Plant extract
The fruits of Cucumis trigonus Roxb. were collected in August 2008 from Beed, Maharashtra State, India. The plant was authenticated by Dr Harsha Hegde Research officer, regional medical research centre, belgaum, karnataka, india and the voucher specimen has been deposited in the herbarium of the Department of Pharmacognosy and Phytochemistry, K.L.E.S’s College of Pharmacy, Belgaum, Karnataka, India. The collected fruits were shade dried at room temperature.The two hundred grams of dried powdered fruits of Cucumis trigonus were extracted by continuous hot extraction process using soxhlet apparatus with petroleum ether, chloroform and alcohol. The powder was finally macerated with chloroform-water IP (As per Indian Pharmacopeia) .The extracts were filtered and concentrated under reduced pressure and low temperature (40oC) on a rotary evaporator.
Phytochemical analysis
The extracts of the plant material were screened for various classes of natural products using standard qualitative methods as described by Harborne (
9).
Experimental animals
Female albino Wistar rats weighing between 180 and 200 g were obtained from animal house, Department of Livestock Production, Government Veterinary College, Hebbal, Bangalore, India. Animals were maintained on a standard laboratory diet. Food and water were given ad libitum. They were housed in standard stainless-steel cages at a 12 h cycle of light and dark. Room temperature was kept at 22 ± 2°C and humidity maintained at 50%. All the chemicalsused were of the analytical grade from standard companies.
Treatment of animals
Rats were randomly divided into 7 groups with 6 animals in each group. Group 1 served as negative control and was administered a single daily dose of distilled water by oral gavage for seven days. Liver damaged was induced by administration of CCl
4 (2 mL/kg, IP as 50 : 50 solution in olive oil) on 1
st, 4th and 7
th day to the animal of remaining group. Group 2 received only CCl
4, group 3 received CCl
4 and standard reference Liv-52 4 mL/kg. p.o. for 7 days. The drug control groups (4, 5, 6 and 7) were given the plant extracts orally in doses of 300 mg/kg/0.2 mL (in distilled water), respectively, one hour after the administration of carbon tetrachloride, for 7 days (
10,
11). Twenty four h after CCl
4 injection animals were anaesthetized by light ether anaesthesia and blood was collected from the vena cava, and the serum was separated for subsequent use for different enzyme measurements. The rats were then decapitated and the livers were carefully dissected and cleaned of extraneous tissues. Part of the liver tissue was immediately transferred to 10% formalin for histopathological assessments.
Assessment of liver damage
Liver damage was assessed by the estimation of serum activities of AST, ALT, ALP and total bilirubin according to the method of Reitman, Kind and Mally by using commercially available test kits (
12-
14).
The livers were removed from the animals and the tissues were fixed in 10% formalin for at least 24 h. Then, the paraffin sections were prepared (Automatic tissue processor, Autotechnique) and cut into 5 μm thick sections using a rotary microtom. The sections were then stained with Haematoxylin-Eosin dye and studied for histopathological changes, such as necrosis, fatty changes, ballooning degeneration and lymphocyte infiltration. Histological damages were scored as: Ø, absent; +, mild; ++, moderate; +++, severe; ++++, extremely severe (
15).
Statistical analysis
Data were analyzed by one-way analysis of variance (ANOVA), followed by the Tuky’s test for individual comparisons using SPSS software and p ≤ 0.01 was regarded as significant.