475.
Cai, Y.; Sun, M.; Corke, H., 2003, Antioxidant
26
27
28
Nadlergasse 1, A-1090 Vienna, Austria. Tel +43 1 4082633; Fax: +43 1 4081366; E-mail:
helmut.sinzinger@chello.at
Abstract
Used in traditional medicine since long,
Opuntia and compounds derived from it have
shown under experimental conditions as well
as in human that a variety of metabolic
parameters are beneficially affected. The
underlying responsible compound, however,
fruit or cactus itself, which type, the
preparation, the amount necessary per day are
not well defined. There is, however, certain
evidence that Opuntia consumption besides
improving glucose metabolism exerts multiple
beneficial actions on lipid metabolism. A
decrease in total- and LDL-cholesterol and a
decreased oxidation of lipoproteins is
consistently reported. Main mechanism of
action could be an increase in hepatic LDLbinding eventually associated with a decreased
absorption. Radical scavenging capacity may
decrease atherogenicity of lipoproteins.
Evidence based data from prospective
controlled should be collected in order to
assess the mechanism as well as the extent of
action of cactus.
In view of the ever growing (semi-)arid regions
and the expected climatic change the intake of
cactus as crop as well as dietary nutrient will
gain great relevance.
Key words: atherosclerosis hyperlipidemia
cactus LDL-receptor prickly pear radical
scavenger
Introduction
The role of natural products in medicine and
pharmacology is tremendously increasing in
these days. On the one hand, since long drugs
have been derived from various plants, on the
other hand, fruits and nutrients since long used
by local people for various health issues, are
gaining increasing attention and also
commercial interest. Among them: cacti.
Cactus can be considered as an important
crop in (semi-)arid regions and as a natural
source of fatty acids with a variety of beneficial
biological actions. The large number of
Available information
History
The
investigation
of
prehistoric
diets
(Danielson and Rainhard, 1998) indicates that
already in this period about 6000 years ago
prickly pear was widely consumed by the
29
Current use
Nopalitos (young sprouts) of Opuntia ficusindica are widely used in Mexico as
vegetables. The Mexicans have more than 100
recipes for the preparation of nopalitos. Also in
South Korea Opuntia ficus-indica is a
traditional health fruit which also has been
used to prevent various diseases for a long
time (Han et al., 2001; Oh and Lim, 2006).
Background
Elevated lipids and lipoproteins, in particular
after oxidative modification, have been shown
to be a key risk factor for the development of
atherosclerosis. A decrease in total cholesterol
of only 1% results in a 3-percent decreased
vascular risk. Thus, nutritional measures being
able to modulate total- and LDL-cholesterol are
of key relevance on a population base.
Experimental findings
In rats, an extract from Opuntia fuliginosa was
purified and shown to normalize blood glucose.
The low amount of substance administered (1
mg/kg body weight) excludes a relevant role of
dietary fiber (Trejo-Gonzalez et al., 1996). On
the other hand, prickly pear pectin was
demonstrated to improve lipid metabolism at
the hepatic receptor level (Fernandez et al.,
1992; Fernandez et al., 1994). In Wistar rats
(Li et al., 2005) Opuntia powder decreased
total cholesterol, LDL, triglycerides, and
malondialdehyde. The hypolipidemic action
observed was dose-dependent.
In guinea pigs, the addition of prickly pear
pectin
decreases
LDL-cholesterol
by
increasing the expression of hepatic apo-B,E
receptor (Fernandez et al., 1994). Fernandez
et al. (Fernandez et al., 1992) showed in
guinea pigs that after prickly pear pectin
administration hepatic apo-B,E receptor
expression (Bmax) was 60% increased and the
fractional catabolic rate by 190%.
In mice, Opuntia ficus-indica glycoprotein with
a molecular mass of about 90 kDa has been
shown to act as radical scavenger decreasing
thiobarbituric acid reactive substances and
increasing nitric oxide (Oh et al., 2006). It was
also claimed that via blocking lipid peroxidation
endothelial function may be improved by
increasing relative local NO availability.
Furthermore, this glycoprotein has been shown
to decrease blood total cholesterol, LDLcholesterol and triglycerides. We found
(unpublished data) that in rat aortic
prostaglandin I2-formation was significantly
Human data
In a randomized cross-over double-blind study
in 18 healthy volunteers receiving either 250 g
fresh pulp of Opuntia ficus-indica or 75 mg
vitamin C for 2 weeks daily there was a
comparable increase in vitamins E and C. 8epi-PGF2
(an
isoprostane)
and
malondialdehyde indicators of oxidative stress
dropped by about 30 and 75%, respectively
(Tresoriere et al., 2004). Opuntia streptacantha
was able to decrease the area under the
glucose
tolerance
curve
and
the
hyperglycaemic peak (Roman-Ramos et al.,
1995).
It remains to be elucidated, whether the
antiplatelet action reported is due to the
hypolipemic and/or the antioxidant effect or a
direct antiplatelet action (Wolfram et al., 2003).
