Coccinia
indica- A Phytopharmacological
Review.
Raje VN1*,
Yadav AV2, Shelar
PA2
1Gorishankar Education
society’s College of Pharmacy (D. Pharm) Limb, Satara, India-415015.
2Gourishankar
Institute of Pharmaceutical Education & Research, Limb, Satara,
India-415015.
ABSTRACT:
Coccinia indica belonging to family Cucurbitaceae is distributed all over India, it is commonly
known as Ivy gourd and the leaves, roots, fruits and bark has been used for
various disorders in traditional and folk medicine. The plant is used as
cathartic, antispasmodic, expectorant, etc. The leaves are used as anthelmintic, antispasmodic, expectorant, and antiulcer.
Fruits are used as laxative, antiemetic, anti-inflammatory, antileprotic.
Roots are used as cathartic, antiarthritic,
hypoglycemic.
The plant is known to possess various active constituents like steroids,
alkaloids, flavonoids, glycosides, tannins and Phenolic compounds. The plant is screened for hepatoprotective, antimicrobial, anthelmintic,
antibacterial, anti-inflammatory, antioxidant and antiulcerogenic
activity. The present review is therefore, an effort to give a detailed survey
of the literature on the microscopical, phytochemical and pharmacological properties of Coccinia indica.
This review supports all updated information on its phytochemical
and pharmacological activities, traditional uses and scientific approach. Coccinia indica is one
of the most important controversial and effective natural origin
that has a tremendous future for research. The plant part contains important
constituents and has been widely used for the treatment of large number of
human ailments. The applicability of Coccinia indica is hidden and thus such things should be
overcome through modern scientific concepts.
KEYWORDS: Coccinia indica, Traditional uses, Phytoconstituents,
hepatoprotective activity, hypoglycemic activity,
antioxidant activity.
INTRODUCTION:
Coccinia indica belonging to family
Cucurbitaceae, commonly called as Ivy gourd
(English), Kundasu (Hindi), Bimbi (Sanskrit).1 Coccinia indica is a
perennial, scandent or prostrate, much branched,
roots are thick, stems are grooved, slender, glabrous. The leaves are 5-10cm
long and broad, bright green above, paler beneath, studded and sometimes rough
with papillae. Fruits are in fusiform, ellipsoid, slightly beaked, marked when immature
with white streaks, bright scarlet when fully ripe. Seeds are obovoid, rounded at the apex, slightly papillose,
much compressed, yellowish grey in colour.2
The plant is used as cathartic, antispasmodic,
expectorant, etc. The leaves are used as anthelmintic,
antispasmodic, expectorant, and antiulcer. Fruits are used as laxative,
antiemetic, anti-inflammatory, antileprotic. Roots
are used as cathartic, antiarthritic, hypoglycemic.1,
2, 3,
Ø Regional names:1
The plant is known by various names in different
languages as follows:
Hindi name
: Kundasu
Sanskrit name
: Bimbi
English name
: Ivy gourd
Tamil name
: Kobai, Kai
Telgu
name :
Donda, Kapa
Ø Scientific
classification:4
Kingdom
: Plantae
(Unranked) :
Angiosperms
(Unranked) :
Eudicots
(Unranked) :
Rosids
Order
: Cucurbitales
Family
: Cucurbitaceae
Genus
: Coccinia
Species
: indica
Botanical name :
Coccinia indica
Macroscopy (Fig-1):-5
Stem:
Smooth, cylindrical and slightly flattened at
the extremities, longitudinal striations on the external surface, fibrous with
presence of leaf tendrils.
Leaves:
Alternate, sagittate, margins crenate, 6 to 13
cm. or more long, 10 to 14 cm. wide, lower surface smooth with reticulate
venation, mucronate apex (Fig:1)
Flowers:
1 to 2 cm. in diameter, solitary or in
densely crowded auxiliary heads.
(i)Pedicles:1 to 2 cm. slender, joined near the middle.
(ii)Calyx: Persistent and 5 lobed
(iii)Sepals :Pale green, triangular, acute,
about 6mm. long.
(iv)Petals: Five, joined at base, 6 to 9
mm. or more long, white or pale yellow, with a shallow notch at the apex.
(v)Ovary :Eight celled, one ovulate.
