chapter-iii - shodhganga : a reservoir of indian theses...
TRANSCRIPT
Introduction to plant
and its review of
literature
Chapter-III
"The real act of discovering is not in finding in new lands, but in seeing with new eyes."
Chapter-3 Review of Literature
Bhagwant University PhD Thesis 41
3. REVIEW OF LITERATURE
3.1 Syzygium cumini Linn.
Jamun is a very common, large evergreen beautiful tree of Indian subcontinent. The
scientific name of Jamun is Eugenia jambolana Lam. or Syzygium cumini Linn. and it
belongs to the family myrtaceae. Common names are Java plum, Black plum, Jambul
and Indian Blackberry1,2
.
A. Common names from world wide
Brazil - Azeitona
Pakistan - Jaman
West Indies - Jambol
Nepal - Java plum
Thailand - Lukwa
Japan - Madan
Madagascar - Rotra
B. Other names
Hindi - Jaman, Jam
Bengali - Jam, Kalajam
Gujarati - Jambu, JamLi
Telugu - Jambuvu
Marathi - Jaman, Jambul
C. Taxonomic classification3
Kingdom: Plantae
Division : Magnoliophyta
Class : Magnoliopsida
Order : Myrtales
Family : Myrtaceae
Genus : Syzygium
Species : Cumini
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Figure 3.1: Jamun leaves with fruit
D. Occurrence and distribution
The original home of jamun is India, distributed throughout India, in forest up
to 1800m usually along the bank and moist localities, also cultivated as shade trees
along road sides. It is widely cultivated in Haryana as well as the rest of the Indo-
Gangetic plains on a large scale. Its habitat starts from Myanmar and extends up to
Afghanistan.
It is also found in Thailand, Philippines, Madagascar and some other country.
The plant has been successfully introduced into many other tropical countries such as
the West Indies, West Africa and some subtropical regions including Florida,
California, Algeria and Israel4. It was cultivated in England by Miller in 1768
5.
E. Description6,7
Plant introduction
Botanical name : Syzygium cumini Linn or Eugenia jambolana Lam
Family : Myrtaceae
Synonym : Black plum, Java plum, Jaman, Jambolan.
Distribution : Native of India and Indonesia
Botanical characters
Habitat : Tropical Asia (mainly India and Indonesia)
Leaves : Leaves are opposite simple, glossy, smooth, somewhat leathery,
coriaceous, shiny, entire, oval, Elliptic-oblong, and lanceolate, 7.5 to
15 cm long
Bark : Bark is scaly gray or brown and smooth.
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Flowers: Are greenish white, tetramerous, in 3- flowered cymes, arranged in
broad trichotomous panicles
Fruit : Berry oblong or subglobose, purple or black, succulent, Smooth when
ripe
Seed : cream colored, coriaceous covering, smooth, oval or roundish.
F. Chemical constituents
Leaves of E. jambolana contain isolated 15 polyphenols and two acetylated flavonol
glycosides identified as 3-O- (4”-Oacetyl)- alpha-L-rhamnopyranosides of mearnsetin
(myricetin 4’-methyl ether) and myricetin 3-O- (4”-Oacetyl-2”-O-galloyl)–alpha-L-
rhamnopyranoside from8 and subsequently Timbola et al
9 isolated quercetin
(0.0085%), myricetin (0.023%), myricitrin (0.009%), and a flavonol glycosides
myricetin 3-O-(4”-acetyl)-α- L-rhamnopyranosides (0.059%) from its leaves.
Seeds of E. jambolana contain glycosides, a trace of pale yellow essential oil, fat,
resin, albumin, chlorophyll2, an alkaloid- jambosine
3, gallic acid, ellagic acid,
corilagin and related tannin,3,6-hexahydroxydiphenoylglucose and its isomer 4,6-
hexahydroxydiphenoylglucose, 1-galloylglucose, 3-galloylglucose, quercetin10
and
elements such as zinc, chromium, vanadium, potassium and sodium11
.Unsaponifiable
matter of seed fat contains β-sitoterol12
.
Fruits of E. jambolana have been reported with raffinose, glucose, fructose13
, citric
acid14
, mallic acid and gallic acid15
. The sourness of fruits may be due to presence of
gallic acid. Venkateswarla (1952) reported that the color of the fruits might be due to
the presence of anthocyanins namely delphinidin-3-gentiobioside and malvidin-3-
laminaribioside along with petunidin-3-gentiobioside16,17
. Betulinic acid, friedelin,
friedelan-3-α-ol and β-sitosterol from petroleum ether extract and kaempferol and its
3-o-glycoside, β-sitosterol-Dglucoside, sucrose, gallic acid, ellagic acid, gallotannin
and ellagitannin from alcohol extract18
and myricetine in small amount have been
reported from stem bark of E. jambolana19
.
Bark
Tannins like gallic and ellagic acid and derivatives including 3-3 di-o-methyl ellagic
acid.
Steroids: sterols including -sitosterol, -sitosterol glucoside.
Triterpenes: betulinic acid, friedelin, friedelan-3--ole, epi-triedelanol eugenin.
Flavanoids: including myricetin, kaempferol, quercetin, astragalin15
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Roots of syzygium cumini contain myricetin 3-o-glucoside and the new flavanoid
myricetin 3-o-robinoside17
.
G. Traditional uses
Most of the plant parts of E. jambolana are used in traditional system of
medicine in India. According to Ayurveda, its bark is acrid, sweet, digestive, and
astringent to the bowels, anthelmintic and in good for sore, throat, bronchitis, asthma,
thirst, biliousness, dysentery, blood impurities and to cure ulcers1. Its bark is used as
decoction in case of chronic diarrhoea and dysentery. It is also acts as a gargle in sore
throat, spongy gums etc. and when externally used, bark shows good wound healing
properties2,3
.
The fruits are acrid and sweet, cooling, dry and astringent to bowels. They
increase Vata” and remove bad smell from the mouth. The riped fruits are considered
to be the good diet in convalescence diarrohea and dysentery. Syrup or vinegar
prepared from them is also useful in spleen enlargement and it is effective in chronic
diarrhoea2. As per Unani system of medicine they acts as liver tonic, enriches blood,
strengthens teeth and gums and forms good lotion for removing ringworm infection of
the head.
The seeds are sweet, astringent to bowels and good for diabetes. The sprouts
are refrigerant, carminatives & astringent to bowels. Powdered seeds are used as a
remedy in diabetes and in metrorrhagia1,2,3
. Seed powdered in combination with
mango kernels were administered with curd to overcome the problem of diarrohea and
dysentery, enlargement of spleen and as diuretic in scanty20
.
REVIEW OF LITERATURE
Kirtikar and Basu1 have suggested that according to Ayurveda, jamun bark is
acrid, sweet, digestive, astringent to the bowels, anthelmintic and in good for sore,
throat, bronchitis, asthma, thirst, biliousness, dysentery, blood impurities and to cure
ulcers. Leaves are acts as liver tonic, enrich blood, strengthen teeth and gums and
forms good lotion for removing ringworm infection of the head.
Priyavtra Sharma and Mehta3 described fruits are acrid and sweet, cooling, dry
and astringent to bowels. They increase “Vata” and remove bad smell from the
mouth. As per Unani system of medicine they acts as liver tonic, enriches blood,
strengthens teeth and gums and forms good lotion for removing ringworm infection of
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the head. The vinegar prepared from the fruit is tonic, astringent, carminative and
useful in spleen diseases. The seeds are sweet, astringent to bowels and good for
diabetes. The sprouts are refrigerant, carminatives & astringent to bowels.