In one study, the edible pulp of Opuntia
robusta given for 4 weeks at 250 g per day
showed a significant lowering of total (p < 0.01)
and LDL-cholesterol (p < 0.04), while HDL and
triglycerides remained unchanged. The
observed decrease in plasma, serum and
urinary
isoprostane
(IP)
8-epi-PGF2
(Budinsky etv al., 2001) indicated that
significant lowering of oxidation injury. There
was a significant correlation of IP with total
cholesterol and even more close to LDLcholesterol, and a negative one to HDL, the
vitamin content being unable to explain the
benefit. Using radioiodine labelled LDL shows
a significant upregulation of LDL binding sites
in men (16) determined via in-vivo gamma
camera imaging. The same design used in 10
patients with isolated heterozygous familial
hypercholesterolemia for 6 weeks showed a
significant (p < 0.0001) increase in LDL uptake
by the liver and an enhanced decay in
circulating blood. Total cholesterol was
lowered from a mean of 298.0 to 268.0 mg/dl
(p < 0.0001) and LDL-cholesterol from 210.5 to
176.4 mg/dl (p < 0.0001). Again, triglycerides
and HDL were unaffected.
In another paper of the same group, mainly
aimed to study the effect on glucose and lipid
metabolism in non-diabetics, a decrease of
total cholesterol by 12% LDL-cholesterol by
30
15% and apolipoprotein B (-9%), fibrinogen (11%), blood glucose (-11%), insulin (-11%)
and uric acid (-10%) was found. HDL, apo-A 1,
lipoprotein(a) and triglycerides, in contrast,
remained unchanged.
Capsules
Various preparations of nopal capsules are
available around the world. The application of
commercial dried nopal capsules in diabetics
versus placebo was not able to acutely
improve lipid or glucose metabolism despite
using the impractical dose of 30 capsules at a
single application (Frati Munari et al., 1992;
Frati Munari et al., 2004). In contrast, 500 g of
broiled stems of Opuntia streptacantha given
orally in 8 type II diabetics versus 6 healthy
volunteers induced a significant decrease in
glucose the diabetics versus the controls (Frati
Munari et al., 1992). No scientific data on lipid
metabolism of nopal capsules are available.
Meckes-Lozoya et al. (Meckes-Lozoya aand
Ibanez-Camacho, 1989) investigated the
hypoglycaemic
activity
of
Opuntia
streptacantha and did not find seasonal
variations concerning this effect.
Discussion
Already in 1989 Moore and coworkers (Moore,
1989) wrote that a benefit of prickly pear
consumption in diabetes is clinically verifiable.
Fernandez et al. (Fernandez et al., 1994) were
the first to claim that prickly pear pectin intake
decreases LDL-cholesterol by increasing the
hepatic apo-B,E receptor expression in guinea
pigs fed a hypercholesterolemic diet. The
absorption,
however,
was
unaffected.
Furthermore, Opuntia humifusa for example,
was reported to exert a direct scavenging
activity and inhibition of reactive species
generation resulting in a decreased expression
of cytokines (Cho et al., 2006).
Conclusion
Consistently, in animal experiments as well as
in men cactus products seem to improve lipid
metabolism (lowering total- and LDLcholesterol) and decreasing the extent of
lipoprotein oxidation. This review focuses on
lipid action of cactus (products) in experimental
animals and human. Unanimously, a beneficial
effect on total- and LDL-cholesterol is reported
which may be due to an increase in hepatic
LDL-binding and a decreased absorption.
Compositional changes and antioxidant action
on lipoproteins may add a further piece to the
antiatherosclerotic actions.
References
Budinsky A, Wolfram R, Oguogho A, Efthimiou Y,
Stamatopoulos Y, Sinzinger H., 2001.
Regular ingestion of Opuntia robusta
lowers oxidation injury. Prostagl Leukotr
Essential Fatty Acids, 65, 45-50.
Cho JY, Park SC, Kim TW, Kim KS, Song JC, Kim
SK, Lee HM, Sung HJ, Park HJ, Song YB,
Yoo ES, Lee Ch, Rhee MH., 2006. Radical
scavenging and anti-inflammatory activity
of extracts from Opuntia humifusa Raf. J
Pharm Pharmacol; 58: 113-119.
Danielson DR, Reinhard KJ., 1998. Human dental
microwear caused by calcium phytoliths in
prehistoric diet of the lower Pecos region,
Texas. Am J Phys Anthropol; 107, 297304.
Ennouri M, Fetoui H, Bourret E, Zeghal N, Attia H.
2005. Evaluation of some biological
parameters of Opuntia ficus-indica. 1.
Influence of a seed oil supplemented diet
on rats. Bioresour Technol, 26, 189-193.
Fernandez ML, Lin EC, Trejo A, McNamara DJ.,
1992. Prickly pear (Opuntia sp.) pectin
reverses low-density lipoprotein receptor
suppression
induced
by
a
hypercholesterolemic diet in guinea pigs. J
Nutr , 122, 2330-2340.
Fernandez ML, Lin EC, Trejo A, McNamara DJ.,
1994. Prickly pear (Opuntia sp.) pectin
alters
hepatic cholesterol metabolism
without affecting cholesterol absorption in
guinea pigs fed a hypercholesterolemic
diet. J Nutr; 124, 817-824.
Feugang JM, Konarksi P, Zou D, Stintzing FC, Zou
C., 2006. Nutritional and medicinal use of
Cactus pear (Opuntia spp.) cladodes and
fruits. Front Biosci, 11, 2574-2589.
Frati Munari AC, Xilotl Diaz N, Altamirano P, Ariza
R., Lopez Ledesma R., 1991. The effect of
two
sequential
doses
of
Opuntia
streptacantha upon glycemia. Arch Invest
Med Mex; 22, 333-336.
