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Comparative Hepatoprotective Evaluation of Calotropis gigantea Root and Portulaca oleracea Foliated-Stem Extracts, Alone and in Combination, Against Carbon Tetrachloride-Induced Hepatotoxicity in Wistar Rats
Subject area: Biological & Medical Sciences · Area of research: Pharmacy
Abstract
Carbon tetrachloride (CCl4)-induced hepatotoxicity is a well-established experimental model for evaluating hepatoprotective agents, given its reproducible induction of oxidative hepatocellular injury via cytochrome P450-mediated bioactivation to the trichloromethyl free radical [3-6]. This study evaluated the comparative and combined hepatoprotective potential of methanolic extracts of Calotropis gigantea root and Portulaca oleracea foliated stem against CCl4-induced hepatotoxicity in Wistar rats. Extracts were obtained by cold maceration (6.30% w/w and 8.40% w/w yield respectively) and screened for phytoconstituents, both testing positive for flavonoids, alkaloids, glycosides, saponins and tannins. Acute oral toxicity testing (OECD 423) confirmed safety up to 2000 mg/kg, and doses of 100, 200 and 400 mg/kg were selected for the main study. Sixty male Wistar rats were divided into ten groups (n = 6): normal control, CCl4 toxic control, silymarin (50 mg/kg), three dose levels each of C. gigantea and P. oleracea, and a low-dose combination. CCl4 administration markedly elevated serum ALT, AST, ALP and bilirubin and hepatic malondialdehyde while depleting glutathione and body/liver-weight indices; both extracts dose-dependently attenuated these changes, with C. gigantea 400 mg/kg (74.6% hepatoprotection), P. oleracea 400 mg/kg (78.5%) and particularly the combination (85.4%, approaching silymarin's 87.7%) producing the most pronounced normalisation, corroborated by histopathological improvement from severe centrilobular necrosis to near-normal architecture. These findings support a synergistic, antioxidant-mediated hepatoprotective action for the combined extracts, comparable to standard silymarin therapy.
Keywords
Calotropis gigantea; Portulaca oleracea; hepatoprotective activity; carbon tetrachloride; oxidative stress; silymarin; polyherbal combination; Wistar rats
References
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How to cite this paper
@article{1724049,
author = {Niketa, Prashant Kumar Singh},
title = {Comparative Hepatoprotective Evaluation of Calotropis gigantea Root and Portulaca oleracea Foliated-Stem Extracts, Alone and in Combination, Against Carbon Tetrachloride-Induced Hepatotoxicity in Wistar Rats},
journal = {Iconic Research And Engineering Journals},
year = {2026},
volume = {10},
number = {4},
pages = {2501-2510},
issn = {2456-8880},
url = {https://www.irejournals.com/formatedpaper/1724049.pdf},
abstract = {Carbon tetrachloride (CCl4)-induced hepatotoxicity is a well-established experimental model for evaluating hepatoprotective agents, given its reproducible induction of oxidative hepatocellular injury via cytochrome P450-mediated bioactivation to the trichloromethyl free radical [3-6]. This study evaluated the comparative and combined hepatoprotective potential of methanolic extracts of Calotropis gigantea root and Portulaca oleracea foliated stem against CCl4-induced hepatotoxicity in Wistar rats. Extracts were obtained by cold maceration (6.30% w/w and 8.40% w/w yield respectively) and screened for phytoconstituents, both testing positive for flavonoids, alkaloids, glycosides, saponins and tannins. Acute oral toxicity testing (OECD 423) confirmed safety up to 2000 mg/kg, and doses of 100, 200 and 400 mg/kg were selected for the main study. Sixty male Wistar rats were divided into ten groups (n = 6): normal control, CCl4 toxic control, silymarin (50 mg/kg), three dose levels each of C. gigantea and P. oleracea, and a low-dose combination. CCl4 administration markedly elevated serum ALT, AST, ALP and bilirubin and hepatic malondialdehyde while depleting glutathione and body/liver-weight indices; both extracts dose-dependently attenuated these changes, with C. gigantea 400 mg/kg (74.6% hepatoprotection), P. oleracea 400 mg/kg (78.5%) and particularly the combination (85.4%, approaching silymarin's 87.7%) producing the most pronounced normalisation, corroborated by histopathological improvement from severe centrilobular necrosis to near-normal architecture. These findings support a synergistic, antioxidant-mediated hepatoprotective action for the combined extracts, comparable to standard silymarin therapy.},
keywords = {Calotropis gigantea; Portulaca oleracea; hepatoprotective activity; carbon tetrachloride; oxidative stress; silymarin; polyherbal combination; Wistar rats},
month = {October},
}