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Research Article

Metformin ameliorates acetaminophen-induced sub-acute toxicity via antioxidant property

, , , , , , & show all
Pages 52-60 | Received 04 Jul 2019, Accepted 10 Aug 2019, Published online: 02 Sep 2019
 

Abstract

Acetaminophen or N-acetyl-p-amino-phenol (APAP) is a drug which is available over-the-counter for fever and pain. Its overdosing causes oxidative stress and subsequent acute liver damage. In the present study, we scrutinized the protective effect of metformin co-treatment in APAP induced blood and liver sub-acute toxicity. This is a pre-clinical study in which male Wistar Rats (BW: 300 ± 20 g) were orally co-treated with APAP (1 g/kg/day) and metformin (300 mg/kg/day) for 28-days. Pro- and anti-oxidant markers viz reactive oxygen species, protein carbonyl, malondialdehyde (MDA), the ferric reducing ability of plasma (FRAP), plasma membrane redox system(PMRS) and reduced glutathione (GSH) were evaluated in blood. Additionally, in liver tissue, catalase (CAT), superoxide dismutase (SOD), MDA and GST level were also evaluated. Histological study and estimation of alanine aminotransferase (ALT), and aspartate aminotransferase (AST) level in serum were performed. APAP induces pro-oxidant markers as well as reduces anti-oxidant markers in blood and liver. Hepatic tissues degeneration and vacuolization of hepatocytes were evident after APAP treatment. Metformin treatment reduces pro-oxidant markers as well as increases anti-oxidant markers in both tissues. It also improves liver tissue architecture after treatment. The outcome of this study suggests that metformin has protective capability against APAP-induced blood and liver toxicity. Thus, metformin co-treatment with APAP attenuates oxidative stress and its consequences

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was also supported by a research grant to SIR from SERB-DST, Govt of India (EMR/2016/006470). Dr D.S. Kothari Post-Doctoral Fellowship scheme of University Grant Commission (UGC), New Delhi, India, is also acknowledged for providing financial support (F(0).4–2/2006 (BSR)/BL/17–18/0381) to SST. The Department of Biochemistry is supported by FIST grant of DST, New Delhi, and SAP DRS I from UGC, India.

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