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Impact of chronic low dose exposure of monocrotophos in rat brain: Oxidative/ nitrosative stress neuronal changes and cholinesterase activity

机译:久效磷长期低剂量暴露在大鼠脑中的影响:氧化/亚硝化应激神经元变化和胆碱酯酶活性

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摘要

Monocrotophos (MCP) is an organophosphate mainly used as insecticides in agriculture, and veterinary practice to control pests. Exposure to MCP is known to induce significant systemic toxicity in animals and humans. Short term exposure to a high dose of MCP has been reported to cause systemic toxicity, however limited information is available regarding low dose long term exposure in rats. We studied the effects of low dose long term exposure to MCP on oxidativeitrosative stress, cholinesterase activity and neuronal loss in rat. Male rats were exposed to MCP (0.1 μg or 1 μg/ml) via drinking water for 8 weeks. The pro-oxidant markers such as reactive oxygen species (ROS), lipid peroxidation (MDA), nitrite level and antioxidant markers such as reduced glutathione (GSH), superoxide dismutase (SOD), catalase (CAT) and inhibition of cholinesterase activities were measured to evaluate the effects of MCP on brain along with plasma cholinesterase activity. Neuronal loss was analyzed in cortical region using H&E stained slices. The results suggested that exposure to MC even at the low dose, increased reactive oxygen species, thiobarbituric acid reactive substance levels and decreased glutathione, superoxide dismutase, catalase and cholinesterase activities in brain. No significant effect however, was observed on nitrite levels. Histological analysis revealed that low dose MCP exposure lead to structural changes in the cortical neurons in rats. It can be concluded from the study that low dose long term exposure (lower than No Observed Effect Level) of MCP may lead to the generation of oxidative stress by elevation of pro-oxidants markers and depletion of antioxidant enzymes markers along with inhibition of cholinesterase activity. These changes might thus be considered as the possible mechanism of cortical neuronal loss in these animals.
机译:久效磷(MCP)是一种有机磷酸盐,主要在农业中用作杀虫剂,在兽医实践中用于控制有害生物。已知接触MCP会在动物和人类中引起明显的全身毒性。据报道,短期暴露于高剂量的MCP会引起全身毒性,但是关于大鼠长期低剂量暴露的信息有限。我们研究了低剂量长期暴露于MCP对大鼠氧化/亚硝基应激,胆碱酯酶活性和神经元丢失的影响。雄性大鼠通过饮用水接触MCP(0.1μg或1μg/ ml)8周。测量了活性氧标记物(ROS),脂质过氧化(MDA),亚硝酸盐水平的抗氧化剂标记物,以及还原型谷胱甘肽(GSH),超氧化物歧化酶(SOD),过氧化氢酶(CAT)和抗胆碱酯酶活性的抗氧化剂标记物评估MCP对大脑的影响以及血浆胆碱酯酶活性。使用H&E染色切片分析皮质区域的神经元丢失。结果表明,即使在低剂量下接触MC,大脑中的活性氧种类,硫代巴比妥酸反应性物质含量也会增加,谷胱甘肽,超氧化物歧化酶,过氧化氢酶和胆碱酯酶活性降低。然而,未观察到对亚硝酸盐水平的显着影响。组织学分析表明,低剂量的MCP暴露可导致大鼠皮质神经元发生结构变化。从研究中可以得出结论,低剂量长期接触MCP(低于未观察到的作用水平)可能通过升高促氧化剂标记物和减少抗氧化酶标记物以及抑制胆碱酯酶活性而导致氧化应激的产生。 。这些变化因此可以被认为是这些动物皮质神经元丢失的可能机制。

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