Nadkarni2 has investigated powdered seeds are used as a remedy in diabetes
and in metrorrhagia. Seed powdered in combination with mango kernels were
administered with curd to overcome the problem of diarrohea and dysentery,
enlargement of spleen and as diuretic in scanty or suppressed urine and oil of leaves is
useful in skin diseases.
Chopra et al9 has determined that the bark is used in diarrhoea and dysentery,
astringent to bowels, carminative, diuretic, digestive, febrifuge, constipating,
anthelmintic, good for bronchitis, asthama, thrist, fever, gastropathy, dermatopathy, to
treat sore throat, diabetes and blood impurities. Seeds are hypoglycemic and allay
thrist in diabetes. It has astringent and carminative properties, diuretic, stops urinary
discharge (yunani), powdered seeds are mainly used in diabetes and reduce the
quantity of sugar in urine.
Prajapati et al8 has suggested that seeds are hypoglycaemic and allays thrist in
diabetes. It has astringent and carminative properties, diuretic, stops urinary discharge
(yunani), powdered seeds are mainly used in diabetes and reduce the quantity of sugar
in urine, fruits and seeds are tonic, used in diabetes, diarrhoea, splenopathy,
ringworm, pharyngitis, The roots are reported to be antidiuretic in nature. Fruits juice
used as carminative, diuretic and stomachic, als used in diarrhoea and spleen
enlargement.
Parrotta9 has found that leaves are antidysentric, antibacterial. Ash of leaves is
used for strengthing the teeth and gums.seeds are hypoglycaemic and allays thrist in
diabetes. It has astringent and carminative properties, diuretic, stops urinary discharge
(Unani), powdered seeds are mainly used in diabetes and reduce the quantity of sugar
in urine, fruits and seeds are tonic, the bark is used in diabetes, diarrhoea,
splenopathy, ringworm, pharyngitis. Diabetes and blood impurities, used for making
mouth wash and gargles, also acts as antibacterial.
Elizabeth and Williamson7 has evaluated the bark is acrid and sweet,
decoction is used in diarrhoea and dysentery, astringent to bowels, carminative,
diuretic, digestive, febrifuge, constipating, anthelmintic, good for bronchitis, asthama,
thrist, fever, gastropathy, dermatopathy, to treat sore throat, diabetes and blood
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impurities, used for making mouth washes and gargles, also acts as antibacterial.
Leaves are antidysentric, antibacterial. Ash of leaves is used for strengthing the teeth
and gums. Tender leaves for vomiting. Fruits and seeds are tonic, used in diabetes,
diarrhoea, splenopathy, ringworm, pharyngitis.
Chopra9 has found that seeds are hypoglycaemic and allays thrist in diabetes.
It has astringent and carminative properties, diuretic, stops urinary discharge (Unani),
powdered seeds are mainly used in diabetes and reduce the quantity of sugar in urine,
fruits and seeds are tonic, used in diabetes, diarrhoea, splenopathy, ringworm.
Longman21
has described, the bark is acrid and sweet, decoction is used in
diarrhoea and dysentery, astringent to bowels, carminative, diuretic, digestive,
febrifuge, constipating, anthelmintic, good for bronchitis, asthama, thrist, fever,
gastropathy, dermatopathy, to treat sore throat, diabetes and blood impurities, Leaves
are antidysentric, antibacterial. Ash of leaves is used for strengthing the teeth and
gums. Tender leaves for vomiting. The seeds and fruits are used in the treatment of
diabetes, pharyngitis, splenopathy.
Tirtha22
has written in the text that the bark is used in diarrhoea and
dysentery, astringent to bowels, carminative, diuretic, digestive, febrifuge,
constipating, anthelmintic, good for bronchitis, asthama, thrist, fever, gastropathy,
dermatopathy, to treat sore throat, diabetes and blood impurities. Seeds are
hypoglycaemic and allay thrist in diabetes discharge (Unani), powdered seeds are
mainly used in diabetes and reduce the quantity of sugar in urine.
Scartezzini and Speroni23
have discussed that seeds are hypoglycaemic and
allays thrist in diabetes. It has astringent and carminative properties, diuretic, stops
urinary discharge (yunani), powdered seeds are mainly used in diabetes and reduce
the quantity of sugar in urine, fruits and seeds are tonic, used in diabetes, diarrhoea,
splenopathy, ringworm, pharyngitis.
Trease and Evans24
have shown that the seeds are astringent, diuretic and stops
urinary discharge. Powdered seeds are used as a remedy in diabetes and in
metrorrhagia. Ash of leaves is used for strengthing the teeth and gums. Tender leaves
for vomiting. Fruits juice used as carminative, diuretic and stomachic, also used in
diarrhoea and spleen enlargement. The seeds and fruits are used in the treatment of
diabetes.
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Anti diabetic
Sharma et al25
was investigated the oral antihyperglycemic effect of the water
and ethanolic extracts of the fruit-pulp of Eugenia jambolana (EJ) in alloxan-induced
diabetic with fasting blood glucose between 120 and 250 mg/dl as well as severely
diabetic rabbits (fasting blood glucose above 250 mg/dl).Water extract was found to
be more effective than the ethanolic extract in reducing fasting blood glucose and
improving blood glucose in glucose tolerance test.
Ravi et al26
has evaluated the hypoglycemic activity of the inorganic part of E.
jambolana seeds on streptozotocin-induced diabetes and analyze the inorganic trace
elements present in Eugenia jambolana seeds. The conclusion that the inorganic
constituents might play a important role in the antidiabetic nature E. jambolana seeds
was reached.
Prince et al27
has designed the antidiabetic and antihyperlipidaemic effect of
an alcoholic extract of Syzigium cumini seeds (JSEt) in alloxan diabetic rats. Thus, our
investigation clearly shows that alcoholic JSEt has both antidiabetic and
antihyperlipidaemic effects.
Sharma et al28
has investigated the hypoglycaemic and hypolipidemic effect of
ethanolic extract obtained from seeds of E. jambolana in alloxan-induced diabetic
rabbits. The ethanolic extract of seeds also exhibited significant hypolipidemic effect
as evident from fall in total serum cholesterol (TC)/high density lipoprotein
cholesterol (HDL-c) ratio, serum low density lipoprotein cholesterol (LDL-c) levels
and decreased activity of HMG-CoA reductase.
Vikrant et al29
has undertaken the study to find out the effects of different
doses (100,200 and 400 mg per day) of alcoholic and aqueous extracts of Momordica
charantia (MC) and Eugenia jambolana (EJ) on the metabolic parameters (body
weight and serum glucose, insulin and triglycerides levels) of fructose fed rats.
Treatment with 400 mg per day of aqueous extracts of MC and EJ for 15 days
substantially prevented hyperglycemia and hyperinsulinemia induced by a diet high in
fructose.
Pepato et al30
has shown lack of antidiabetic effect of a Eugenia jambolana
leaf decoction on rat streptozotocin diabetes. We conclude that, at least in this
experimental model, Eugenia jambolana leaf decoction has no antidiabetic activity.
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Prince et al31
has shown that Jamun seed extract (JSEt) has hypoglycaemic
action. The effect of JSEt was most prominently seen in the case of animals given 5.0
g/kg body weight. JSEt was more effective than glibenclamide.
