两种不同剂量氰钴胺素对大鼠甲氨蝶呤肾毒性的可能保护作用

Noor Mohammed Alduboni, Nada N. Al-Shawi
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引用次数: 1

摘要

肾毒性被定义为肾功能的快速恶化。它源于直接接触药物或其代谢物。甲氨蝶呤是一种著名的化疗药物,具有抗炎和免疫抑制的特性。大剂量甲氨蝶呤引起的肾功能不全可能危及生命。氰钴胺素是维生素B12的一种形式,在细胞质中充当同型半胱氨酸转化为蛋氨酸的辅酶,在线粒体中将甲基丙二酰辅酶a转化为琥珀酰辅酶a。本研究旨在通过Nrf2/keap1分子机制,探讨两种不同剂量氰钴胺素与甲氨蝶呤(20mg /kg)共给药对大鼠肾毒性的影响。实验用大鼠随机分为4组,每组10只;1组(对照组)大鼠腹腔注射生理盐水0.5ml,每日1次,连续7天。2组:大鼠腹腔注射生理盐水0.5ml,每日1次,连续7天;第2天,单次腹腔注射甲氨蝶呤(20mg/kg)。3组:大鼠腹腔注射氰钴胺素0.5mg/kg,每天1次,连续7天,第2天腹腔注射甲氨蝶呤单次剂量(20mg/kg)。第4组:大鼠腹腔注射氰钴胺素2mg/kg,每天1次,连续7天,第2天腹腔注射甲氨蝶呤单次剂量(20mg/kg)。氰钴胺0.5mg/kg和2mg/kg剂量与甲氨蝶呤共给药组丙二醛显著降低(P<0.05),谷胱甘肽降低水平显著升高(P<0.05),肾Nrf2表达显著上调,肾keap1表达显著下调(P<0.05)。总之,本研究表明,氰钴胺素以两种不同剂量与MTX共同给药,通过利用选定的参数可以减弱其肾毒性。关键词:肾毒性,甲氨蝶呤,氰钴胺素,丙二醛,谷胱甘肽,Nrf2, Keap1
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possible protective effects of two different doses of cyanocobalamin against methotrexate nephrotoxicity in rats
Abstract    Nephrotoxicity is defined as rapid deterioration in kidney functions. It arises from direct exposure to drugs or their metabolites. Methotrexate is a famous chemotherapeutic drug with anti-inflammatory and immunosuppressive properties. A high-dose methotrexate-induced renal dysfunction can be life threatening. Cyanocobalamin, one of the forms of vitamin B12, acts as a coenzyme in the conversion of homocysteine to methionine in the cytosol, and the conversion of methylmalonyl-CoA to succinyl-CoA in the mitochondrion. This study is designed to examine the effect of cyanocobalamin in two different doses each co-administered with methotrexate at 20 mg/kg induced nephrotoxicity in rats through the involvement of Nrf2/keap1 molecular mechanism in this respect. Rats utilized in this study were randomized into 4 groups (ten rats per each group); Group 1- (Control) rats intraperitoneally injected with 0.5ml normal saline once daily for 7 consecutive days. Group 2- Rats intraperitoneally injected with 0.5ml normal saline once daily for 7 consecutive days; and at day 2, a single intraperitoneal dose of methotrexate (20mg/kg) is to be injected. Group 3- Rats intraperitoneally injected with a 0.5mg/kg cyanocobalamin once daily for 7 consecutive days, and at day 2, a single intraperitoneal dose of methotrexate (20mg/kg). Group 4- Rats intraperitoneally injected with a 2mg/kg cyanocobalamin once daily for 7 consecutive days, and at day 2, a single intraperitoneal dose of methotrexate (20mg/kg). Co-administration of cyanocobalamin at doses cyanocobalamin 0.5mg/kg and 2mg/kg with methotrexate showed significant  reduction  (P<0.05) in malondialdehyde, significant elevation (P<0.05)  in reduced glutathione level, significant upregulation in  renal Nrf2 expression and significant down regulation in renal keap1 expression each compared to corresponding levels in methotrexate-only treated group. In conclusion this study demonstrated that co-administration of cyanocobalamin at two different doses with MTX resulted in attenuation of its nephrotoxicity by the utilization of selected parameters. Keywords: Nephrotoxicity, methotrexate, cyanocobalamin, malondialdehyde, glutathione, Nrf2, Keap1.
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