(vi) Stamens :Many filaments arising from a
tube.
(vii)Style :Divided to 6 branches. (Fig:1)
Fruits:
Outer surface of the fruit is dark green colour
and inner surface is yellowish-pink colour. Somewhat
curved from base and are having smooth surface. Fruits contain: Pericarp, Epicarp, and Mesocarp. The fruits also contain Endocarp, Placenta, and Unilocular ovary. (Fig:1)
Seeds :
Small, roughly triangular, 1.5 mm. long with
a deep depression on each sides, reddish brown or black.
Root : Strong Taproot.
Microscopy:-5
The T.S. of leaf consists of Lamina and Midrib and report mentioned in
Fig.no-2.
Lamina:
(1) The upper and lower epidermis consists of single layer of tabular
cells, covered with smooth cuticle.
(2) Just below the upper epidermis single layer of palisade parenchyma
(Upper palisade) was present and it was not
continuous over the midrib
region.
(3) Rest part of the lamina is filled with loosely arranged parenchymatus cells having large intra cellular spaces
(Spongy Parenchyma), few cells contains calcium oxalate crystals.
(4) No lower palisade
cells were observed.
Midrib:
The midrib was having
slight projection on the upper side and lower side was wider.
(1) Upper epidermis
composed of single layer tabular cells with smooth cuticle. Below the upper
epidermis in the projection area 3-4 layers of collenchymatous
tissue were observed, followed by layers of cortical parenchymatous
cells.
(2)
. Palisade cells were absent at the midrib region.
(3) The secondary
vascular bundle consists of xylem vessels. Surrounded by inter xylary parenchymatous cells,
phloem composed of 3-4 layers of polyhedral closely arranged cells and 3-4
layers of pericyclic sclerenchymatous
cells. It is present towards the ventral side.
(4) The primary
vascular bundle consists of xylem vessels. Surrounded by inter xylary parenchymatous cells,
phloem composed of 3-4 layers of polyhedral closely arranged cells which are
slightly bigger then the secondary vascular bundle.
(5) The space between
the endodermis and collenchymatus layer is filled
with cortical parenchyma.
(6) Lower epidermis
consisted of single layer irregular shaped cells with smooth cuticle and just
above the lower epidermis 2-3 layers of parenchymatous
cells followed by the layers of collenchymatous cells
were present.
(7) Prismatic
calcium-oxalate crystals were found in the midrib region inside collenchymatous cells.
Powder Microscopy-5
The powder characters
of a drug are mainly used in the identification of the drug in the powder from.
The leaf powder was green in colour, characteristic
in odour with in mucilaginous and slightly bitter in
taste on microscopical examination the powder showed animocytic stomata, Spongy parenchyma containing calcium
oxalate prisms, Spiral Xylem vessel, Prismatic calcium oxalate crystals, collenchymatous cells and cortical parenchymatus
cells and report mentioned in Fig.no-3.
Physical evaluation-5
The Loss on Drying,
Ash Values likes (Total Ash, Acid insoluble ash, Water soluble ash, Sulphated ash) Water soluble extractive, Methanol soluble
extractive, Pet. Ether soluble extractive and Swelling Index of leaf powder are
given in table-1.
Acute Toxicity Study: 6
Acute oral toxicity
was performed as per OECD-423 guidelines. Animals are distributed into one
control and three treated groups. Animals in control group received vehicle
while animals in other groups received 100, 500, 1000mg/kg body weight aqueous
extract. In the acute toxicity test of
aqueous extract there was no mortality or any signs of behavioral changes or
toxicity observed after oral administration of the extract up to the dose of
2000mg/kg body weight in mice.
Chemical Constituents:-
Coccinia indica has been explored phytochemically by various researchers and found to posses number of chemical constituents.
The plant contains Saponins, flavonoids, sterols and alkaloids.
The various
plant constituents reported are cephalandrol, tritriacontane, lupenol,, β-sitosterol, cephalandrin A, cephalandrin B,
stigma-7-en-3-one, taraxeron and taraxerol.6
The roots are found to contain Triterpenoids,
saponin coccinioside, flavonoid glycoside ombuin
3-o-arabinofuranoside, lupenol, β-amyrin, β-sitosterol,
stigmast-7-en-3-one.7-10
The fruits are found to contain Taraxerone, taraxerol, and
(24R)-24- ethylcholest- 5- en- 3β- ol glucoside.
