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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

Niketa Prashant Kumar Singh

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

Niketa, Prashant Kumar Singh "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" Iconic Research And Engineering Journals Volume 10 Issue 4 2026 Page 2501-2510
Niketa, Prashant Kumar Singh "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" Iconic Research And Engineering Journals, vol. 10, no. 4, Oct. 2026
Niketa, Prashant Kumar Singh (2026). 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. Iconic Research And Engineering Journals, 10(4).
Niketa, Prashant Kumar Singh "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" Iconic Research And Engineering Journals, vol. 10, no. 4, Oct. 2026.
@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},
  }