Frati Munari AC, Vera Lastra O, Ariza Andraca CR.,
1992. Evaluation of nopal capsules in
diabetes mellitus. Gaceta Med Mex, 128,
431-436.
Frati Munari AC, Fernndez-Harp JA, de la Riva H,
Ariza-Andraca R, del Carmeritorres M.
2004. Effect of nopal (Opuntia sp.) on
serum lipids, glycaemia and body weight.
Am J Clin Nutr; 80, 668-673.
Han YN, Choo Y, Lee YC, Moon YI, Kim SD, Choi
JW., 2001. Monoamine oxidase B inhibitors
from the fruits of Opuntia ficus-indica var.
saboten. Arch Pharm Res, 24, 51-54.
Li CY, Cheng XS, Cui MZ, Yan YG, 2005.
Regulative effects of Opuntia powder on
blood lipids in rats and its mechanism.
Zhongguo Thong Yao Za Zhi, 30, 694-696.
Meckes-Lozyoa M., Ibanez-Camacho R., 1989.
Hypoglucaemic
activity
in
Opuntia
31
32
Abstract
BIO SERAE Laboratories, French company
established in 1984, has been working since
the end of the 90s in the field of
nutraceuticals, to develop innovative &
original active ingredients. Obesity and
associated disorders being one of the major
issues of developed countries populations,
its R&D team focused its research on weight
management ingredients, and particularly on
dietary fibers. After comparative studies, they
chose Opuntia ficus-indica for its assets as a
lipophilic fiber, and developed NeOpuntia
This article will have a look on the research
works made on this cactus-based ingredient,
and will particularly focus on the latest
clinical study conducted syndrome X
related.
Introduction
NeOpuntia is a functional ingredient resulting
from a long step by step development process.
It is made from dehydrated leaves of cactus
Opuntia ficus-indica via a patented process
(PCT / FR02 / 01254).
NeOpuntia is an original complex of insoluble
and soluble dietary fibers which offers
interesting lipophilic properties. NeOpuntia
can indeed be involved to reduce fat absorption
into the body, with instant efficiency starting in
Scientific background
NeOpuntia is backed by strong scientific
33
Methods
The objective of this clinical study was to
evaluate the efficacy of NeOpuntia on blood
lipid parameters. It was conducted in France
between May and June 2006 on 68 females
with a BMI (Body Mass Index) between 25 and
40, and diagnosed with Metabolic Syndrome
as defined by the International Diabetes
Federation in 2005.
The study was monocentric, randomised,
placebo-controlled, in parallel double blind
format. Several lipid parameters were
measured: changes in HDL cholesterol, serum
triglycerides. At the end of the study the
participants were re-evaluated for metabolic
syndrome.
During the 6 week study, half of the females
consumed 1,6 g of NeOpuntia per meal and
the other half consumed a placebo. The
placebo and NeOpuntia were given in the form
of capsules. All along the study, volunteers had
to follow dietary advice in order to respect a
balanced diet (average caloric input of 2000
kcal, lipid input limitation) and to have minimum
physical activity (30 min per day). During this
study, several blood lipid parameters were
controlled (D0, D+14 et D+42), in particular the
evolution of HDL cholesterol, triglycerides and
metabolic syndrome diagnostic.
34
HDL, g/l
0.04
0.02
0
-0.047
-0.04
-0.06
NeOpuntia
40%
30%
39%
20%
Placebo
NeOpuntia
10%
8%
0%
Placebo
NeOpuntia
Conclusion
0.0217
-0.02
Results
Placebo
35
Abstract
The purpose our investigation concern the
evaluation of the effects of diets enriched with
cactus pear oil (CPO) or seeds (CPS) on
serum and liver lipid parameters compared to
those of adult rats submitted to standard diet
were tested. Male rats were divided into three
groups, the first group represented control
group, fed with standard diet, the second group
was fed with control diet supplemented with
CPO (2.5%, wt/wt) and the third group fed
control diet supplemented with CPS (33%,
wt/wt), for nine weeks. Feed intake and body
weight of rats were measured every two days.
Cholesterol, HDL and triglycerides levels were
determined by enzymatic methods. Liver and
serum lipid extracts were analysed for their
fatty acid composition for the three groups of
rats.
The tested diets decreased significantly the
atherogenic index compared to control diet,
whereas serum cholesterol level was only
reduced by the supplementation with CPO diet.
No variations in serum lipids were observed
among the groups, whereas liver lipids showed
slight variations. Accordingly, these results
indicated that the supplementation with CPO or
CPS could be effective in decreasing the
atherogenic risk factors in rats
Key words: Opuntia ficus-indica seeds; Fatty
acids profile; Liver; Serum; Cholesterol
Introduction
Cactus pear (Opuntia ficus-indica) grows
throughout Tunisia and the fruits are
consumed exclusively as fresh fruit. The seeds
are rich in oil, known for its content in
polyunsaturated fatty acids.
The seeds are made of two different tissues,
the endosperm and the pericarp in the relative
proportion of 1:9 respectively. Analysis of the
main constituents of prickly pear seeds
showed
a
significant
amount
of
polysaccharides, cellulose and hemicelluloses,
36
Results
Chemical composition of diets
Table 1 shows the chemical composition of fed
diets substituted with oil (CPO) or seed powder
(CPS) and the control diet. The CPS diet was
rich in lipids and fiber compared to control. The
CPO diet was also rich in lipids compared to
control.
