Reno-protective effect of mangiferin against methotrexate-induced kidney damage in male rats: PPARy-mediated antioxidant activity

被引:6
|
作者
Attia, Seba Hassan [1 ]
Elshazly, Shimaa Mustafa [2 ]
Abdelaal, Mahmoud Mohamed [3 ]
Soliman, Eman [2 ]
机构
[1] Zagazig Univ, Fac Med, Clin Pharmacol Dept, Zagazig, Egypt
[2] Zagazig Univ, Fac Pharm, Pharmacol & Toxicol Dept, Zagazig, Egypt
[3] Zagazig Univ, Fac Pharm, Pharmacogonosy & Phytochem Dept, Zagazig, Egypt
关键词
Mangiferin; Methotrexate; Nephrotoxicity; Peroxisome proliferator-activated receptor-y(PPAR-y); Oxidative stress; PROLIFERATOR-ACTIVATED-RECEPTOR; OXIDATIVE STRESS; GENE-EXPRESSION; GAMMA; INJURY; ACID; APOPTOSIS; PATHWAY; NRF2;
D O I
10.1016/j.jsps.2022.06.026
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methotrexate (MTX) is an immunosuppressant used for the treatment of cancer and autoimmune dis-eases. MTX has a major adverse effect, acute kidney injury, which limits its use. Mangiferin (MF) is a nat-ural bioactive xanthonoid used as a traditional herbal supplement to boost the immune system due to its potent anti-inflammatory and antioxidant activity. The present study evaluates the protective effect of MF against MTX-induced kidney damage. Male Wistar rats received MTX to induce nephrotoxicity or were pretreated with MF for 10 constitutive days before MTX administration. MF dose-dependently improved renal functions of MTX-treated rats and this activity was correlated with increased renal expression of PPARy, a well-known transcriptional regulator of the immune response. Pretreating rats with PPARy inhibitor, BADGE, reduced the reno-protective activity of MF. Furthermore, MF treatment sig-nificantly reduced MTX-induced upregulation of the pro-inflammatory (NFKB, interleukin-1 ss, TNF-a, and COX-2), oxidative stress (Nrf-2, hemoxygenase-1, glutathione, and malondialdehyde), and nitrosative stress (nitric oxide and iNOS) markers in the kidney. Importantly, BADGE treatment significantly reduced the anti-inflammatory and antioxidant activity of MF. Therefore, our data suggest that the reno-protective effect of MF against MTX-induced nephrotoxicity is due to inhibition of inflammation and oxidative stress in a PPAR-y-dependent manner.(c) 2022 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1252 / 1261
页数:10
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