Antiulcer
Chaturvedi et al32
has studied the effect of ethanolic extract of seeds of E.
jambolana (EJE) against gastric ulcers in rats. The result of the present study indicates
that E. jambolana seed has gastro-protective properties mainly through promotion of
mucosal defensive factors and antioxidant status and decreasing lipid peroxidation.
Ramirez and Roa33
has determined the gastroprotective effect of quantified
tannins (13.4%) from Syzygium cumini. These findings suggest that tannins extracted
from S. cumini have gastroprotective and anti-ulcerogenic effects.
Anti-inflammatory
Muruganandan et al34
investigated the ethanolic extract of the bark of
Syzygium cumini for its anti-inflammatory activity in animal models. Thus, the
present study demonstrated that S. cumini bark extract has a potent anti-inflammatory
action against different phases of inflammation without any side effect on gastric
mucosa.
Modi et al35
has evaluated anti-inflammatory activity of the methanolic and
aqueous extracts of the seeds of Syzygium cumini Linn in wistar rats using the
carrageenan induced left hind paw edema. The methanolic and aqueous extracts of
Syzygium cumini at the dose of 250mg/kg body wt reduced the edema induced by
carrageenan by 48.29 % and 68.85 % respectively on oral administration of 250
mg/kg body wt, as compared to the untreated control group. Diclofenac sodium at 100
mg/kg body wt inhibited the edema volume by 75.08 %. The results indicated that the
aqueous extract shows more significant anti-inflammatory activity then methanolic
extracts when compared with the standard and untreated control.
Kumar et al36
has evaluated the anti-inflammatory activity of ethyl acetate and
methanol extracts of S. cumini seed in carrageenan induced paw oedema in wistar rats
at the dose level of 200 and 400 mg/kg administrated orally. Both the extracts
exhibited significant anti-inflammatory activity, which supports the traditional
medicinal utilization of the plant. This study established anti-inflammatory activity of
the seed of S. cumini.
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Antioxidant
Veigas et al37
has studied anthocyanin pigments from Syzygium cumini fruit
peels were characterized and evaluated for their antioxidant efficacy.
Sunilu Vasi and Anoop Austin38
have studied the Antioxidant potential of
Eugenia jambolana using various in vitro models. Ethanolic (50%) extract showed
maximum scavenging activity in all models. The finding justifies the therapeutic
application of the plant in the indigenous system of medicine, augmenting its
therapcutic value.
Bhatia et al39
has described that jamun leaf and seed contain gallic acid,
ellagic acid, chebulic acid, corilagin and related ellagitannins and its two isomeric
forms, galloylglucose and quercetin, The presence of gallic acid,
hexahydroxydiphenic acid, chebulic acid and isohexahydroxydiphenic acid as the
building blocks of the tannins in the seeds has been confirmed from chromatographic
studies of the tannin hydrolysates.
Antipyretic activity
Vila-Pena et al40
has evaluated analgesic potential of leaf hydro-alcoholic
extracts in rats by hot plate and formalin tests. In the hot plate test, Syzygium jambos
extract produced a significant increase in the withdrawal response latencies in a dose-
dependent manner and with a maximal effect (analgesic efficacy) similar to that of
morphine. The extract (i.p.) significantly reduced pain scores in all the phases of the
formalin test with an analgesic efficacy higher than that shown by diclofenac.
Moresco et al41
has designed study to evaluate the effect of the aqueous
Syzygium cumini leaf extract, given either as a single dose or by 7 days of
pretreatment, on hepatotoxicity induced by carbon tetrachloride in rats. This suggests
that the extract may be useful for liver protection but needs to be given over a
significant period and prior to liver injury.
Jasmineet et al42
has revealed that crude extracts of seeds of this plant
demonstrated zones of inhibition in the range of 14– 21 mm against the isolated β-
lactamase-producing drug-resistant bacteria. Thus, the use of this plant by tribals to
treat bacterial infections has some scientific basis.
Kumar et al43
was intended to evaluate the anti-inflammatory activity of ethyl
acetate and methanol extracts of S. cumini seed in carrageenan induced paw oedema
in wistar rats at the dose level of 200 and 400 mg/kg administrated orally. Both the
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extracts exhibited significant anti-inflammatory activity, which supportsthe traditional
medicinal utilization of the plant.
3.2. Cissus quadrangularis Linn.
Cissus quadrangulairs (Vitaceae) is an indigenous medicinal plant of India.
Cissus quadrangularis L. (A genus of about 200 species found in tropical and warm
locations.)44
. This perennial climber with a thick, succulent, quadrangular stem that is
winged, but constricted at the nodes, is nearly leafless, except on new growth. Its
tendrils are long, slender and simple. The deciduous leaves are variable, ranging from
ovate to cordate to tri-lobed and from 3-5 cm in length. The inflorescence is a
compound cyme, with four-petaled pink or white 2 mm long flowers. The 6-10 mm in
diameter fruit is a very acidic, globose, one-seeded red berry45
.
It has been prescribed in ancient Ayurvadic texts by Bhava Prakash and
Chakra Dutt as a general tonic especially for the fractured patient46
. The stem is also
reputed in Ayurvadic alterative, anthelmintic, dyspeptic, digestive, tonic, analgesic in
eye and ear diseases, in the treatment of irregular menstruation and asthma, and in
complaints of the back and spine47,48,49
.
A. Vernacular names
Sanskrit : Vajravalli, Chaturdhara
Bengali : Hadjora
Gujrati : Hadasankala
Hindi : Hadjod
Marathi : Kandvel
Tamil : Perandai
B. Taxonomic classification
Kingdom : Planate
Division : Magnoliophyta
Class : Magnoliopsida
Order : Vitales
Family : Vitaceae
Genus : Cissus
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Stem:
Stern is quadrangular, 4-winged,
internodes constricted at nodes;
A tendril occasionally present at nodes;
Internodes 4-15 cm long and 1-2 cm thick;
Surface smooth, glabrous, buff coloured
with greenish tinge, angular portion
reddish-brown;
Taste: None
Odour: None.
Leaf:
Leafless when old, leaves are 5 – 15 cm
long, cordate, broadly ovate or reniform,
crenate – serrate, sometimes 3 – 7 lobes,
glabrous, 2.5 – 7.5 cm X 3 – 9 cm. Flowers are small, greenish white, in short
umbellate cymes. Berries are obovoid or globose in shape, succulent, very acrid, pea -
sized.
Figure 3.3: Leaves of Cissus quadrangularis
Figure 3.2: Stem of Cissus quadrangularis
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C. Description
B.S: Drug consists of dried stems of Cissus quadrangularis Linn.
Family: Vitaceae.
Habitat: It is found throughout the hotter parts of india.
Distribution: Cissus quadrangularis is an ancient medicinal plant native to the
hotter parts of Ceylon and India.
a) Macroscopic
Drug occurs as pieces of stem of varying lengths; stem quadrangular, 4-
winged, internodes constricted at nodes; a tendril occasionally present at nodes;
internodes 4-15 cm long and 1-2 cm thick; surface smooth, glabrous, buff coloured
with greenish tinge, angular portion reddish brown, no taste and odour 50
.
