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氯菊酯改变成年大鼠纹状体中 mRNA 的表达谱:一种可能的机制是出生后预暴露,然后在成年期再次暴露增强神经退行性变。

Cypermethrin alters the expression profile of mRNAs in the adult rat striatum: a putative mechanism of postnatal pre-exposure followed by adulthood re-exposure-enhanced neurodegeneration.

机构信息

CSIR-Indian Institute of Toxicology Research, Mahatma Gandhi Marg, Post Box-80, Lucknow 226 001, Uttar Pradesh, India.

出版信息

Neurotox Res. 2012 Nov;22(4):321-34. doi: 10.1007/s12640-012-9317-8. Epub 2012 Apr 21.

Abstract

This study was undertaken to investigate the effect of cypermethrin on the expression patterns of mRNAs in the striatum of adulthood alone and postnatal pre-exposed followed by adulthood re-exposed rats using discover chips rat microarrays. The expression patterns of V-akt murine thymoma viral oncogene homolog 1, B-cell lymphoma 2 (BCL-2), BCL-2-associated X protein, caspase 1, caspase 9, death-associated protein 3 and interleukin-1β were validated by the qRT-PCR. The expressions of inducible nitric oxide synthase (iNOS) and major histocompatibility complex (MHC) II were assessed immunohistochemically; however, tumour protein p53 and cytochrome c (mitochondrial and cytosolic) expressions were checked at protein level by western blotting. Cypermethrin differentially regulated 65 transcripts at one or the other stage of exposure and 21 transcripts exhibited more pronounced alterations in the postnatal pre-exposed and adulthood re-challenged rats. The results of qRT-PCR were in accordance with the microarray observations and the expressions of iNOS, p53 and cytosolic cytochrome c and MHC II positivity were increased while the level of mitochondrial cytochrome c was reduced in adulthood treated animals. The effects were more pronounced in the postnatal pre-exposed followed by adulthood re-exposed rats. The results obtained thus suggest that multiple pathways are involved in the neurodegeneration as well as in enhancing the vulnerability of neurons in cypermethrin pre-exposed postnatal animals upon re-exposure during adulthood.

摘要

这项研究旨在使用Discover 芯片大鼠微阵列,研究氯菊酯对成年期单独和出生后预暴露后再暴露的大鼠纹状体中 mRNA 表达模式的影响。使用 qRT-PCR 验证了 V-akt 鼠胸腺瘤病毒癌基因同源物 1、B 细胞淋巴瘤 2 (BCL-2)、BCL-2 相关 X 蛋白、半胱天冬酶 1、半胱天冬酶 9、死亡相关蛋白 3 和白细胞介素 1β 的表达模式。通过免疫组织化学评估诱导型一氧化氮合酶 (iNOS) 和主要组织相容性复合体 (MHC) II 的表达;然而,肿瘤蛋白 p53 和细胞色素 c(线粒体和细胞质)的表达通过蛋白质水平的 Western blot 进行检查。氯菊酯在一个或另一个暴露阶段差异调节了 65 个转录物,并且 21 个转录物在出生后预暴露和成年期再挑战的大鼠中表现出更明显的改变。qRT-PCR 的结果与微阵列观察结果一致,iNOS、p53 和细胞质细胞色素 c 的表达增加,而成年期处理动物中线粒体细胞色素 c 的水平降低。在出生后预暴露后再暴露的大鼠中,这种影响更为明显。因此,研究结果表明,在成年期再次暴露时,多途径参与了氯菊酯预暴露的新生动物的神经退行性变以及增强神经元的易感性。

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