Β- carotene, lycopene,
cryptoxanthin, and apo- 6’-
lycopenalΒ- sitosterol
and taraxerol.11-13
Aerial parts of the plant contain Heptacosane
Cephalandrol, C29H58O tritriacontane C33H68 Β- sitosterol alkaloids Cephalandrine
a and Cephalandrine b.14,15
The whole plant contain Aspartic acid, Glutamic
Acid, Asparagine, Tyrosine, Histidine,
Phenylalanine And Threonine Valine
Arginine.16
Traditional Uses:
Almost all the parts
of Coccinia indica are of
medicinal importance and traditionally used for the treatment of various
ailments.
This plant is
traditionally used in various diseases like psoriasis, ringworm, itching, small
pox, skin diseases, ulcer, scabies, diabetes, asthma, bronchitis, dysentery,
vomiting, cough and cold.6, 17, 18
Pharmacological Studies:-
Hypoglycemic activity:
Hypoglycemic effect of
Coccinia indica W and
A. and its influence on certain biochemical parameters were studied, where the
alcoholic extract was found to be more active in reducing blood glucose level. 19
Pectin isolated from hydroalcoholic extract of fruits of Coccinia indica upon oral administration at a
dose of 200mg/ 100gmBW/Day showed significant hypoglycemic effect.20
Evaluation of antidiabetic efficacy of coccinia indica in rats shows significant
reduction in blood glucose, serum cholesterol, triglyceride and lipid peroxides
levels and elevation of reduced glutathione and liver glycogen in C. indica
treated group when compared with the diabetic control. The results showed that
the ethanolic extract of C. indica
leaves possessed significant hypoglycaemic, hypolipidemic and antioxidant effects.21
Hypoglycemic activity
of Pectin isolated from the fruit of coccinia indica in normal rats showed highly significant
Glycogen synthetase activity and significant redn. in phosphorylase
activity.22
Antiulcer activity:
The anti–ulcer
activity of ethanolic, aqueous, total aqueous
extracts of leaves of Coccinia grandis
(Linn.), Anti-ulcer activity of the three extracts was studied in rats by using
pylorus ligated ulcer model. The expected result is
to get an anti-ulcer activity of the leaf extracts of Coccinia grandis should owing to the presence of
one or more phytoconstituents, which may reduce the
acidity of the gastric juice and also prevents the mucosal damage and ulcer
formation. The Ethanolic Extract 400mg/kg expected to
showed comparable anti ulcer-activity as that of standard Omeprazole.23
Anthelmintic activity:
The present study was
designed to explore the anthelmintic activity of
different extracts of plant Coccinia indica (fruits) using petroleum ether, ethyl acetate
methanol and water as solvents. Various concentrations (25 and 50mg/ml) of all
the extracts were tested, which involved determination of time of paralysis and
time of death of the worms. It was compared with Albendazole
as standard reference and normal saline as control. The study indicated the
potential usefulness of Coccinia indica
against earthworm infections.18
Antibacterial activity:
In vitro antibacterial
activity of leaves and stem extracts of Coccinia grandis L., has been
investigated against Bacillus cereus, Corynebacterium diptheriae,
Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli (ETEC), Klebsiella
pneumonia, Proteus mirabilis, Pseudomonas aeruginosa,
Salmonella typhi and Shigella
boydii. Water extract of leaves and ethanolic extract of stem showed significant activity
against Shigella boydii and Pseudomonas aeruginosa
respectively.24
The aqueous and organic solvent (Petroleum ether, chloroform and
ethanol) extracts from the leaves of Coccinia
indica (Cucurbitaceae)
were tested against Enterobacter aerogenes, Pseudomonas aeruginosa,
Staphylococcus epidermidis, Bacillus subtilis and Salmonella typhimurium
by agar well diffusion method and broth dilution method. Results showed
promising antibacterial activity against the bacteria tested. Among these,
ethanol and aqueous extracts were found to have a more potent inhibitory effect
comparing with the other extracts.25
Antioxidant activity:
The aim of the present
study was investigating the antioxidant activity of the methanolic
extract of the fruit of Coccinia grandis L.
