谷胱甘肽的抗氧化作用及其保护小鼠肝细胞免受呋喃损伤的能力

Ibrahim Ibrahim, Hend Saleh, Alshaimaa Hamouda
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摘要

呋喃通常存在于多种热处理食品中,食品中呋喃的存在引发了公共卫生问题。目前的研究探讨了谷胱甘肽对小鼠肝脏、肾脏功能和肿瘤标志物的预防作用。/天)、G5(4 毫克呋喃/千克体重/天)、G6(2 毫克呋喃/千克体重/天 +500 毫克谷胱甘肽/千克/天)和 G7(4 毫克呋喃/千克体重/天 +500 毫克谷胱甘肽/千克/天)。研究结束时,即 8 周后,进行麻醉和宰杀,然后进行不同的测试。结果呋喃会明显增加小鼠肝细胞的损伤,表现为小鼠在服用 2 毫克/千克/天的剂量后,转氨酶(AST)和丙氨酸氨基转移酶(ALT)的活性增加。不同剂量(0.5、1、2 和 4 毫克/千克/天)的呋喃会导致丙二醛水平升高,从而促进氧化应激。研究发现,用 500 毫克/千克/天的谷胱甘肽进行预处理可降低小鼠的 AST、ALT 和 MDA 活性,而呋喃水平不会对肾功能产生负面影响。值得注意的是,与对照组(3.1 纳克/毫升)相比,所有水平的呋喃都会增加肿瘤标志物[甲胎蛋白 (AFP)],而谷胱甘肽可将服用呋喃剂量(2 和 4 毫克/千克)组的甲胎蛋白水平降至(3.5 - 3.6 毫克/毫升),而服用呋喃剂量(2 和 4 毫克/千克)但未服用谷胱甘肽的同一组的甲胎蛋白水平则为(4.6 - 4.8 毫克/毫升)。谷胱甘肽对呋喃诱导的肝细胞损伤的保护作用可能是由于其清除自由基的特殊能力。谷胱甘肽具有很强的抗氧化性,有望成为一种治疗和预防呋喃化合物诱发疾病的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glutathione's antioxidant effects and its ability to shield mice's hepatocytes from damage caused by furan
Furan is commonly found in several kinds of heat - treated foods, the existence of furan in food causes public health issues. The current research examines the preventive impact of glutathione on liver, kidney function, and tumor markers against furan - induced injury in mice. Male albino mice were divided into seven groups: a control (G1), G2 (0.5mg furan/ kg b.w./day), G3 (1 mg furan/kg b.w./day), G4 (2 mg furan/kg b.w./day), G5 (4 mg furan/ kg b.w./day), G6 (2 mg furan/kg b.w./day +500 mg glutathione/kg/day), and G7 (4 mg furan/kg b.w./day +500 mg glutathione/kg/day). At the end of the study, after 8 weeks, the anesthetized and sacrificed were done, and then the different tests were conducted. Results: Furan significantly increased hepatocyte damage in mice, as evidenced by increased activities of aminotransferase (AST) and alanine aminotransferase (ALT) after a 2mg/kg/ day dose. Furan promoted oxidative stress due to elevated malondialdehyde levels, occurring at various furan dosages (0.5, 1, 2, and 4mg/kg/day). The study found that pre-treatment with glutathione at 500 mg/kg/day reduced AST, ALT, and MDA activities in mice, while furan levels did not negatively impact kidney functions. It should be noted that all levels of furan increased tumor markers [Alpha Fetoprotein (AFP)] compared to the control (3.1 ng/ml), whereas glutathione reduced the level of AFP in groups taking furan at (2 and 4 mg/kg) to range (3.5 – 3.6 mg/ml) compared to (4.6 – 4.8 mg/ml) for the same groups taking furan at (2 and 4 mg/kg) without glutathione. Glutathione's protective effects against furan - induced hepatocyte damage may be due to its exceptional capacity to scavenge free radicals. Glutathione, with its strong antioxidant properties, has the potential to be a promising therapeutic and preventive agent for diseases induced by furan compounds.
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