Protective effects of melatonin and l-carnitine against methotrexate-induced toxicity in isolated rat hepatocytes

被引:6
作者
Khatab, Lamiaa A. [1 ]
Abdel-Raheem, Ihab T. [1 ]
Ghoneim, Asser I. [1 ]
机构
[1] Damanhour Univ, Dept Pharmacol & Toxicol, Fac Pharm, Damanhour 22514, Egypt
关键词
Hepatocytes; l-Carnitine; Melatonin; Methotrexate; INDUCED OXIDATIVE STRESS; INDUCED LIVER TOXICITY; INDUCED HEPATOTOXICITY; KAPPA-B; INJURY; APOPTOSIS; DAMAGE; ACID; MECHANISMS; EXTRACT;
D O I
10.1007/s00210-021-02176-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study was designed to evaluate the possible protective effects of melatonin (MEL) and/or l-carnitine (L-CAR) against methotrexate (MTX)-induced toxicity in isolated rat hepatocytes. Hepatocytes were prepared using collagenase techniques of perfusion and digestion of rat liver. Trypan blue uptake, as well as, glutathione (GSH), lipid peroxidation (LPO), nitric oxide (NO), and tumor necrosis factor-alpha (TNF-alpha) levels were measured. Caspase-3 activity was also assessed. Pre-incubation of hepatocytes with MEL (1 mM) and/or l-CAR (10 mM) 30 min prior to intoxication with MTX, significantly protected hepatocytes against toxicity. In addition, LPO, NO, TNF-alpha levels, and caspase-3 activity were decreased in comparison to the MTX-intoxicated group. Furthermore, the two drugs increased the MTX-depleted GSH level. MEL and L-CAR prevented MTX-induced hepatocytotoxicity, at least partly, by their antioxidative, antiinflammatory, and antiapoptotic effects. Further studies are recommended on the clinical pharmacologic and toxicologic effects of MEL and L-CAR in patients receiving MTX.
引用
收藏
页码:87 / 97
页数:11
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