Hepatoprotective Potential of <i>Phyllanthus niruri</i> Extracts Against CCl<sub>4</sub>‐Induced Liver Injury in Rats: Insight From Phytochemical Profiling, Molecular Docking, and Oxidative Stress Studies

Phyllanthus niruri, a well-known medicinal plant, has been widely recognized for its hepatoprotective, anti-inflammatory, and antioxidant properties. In the present study, the hepatoprotective potential of ethanol extract of P. niruri (EPN) and hexane extract of P. niruri (HPN) were evaluated against carbon tetrachloride (CCl<sub>4</sub>)-induced hepatotoxicity in rats. Oral administration of both EPN and HPN extracts at the dose of 200 mg/kg body weight and silymarin (50 mg/kg) was assessed for their therapeutic effect on liver function, oxidative stress markers, and inflammatory biomarkers. The results demonstrated that standard drug and P. niruri extracts significantly reduced elevated levels of liver enzymes (ALT and AST), oxidative stress (MDA and NO) markers, and inflammatory markers (TNF-α and TGF-β), along with remarkable restoration of antioxidants (GSH and CAT). Furthermore, histopathological outcomes suggested that the hepatic architecture of liver tissues normalized on extract treatment in comparison to the CCl<sub>4</sub>-treated group. The in silico study revealed that 1H-indole, 4-(3-methyl-2-butenyl)- and α-Amyrin from EPN extract, while phenol, 2,4-bis(1,1-dimethylethyl) and Stigmast-4-en-3-one from HPN extract exhibited high binding affinities against selected proteins, TNF-α and TGF-β. These findings highlight P. niruri L. as a valuable source for the development of natural hepatoprotective drugs, as evidenced by its ability to mitigate CCl<sub>4</sub>-induced liver toxicity in rats primarily by enhancing antioxidant status and stabilizing liver cell integrity.

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Journal
Chemistry & Biodiversity
Published
2025-06-03
DOI
https://doi.org/10.1002/cbdv.202500691
Primary Topic
Drug-Induced Hepatotoxicity and Protection
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article
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article

Hepatoprotective Potential of Phyllanthus niruri Extracts Against CCl4‐Induced Liver Injury in Rats: Insight From Phytochemical Profiling, Molecular Docking, and Oxidative Stress Studies

Ali Arshad, Fakhria A. Al‐Joufi, Tariq Aziz, Asia Kiran et al.
Chemistry & Biodiversity
Drug-Induced Hepatotoxicity and Protection
article

Hepatoprotective Potential of Phyllanthus niruri Extracts Against CCl4‐Induced Liver Injury in Rats: Insight From Phytochemical Profiling, Molecular Docking, and Oxidative Stress Studies

Ali Arshad, Fakhria A. Al‐Joufi, Tariq Aziz, Asia Kiran, Fatima Arshad, Khairiah Mubarak Alwutayd, Sara Zahid, Muhammad Sarwar, Awais Altaf, Ashwag Shami, Maher S. Alwethaynani, Tahir Maqbool
article en

Abstract

Phyllanthus niruri, a well-known medicinal plant, has been widely recognized for its hepatoprotective, anti-inflammatory, and antioxidant properties. In the present study, the hepatoprotective potential of ethanol extract of P. niruri (EPN) and hexane extract of P. niruri (HPN) were evaluated against carbon tetrachloride (CCl<sub>4</sub>)-induced hepatotoxicity in rats. Oral administration of both EPN and HPN extracts at the dose of 200 mg/kg body weight and silymarin (50 mg/kg) was assessed for their therapeutic effect on liver function, oxidative stress markers, and inflammatory biomarkers. The results demonstrated that standard drug and P. niruri extracts significantly reduced elevated levels of liver enzymes (ALT and AST), oxidative stress (MDA and NO) markers, and inflammatory markers (TNF-α and TGF-β), along with remarkable restoration of antioxidants (GSH and CAT). Furthermore, histopathological outcomes suggested that the hepatic architecture of liver tissues normalized on extract treatment in comparison to the CCl<sub>4</sub>-treated group. The in silico study revealed that 1H-indole, 4-(3-methyl-2-butenyl)- and α-Amyrin from EPN extract, while phenol, 2,4-bis(1,1-dimethylethyl) and Stigmast-4-en-3-one from HPN extract exhibited high binding affinities against selected proteins, TNF-α and TGF-β. These findings highlight P. niruri L. as a valuable source for the development of natural hepatoprotective drugs, as evidenced by its ability to mitigate CCl<sub>4</sub>-induced liver toxicity in rats primarily by enhancing antioxidant status and stabilizing liver cell integrity.

Chemistry & BiodiversityVol. 22(10)
Princess Nourah bint Abdulrahman University (SA), University of Lahore (PK), University of Ioannina (GR), Jouf University (SA), Shaqra University (SA), Abbasi Shaheed Hospital (PK)
Openalex Percentile: Top 84%
Drug-Induced Hepatotoxicity and Protection
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