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首页> 外文期刊>Environmental Science and Pollution Research >Oxidative stress and renal toxicity after subacute exposure to decabrominated diphenyl ether in Wistar rats
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Oxidative stress and renal toxicity after subacute exposure to decabrominated diphenyl ether in Wistar rats

机译:亚急性暴露于<强调型=“斜体”> Wistar 大鼠中的亚急性暴露于分溴二苯醚后的氧化应激和肾毒性

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摘要

Abstract Fully brominated diphenyl ether (BDE-209) is a flame retardant widely used in plastics and textiles. Because of its high persistence, humans are exposed to it continuously, mainly via dust ingestion. We investigated effects of BDE-209 on renal function and oxidative stress development in the kidney after subacute exposure in rats. Five groups of animals were given by oral gavage 31.25–500?mg BDE-209/kg b.w./day for 28?days, and relative kidney weight, serum urea and creatinine, and oxidative stress parameters in the kidney were determined. Benchmark-dose approach was used for dose response modeling. Serum creatinine was increased, while results obtained for serum urea were inconclusive. Relative kidney weight was not affected by BDE-209. Kidney reduced glutathione was elevated, while superoxide dismutase activity was not changed after BDE-209 treatment. Also, levels of thiobarbituric acid reactive substances (TBARS) were increased and total -SH groups were decreased, which indicated oxidative imbalance. The critical effect dose (CED)/CEDL ratios for the effects on TBARS and total -SH groups indicated estimated CEDs for these markers can be used in risk assessment of BDE-209. Our study results have shown that a relatively low dose of BDE-209 affects kidney function and that oxidative stress is one of the mechanisms of its nephrotoxicity.
机译:摘要完全溴化二苯基醚(BDE-209)是塑料和纺织品广泛应用的阻燃剂。由于其高持久性,人类持续地暴露于它,主要通过尘埃摄入。我们研究了BDE-209对大鼠亚急性暴露后肾功能和氧化应激发育的影响。通过口服饲养31.25-500〜28-500-500〜28〜28〜28./day,确定肾脏中的肾脏重量,血清尿素和肌酐,以及肾脏中的氧化应激参数。基准剂量方法用于剂量响应建模。血清肌酐增加,而血清尿素的结果不确定。相对肾体重不受BDE-209的影响。肾脏还原谷胱甘肽升高,而BDE-209治疗后,超氧化物歧化酶活性不会改变。此外,硫氨基吡咯酸反应性物质(TBAR)的水平增加,并且总-SH组减少,表明氧化不平衡。对TBAR和总-SH组影响的临界作用剂量(CED)/ CEDL比表明这些标记的估计CED可以用于BDE-209的风险评估。我们的研究结果表明,相对低剂量的BDE-209会影响肾功能,氧化应激是其肾毒性的机制之一。

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