Protective Effects of Momordica charantia (Bitter Melon) against Methotrexate-induced Kidney Damage

被引:0
|
作者
Macit, Caglar [1 ]
Ozbeyli, Dilek [2 ]
Cevik, Ozge [3 ]
Cetin, Melisa [4 ]
Sener, Goksel [5 ]
Ozkan, Sevil [6 ]
机构
[1] Istanbul Medipol Univ, Sch Pharm, TR-34815 Istanbul, Turkiye
[2] Marmara Univ, Vocat Sch Hlth Sci, Istanbul, Turkiye
[3] Adnan Menderes Univ, Sch Med, Aydin, Turkiye
[4] Marmara Univ, Sch Pharm, Istanbul, Turkiye
[5] Fenerbahce Univ, Fac Pharm, Istanbul, Turkiye
[6] Univ Hlth Serv, Haydarpasa Numune Educ & Res Hosp, Clin Internal Med, Istanbul, Turkiye
关键词
Momordica charantia; protective effect; kidney; methotrexate; nephrotoxicity; oxidative damage; OXIDATIVE ORGAN INJURY; CELLS IN-VITRO; STRESS; ANTIOXIDANT; APOPTOSIS; EXTRACTS; PROTEIN; POLYSACCHARIDES; INTERVENTION; CYTOTOXICITY;
D O I
10.2174/1574885518666230112110246
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Methotrexate is a cytotoxic chemotherapeutic agent that has severe side effects, such as nephrotoxicity. Momordica charantia is a bright yellow-orange fruity plant that has been shown to have antioxidant, antidiabetic, and anti-inflammatory properties. Objective This study scrutinized the protective effects of Momordica charantia extract against methotrexate-induced nephrotoxicity. Methods 24 Sprague Dawley male rats were divided into three experimental groups (8 rats in each): Control (C); Methotrexate (MTX); and Methotrexate plus Momordica charantia (MTX+MC). All rats were fed ad libitum and tap water. Methotrexate was administered at 20 mg/kg intraperitoneally as a single dose. In the MTX+MC group, MC was administered at a dose of 50mg/kg for 5 days orally. At the end of the 5th day, the rats were decapitated and kidney samples were taken to analyze glutathione (GSH), malondialdehyde (MDA), myeloperoxidase (MPO), 8-hydroxy-2'-deoxyguanosine (8-OHdG) and caspase-3 activity. Data was analyzed with GraphPad Prism 5.0. Results Findings showed that while there was a significant increase in MDA, MPO, 8-OHdG levels, and an essential reduction in GSH levels in the MTX-treated group when compared with the control group, bitter melon treatment significantly reversed MDA, MPO, and 8-OHdG levels (p< 0.001). GSH level elevation was observed in the MTX-MC group when compared to the MTX-treated group (p< 0.001). Conclusion This study showed that bitter melon is thought to have a protective effect against kidney damage caused by methotrexate. With future studies, we believe that the use of bitter melon extract as a protective agent in kidney damage caused by drug-induced oxidative damage will bring an innovative approach to treatment.
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收藏
页码:231 / 236
页数:6
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