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Targeting redox metabolism: the perfect storm induced by acrylamide poisoning in the brain

机译:靶向氧化还原新陈代谢:丙烯酰胺中毒在大脑中诱导的完美风暴

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Exposure to acrylamide may lead to different neurotoxic effects in humans and in experimental animals. To gain insights into this poorly understood type of neurotoxicological damage, we used a multi-omic approach to characterize the molecular changes occurring in the zebrafish brain exposed to acrylamide at metabolite, transcript and protein levels. We detected the formation of acrylamide adducts with thiol groups from both metabolites and protein residues, leading to a quasi-complete depletion of glutathione and to the inactivation of different components of the thioredoxin system. We propose that the combined loss-of-function of both redox metabolism-related systems configure a perfect storm that explains many acrylamide neurotoxic effects, like the dysregulation of genes related to microtubules, presynaptic vesicle alteration, and behavioral alterations. We consider that our mechanistical approach may help developing new treatments against the neurotoxic effects of acrylamide and of other neurotoxicants that may share its toxic mode of action.
机译:暴露于丙烯酰胺可能导致人类和实验动物的不同神经毒性作用。为了深入了解这种不良类型的神经毒理学损伤,我们使用了一种多OMIC方法来表征在代谢物,转录物和蛋白质水平下暴露于丙烯酰胺的斑马鱼脑中发生的分子变化。我们检测到与代谢物和蛋白质残留的硫醇基团形成丙烯酰胺加合物,导致谷胱甘肽的准完全耗尽并灭活硫氧吡嗪系统的不同组分。我们提出,氧化还原与新陈代谢相关系统的组合函数丧失配置了一个完美的风暴,解释了许多丙烯酰胺神经毒性作用,如与微管,突触前囊泡改变和行为改变相关的基因的失调。我们认为,我们的机械方法可能有助于为丙烯酰胺和其他可共享其有毒作用模式的神经毒性作用的神经毒性作用产生新的治疗。

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