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用二异丙基氟磷酸进行急性和慢性胆碱酯酶抑制对大鼠纹状体毒蕈碱、多巴胺和GABA受体的影响。

Effect of acute and chronic cholinesterase inhibition with diisopropylfluorophosphate on muscarinic, dopamine, and GABA receptors of the rat striatum.

作者信息

Sivam S P, Norris J C, Lim D K, Hoskins B, Ho I K

出版信息

J Neurochem. 1983 May;40(5):1414-22. doi: 10.1111/j.1471-4159.1983.tb13584.x.

DOI:10.1111/j.1471-4159.1983.tb13584.x
PMID:6300336
Abstract

The effects of acute and chronic administration of diisopropylfluorophosphate (DFP) to rats on acetylcholinesterase (AChE) activity (in striatum, medulla, diencephalon, cortex, and medulla) and muscarinic, dopamine (DA), and gamma-aminobutyric acid (GABA) receptor characteristics (in striatum) were investigated. After a single injection of (acute exposure to) DFP, striatal region was found to have the highest degree of AChE inhibition. After daily DFP injections (chronic treatment), all brain regions had the same degree of AChE inhibition, which remained at a steady level despite the regression of the DFP-induced cholinergic overactivity. Acute administration of DFP increased the number of DA and GABA receptors without affecting the muscarinic receptor characteristics. Whereas chronic administration of DFP for either 4 or 14 days reduced the number of muscarinic sites without affecting their affinity, the DFP treatment caused increase in the number of DA and GABA receptors only after 14 days of treatment; however, the increase was considerably lower than that observed after the acute treatment. The in vitro addition of DFP to striatal membranes did not affect DA, GABA, or muscarinic receptors. The results indicate an involvement of GABAergic and dopaminergic systems in the actions of DFP. It is suggested that the GABAergic and dopaminergic involvement may be a part of a compensatory inhibitory process to counteract the excessive cholinergic activity produced by DFP.

摘要

研究了对大鼠急性和慢性给予二异丙基氟磷酸酯(DFP)后,其对乙酰胆碱酯酶(AChE)活性(在纹状体、延髓、间脑、皮质和髓质中)以及毒蕈碱、多巴胺(DA)和γ-氨基丁酸(GABA)受体特性(在纹状体中)的影响。单次注射(急性暴露于)DFP后,发现纹状体区域的AChE抑制程度最高。每日注射DFP(慢性治疗)后,所有脑区的AChE抑制程度相同,尽管DFP诱导的胆碱能活性亢进有所消退,但该抑制程度仍保持稳定。急性给予DFP增加了DA和GABA受体的数量,而不影响毒蕈碱受体特性。然而,慢性给予DFP 4天或14天会减少毒蕈碱位点的数量,但不影响其亲和力,DFP治疗仅在治疗14天后导致DA和GABA受体数量增加;然而,增加幅度明显低于急性治疗后观察到的增加幅度。在体外向纹状体膜中添加DFP不影响DA、GABA或毒蕈碱受体。结果表明GABA能和多巴胺能系统参与了DFP的作用。提示GABA能和多巴胺能的参与可能是一种代偿性抑制过程的一部分,以抵消DFP产生的过度胆碱能活性。

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