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毒死蜱诱导大鼠皮质神经元凋亡,这种凋亡由p38与ERK/JNK丝裂原活化蛋白激酶之间的平衡调节。

Chlorpyrifos induces apoptosis in rat cortical neurons that is regulated by a balance between p38 and ERK/JNK MAP kinases.

作者信息

Caughlan Anne, Newhouse Kathleen, Namgung Uk, Xia Zhengui

机构信息

Toxicology Program in the Department of Environmental and Occupational Health Sciences, University of Washington, Seattle, Washington 98195-7234, USA.

出版信息

Toxicol Sci. 2004 Mar;78(1):125-34. doi: 10.1093/toxsci/kfh038. Epub 2003 Dec 22.

Abstract

Chlorpyrifos, an acetylcholinesterase (AChE) inhibitor, is a widely used organophosphate pesticide. Recent concern has focused on its neurotoxicity that is not attributable to AChE inhibition. Here, we report that chlorpyrifos and chlorpyrifos-oxon, but not 3,5,6-trichloro-2-pyridinol (TCP; the breakdown product of chlorpyrifos and chlorpyrifos-oxon), induce apoptosis in primary cortical neurons cultured from embryonic day 17 or newborn rats. It is generally agreed that chlorpyrifos-oxon is approximately three orders of magnitude more potent than chlorpyrifos in inhibition of brain acetylcholinesterase activity. However, our data demonstrate that chlorpyrifos-oxon is only slightly more potent than chlorpyrifos in inducing apoptosis. This indicates that chlorpyrifos-induced apoptosis may occur independently of AChE inhibition, although AChE activity was not measured in this study. Furthermore, chlorpyrifos activates the ERK1/2 and p38 MAP kinases. Surprisingly, blocking ERK1/2 activation by the MEK inhibitor SL327 caused a small but statistically significant inhibition of apoptosis, while blocking p38 with SB202190 significantly accelerated apoptosis induced by chlorpyrifos. This suggests a pro- and anti-apoptotic role for ERK1/2 and p38, respectively. Although chlorpyrifos did not stimulate total JNK activity, it caused a sustained activation of a sub-pool of JNK in the nucleus and stimulated phosphorylation of c-Jun, a downstream target of JNK. Transient expression of a dominant negative c-Jun mutant inhibited chlorpyrifos-induced apoptosis, suggesting a role for JNK and JNK-mediated transcription in this cell death. Together, our data suggest apoptosis as a novel toxic endpoint of chlorpyrifos neurotoxicity in the brain that may be independent of AChE inhibition. Furthermore, activation of the ERK1/2 and JNK MAP kinases contributes to, while activation of the p38 MAP kinase counteracts chlorpyrifos-induced apoptosis in cortical neurons.

摘要

毒死蜱是一种乙酰胆碱酯酶(AChE)抑制剂,是一种广泛使用的有机磷农药。最近的关注焦点集中在其与AChE抑制无关的神经毒性上。在此,我们报告毒死蜱和毒死蜱氧磷,但3,5,6 - 三氯 - 2 - 吡啶醇(TCP;毒死蜱和毒死蜱氧磷的分解产物)不会,诱导来自胚胎第17天或新生大鼠的原代皮质神经元凋亡。一般认为,毒死蜱氧磷在抑制脑乙酰胆碱酯酶活性方面比毒死蜱强约三个数量级。然而,我们的数据表明,毒死蜱氧磷在诱导凋亡方面仅比毒死蜱稍强。这表明,尽管本研究未测量AChE活性,但毒死蜱诱导的凋亡可能独立于AChE抑制而发生。此外,毒死蜱激活ERK1/​2和p38丝裂原活化蛋白激酶。令人惊讶的是,MEK抑制剂SL327阻断ERK1/​2激活导致凋亡受到轻微但具有统计学意义的抑制,而用SB202190阻断p38则显著加速毒死蜱诱导的凋亡。这分别表明ERK1/​2和p38具有促凋亡和抗凋亡作用。尽管毒死蜱未刺激总的JNK活性,但它导致细胞核中JNK亚群的持续激活,并刺激JNK的下游靶点c-Jun的磷酸化。显性负性c-Jun突变体的瞬时表达抑制了毒死蜱诱导的凋亡,表明JNK和JNK介导的转录在这种细胞死亡中起作用。总之,我们的数据表明凋亡是毒死蜱在脑中神经毒性的一个新的毒性终点,可能独立于AChE抑制。此外,ERK1/​2和JNK丝裂原活化蛋白激酶的激活促进了皮质神经元中毒死蜱诱导的凋亡,而p38丝裂原活化蛋白激酶的激活则起到抵消作用。

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