Conclusion
Our studies demonstrated for the first time that
the enrichment of diet with CPS had a very
pronounced hypolipidemic effect as compared
to the CPO diet. It could significantly decrease
the levels of triglycerides in serum and total
37
Control
CPO
x
CPS
x
Lipids
3.37 0.17
5.90 0.10
5.87 0.36y
Protein
15.23 1.35x
14.68 0.52x
11.95 1.12x
Ash
4.63 0.09x
4.50 0.15x
3.53 0.11x
Cellulosic polysaccharides
5.12 1.06x
5.20 0.09x
23.41 1.25y
Starch
11.75 1.86x
11.63 1.50x
8.30 1.32x
Table 2. Initial body weight, body weight gain and feed intake in control, CPO and CPS groups
a
after 9 weeks of treatment .
Parameters
Control
CPO
x
CPS
x
123.8 0.7x
122.35 1.61
123.7 0.9
143.3 31.2x
141.8 22.6x
93.7 15.5y
20.7 4.6x
18.6 1.5y
25.2 3.7z
Table 3. Lipid parameters in serum of rats in CPO, CPS and control groups.
Parameters
Control
CPO
CPS
Cholesterol (g/l)
0.66 0.03x
0.43 0.06y
0.76 0.03y
0.36 0.03x
0.35 0.08x
0.48 0.03y
0.55 0.06x
0.81 0.20y
0.64 0.02z
Triglycerides (g/l)
0.717 0.079x
1.384 0.182y
0.333 0.075z
Athero. Index*
0.822 0.204x
0.505 0.205y
0.564 0.071y
38
Table 4. Fatty acid composition of prickly pear seed oil (g / 100 g of total fatty acid) (Ennouri et
al., 2005)
Fatty acid
Lauric C12:0
Myristic C14:0
Palmitic C16:0
9.320.19
Palmitoleic C16:1
1.420.01
Stearic C18:0
3.110.04
Oleic C18:1
16.770.47
Linoleic C18:2
70.290.60
12.430.12
MFA
18.190.47
PFAe
70.290.60
SFA
Table 5. Serum fatty acid composition of rats in CPO, CPS and control groups (g/100 g of total
a
fatty acid) .
Fatty acid
SFA
Control
32.0 5.75
CPO
x
CPS
x
32.440 0.878
34.891 0.236y
0.45 0.00x
0.409 0.002y
0.501 0.049z
21.2 0.31x
19.98 0.84y
20.3 1.02y
9.23 0.35x
11.04 0.01y
12.69 0.68z
18.67 0.7x
14.75 1.02y
16.67 2.46x
1.98 0.53x
0.7 0.50y
1.26 0.03y
15.81 0.47x
13.49 0.71a
13.1 2.41
52.01 1.36x
52.7 2.35x
47.6 2.25y
24.02 1.23x
22.71 1.43y
17.18 0.45z
0.80 0.04x
0.73 0.01y
0.95 0.18z
0.26 0.01x
0.92 0.36y
0.71 0.17y
23.771 0.86x
25.25 2.36x
25.72 2.99x
0.16 0.07x
0.16 0.07x
0.33 0.10x
0.71 0.02x
0.82 0.02y
0.77 0.03x
2.130 0.226x
1.109 0.516y
2.08 0.42z
1.613 0.027x
1.626 0.108x
1.36 0.05y
MUFA
PUFA
PUFA/SFA
39
Table 6. Liver fatty acids composition of rats in CPO, CPS and control groups (g/100 g of total
a
fatty acid) .
Fatty acid
Control
SFA
38.88 2.99
CPO
x
36.53 0.32
CPS
x
44.9 3.82z
0.26 0.06x
0.51 0.05y
0.23 0.04x
18.93 0.64x
19.44 0.18x
20.66 1.69x
18.0 2.64x
15.24 0.1y
22.90 2.09y
10.6 2.56x
15.0 0.46y
10.12 0.91x
0.77 0.14x
0.97 0.34x
0.72 0.07x
8.62 2.60x
13.6 0.34y
7.74 1.26x
50.1 0.46x
48.18 0.47y
46.43 2.43y
17.51 1.70x
17.33 0.48x
14.43 1.69y
0.48 0.07x
0.25 0.17y
0.28 0.01y
0.34 0.11x
0.58 0.02y
0.42 0.03x
23.42 1.04x
22.46 0.16x
24.0 2.15x
0.43 0.32x
0.06 0.05y
0.11 0.04x
1.29 0.1.21x
1.52 0.34x
1.15 1.06x
4.76 0.13x
4.11 0.54x
4.21 0.38x
1.29 0.08x
1.32 0.02x
1.04 0.14y
MUFA
PUFA
PUFA/SFA
30
25
Control
CPO
***
(7)
20
15
**
(7)
CPS
(7)
10
5
0
Serum
200
160
120
Control
**
(7)
CPO
CPS
(7)
***
(7)
80
40
0
liver
40
References
Barter,
41
Abstract
Extract of Cactus (Opuntia ficus-indica)
cladode was given alone or simultaneously
with a toxic chlorpyrifos dose to Balb/c mice
and was evaluated for its ability to restore
damages induced by this organophosphorus
insecticide. The experimental approach
consisted of six treatments of six mice: one
group have received chlorpyrifos at 10 mg/kg
(bw) combined with extract of cactus cladodes
100 mg/kg (bw). Another group have received
chlorpyrifos at 150 mg/kg (bw) combined with
extract of cactus cladodes 1.5 g/kg (bw). Two
groups have received chlorpyrifos alone at 10
mg/kg and 150 mg/kg (bw) respectively. The
rest of groups are control groups, (water, and 5
g/kg bw of extract of cactus cladodes). Twenty
four hours after treatment, Liver damage was
evaluated by the liver weight and the measure
of some enzymes in serum. Immunotoxicity
was estimated by the count of stem cells in the
bone marrow and the weight of thymus. An
increase in enzyme levels and liver weight, a
decrease of the stem cells number in the bone
marrow and the thymus weight were noticed in
only chlorpyrifos treated animals compared
with the control animals. For groups treated
with chlorpyrifos and cactus, there was a
recovery in all parameters, so this extract
contains active components that reduce
damages caused by this insecticide.
