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Effects of Short Term Exposure of Atrazine on the Liver and Kidney of Normal and Diabetic Rats

机译:短期暴露于r去津对正常和糖尿病大鼠肝肾的影响

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摘要

The present study evaluates the effects of short term (15 days) exposure of low dose (300 μg kg−1) of atrazine (2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine) on antioxidant status and markers of liver and kidney damage in normal (nondiabetic) and diabetic male Wistar rats. Rats were divided into four groups: Group I as normal control, Group II as atrazine treated, Group III as diabetic control, and Group IV as atrazine treated diabetic rats. Atrazine administration resulted in increased MDA concentration as well as increased activities of SOD, CAT, and GPx in both liver and kidney of atrazine treated and atrazine treated diabetic rats. However, GSH level was decreased in both liver and kidney of atrazine treated and atrazine treated diabetic rats. Atrazine administration led to significant increase in liver damage biomarkers such as AST, ALT, and ALP as well as kidney damage biomarkers such as creatinine and urea in both normal and diabetic rats, but this increase was more pronounced in diabetic rats when compared to normal rats. In conclusion, the results of the present study demonstrate that short term exposure of atrazine at a dose of 300 μg kg−1 could potentially induce oxidative damage in liver and kidney of both normal and diabetic rats.
机译:本研究评估了低剂量(300μgkg -1 )小剂量r去津(2-氯-4-乙基氨基-6-异丙基氨基-1,3, 5-三嗪)对正常(非糖尿病)和糖尿病雄性Wistar大鼠抗氧化状态以及肝肾损害标志物的影响。大鼠分为四组:第一组为正常对照组,第二组为阿特拉津治疗的糖尿病组,第三组为糖尿病对照组,第四组为阿特拉津治疗的糖尿病大鼠。施用阿特拉津导致糖尿病大鼠和阿特拉津治疗的糖尿病大鼠的肝脏和肾脏中MDA浓度增加以及SOD,CAT和GPx的活性增加。然而,在阿特拉津治疗和阿特拉津治疗的糖尿病大鼠的肝脏和肾脏中,GSH水平均降低。在正常和糖尿病大鼠中,阿特拉津的给药均导致肝脏损伤生物标志物(例如AST,ALT和ALP)以及肾脏损伤生物标志物(例如肌酐和尿素)显着增加,但与正常大鼠相比,这种增加在糖尿病大鼠中更为明显。综上所述,本研究结果表明,短期暴露于300μggkgkg -1 剂量的r去津有可能在正常和糖尿病大鼠的肝脏和肾脏中引起氧化损伤。

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