D. Chemical constituents51
:
The identification of chemical compounds have been reported such as
carotene, vitamin A, vitamin C, calcium oxalate crystal, triterpene, steroid,
tetracyclic, triterpenoid, saponins, flavonol, stilbene and miscellaneous
compound. Recent study found two new iridoids 6 – 0 [ 2,3 – dimethoxy] –
trans – cinnamoyl catalpol, 6 – O – meta – methoxy – benzyl catalpol along
with a known iridoid picoside 1, two stilbenes quadrangularis A, pallidol,
quercitin, quercitrin, beta sitisterol and beta – sitosterol glycoside were
isolated from Cissus quadrangularis.
Phytochemical tests on the plant revealed the presence of alkaloids, saponins,
tannins, flavonoids, glycosides with the absence of cyanogenic glycosides.
Terpenoids to large stilbene derivatives have been isolated from the plant, The
stem of plant has phenolics compound tannin, vitamin C and beta – carotene
that known to be excellent anti oxidants may have positive effects in oxidative
stress related pathologies.
Stilbene derivatives likr Quadrangularis A, Band C, resveratrol, piceatannol,
pallidol and parthenocissin are present in the stem.
E. Ethenomedical uses
Plant is bitter, sweet, sour, thermogenic, alternate, laxative, anthelmentic,
carminative, digestive, depurative, haemostatic, analgesic, antiinflammatory,
aphrodisiac, ophthalmic and useful in vitiated condition of vata, helminthiasis,
anorexia, dyspepsia, colic, flatulence, skin disease, leprosy, haemorrhages,
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ophthalmopathy, chronic ulcer, tumours, epilepsy, convulsion, fracture, swelling and
vitiated condition of kapha52,
53
. External as paste applied over fractures extract has
acetyl choline like action54
.
REVIEW OF LITERATURE
Anti-inflammatory and analgesic activity
Panthong et al55
has evaluated that Cissus quadrangularis is used for the
treatment of hemorrhoid. The effects associated with hemorrhoid, i.e. analgesic and
anti-inflammatory activities as well as the venotonic effect of the methanol extract of
C. quadrangularis (CQ) were assessed in comparison with reference drugs. In the
analgesic test, CQ provoked a significant reduction of the number of writhes in acetic
acid-induced writhing response in mice. CQ also significantly reduced the licking
time in both phases of the formalin test. The results obtained confirmed the traditional
use of C. quadrangularis for the treatment of pain and inflammation associated with
hemorrhoid as well as reducing the size of hemorrhoids.
Rao et al56
has evaluated the effect of alcoholic extract of Cissus
quadrangularis (CQ) on the intrauterine growth of trabeculae in the long bones in
rats. Pregnant rats were administered with Ethanol extract of CQ, orally, at the dose of
750 mg/kg body weight from 9th
day of gestation till delivery. Femur bone of the
newborn pups were collected, decalcified and processed for paraffin sectioning.
Results showed a significantly increase in thickness of the cortical bone at mid shaft
level compared to control rats. The thickness of individual trabecula was increased
significantly. The present study demonstrates enhanced bone formation during fetal
growth by CQ, which may be related to rich content of calcium, phosphorus and
phytoestrogenic property of the plant.
Anti neoplastic activity
Opoku et al57
has evaluated that aqueous and methanol extracts of nine
traditional Zulu medicinal plants, all belonging to the [Vitaceae] family for their
anti neoplastic activity. The anti proliferative activity in vitro against HepG2 cells was
determined. Higher degrees of growth inhibition were found in aqueous root extracts
in comparison with the methanol extracts of the same plant parts. The results show
potential anti neoplastic activity, indicating some scientific validation for traditional
usage.
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Anti nociceptive activity
Mate et al58
has evaluated that chloroform:water (20:80) extract of Cissus
quadrangularis Linn. (Vitaceae) was centrally acting analgesics by using the hot plate
method, formalin test and acetic acid-induced writhing method for peripherally acting
analgesics. The doses administered were 250 mg/kg and 350 mg/kg. The animal that
administered both the doses showed significant analgesic activity. The animal that
administered a dose of 350 mg/kg has shown the maximum analgesic activity which
is comparable to the standard.
Anti osteoporotic activity
Thavani et al59
has evaluated that Clinical trial on 60 patients to prove the
efficacy of Cissus quadrangularis (CQ) in fracture healing. Fractures of long bones
were treated topically with CQ. CQ treated patients showed good callus formation in
30-40 percent less time than the non-treated.
Gharpure et al60
has studied that Cissus quadrangularis also known as Hadjod.
Asthisamhariis commonly used in Indian traditional medicine for bone healing.
Recent animal studies and human trials with its extract have shown promising results
in fracture healing and osteoporosis.
Potu et al61
has evaluated Cissus quadrangularis significantly increased the
force required to break the femur (p<0.001) and significantly increased the thickness
of both cortical (p<0.001) and trabecular bone (p<0.001). This action of CQ was
comparable to the action of raloxifene. The petroleum ether extract of CQ stem seems
to possess anti-osteoporotic activity in rats.
Potu et al62
has evaluated treatment with 100, 200 or 300 mg/mL petroleum
ether extract of Cissus quadrangularis enhanced the differentiation of marrow
mesenchymal stem cells into ALP-positive osteoblasts and increased extracellular
matrix calcification. Treatment with 300 µg/mL petroleum ether extract of Cissus
quadrangularis also enhanced the proliferation rate of the marrow mesenchymal stem
cells. Cissus quadrangularis stimulates osteoblastogenesis and can be used as
preventive/ alternative natural medicine for bone diseases such as osteoporosis.
Potu et al63
has evaluated petroleum ether extract of Cissus quadrangularis
Linn. (CQ) on an osteoporotic rat model developed by ovariectomy. The osteoclastic
activity was confirmed by TRAP staining, and the bone formation was assessed by
ALP staining in the femur sections. The color intensity of TRAP and ALP enzymes
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from the images were evaluated by image analysis software developed locally. The
effect of CQ was found to be effective on both enzymes, and it might be a potential
candidate for prevention and treatment of postmenopausal osteoporosis. The
biological activity of CQ on bone may be attributed to the phytogenic steroids present
in it.
Potu et al64
has found maternal administration of Cissus quadrangularis
petroleum ether extract during pregnancy can stimulate the development of fetal bone
growth during the intra uterine developmental period.
Parisuthiman et al65
has evaluated Cissus quadrangularis Linn. has been
implicated as therapeutic agent for enhancing bone healing. Though its osteogenic
activity has been suggested, the underlying mechanism still remains unclear. In the
present study, the effects of ethanol extract of C. quadrangularis (CQE) on osteoblast
differentiation and function were analyzed using murine osteoblastic cells. The results
indicated that mRNA expressions of osteoblast related genes were not affected by the
CQE treatment. However, alkaline phosphatase (ALP) activity and the extent of
mineralized nodules were significantly increased in treated cells compared with
controls. These results suggested that CQE may regulate osteoblastic activity by
enhancing ALP activity and mineralization process.
Shirwaikar et al66
has suggested Ethanol extract of Cissus quadrangularis was
evaluated for its anti-osteoporotic activity in ovariectomized rat model of osteoporosis
at two different dose levels of 500 and 750 mg/kg per day. Healthy female albino rats
were divided into five groups of six animals each. First group was sham operated and
served as control. All the remaining groups were ovariectomized. Group 2 was fed
with equivolume of saline and served as ovariectomized control. Groups 3-5 were
orally treated with Raloxifen (5.4 mg/kg) and ethanol extract of Cissus
quadrangularis (500 and 750 mg/kg), respectively. The findings assessed on the basis
of biochemical and histopathological parameters showed that the ethanol extract of
the plant had a definite antiosteoporotic effect.