Key words: cactus, chlorpyrifos, liver, thymus,
bone marrow
1. Introduction
Natural product and health foods have recently
received a lot of attention both by health
professionals and the common population for
improving overall well-being, as well as in the
prevention of diseases. Cactus (Opuntia) has
been used for many years as a common
vegetable and as medicine by the native
Americans and Mexicans (Cornett 2000, Kay
3. Results
2.1. Chemicals
Chlorpyrifos CPF was purchased as an
agricultural product used in our country
(Duracid) from STEC society. Marker enzymes
of liver damage, alkaline phosphatase (AkP),
alanine
aminotransferase
(ALAT)
and
aspartate aminotransferase (ASAT) were
measured by standard kits provided by BioMagreb.
2.2. Animals
In this study, 36 male SWISS mices (SEXUAL,
St Doulchard, France) were used. Their weight
was about 25g and they were 4 to 5 weeks old.
Animals were housed in plastic cages, fed ad
libitum and allowed to adjust to the new
environment for 2 weeks time before starting
the experiment. Then, they were divided into 6
treatment groups, each of six mice as follow:
1. Mice given granulated chow and
drinking water ad libitum= control group
(Cont. G1)
2. Mice given CPF at 10mg/kg (bw) (G2)
3. Mice given 10mg/kg (b.w) CPF with
100mg/kg (b.w) cactus (G3)
4. Mice given 150 mg/kg (b.w) CPF (G4)
5. Mice given 150 mg/kg (b.w) CPF with
1.5 g/kg cactus (G5)
6. Mice given 5g/kg cactus (G6)
Group 6 was chosen to test the toxicity of
cactus through lethality of mice parameter.
Both CPF and cactus were dissolved in water
Concerning
lethality
essays,
LC50
of
chlorpyrifos was confirmed, it is about
150mg/kg bw. No death occurred in groups
treated with cactus alone or cactus with CPF
(groups 5 and 6) indicating that this natural
plant is not toxic (Viala 1980). As shown in
table 1, results of serum biochemical analysis
showed an increase of the biochemical
parameters of interest in groups treated only
with CPF (groups 2 and 4) compared to the
control group (group 1), which indicates a liver
damage. However, treatment by cactus
restores this increase in groups treated by CPF
and cactus (groups 3 and 5) in values similar
to normal. The relative liver weight increases in
CPF treated groups (groups 2 and 4)
compared to the control (group 1). This trend
was not seen in groups 3 and 5 (table 1),
which can confirm the CPF toxicity (Mahaboob
et al. 2005) and the protective role of cactus.
The immunotoxicity was investigated through
thymus and the bone marrow. The weight of
thymus diminished in group 2, in group 4, this
organ was totally deleted. However, it was
obvious that the thymus atrophy was
minimized in groups 3 and 5 (figure 1).
For the bone marrow, action of this insecticide
was noticed essentially in the group 4: the
number of stem cells of the group 4 animals
femur decreased compared with none treated.
This decrease is less important when cactus is
administrated (group 5) (figure 2). Thus, these
results confirm immunotoxicity of CPF (Blakely
et al. 1999) and allow us to say that cactus
stem extract is also reliable counter harmful
action of CPF.
43
Thymus
relative
weight in %
0,35
0,3
0,25
0,2
0,15
0,1
0,05
0
Groupe 1
Groupe 2
Groupe 3
Groupe 4
Groupe 5
Groups
Groupe 1
Groupe 4
Groupe 5
Groups
4. Discussion
In the present study, both lethal LC50 and the
th
sub-lethal (1/10 of LC50: almost 10mg/kg)
concentrations were studied. For the LC50
treatment (group 4), mortality was observed
and touched half of animals, so we confirm
results found by other studies (McCollister et
al. 1995) With sub-lethal concentration, no
mortality was observed during the experiment
tenure. However, an increase in liver specific
enzymes was noticed. Elevation in these
44
5. References
Amacher D.E, Schomaker S.J and Burkhardt J.E.
