Dichloromethane and ethanol co-exposure aggravates oxidative stress indices causing hepatic and renal dysfunction in pubertal rats.

S. Owumi, Eseroghene S. Najophe
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引用次数: 7

Abstract

Toxicological effects from chemical interaction may result in weaker or stronger effects. The present study investigated the influence of acute oral co-exposure to dichloromethane (DCM) and ethanol (EtOH) in rats. Four groups of rats were treated for seven consecutive days with corn oil, DCM at 150 mg/kg alone, EtOH at 5 g/kg alone, and both DCM and EtOH, respectively. Subsequently, biomarkers of hepatic and renal functions, cellular antioxidant defense systems, and oxidative stress indices were analyzed in the liver and kidney samples. Results indicated that the significant (p < 0.05) elevations in the biomarkers of hepatic and renal toxicity following exposure of rats to DCM alone and EtOH alone were aggravated in the co-exposure group. Further, the significant reductions in the antioxidant status and the increase in lipid peroxidation in the liver and kidney of rats following exposure to DCM alone and EtOH alone were aggravated in the co-exposure group. Histological alterations of rats treated with DCM alone and EtOH alone were worsened in the co-exposure group. In summary, co-exposure to DCM and EtOH elicited more harmful effects on the liver and kidney than the individual chemical exposure, which is attributable to the intensified oxidative stress in the treated rats.
二氯甲烷和乙醇共暴露可加重青春期大鼠氧化应激指标,引起肝肾功能障碍。
化学相互作用产生的毒理学效应可能导致更弱或更强的效应。本研究探讨了急性口服二氯甲烷(DCM)和乙醇(EtOH)对大鼠的影响。四组大鼠分别给予玉米油、DCM单独剂量150 mg/kg、EtOH单独剂量5 g/kg、DCM和EtOH同时给药,连续7 d。随后,研究人员分析了肝脏和肾脏样本中肝脏和肾脏功能、细胞抗氧化防御系统和氧化应激指标的生物标志物。结果表明,DCM和EtOH共暴露组大鼠肝脏和肾脏毒性生物标志物的显著升高(p < 0.05)加剧。此外,单独暴露于DCM和EtOH后,大鼠肝脏和肾脏抗氧化状态的显著降低和脂质过氧化的增加在共暴露组中加剧。DCM和EtOH共暴露组大鼠组织学改变加重。综上所述,DCM和EtOH共暴露比单独暴露对肝脏和肾脏的有害影响更大,这是由于处理大鼠的氧化应激加剧。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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