Deka et al67
has studied the effect of methanolic extract of Cissus
quadrangularis Linn (CQ) on the healing process of experimentally fractured radius
ulna of dog. CQ treated animals revealed faster initiation of healing process than the
control animals on radiological and histo pathological examinations. The treated
group also revealed a decrease in serum calcium level to a greater extent than the
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control group. Healing was almost complete on 21st
day of fracture in the treated
animals and remained incomplete in the control animals.
Anti oxidant activity
Chidambara Murthy et al68
has evaluated Extracts of Cissus quadrangularis L.
were tested for antioxidant activity by beta-carotene linoleic acid model and also by
1,1-diphenyl-2-picrylhydrazyl model. The ethyl acetate fraction of both fresh and dry
stem extracts at a concentration of 100 ppm showed 64.8% antioxidant activity in the
beta-carotene linoleic acid system and 61.6% in the 1, 1-diphenyl-2-picrylhydrazyl
system. The antioxidant activity of methanol extract and aqueous extract were
comparatively less significant than that of ethyl acetate extract, and n-hexane extract
showed the least activity. The results of the study have implications in the use of C.
quadrangularis as an antibacterial agent and more so as an antioxidant in several
applications requiring these properties.
Anti ulcer activity
Austin et al69
has determined anti peptic ulcer activity of Cissus
quadrangularis Linn. against Helicobacter pylori (Hp) human isolates. Flowering and
vegetative period samples were analyzed. Aqueous (hot and cold) and solvent extracts
(acetone, chloroform and methanol) were screened. Among them chloroform was
observed to recover bioactive principles with low MIC. Extracts from samples
collected during flowering period were better than that of vegetative period. The
results confirm the traditional use of the plant in peptic ulcer.
Jainu et al70
has discussed that Cissus quadrangularis is well known for the
treatment of gastric disorders in traditional medicine. Ethanol extract of Cissus
quadrangularis (CQE) against the gastric toxicity induced by aspirin in rats. The
optimum protective dose of 500 mg/kg of extract was selected by the pre treatment of
gastric ulcers with different doses of CQE (250, 500 and 750 mg/kg) for 7 days which
showed ulcer protection by 40, 71.2 and 72.6 percent, respectively, as compared to
ranitidine (RTD) (30 mg/kg) by 71.9 percent in the aspirin model. These findings
suggest that the gastro protective activity of CQE could be mediated possible through
its antioxidant effect as well as by the atenuation of the oxidative mechanism and
neutrophil infiltration.
Jainu et al71
has designed pre-treatment with Cissus quadrangularisextract
(CQE) significantly prevented the gastric mucosal lesion development and decreased
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the gastric toxicity produced by ulcerogen. Histological studies confirmed the results.
The present finding suggests that CQE promotes ulcer protection by the decrease in
ulcer index, gastric secretions and increase in the glycoprotein level, gastric mucin
content. CQE may protect the gastric mucosa against ulceration by its antisecretory
and cytoprotective property.
Jainu et al72
has studied the ulcer protective effect of a methanolic extract of
C. quadrangularis (CQE) was comparable to that of the reference drug sucralfate.
Further, gastric juice and mucosal studies showed that CQE at a dose of 500 mg/kg
given for 10 days significantly increased the mucosal defensive factors like mucin
secretion, mucosal cell proliferation, glycoproteins, and life span of cells. The present
investigation suggests that CQE not only strengthens mucosal resistance against
ulcerogens but also promotes healing by inducing cellular proliferation. Thus, CQE
has potential usefulness for treatment of peptic ulcer disease.
Jainu et al73
has showed effect of ascorbic acid, the major bioactive
component isolated from Cissus quadrangularis extract (CQE) on inflammatory
cytokines and growth factors in non-steroidal anti-inflammatory drug (NSAID)
induced gastric ulcer. Analysis of serum cytokine profile using Enzyme Linked
Immune Sorbent Assay (ELISA) showed a drastic increase in interleukin (IL)-1beta,
IL-6, tumour necrosis factor-alpha (TNF)-alpha, interferon-gamma (IFN-gamma) and
decrease in IL-10, Il-4 and prostaglandin E2 (PGE2) levels in NSAID (aspirin) treated
rats. Administration of CQA produced significant protection against aspirin induced
gastric toxicity by showing significant increase in PGE2, TGF-alpha, VEGF
expression and accompanied by a significant inhibition of nitric oxide and regulating
the levels of cytokines in rats. These findings suggest that CQE prevents gastric ulcer
formation due to its immunemodulatory effect, antioxidant activity along with the
ability to modulate PG synthesis and up-regulation of the growth factors.
Phytochemical review
Gupta et al74
has isolated seven new compounds, from Cissus quadrangularis
have been characterized as 4-hydroxy-2- methyl-tricos-2-en-22-one, 9-methyl-
octadec-9-ene, heptadecyl octadecanoate, icosanyl icosanoate, 31-methyl-
tritriacontan-l-0l, 7-hydroxy-20-oxo-docosanyl cyclohexane and 31-
methyltritriacontanoic acid. Taraxeryl acetate, friedelan-3-one, taraxerol and iso-
pentacosanoic acid also isolated for the first time from this plant.
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Bhutani et al75
has isolated two new unsymmetric tetracyclic triterpenoids
onocer-7-ene-3a, 21β-diol and onocer-7-ene-3 β,21a-diol together with sitosterol, δ-
amyrin and δ -amyrone from Cissus quadrangularis. The structures of the new
compounds were elucidated on the basis of HNMR, mass spectral and chemical
evidence.
Gupta et al76
has isolated a new unsymmetrrcal tetracyclic triterpenoid, 7-oxo-
onocer- & ene-3β, 21α-diol, from Cissus quadrangularis. The structure will
elucidated on the basis of spectral and chemical evidences
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3.3 Moringa oleifera Lam.
A. Biological source77,78,79
It consists of fresh or dried leaves, pods, flowers, roots, seeds and bark of
Moringa oleifera Lam. (Syn. Moringa pterygosperma Gaertn.), Belongs to family
Moringaceae.
B. Geographical source92,93,94,80,81
A small or medium sized tree, about 10 mt. high and cultivated all over plains
of India. Moringa oleifera is the most widely cultivated species in the sub-Himalayan
tracts of India, Pakistan, Bangladesh and Afghanistan. This rapidly-growing tree was
utilized by the ancient Romans, Greeks and Egyptians; it is now widely cultivated and
has become naturalized in many locations in the tropics. It is a perennial softwood
tree with timber of low quality, but which for centuries has been advocated for
traditional medicinal and industrial uses. It is already an important crop in India,
Ethiopia, the Philippines and the Sudan, and is being grown in West, East and South
Africa, tropical Asia, Latin America, the Caribbean, Florida and the Pacific Islands.
All parts of the Moringa tree are edible and have long been consumed by humans95
.
C. Vernacular names 92,93,94,96
Sansk. : Sobhanjana, Bahola, Sakapatra, Sigru
Guj. : MidhoSaragvo, Saragavo, Segto, Seyla
Hin. : Sahijana
Eng. : Horse radish tree, Drum-stick tree
Kann. : Nugge
Tam. : Murungai
Tel. : Sajana, Munaga
Konk. : Maissang, Moring, Moxing
D. Scientific classification95
Kingdom : Plantae
Division : Magnoliophyta
Class : Magnoliopsida
Family : Moringaceae
Genus : Moringa
Species : Oleifera
Scientific name: Moringa oleifera Lam
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E. Morphology
M. oleifera is a fast growing deciduous shrub or small tree up to 12 m tall and
30 cm in diameter with an umbrella-shaped open crown (unless repeatedly coppiced).
