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首页> 外文期刊>Journal of biochemical and molecular toxicology >Splice variant specific increase in Ca2+/calmodulin-dependent protein kinase 1-gamma mRNA expression in response to acute pyrethroid exposure.
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Splice variant specific increase in Ca2+/calmodulin-dependent protein kinase 1-gamma mRNA expression in response to acute pyrethroid exposure.

机译:响应急性拟除虫菊酯暴露,Ca2 + /钙调蛋白依赖性蛋白激酶1-γmRNA表达的剪接变体特异性增加。

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In mammals, pyrethroids are neurotoxicants that interfere with ion channel function in excitable neuronal membranes. Previous work demonstrated increases in the expression of Ca(2+)/calmodulin-dependent protein kinase 1-gamma (Camk1g) mRNA following acute deltamethrin and permethrin exposure. In the rat, this gene is expressed as two distinct splice variants, Camk1g1 and Camk1g2. The present study tests the hypothesis that changes in Camk1g mRNA expression in the rat following acute pyrethroid exposure are due to a specific increase in the Camk1g1 splice variant and not the Camk1g2 splice variant. Long-Evans rats were acutely exposed to permethrin, deltamethrin, or corn oil vehicle. Frontal cortex was collected at 6 h postdosing. In addition, rats were exposed to permethrin (100 mg/kg) or deltamethrin (3 mg/kg), and frontal cortex was collected at 1, 3, 6, 9, 12, or 24 h along with time-matched vehicle controls. Expression of Camk1g1 and Camk1g2 mRNA was measured by quantitative real-time RT-PCR and quantified using the 2(-Delta Delta C)T method. Dose-dependent increases in Camk1g1 mRNA expression were observed for both pyrethroids at 6 h. In addition, a dose-dependent increase in Camk1g2 was observed at 6 h although it was very small in magnitude. The increases in Camk1g1 expression for deltamethrin and permethrin peak between 3 and 6 h postexposure and returns to control levels by 9 h. There was no increase in CAMK1G1 protein as measured with Western blots. The present data demonstrate that pyrethroid-induced changes in Camk1g are driven mainly by increased expression of the Camk1g1 splice variant.
机译:在哺乳动物中,拟除虫菊酯是神经毒性物质,会干扰可激发神经元膜中的离子通道功能。先前的工作表明急性溴氰菊酯和氯菊酯暴露后Ca(2 +)/钙调蛋白依赖性蛋白激酶1-γ(Camk1g)mRNA的表达增加。在大鼠中,该基因表达为两个不同的剪接变体Camk1g1和Camk1g2。本研究测试了以下假设:在急性拟除虫菊酯暴露后,大鼠Camk1g mRNA表达的变化是由于Camk1g1剪接变体而不是Camk1g2剪接变体的特定增加所致。 Long-Evans大鼠急性暴露于苄氯菊酯,溴氰菊酯或玉米油媒介物中。在给药后6小时收集额皮质。此外,将大鼠暴露于苄氯菊酯(100 mg / kg)或溴氰菊酯(3 mg / kg),并在1、3、6、9、12或24 h与时间匹配的媒介物对照一起采集额叶皮层。通过定量实时RT-PCR测量Camk1g1和Camk1g2 mRNA的表达,并使用2(-Delta Delta C)T法进行定量。两种拟除虫菊酯在6 h观察到Camk1g1 mRNA表达的剂量依赖性增加。此外,尽管在6小时内Camk1g2的量很小,但仍呈剂量依赖性。溴氰菊酯和氯菊酯的Camk1g1表达增加在暴露后3至6小时达到峰值,并在9小时后恢复到对照水平。用Western印迹法测得CAMK1G1蛋白没有增加。本数据表明拟除虫菊酯引起的Camk1g的变化主要由Camk1g1剪接变体的表达增加驱动。

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