The Relationship Among Microsomal,
enzyme Induction, Liver Weight and
Histological Change in Rat Toxicology
Studies. Food and Chemical Toxicology. 36
9-10 (1998) 831-839
Blakely B.R, Yole M.J, Brousseau P, Boermans H,
45
Table 1: Effect of cactus stem extract and its protective role against hepatotoxicity in male
SWISS mice treated at 10mg/kg (b.w) and 150 mg/kg (b.w) with CPF
CPF
CPF + cactus
Control
Cactus
(G1)
1.5g/kg
10mg/kg
150mg/kg
10mg/kg CPF
150mg/kg
(G6)
(G2)
(G4)
+ 100 mg/kg
CPF +1.5
cactus (G3)
g/kg cactus
(G5)
ALAT (UI/ml)
13713
13618
21017*
34917*
16013
23010*
12826
1255
23653*
47593*
23653
39143*
LDH (UI/l)
1644384
1703225
3156161*
3993123*
2293407
311640*
PAL (UI/l)
9614
1036
20649*
28328*
12110
19921*
ASAT (UI/ml)
46
47
ROS
e stress
Oxidativ
Bax
Membrane
damage
Mitochondria
Oxidative DNA
Damage
Nucleus DNA
Fragmentation
Cell cycle
arrest
Cytochrome-c
Caspase-9,10
Caspase 3
Necrosis
Apoptosis
48
49
sanguigna
RED FRUIT
surfarina
8 % OF PRODUCTION
CH2OH
O
H
O
H
OH H
OH
H
H
OH HO
YELLOW FRUIT
90% OF PRODUCTION
+
N
2% OF PRODUCTION
+
N
COOH
COOH
HOOC
Betanin
N
H
COOH
HOOC
N
H
COOH
Indicaxanthin
50
Introduction
1. Methodology
The sources of information presented in this
paper are:
-
2. Results
2.1. Documented data
Cactus was introduced into morocco by the
XVIth century; so most documents referring to
this specie are relatively recent in comparison
with many other medicinal plants, as Aloe vera
for instance, which, by the way, is called
Assabr in Arabic, a word similar to Assobar,
the cactus Arabic name. This precision is
important because Assobar is used sometimes
to name the two species. Consequently, some
authors make confusion between virtues of
these succulent plants.
51
Penduletin, Rutin,..).
Authors
Zahouili (1997)
Pads
Bellakhdar (1997)
Flowers
Boujenah (2005)
Seeds
Protein: 11.8 %
Seed oil
Fatty acids (%): C16:0 (11.9); C16:1 (0.6); C18:0 (3.7); C18:1
(21.3); C18:2 (61.1); C18:3 (0.3); C20:0 (0.3); C20:1 (0.2)
Personal observation
2.1.1. Fruit
Fresh pear is used to stop diarrhoeas and
intestinal colic (Boulous, 1983; Sijelmassi,
1996; Bellakhdar, 1997) astringent (Boulous,
1983) and anti-diabetic (Eddouks et al., 2004).
There is no detail about how a sugar-rich fruit
might be useful to prevent diabetes, but it
seems that this ability is due to the pulp fiber.
Some side-effects are however reported, they
are related to fig seeds which might cause
digestive disturbances such as constipation.
2.1.2. Flowers
Dried flower is mentioned among the
Moroccan exported products. It is the part of
Under 20 20 to 40
3 (12%)
Over 40
6 (24%) 11 (44%)
Equal
5 (20%)
Total
25 (100%)
53
Low cost
12.90
Sweet taste
15
48.39
Treat
or/and
Prevent
Digestive
troubles
19.35
Diabetes
16.13
Cholesterol
03.23
31
100
Total
54
5. References
- Diffusion
proprieties:
of
Medias:
internet
TV
programs,
about
cactus
newspapers,
55
56
Abstract
Opuntia ficus indica (prickly pear cactus) is a
highly productive plant?and it is cultivated as a
food source for both human and animals. Also
cactus has important ecological roles in
combating land degradation, and it is adopted
and integrated in the agricultural production
system of arid and semi arid zones. This work
aims at developing an environmentally friendly
corrosion inhibitors where the aqueous extract
of Opuntia stem is used. The inhibitive action
of the Opuntia extract, toward corrosion of iron
in 3% sodium chloride is tested using
polarisation technique and electrochemical
impedance
measurement.
The
extract
examined performed important inhibitor
efficiency (82-86%).
Keywords: iron, corrosion inhibition, Opuntia
extract
Introduction
Corrosion is defined as the destruction or
deterioration of metals by chemical means in
environments to which they are exposed
(Fontana, 1987). Corrosion causes enormous
damages and economic losses. Corrosion
inhibitors reduce or prevent these reactions,
they are adsorbed on the metal surface, and
act by forming a barrier to oxygen diffusion and
reducing the reaction with moisture. This
inhibition effect may take place with adsorption
phenomenon on metal surface and ion
complex formation. Some of the inhibitors
facilitate the formation of a passivating film on
the metal surface (Quraishi et al., 2002).
Many of the available corrosion inhibitors are
highly toxic, pollute environment, and some of
them are suspected as cancer causing agents.
All these facts call for the research on cheap
and
environmentally
friendly
corrosion
inhibitors.
There are only few trials investigating the use
of natural products as corrosion inhibitors
(Awad, 1985; Bouyanzer and Hammouti,
2004). In this respect the corrosion inhibition
57
Potentiodynamic Measurements
Figure 1 represents (a) anodic and (b) cathodic
polarization curves of iron in 3% NaCl solution
containing different concentration of Opuntia
extract. The curves were plotted after
immersion for 30 min in solution at the
corrosion potential and under constant
agitation.