It is a softwood tree with timber of low quality. The bark is corky and gummy. Leaves
are alternate, oddly bi- or tri-pinnate compound, triangular in outline and 20– 70 cm
long.
Each pinnae has 3–9 pairs of 1–2
cm long ovate leaflets, soft dark green
above and whitish below. The white,
fragrant flowers that are obliquely
monosymmetric and papilionoid (the
median petal is adaxial) with five stamens,
are in axillary pendulous panicles 1.5–2
cm long from leaf corners82
.
The fruit pods, called “drumsticks” are
15–45 cm long, 9-ribbed capsules opening
by three valves to release the seeds.
Each tree can produce 15’000 – 25’000 seeds per year.
All parts of the Moringa tree are edible but the roots, which are used as a
condiment in the same way as horseradish, contain the alkaloid spirochin, a
potentially fatal nerve paralyzing agent97
.
F. Chemical constituents
Phytochemicals are, in the strictest sense of the word, chemicals produced by
plants. In particular, this plant family is rich in compounds containing the simple
sugar, rhamnose, and it is rich in a fairly unique group of compounds called
glucosinolates and isothiocyanates83,84
.
Leaves contains two nitrile glycosides, niazirin and niazirinin and three
mustard oil glycosides, 4-[(4’-O-acetyl- α -L- rhamnosyloxy) benzyl]
isothiocyanate, niaziminin A and B85
.4-(a-L-rhamnopyranosyloxy) benzyl
isothiocyanate86
, niazimicin87
, pterygospermin88
, benzyl isothiocyanate89
, and 4-
(α-L-rhamnopyranosyloxy) benzyl glucosinolate90
.
Nitrile glycosides: niazirin, niazirinin94
. mustard oil glycosides: niaziminin A&
B.91,92
Figure 3.4: Moringa oleifera - leaves
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Phenolic flavonoids- Quercetin & its glucosides, kaempferol & its glucosides, 3-
caffeoylquinic and 5- caffeoylquinic acid94,99
.
Vitamins: Carotene (Vit. A), Ascorbic acid (Vit. C), Riboflavin (Vit. B2),
Tocopherols (Vit. K), Nicotinic acid (Vit. B3)92, 100
.
Essential Amino Acids, Proteins92
, Calcium, Phosphorus, iron, copper & Iodine92
.
Structures
4-(4'-O-acetyl-α-L-rhamnopyranosyloxy) Pterygospermin
benzyl isothiocyanate
Niazimicin Benzyl isothiocyanate
4-(α -L-rhamnopyranosyloxy) benzyl glucosinolate
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G. Ethnomedical uses
Gupta AK et al93
described leaves are emetic and their juice with black pepper
is used in headache. The poultice of leaves is used in reducing glandular swelling.
Goyal BR et al94
shows, the leaves are anthelmintic, aphrodiastiac, cures
hallucinations, dry tumors, cough and asthma. Decoction of dried leaves is taken
orally for abortion, externally for rheumatism, and for wound healing. Leaves made in
to a paste with salt are used to treat edema94
. Leaves used in scurvy and catarrhal
affection95
. The leaves are anti-inflammatory, anthelmintic, opthalmic and rich in
vitamin A and C. They are used in wound, tumor, helminthasis96
. The crushed leaves
are taken in the form of a tablet to relieve stomach pain in menstruation by women in
north western Karnataka. A paste of the leaves is applied externally to promote
healing of wounds. The juice extracted from leaves has a strong antibacterial and
antimicrobial properties97
. All parts of the tree are considered to possess medicinal
properties and used in treatment of Ascites, rheumatism, and venomous bites and as
cardiac and circulatory stimulants. The root is laxative, expectorant, diuretic and good
for inflammations, throat, bronchitis, piles, cure stomatitis, urinary discharges, and
obstinate asthama93
. Root bark is useful in heart complaints, eye diseases, all tridosha
fevers, inflammation, dyspepsia and enlargement of spleen. The root and barks are
abortifacient98
. The flowers cure inflammations and muscles diseases, the fruit cures
biliousness pain, leucoderma and tumor. The flowers, fruits and seeds cure capha and
vata. The seeds cure eye diseases and head complaints. Oil is useful in letrous ulcers
and as external aplications for rheumatism93
.
LITERATURE REVIEW
Chemical review
Faizi et al105
(1994), Bioassay-guided analysis of an ethanolic extract of leaves
showed the presence of two nitrile glycosides, niazirin and niazirinin and three
mustard oil glyosides,4-[(4’-0-acetyl-α-L-rhmnosyloxy) benzyl] isothiocyanate,
niaziminin A &B106
.
α-L-Rhamnosides of 4 hydroxy benzyl compounds with nitrile,
carbamate and thiocarbamate groups occurring in leaf extract and the α-L-rhmnoside
of anisaldehyde derivatives were synthasized99
.
Moringa oleifera was analysed for glucosinolates and phenolics (flavanoids,
anthocyanins, proanthocyanidin and cinnamates). Leaves contain 4-(α-rhamnos-
pyranosyloxy)-benzylglucosinolate and three monoacetyl isomers of this glcosinolate.
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The leaves contain queretin 3-O-glucosides and quercetin-3-O-(6”-malonyl-
glucoside), and lower amount of kaempferol-3-O-glucosides and kaempferol-3-O-(6”-
malonyl-glucoside). They also contained 3-caffeoylquinic and 5-caffeoylquinic acid97
.
Moringa oleifera leaves on ethanolic extraction yielded a no. of amino acids
viz., aspartic acid, glutamic acid, serine, glycine, threonine, α-alanine, valine, leucine,
isoleucine, histidine, lysine, arginine, phenylalanine, tryptophan, cystine, and
methionine. the ether extract of leaves yielded α and β-carotene100
.
Moringa oleifera leaves were found to be devoid of tannins101
, rich sourse of
vitamin C102
, than those of Moringa concanensis103
. Roots of Moringa oleifera have
high concentration of both 4-(α-L-rhamnopyranosyloxy) -Benzylglucosinolate and
Benzylglucosinolate104
. The stems contains 4 Hydroxymellein, vanillin, β-Sitosterol,
Octacosanic acid and β-sitosterol105
.
The bark contains 4-(α-L-rhamnopyranosyloxy)-benzylglucosinolate118
The
purified, whole- gum exudates from the drumstick plant contains- L-arabinose, D-
galactose, D- glucuronic acid, L- rhamnose, D- mallose & D- xylose in the molar
ratios of approx. 14.5:11.3:3.2:1.1106
. A leucoanthocyanin characterized as
leucodelphinidin-3-o-β-D- galactopuranosy (1-4)-o- β-D-glucopuranoside is also
present in gum107
.
The aqueous extract of mature flowers contains free natural sugars, D-
mannose and D-glucose in the ratio of 1:5 and two unidentified carbohydrates bearing
materials aong with protein and ascorbic acid of the above materials with varying
proportion. It also contains polysaccharides which on hydrolysis gives D-galactose,
D-glucose & D-glucuronic acid in molar ratio of 1:1.9:0.9108
.
