首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Repression of Activity-Dependent c-fos and Brain-Derived Neurotrophic Factor mRNA Expression by Pyrethroid Insecticides Accompanying a Decreases in Ca~(2+) Influx into Neurons
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Repression of Activity-Dependent c-fos and Brain-Derived Neurotrophic Factor mRNA Expression by Pyrethroid Insecticides Accompanying a Decreases in Ca~(2+) Influx into Neurons

机译:拟除虫菊酯类杀虫剂伴随Ca〜(2+)流入神经元的减少,抑制活性依赖性c-fos和脑源性神经营养因子mRNA的表达。

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摘要

Permethrin, a type I pyrethroid insecticide, is known to affect sodium channels of neurons and prolong sodium currents. On the other hand, the expression of brain-derived neurotrophic factor (BDNF) and c-fos genes is activated through Ca2+ influx into neurons, in an activity-dependent manner. In this study, therefore, we investigated whether permethrin influenced the Ca~(2+) signal-induced expression of these genes. In primary culture of mouse cerebellar granule cells (CGCs), stimulation with veratridine, a potent agonist for sodium channels, which causes membrane depolarization in neurons, induced c-fos and BDNF mRNA expression accompanying the Ca~(2+) influx into neurons. Pretreatment with permethrin at doses nontoxic to CGCs repressed the induction of these genes dose depen-dently, with trans-permethrin more potent than cis-permethrin. Consistent with this, the increase in Ca2+ influx caused by veratridine was repressed by permethrin. The membrane de- polarization induced by elevating the potassium (K+) concen- tration in medium (high K+) caused the activation of c-fos and BDNF genes, which was also repressed by permethrin. Immu- noblotting analysis of c-Fos and a gel-mobility assay of AP-1 DNA-binding activity supported the decrease in c-Fos synthe- sis in permethrin-treated CGCs. The type II pyrethroid cyper- methrin also affected the expression of these genes but less effectively than permethrin. Thus, pyrethroids inhibit the activ- ity-dependent gene expression in neurons.
机译:氯菊酯(一种I类拟除虫菊酯杀虫剂)会影响神经元的钠通道并延长钠电流。另一方面,脑源性神经营养因子(BDNF)和c-fos基因的表达通过Ca2 +流入神经元而以活动依赖的方式被激活。因此,在这项研究中,我们调查了氯菊酯是否影响Ca〜(2+)信号诱导的这些基因的表达。在小鼠小脑颗粒细胞(CGC)的原代培养中,使用藜芦啶(一种有效的钠通道激动剂)进行刺激,引起神经元膜去极化,并伴随Ca〜(2+)流入神经元而诱导c-fos和BDNF mRNA表达。用对CGC无毒的剂量的苄氯菊酯进行预处理,可以抑制剂量相关的这些基因的诱导,反式苄氯菊酯的效力比顺式苄氯菊酯更高。与此一致,氯菊酯抑制了由藜芦定引起的Ca 2+内流增加。通过升高培养基(高K +)中的钾(K +)浓度而引起的膜去极化导致c-fos和BDNF基因的激活,氯菊酯也抑制了该激活。对c-Fos的免疫印迹分析和对AP-1 DNA结合活性的凝胶迁移分析支持了用氯菊酯处理过的CGC中c-Fos合成的减少。 II型拟除虫菊酯氯氰菊酯也影响这些基因的表达,但效果不及氯菊酯。因此,拟除虫菊酯抑制神经元中依赖于活性的基因表达。

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