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首页> 外文期刊>Toxicology Letters: An International Journal Providing a Forum for Original and Pertinent Contributions in Toxicology Research >Detection of Purkinje cell loss following drug exposures to developing rat pups using reverse transcriptase-polymerase chain reaction (RT-PCR) analysis for calbindin-D28k mRNA expression.
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Detection of Purkinje cell loss following drug exposures to developing rat pups using reverse transcriptase-polymerase chain reaction (RT-PCR) analysis for calbindin-D28k mRNA expression.

机译:使用逆转录酶-聚合酶链反应(RT-PCR)分析calbindin-D28k mRNA表达,检测药物暴露于发育中的幼鼠后的Purkinje细胞损失。

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摘要

A technique is described that allows for the identification and quantification of Purkinje cell loss in cerebellum subsequent to developmental toxic exposures. This technique relies upon the extensively validated findings that the Purkinje cell is the only site of expression in the cerebellum of the calcium binding protein calbindin-D28k. Thus, analysis of mRNA expression specific to this protein by comparison to matched controls provides a reliable means of determining whether cell loss has occurred. Purkinje cell loss was induced in rat pups by ethanol exposure on postnatal day (PN) 4 or valproic acid administration to pregnant dams on gestational day 13. Analysis was conducted on PN5 or PN10 and the results compared to parallel groups of pups where the Purkinje cells were counted by traditional means. When compared to matched control rat pups the decrease in calbindin-D28k mRNA expression indicates Purkinje cell loss regardless of whether the cell loss was induced by prenatal valproic acid or postnatal ethanol exposure. The availability of a biochemical alternative to histological cell counting allows for more detailed analyses of the mechanisms of Purkinje cell death induced by these two toxicants, including analyses of the early alterations in signal transduction proteins.
机译:描述了一种技术,该技术可以识别和量化发育性毒性暴露后小脑中的浦肯野细胞损失。该技术依赖于广泛验证的发现,即浦肯野细胞是钙结合蛋白calbindin-D28k在小脑中唯一的表达位点。因此,与匹配的对照相比,对该蛋白特异的mRNA表达的分析提供了确定是否发生细胞损失的可靠方法。在出生后第4天暴露于乙醇或在妊娠第13天将丙戊酸暴露于妊娠母鼠,引起幼鼠Purkinje细胞丢失。对PN5或PN10进行分析,并将结果与​​平行组的幼犬进行比较是用传统方式计算的。当与匹配的对照幼犬比较时,无论钙钙蛋白-D28k mRNA表达的下降是由产前丙戊酸还是产后乙醇暴露引起的,都表明浦肯野细胞损失。组织学细胞计数的生化替代方法的可用性允许对这两种有毒物质诱导的浦肯野细胞死亡的机制进行更详细的分析,包括分析信号转导蛋白的早期改变。

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