The whole pods reported to contain nitrile and isothiocyanate and
thiocarbonates106,107
and O - [ 2 ’- hydroxy - 3’ - (2” – heptenyloxy ) ] –
propylumdecanoates and O-ethyl-4-[ (α-L- rhamnosyloxy) -benzyl] carbontes, methyl
–p- hydroxybenzoate & β-sitosterol109
. The mucilage from the pods designated as
drumstick polysaccharides, the investigation of which revealed the presence of
galactose, dextrose, xylose and sodium, potassium, magnesium, calcium salts of
glucuronic acid. Contrary to the definition of mucilage, the presence of dextrose was
an exception110
.
The mature seeds contain 332.5 gm. crude protein, 412.0 gm. crude fats, 212.2
gm. carbohydrates and 44.3 gm. ash per kg. dry matter. The essential amino acid
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profile showed deficiency of lysine, threonine and valine. The content of methionine,
cysteine (43.6 gm/ kg protein), however, was exceptionally high and closed to that of
human milk, chicken eggs, and cow’s milk111
. Seeds have high concentration of both
4-(α-L-rhamnopyranosyloxy) benzyl glucosinolate and benzyl glucosinolate118
.
Drumstick seeds contain 38.16 % oil which contain Vitamin E (0.01 %), & β-
Carotene (0.014 %), the precursor of Vitamin A112
Mono palmitic and Di- oleic
triglycerides have been isolated from the benzene extract of semi-dried seeds113
.
Results of physical and chemical parameters of the extracted oil: iodine value:
68-71.80; refractive index (400C): 1.4590-1.4625; density (24
0C): 0.9036-0.9080
mg/mL.; saponification value: 180.60-190.50; unsaponifiable matters: 0.70-1.10 %;
and colour (1 in .cell), 0.95-1.10R+20.00-35.30Y. Tocopherols (α, γ and δ) in the oil
were up to123.50-161.30, 84.07-104 and 41.00-56.00 mg/kg. respectively. The oil
was found to contain high levels of oleic acid (up to 78.59 %) followed by palmitic
acid (7.00 %), stearic acid (7.50 %), behenic acid (5.99 %) and arachidic acid (4.21
%)114
.
From the row seeds by hot water extraction 4-(α-L-rhamnosyloxy) benzyl
isothiocyanate and 4-(α-L-rhamnosyloxy) phenylacetonitrile were isolated115
. 4-(α-L-
rhamnosyloxy) benzyl glucosinolate and its thermal degradation product 4-(α-L-
rhamnosyloxy) phenylacetonitrile were also reported116
. Starting from L-rhamnose ,
the first synthesis of the major glucosinolate isolated from drumstick seeds was
completed in seven steps117
.
Anti-inflammatory activity
Caceres A et al118
has showed anti-inflammatory activity of hot water infusion
of leaves against carrageenan induced hind paw edema. The crude ethanolic extract of
Moringa dried seeds was tested for antiinflammatory activity using carrageenan
induced inflammation the hind paw of mice by various workers and found to inhibit
85 % of inflammation at a dose of 3 mg/kg. body weight, while the mature green
seeds inhibited edema by 77 % at the same dose.
Siddhuraju P et al 119
has evaluated water, aqueous methanol and aqueous
ethanol extracts of freeze-dried leaves of Moringa oleifera Lam. from different
agroclimatic regions were examined for free radical scavenging capacities and
antioxidant activities. All leaf extracts were capable of scavenging peroxyl and
superoxyl radicals. Among the three different moringa samples, both methanol and
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Bhagwant University PhD Thesis 65
ethanol extracts of Indian origins showed the highest antioxidant activities, 65.1 and
66.8%, respectively, in the beta-carotene-linoleic acid system. On the basis of the
results obtained, moringa leaves are found to be a potential source of natural
antioxidants due to their marked antioxidant activity.
Ahemad B et al120
has studied methanol extract of the Moringa fruit was also
screened for antiinflammatory effect using the rat paw edema and the rat 6 days at
pouch inflammatory models following oral administration, the extract inhibited
carrageenan induced rat pow edema in a dose dependant manner, with IC50 of 660
mg/kg in the six day at pouch acute inflammation model induced with carrageenan,
the extract was much more potent, with IC50 values of 302.0 mg/kg and 315.5 mg/kg,
for the inhibition of cellular accumulation and fluid exudation, respectively. It
contents antiinflammatory principle that may be useful in the treatment of both the
acute and chronic inflammatory conditions. Moringa oleifera Lam. (moringaceae)
was investigated for analgesic effect against thermal stimuli using Eddy’s hot plate
test and Analgesiometer test and for antipyretic effect.
Ezeamuzie IC et al121
has screened methanol extract of the root of the plant
Moringa oleifera Lam. for anti inflammatory effect using the rat paw edema and the
rat 6-day air pouch inflammatory models. Following oral administration, the extract
inhibited carrageenan induced rat paw edema in a dose-dependent manner, with 50%
inhibitory concentration IC50 of 660 mg/kg. Maximum inhibition obtained with 600
mg/kg was 83.8% and 80.0%, respectively. These results suggest that the root of
Moringa oleifera contains anti inflammatory principle(s) that may be useful in the
treatment of both the acute and chronic inflammatory conditions.
Armando C et al122
has designed antispasmodic, antiinflammatory and diuretic
activity of Moringa oleifera hot water infusions of flowers, leaves, roots, seeds and
stalks or bark. The antispasmodic activity was demonstrated using isolated duodenum,
oral anti-inflammatory activity by carragenan left hind paw edema and oral diuretic
activity by urine output in metabolic cages. The seed infusion showed a significant
inhibition of acetylcholine-induced contraction with an ED of 65.6 mg/mL bath
concentration, inhibition of carrageenan-induced edema at 1000 mg/kg and diuretic
activity at 1000 mg/kg. Some activity was also demonstrated in the roots. All doses
expressed here are as equivalents of dried starting plant material.
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Sutar NG et al123
has evaluated antipyretic activity of an ethanolic extract of
Moringa oleifera Lam. seeds at normal body temperature and yeast induced pyrexia,
in albino rats. The ethanol extract of Moringa oleifera at dose of 100, 200 and
300mg/kg body wt p.o. showed significant dose dependent reduction in normal body
temperature and yeast-provoked elevated temperature. The effect extended upto 5 hrs
after drug administration. The antipyretic effect of an ethanolic extract of seeds of
Moringa oleifera, was comparable to that of Paracetamol (150 mg/kg body wt, p.o.), a
standard antipyretic agent.
Antioxidant activity
Lalas S et al124
has described that aqueous, methanol (80 %) & ethanol (70%)
extract of freeze-dried Moringa oleifera leaves showed radical scavenging and anti
oxidant activities. All the extracts were capable of scavenging peroxyl and superoxyl
radicles. The major bioactive compounds were found to be quercetin and kaempferol.
The oil from the dried seeds showed higher antioxidant activity than butylated
hydroxyl toluene and α-tocopheol.
Siddiq A et al125
has studied the antioxidant activity of different solvent
extracts of Moringa oleifera leaves under accelerated storage of sunflower oil.
Methanolic and acetone (80 to 100%) extracts of Moringa oleifera leaves were added
at the concentration of 0.06% (w/w) into the refined, bleached and deodorized
sunflower oil. The overall order of antioxidant efficacy of the extract of Moringa
oleifera leaves assessed by various oxidation parameters was followed as, 80%
methanolic extract >100% methanolic extract > 80% acetone extract > 100% acetone
extract. The antioxidant activity of Moringa oleifera leaves might be attributed by the
presence of high amount of flavonoids, polyphenolics and tocopherol contents. The
results of present study revealed that M. oleifera leaves might be explored as a viable
source of natural antioxidants and nutraceuticals.
