Melatonin mitigated methotrexate-induced hepatotoxicity through interrelated biological processes
- PMID: 39039363
- DOI: 10.1007/s11033-024-09792-z
Melatonin mitigated methotrexate-induced hepatotoxicity through interrelated biological processes
Abstract
Background: Hepatotoxicity associated with methotrexate (MTX) is mainly due to disruption of redox balance and development of oxidative injury to hepatocytes. Melatonin (MLT) is a potent antioxidant and regulates wide range of biological functions, processes and utilized as adjuvant for number of medical applications VSports手机版. The current study investigated the mitigating effect of MLT on the MTX-induced hepatotoxicity. .
Methods and results: Adult male rats received MLT (25 mg/kg, orally) for seven days flowed by single injection of MTX (20 mg/kg, ip) then treat with MLT continued for additional 7 days. The present result showed MLT treatment mitigated histopathological changes in the liver that associated with normalization of ALT and AST activity as well as bilirubin, albumin and alfa-fetoprotein levels in serum of MLT + MTX-treated rat to comparable control level. MLT treatment significantly reduced MDA content and myeloperoxidase activity while enhanced the activity of superoxide dismutase, catalase and glutathione content in the liver indicating the empowerment of the antioxidant status V体育安卓版. Amelioration of MLT-induced oxidative stress resulted in a reduction in the inflammatory response due to antioxidant restoration and inhibited apoptosis indicated by downregulation of caspase-3 expression. The replenishment of antioxidant content powers the defense system of the hepatocytes. As a result, apoptosis is reduced which might be due to the ability of MLT protect DNA integrity thus maintaining hepatocyte functions and structure. Consequently, liver histology was protected. .
Conclusions: In summary, MLT modulates liver function and structure by orchestrating linked processes, including redox balance, inflammatory response, suppression of caspase-3, and DNA damage V体育ios版. .
Keywords: Alfa-fetoprotein; Caspase-3; DND damage; Inflammatory cytokines; Liver; Oxidative stress. VSports最新版本.
© 2024. The Author(s), under exclusive licence to Springer Nature B. V V体育平台登录. .
References
-
- Maksimovic V, Pavlovic-Popovic Z, Vukmirovic S, Cvejic J, Mooranian A, Al-Salami H, Mikov M, Golocorbin-Kon S (2020) Molecular mechanism of action and pharmacokinetic properties of methotrexate. Mol Biol Rep 47(6):4699–4708 - PubMed
-
- Di Martino V, Verhoeven DW, Verhoeven F, Aubin F, Avouac J, Vuitton L, Liote F, Thevenot T, Wendling D (2023) Busting the myth of methotrexate chronic hepatotoxicity. Nat Rev Rheumatol 19(2):96–110 - PubMed
-
- Khawaja G, El-Orfali Y (2024) Silibinin’s effects against methotrexate-induced hepatotoxicity in adjuvant-induced arthritis rat model. Pharmaceuticals (Basel) 17(4):431 - PubMed
-
- Kayali A, Bora ES, Acar H, Yilmaz G, Erbas O (2024) Fisetin ameliorates methotrexate induced liver fibrosis. Eur Rev Med Pharmacol Sci 28(8):3112–3119 - PubMed
MeSH terms
- Actions (V体育官网)
- V体育官网入口 - Actions
- "V体育官网入口" Actions
- "VSports注册入口" Actions
- "V体育官网入口" Actions
- Actions (V体育安卓版)
- "V体育平台登录" Actions
- V体育2025版 - Actions
Substances
- "V体育官网" Actions
- "V体育2025版" Actions
- "V体育平台登录" Actions
- "VSports在线直播" Actions
LinkOut - more resources (VSports最新版本)
Full Text Sources (V体育官网)
Medical
Research Materials