Effects of omega-3 and vitamin c on methotrexate-induced liver injury

D. Mohammed, A. Al-Gareeb
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Abstract

Context: Methotrexate (MTX)-induced liver injury is a serious side effect characterized by the increased level of hepatic biomarkers and resulted in acute liver failure. Omega 3 and Vitamin C act as antioxidant that participate in the fighting of free radicals generation during the inflammatory process. Aims: To evaluate the effect of omega 3 and Vitamin C on hepatotoxicity induced by MTX. Settings and Design: 42 (Swiss albino mice) used and divided into six groups (7 mice each): First: Maintained with normal saline, second: Received a single dose injection of MTX (20 mg/kg, intraperitoneally), third: Pretreated with omega 3 100 mg/kg, fourth: Pretreated with omega 3 200 mg/kg, fifth: Pretreated with Vitamin C 100 mg/kg, sixth: Pretreated with Vitamin C 200 mg/kg, then these group injected with MTX on day 10. Subjects and Methods: MTX as 50 mg injection. Omega 3 as capsule 1000 mg. Vitamin C as powder 1000 mg. Assessment of liver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST], and alkaline phosphatase [ALP]) made using automated computering device (Flexor–EL80) provider by Vitalab (South Africa). Assessment of oxidative stress markers (malondialdehyde [MDA], superoxide dismutase [SOD], reduced glutathione [GSH]) and lactate dehydrogenase (LDH) made by using competitive ELISA kits using (ELISA microplate Humareader). Results: This study showed a significant increase in the liver enzymes (ALT, AST, ALP, and LDH) as well oxidative stress markers (MDA, SOD, and GSH) with severe changes in the histopathological findings (severe inflammatory cell necrosis) among group injected with MTX as compared with control group and illustrated improvement in serum level of ALT, ALP, LDH, MDA, SOD and reduced GSH; besides improved histopathological findings (mild and moderate changes) for a group of mice pretreated with omega 3 and Vitamin C. Conclusions: This study concluded that pretreatment with omega 3 (which was strong antioxidant supplement) and Vitamin C (which was dose-dependent manner with beneficial antioxidant action) exert more hepatoprotective effect against oxidative tissue damage induced by MTX.
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ω-3和维生素c对甲氨蝶呤肝损伤的影响
背景:甲氨蝶呤(MTX)诱导的肝损伤是一种严重的副作用,其特征是肝脏生物标志物水平升高,并导致急性肝衰竭。欧米茄3和维生素C作为抗氧化剂,在炎症过程中参与对抗自由基的产生。目的:评价ω3和维生素C对MTX肝毒性的影响。设置和设计:使用42只(瑞士白化病小鼠),并分为六组(每组7只):第一组:用生理盐水维持,第二组:接受单剂量MTX注射(20 mg/kg,腹膜内),第三组:用ω3 100 mg/kg预处理,第四组:用Ω3 200 mg/kg预处理,然后这些组在第10天注射MTX。受试者和方法:MTX 50 mg注射液。Omega 3胶囊1000 mg。维生素C粉末1000 mg。使用Vitalab(南非)提供的自动计算机设备(Flexor–EL80)对肝酶(丙氨酸氨基转移酶[ALT]、天冬氨酸氨基转移酶/AST]和碱性磷酸酶[ALP])进行评估。氧化应激标志物(丙二醛[MDA]、超氧化物歧化酶[SOD]、还原型谷胱甘肽[GSH])和乳酸脱氢酶(LDH)的评估通过使用竞争ELISA试剂盒使用(ELISA微孔板Humarader)进行。结果:与对照组相比,注射MTX组的肝酶(ALT、AST、ALP和LDH)和氧化应激标志物(MDA、SOD和GSH)显著增加,组织病理学表现(严重炎症细胞坏死)发生严重变化,血清ALT、ALP、LDH、MDA、SOD水平提高,GSH减少;此外,用ω3和维生素C预处理的一组小鼠的组织病理学结果(轻度和中度变化)也有所改善。结论:本研究得出结论,ω3(一种强抗氧化剂补充剂)和维生素C(具有有益抗氧化作用的剂量依赖性方式)预处理对MTX诱导的氧化组织损伤具有更大的肝脏保护作用。
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