0,1
1E-3
0,01
1E-5
1E-6
1E-7
-0,80
I(A/Cm2)
I(A/Cm2)
1E-4
(0% inh)
(6% inh)
(8% inh)
(12% inh)
(16% inh)
-0,75
-0,70
1E-3
(0%inh)
(6%inh)
(8%inh)
(12%inh)
(16%inh)
1E-4
1E-5
1E-6
-0,65
-0,60
-0,55
-0,50
-0,60
-0,45
-0,55
-0,50
-0,45
-0,40
-0,35
-0,30
-0,25
-0,20
-0,15
E(V/Ag/AgCl)
E(V/Ag/AgCl)
Figure 1. Polarization curves (a/left) anodic, (b/right) cathodic, of iron in 3% NaCl containing
different concentration of Opuntia extract.
Table 1. Electrochemical parameters of iron corrosion in free and inhibited 3% NaCl solutions
NaCl %
-Ecorr
mV /Ag-AgCl
Icorr
A/Cm2
-bc
mV/dcade
566
176
42
507
72.4
76
59
538
49
79
72
12
509
40.7
79
77
16
551
31.4
70
82
E
%
58
Electrochemical Impedance
Measurements
Impedance diagrams obtained for the
frequency range 10 mHz-65 KHz at Ecorr for
iron in 3% NaCl, are shown in figure 2.
Figure 2 (a) represents impedance diagram
shape obtained for the iron in 3% sodium
chloride interface in the absence of the
inhibitor.
Two capacitive loops appear. In the context of
detailed study published elsewhere (Bonnel et
al., 1983), the high frequency (HF) capacitive
loop is attributed to a charge transfer process,
while that observed at low frequency (LF) is
interpreted in terms of the mass transport
which is occurring at the same time in the
liquid and solid phase through the layer of
corrosion products formed (Srhiri, 1985).
extract:
three
Reference surface
Iron surface in 3%
NaCl after 6 h of
immersion
3% NaCl
containing 6% of
inhibitor after 6 h
of immersion
3% NaCl
containing 12% of
inhibitor after 6 h
of immersion
3% NaCl
containing 16% of
inhibitor after 6h
of immersion
59
Impedance diagram
100
NaCl 3%
90
80
-Im(ohm cm )
70
60
50
40
30
0.1Hz
1 Hz
20
0.01Hz
10
0
0
10
20
30
40
50
60
70
80
Re(ohm cm )
Figure 2 (a)
Figure 2 (b)
200
8% inh
180
160
-Im(ohm cm )
140
120
100
0.01Hz
80
60
0.1Hz
40
1Hz
20
0
0
20
40
60
80
100
120
140
160
180
200
220
240
Re(ohm cm2)
Figure 2 (c )
Figure 2 (d)
240
16% inh
220
200
160
-Im(ohm cm )
180
140
120
0.01Hz
100
1Hz
80
0.1Hz
10Hz
60
40
20
0
0
20 40 60 80 100 120 140 160 180 200 220 240 260 280 300 320 340 360
2
Re(ohm cm )
Figure 2 (e)
Conclusion
The Opuntia extract is a good inhibitor for
corrosion of iron in 3% chloride sodium
solution. The results show an important
inhibition efficiency about 86%. The inhibitive
action increases with increasing extract
concentration. This action is probably
performed via adsorption of the extracts
compounds on iron surface.
References
Fontana,
M.G.,
1987.
Corrosion
Engineering,
60
Abstract collection:31
Mc Garvie, D. et Parolis, H. ; 1979. Carbohydrate
Research 69(1) : 171-179.
Mc Garvie, D. et Parolis, H. ; 1981. Carbohydrate
Research 88(2) : 305-314.
Trachtenberg,
S.
et
Mayer ,
A. ;
1981.
Phytochemistry, 20(12) :2665-2668 .
Srhiri A., Derbali, Y. and Picaud, T.; 1995. Corrosion
Science, 51(10) :788-796
61
Network News
The most salient event of the year was the
organization of the The VI International Congress on
Cactus Pear and Cochineal and the VI General
Meeting of the International Committee of the
International Technical Cooperation Network on
Cactus (FAO-CACTUSNET) held in Joo Pessoa
Brazil, from October 22nd to 26th, 2007.
Five partners took part in the organization of the
congress: Federao da Agricultura e Pecuria da
Paraba (FAEPA), Universidade Federal da Paraba
(UFPB), Food and Agriculture Organization of the
United Nations (FAO), Technical Cooperation
Network on Cactus Pear (CACTUSNET), and
International Society for Horticultural Science
(ISHS).
The event gathered 533 participants among
producers, students and national and international
researchers. The Congress also counted with the
presence of national and international institutions of
great importance in the area, such as the INSA,
ICARDA and FAO.
The Scientific Program, under the congress theme Production of Cactus Pear and other cactus in
the different ecosystems in the world: challenges and technological progress, was presented in 10
Sessions, with 34 lectures and more than 230 papers presented as poster.
All abstracts were published in a cd-rom that was distributed to all participants of the congress.The
program was enriched by the participation of invited speakers of great importance and large
experience in the area.
