Possible protective effects of two different doses of cyanocobalamin against methotrexate nephrotoxicity in rats

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

Abstract

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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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
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
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