Curriculum in Toxicology, University of North Carolina at Chapel Hill, CB 7270, Chapel Hill, NC 27599, USA.
J Biochem Mol Toxicol. 2010 May-Jun;24(3):174-86. doi: 10.1002/jbt.20324.
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.
在哺乳动物中,拟除虫菊酯是神经毒素,会干扰可兴奋神经元膜中的离子通道功能。先前的工作表明,急性使用氯菊酯和氯氰菊酯后,Camk1g 信使 RNA 的表达增加。在大鼠中,该基因表达为两种不同的剪接变体,即 Camk1g1 和 Camk1g2。本研究检验了以下假设:急性接触拟除虫菊酯后,大鼠 Camk1g 信使 RNA 表达的变化是由于 Camk1g1 剪接变体的特异性增加而不是 Camk1g2 剪接变体的增加所致。长爪沙鼠急性暴露于氯菊酯、氯氰菊酯或玉米油载体中。在给药后 6 小时采集额皮质。此外,大鼠暴露于氯菊酯(100mg/kg)或氯氰菊酯(3mg/kg),并在 1、3、6、9、12 或 24 小时时采集额皮质,同时采集时间匹配的载体对照。通过实时定量 RT-PCR 测量 Camk1g1 和 Camk1g2 信使 RNA 的表达,并使用 2(-Delta Delta C)T 方法进行定量。两种拟除虫菊酯在 6 小时时均可观察到 Camk1g1 信使 RNA 表达的剂量依赖性增加。此外,在 6 小时时观察到 Camk1g2 的剂量依赖性增加,尽管其幅度非常小。氯氰菊酯和氯菊酯引起的 Camk1g1 表达增加在暴露后 3 至 6 小时之间达到峰值,并在 9 小时时恢复到对照水平。Western blot 分析未检测到 CAMK1G1 蛋白增加。本数据表明,拟除虫菊酯诱导的 Camk1g 变化主要是由 Camk1g1 剪接变体的表达增加驱动的。