Voigt. (Cucurbitaceae). The
antioxidant activity of the fruit has been evaluated by using three in vitro
assays and was compared to standard antioxidant, Butylated
hydroxyanisole (BHA). All the fractions showed
effective H-donor activity, reducing power, free radical scavenging activity.
The antioxidant property depends upon concentration and increased with
increasing amount of the fractions. The free radical scavenging and antioxidant
activities may be attributed to the presence of flavonoids
present in the fractions.26
Antitussive activity:
The a antitussive effect of aerosols of
two different concentrations (2.5%, 5%w/v) of methanol extract of Coccinia grandis
fruits were tested by counting the numbers of coughs produced due to
aerosols of citric acid, 10 min after exposing the male guinea pigs to aerosols
of test solutions for 7 min. In another set of experiment methanol extract was
investigated for its therapeutic efficacy on a cough model induced by sulfur
dioxide gas in mice. The results showed significant reduction of cough number
obtained in the presence of both concentrations of methanol extract as that of
the prototype antitussive agent codeine phosphate.27
Antihepatotoxic activity:
Ethanolic extract of fruit and
leaves of Coccinia indica
revealed the presence of saponins. The purified
fraction Ci from ethanolic
extract by gradient silica gel column chromatography in the dose 25 mg/kg
(Ci-1) and 50 mg/kg (Ci-2) (p.o.) showed significant
dose dependent reduction in SGPT, SGOT, bilirubin,
total protein, liver weight and lipid peroxide levels with reference to the
standard, silymarin (25 mg/kg, p.o).The
Ci compound also revealed significant dose dependent
reduction in the hepatic antioxidant enzyme activities such as super oxide
dismutase, glutathione, catalase, and peroxidase. The structural characterization of Ci compound by microanalysis, UV, IR, 1H NMR, 12C NMR spectroscopy and
Mass spectrometry revealed structure with molecular formula C29 H50
O (β sitosterol). Hepatoprotective
potential of Ci compound, β sitosterol
was inferred from it's antihepatotoxic activities on serum transaminases
and hepatic antioxidant enzymes in CCl4 intoxicated rats.28
Anti-inflammatory, analgesic and antipyretic activity:
Anti-inflammatory,
analgesic and antipyretic activity of aqueous extract of fresh leaves of Coccinia indica. The anti-inflammatory
activity was studied by using Carrageenan- induced
paw oedema method, analgesic activity was studied by
using Tail flick model in rats and antipyretic activity was studied by using
Yeast induced hyperpyrexia in rats. The aqueous extract of fresh leaves was
found to be effective as anti-infflamatory, analgesic
and antipyretic.29
Figure 1: Macroscopy
of Coccinia indica.
Fig-2. Microscopy of Coccinia indica leaf
SP-Spongy Parenchyma, LE-Lower Epidermis, VB-Vasucular
Bundle, CH- Collenchyma,,
LEC-Lower
Epidermis with Cuticle, UEC-Upper Epidermis With
Cuticle, PF-Pericyclic Fibers, UP-Upper Palisade.
Fig-3. Powder Characteristics of Coccinia indica leaf
Table 1: Physical Evaluation.
Sr. No. |
Parameter Values |
(%)(w/w) |
1. |
Loss on Drying |
15.5% |
2. |
Ash Values |
|
A. |
Total Ash |
13.7% |
B. |
Acid insoluble ash |
1.25% |
C. |
Water soluble ash |
7.20% |
D. |
Sulphated ash |
11.5% |
3. |
Extractive Values |
|
A. |
Water soluble
extractive |
20.5% |
B. |
Methanol soluble Exractive |
12.80% |
C. |
Pet.ether soluble Extractive |
3.16% |
4. |
Swelling Index |
0.827 |
CONCLUSION:
Coccionia indica have several
pharmacological properties like, Antidiabetic,
Anti-inflammatory, Analgesic, antipyretic, antioxidant
and hepatoprotective activity. The main chemical
constituents are steroids, alkaloids, flavonoids,
glycosides, tannins and Phenolic compounds. Hence in
this review article, effort has been taken to collect and compile the details
regarding Coccionia indica which
will be useful to the society to venture into a field of alternative systems of
medicine.
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Received on 29.08.2012
Modified on 04.09.2012
Accepted on 19.09.2012
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