Antimicrobial activity
Goel M et al126
has studied leaf extract of Moringa oleifera Lam. in three
different solvents (methanol, ethyl acetate and aqueous) reduced sporulation of some
fungi, aqueous and methanolic extracts were most effective. HPTLC analysis yield
gallic acid in leaves. According to these results, it can be predicted that it has certain
substances inhibitory to the fungal spore germination.
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Eilert U has discussed antimicrobial agent for (α-L-rhamnosyloxy) benzyl
isothiocyanate was identified from the seeds. Defatted and shell free seeds contain
about 8-10 % of 4(α-L-rhamnosyloxy) benzyl isothiocyanate but this amount is
produced when ascorbic acid added during water extraction. The compound acts on
several bacteria and fungi. The minimal bactericidal concentration in vitro is 40
mmol/l for Mycobacterium phlei and 56mmol/l for Bacillus subtilis127
.
Cardiovascular activity
Eilert U et al128
has written that niazinin A, niazimicin, niaziminin A & B
isolated from ethanolic extract of eaves produced hypotensive and bradycardiac effect
in anaesthetized at a dose of 250 mg/kg. i.v. The aqueous extract of stem bark
produced a positive inotropic effect at low concentration and negative inotropic effect
at high concentration on isolated perfused dog heart and it also produced a dose
dependant hypotensive effect on dog blood pressure. Ethanolic and aqueous extracts
of whole pods and their parts namely; fruit, pulp and seeds also showed hypotensive
activity. The activity of the ethanolic extract of both the pods and the seeds was
equivalent at the dose of 250 mg/kg.
Dangi SY et al129
has obtained alkaloids by fractionation of the water extract
of the leaves converted in to their salt form, were tested for theie activity on the
isolated frog hearts. The total alkaloidal salts were found to produce a negative
inotropic effect on the isolated perfused frog heart. This activity was further
characterized by testing it on the isolated guinea pig ileum.
Antihyperlipidaemic activity
Saluja MP et al130
has invented that administration of crude leaf extract along
with high-fat diet decreased the high-fat diet induced increase in serum, liver and
kidney cholesterol level by 14.35 % (115-103.2 mg/100 mL of serum), 6.40 % (9.4-
8.8 mg/g wet wt.) and 11.09 % (1.09-0.97mg/g wet wt), respectively.
Mehta et al131
, fruits of Moringa oleifera were reported to possess
hypolipidaemic effect. They were found to lower the serum cholesterol, phospholipid,
triglycerides, VLDL, LDL, cholesterol to phospholipid ratio and atherogenic index in
hyper cholesterolaemic rabbits, but were found to increase the HDL ratio (HDL/HDL
Total cholesterol) as compared to the corresponding control groups.
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Anticancer activity
Guevara AP et al132
has screened paste of drumstick leaves for its influence
on the carcinogen detoxifying glutathione-S- transferase (GST) activity by more than
78 % in the stomach, liver and oesophagus and showed protective activity against
carcinogenesis.
Antihepatotoxic activity
Pari L et al133
has determined hepatoprotective effect of an ethanolic extract of
leaves of moringa on liver damage induced by antitubercular drugs such as isoniazid,
rifampicin and pyrazinamide in rat has been evaluated. The extract was found to
enhance the recovery from hepatic damage induced by antitubercular drugs.
Kumar NA et al134
has studied the protective effect of Moringa oleifera Lam.
(Moringaceae) on hepatic marker enzymes, lipid peroxidation, and antioxidants was
investigated during antitubercular drug induced toxicity in rats. Administration of
Moringa oleifera extract and silymarin significantly decreased hepatic marker
enzymes and lipid peroxidation with a simultaneous increase in the level of
antioxidants. We speculate that Moringa oleifera extract exerts its protective effects
by decreasing liver lipid peroxides and enhancing antioxidants.
Antidiabetic activity
Patil MB et al135
has evaluated Moringa oleifera leaves extract for their
hypoglycaemic activity in normal rabbits fed with glucose. Acetone extract exhibits
significant hypoglycaemic activity (P more than 0.025), Methanolic extract also
showed hypoglycaemic activity but it was not significant. All other solvent extracts
failed to reduce the blod glucose evel.
Jaiswal D et al136
has studied effect of Moringa oleifera Lam. leaves aqueous
extract on hyperglycemic rats. The dose of 200 mg/kg decreases blood glucose level
(BGL) of normal animals by 26.7 and 29.9% during FBG and OGTT studies
respectively. In sub and mild diabetic animals the same dose produced a maximum
fall of 31.1 and 32.8% respectively, during OGTT. In case of severely diabetic
animals FBG and PPG levels were reduced by 69.2 and 51.2% whereas, total protein,
body weight and haemoglobin were increased by 11.3, 10.5 and 10.9% respectively
after 21 days of treatment. Significant reduction was found in urine sugar and urine
protein levels from +4 and +2 to nil and trace, respectively. The study validates
Chapter-3 Review of Literature
Bhagwant University PhD Thesis 69
scientifically the widely claimed use of M. oleifera as an ethnomedicine to treat
diabetes mellitus
Nootropic activity
Mohan M et al137
has assessed toluene-ethyl acetate fraction of methanolic
extract of Moringa oleifera (Moringaceae) leaves for its nootropic activity using
passive shock avoidance paraigm and elevated plus maze.Extracts (50 and 100 mg/kg)
was compared with Piracetam (100mg/kg), Scopalomine (1mg/kg) was used to induce
cognitive dysfunction. The extract significantly decreased Transfer Latency on Day-2.
The extract reduced the latency to reach the SFZ and the number of mistakes. No
adverse effects were observed up to a dose of 200mg/kg.
Lakshmi V et al138
has determined antidiuretic activity of Moringa oleifera
pods. In the present study the aqueous extract of Moringa oleifera pod was tested in
two oral doses (400mg/kg and 800mg/kg) for its diuretic activity in albino rats and its
diuretic activity was compared with that of a standard drug hydrochlorothiazide. In
our study aqueous extract of Moringa oleifera showed a significant increase in urine
volume and it was comparable to that of hydrochlorothiade. Thus the authors
conclude that Moringa oleifera has diuretic action
Miscellaneous activity
Girija V et al139
has described that hot water infusion of leaves possesses
antispasmodic activity. Availability of carotene (vitamin A) from vegetables was
studied in rats by the liver storage bioassay method. Carotene of Moringa oleifera was
49.1 % active in producing vitamin A. When rats were supplemented with pure
carotene, the Hb level increased. The bio-availability of thiamin and riboflavin from
leaves was higher.
Mossa JS et al140
has showed that Moringa oleifera increased the blood
glucose by 15 % in alloxanized mice.
Kar A et al141
has evaluated that ethanolic extract showed significant blood
glucose lowering effect within 2 weeks in alloxan induced diabetic albino rats. The
blood glucose levels and the corresponding insulin levels in response to drumstick
leaves in southern India were compared to the leaves achieved in response to 75 gm
of glucose in non insulin dependent diabetes mellitus patients. The blood glucose
response was 56% compared to 75 gm of glucose. It was concluded that the reduced
blood glucose response to drumstick leaves is not due to insulin secretion.
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Bhagwant University PhD Thesis 70
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