A field visit to the cities of Juazeirinho and Tapero happened on the last day of the event (October,
26th). More than 200 people participated to the visit and were able to see by themselves all the
potential, advantages and threats of the cactus pear crop.
The Exhibition area was also very important for the event. It was an opportunity for 36 exhibitors
(companies, institutions, researchers, artisans) from different places of Paraba and region, to show
their work and products, always valuing the state and countries culture.
We believe that the objectives of the Congress were reached with success. The access to the most
recent advances in the area and the exchange of scientific results were promoted, many partnerships
were made, as well as future projects to the development of the culture of Cactus in Brazil.
The VI General Meeting of the FAO-CACTUSNET was the occasion to discuss the venue of the VIIth
International Cactus Congress, and to review the composition of the International Committee of the
network. Three countries were candidates to host the next congress, namely Italy, India, and Morocco.
After a long discussion, it was decided that the VII international Congress on Cactus and the VII
General Meeting of Cactus network will be held in India. The review of the international committee of
the network has led to the following modifications: (i) deletion of the working group on socioeconomics and the introduction of a new group dealing with medicinal uses of cactus that will be
leaded by Dra Monica Nazareno from the University of Santiago del Estero, Argentina; (ii) the
replacement of the former coordinator of the working group on pitayas and pitahays by Dr. Noemi
Judith Tel-Zur from Ben Gurion University of the Negev, Israel. The other important decisions of the
network are related to the reinforcement of network activities and to the need to formalize countries
focal points in order to rely more on them for network activities. Participants welcomed and
recommended for both FAO and ICARDA to join their efforts to improve the network efficiency and to
ensure its sustainability. Thus, in the future the network will be FAO-ICARDA Cactusnet. On the
other hand intitiative will be taken by FAO and the network to identify and formalize countries focal
points. Research and development institutions will be approached to have countries suggestions.
62
Group picture of participants to the VIth International Congress on Cactus, Joo Pessoa Brazil, October 22nd to 26th, 2007
63
Welcome to Dr Noemi Judith Tel-Zur, New coordinator of Pitayas and Pitahayas Working Group
Born on 16 February 1965 in Buenos Aires, Argentina, Dr Noemi Tel-Zur
immigrated to Israel at the age of 20. She graduated in 1988 from The Hebrew
University of Jerusalem, faculty of Agriculture and completed her M.Sc. at the
same university in 1992. In 2001, Noemi obtained her Ph.D. from Ben-Gurion
University of the Negev (BGU), Department of Life Sciences on Genetic
relationships between vine-cacti of the genera Hylocereus and Selenicereus.
Her first post-doc fellowship was supported by UCLA-BGU Program of Academic
Cooperation. Her second post-doc period was spent at the Department of
Horticulture, University of Wisconsin, Madison. Currently, Noemi is a lecturer at
The Albert Katz Department of Dryland Biotechnologies, The Blaustein Institutes
for Desert Research, Sede Boqer Campus, BGU.
Her research areas are Plant Cytogenetics and Plant Reproduction with special focus in exotic fruit crops.
Noemi is the recipient of and number of awards: the Pasternak Prize for Agricultural Research (2006), award
for Ph.D. (Future Leadership Program for Fruit Crops in Israel, 1998-2000), and Molcho Center Scholarships
(1997-1998). She is author of many publications in prestigious international journals.
64
New subscribers
CACTUSNET NEWSLETTER
FAO-ICARDA INTERNATIONAL TECHNICAL COOPERATION
NETWORK ON CACTUS
Biodata sheet
Dear subscribers
We are updating our mailing list. Please fill out this page and return it by fax or email so that
you continue receiving the news, and those we have accurately recorded your name and
address. If you have any colleagues interested in receiving CACTUSNET NEWSLETTER,
pass on a copy or send in their address to:
CACTUSNET NEWSLETTER
C/O Ali Nefzaoui, General Coordinator
International Center for Agricultural Research in the Dry Areas (ICARDA)
Rue des Oliviers, 1. El Menzah V. 2037 Tunis, Tunisia
Phone: (++216)71752134/71752099
Fax : (++216)71753170
Cellular : (++216)22347149
Email: ali.nefzaoui@icarda.org.tn; a.nefzaoui@cgiar.org
Fax
Please include brief description of your recent current research related to cactus. We also
welcome comments, stories, abstracts of your work, job or meeting announcements,
requests, etc.
65
Technical Secretary
Regional Coordinators
North America
Dr. Jesus Fuentes, Mexico
jesus_fuentes@hotmail.com
South America
Dr. Judith Ochoa, Argentina
judith@unse.edu.ar
Mediterranean Basin
Dr. Enza Chessa, Italy
Chessa_i@uniss.it
Sub-Saharan Africa
Dr. Johan Potgieter, South Africa
jpot@mweb.co.za, potgieterjp@agricho.norprov.gov.za
West Asia
Dr. Gurbachan Singh, India
gsingh@satyam.net.in
Cochineal
Dr. Liberato Portillo, Mexico
lportill@MAIZ.CUCBA.UDG.MX
Fruit production
Dr. Giovanni Nieddu, Italy
gnieddu@uniss.it
Biology
Dr. Francisco Campos, Brazil.
bioplant@ufc.br
Nopalitos
Dr. Ricardo Valdez, Mexico.
vacrida@hotmail.com
Medicinal uses
Dra. Monica Nazareno, Argentina.
manazar2004@yahoo.com
66