首页> 外文期刊>Molecular biology reports >Caspase 1, Caspase 3, TNF-alpha, p53, and Hif1-alpha gene expression status of the brain tissues and hippocampal neuron loss in short-term dichlorvos exposed rats
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Caspase 1, Caspase 3, TNF-alpha, p53, and Hif1-alpha gene expression status of the brain tissues and hippocampal neuron loss in short-term dichlorvos exposed rats

机译:短期敌敌畏暴露大鼠脑组织的半胱氨酸天冬氨酸蛋白酶1,半胱天冬酶3,TNF-alpha,p53和Hif1-alpha基因表达状态与海马神经元丢失

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摘要

Dichlorvos (DDVP) is an organophosphate compound that causes neurotoxicity. Apoptosis plays an important role in neurotoxic cell death in the brain. The aim of this study was to examine caspase 1, caspase-3 and also cell apoptosis related genes as p53, Tumor Necrosis Factor-alpha, Hypoxia Inducible Factor 1-alpha expressions in hippocampus, cerebellum, cortex, and to estimate total hippocampal neuron number in DDVP treated rats. Ten female albino rats were divided into control (n:5) and dose (n:5) groups. In dose group, single dose of DDVP (25 mg/kg) was administered to the animals via oral gavage. A week later, brains were removed and total neuron number was estimated in the left hippocampus using by optical fractionator method. The right part of the brain was used for gene expression analysis. In dose group, total hippocampal neuron number was significantly decreased compared to control group (p = 0.008). Caspase 1 and TNF-alpha gene expression were increased in all brain tissues and p53 gene expression was decreased in only hippocampus tissue in dose group. Short-term exposure to dichlorvos leads to neuronal loss in hippocampus and TNF-alpha rapidly and potently induces apoptosis and also several caspases as possible participants in the apoptotic cascade.
机译:敌敌畏(DDVP)是一种会引起神经毒性的有机磷酸盐化合物。凋亡在脑神经毒性细胞死亡中起重要作用。这项研究的目的是检查caspase 1,caspase-3以及与细胞凋亡相关的基因,如p53,肿瘤坏死因子-α,缺氧诱导因子1-α在海马,小脑,皮层中的表达,并评估海马总神经元数量在DDVP治疗的大鼠中。将十只雌性白化病大鼠分为对照组(n:5)和剂量组(n:5)。在剂量组中,通过口服管饲法向动物施用单剂量的DDVP(25mg / kg)。一周后,取出大脑,并使用光学分馏仪方法评估左海马中的总神经元数量。大脑的右半部分用于基因表达分析。在剂量组中,与对照组相比,海马总神经元数量明显减少(p = 0.008)。在剂量组中,所有脑组织中Caspase 1和TNF-α基因表达均升高,而仅海马组织中p53基因表达降低。短期暴露于敌敌畏会导致海马神经元丢失,TNF-α会迅速有效地诱导细胞凋亡,还有一些胱天蛋白酶可能参与凋亡级联反应。

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