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急性二异丙基氟磷酸酯(DFP)处理后毒蕈碱受体亚型及磷酸肌醇水解未发生改变。

Lack of alterations in muscarinic receptor subtypes and phosphoinositide hydrolysis upon acute DFP treatment.

作者信息

Cioffi C L, el-Fakahany E E

机构信息

Department of Pharmacology and Toxicology, University of Maryland School of Pharmacy, Baltimore 21201.

出版信息

Eur J Pharmacol. 1988 Oct 26;156(1):35-45. doi: 10.1016/0014-2999(88)90144-6.

Abstract

There was a 25 and 27% reduction in the density of mouse brain muscarinic acetylcholine receptors 18 and 24 h following a single injection of the organophosphate diisopropylfluorophosphate (DFP) when the muscarinic antagonist [3H]N-methylscopolamine ([3H]NMS) was used as the ligand. Down-regulation of specific [3H]NMS binding was rapidly reversible reaching control levels 36 h after DFP administration. Carbamylcholine and pirenzepine competition for the specific binding of either [3H]NMS or [3H]quinuclidinyl benzilate ([3H]QNB) in brain homogenates from untreated and DFP-treated mice demonstrated that the alteration in muscarinic receptor density following acute DFP treatment was not accompanied by a change in a particular muscarinic receptor binding conformation. Furthermore, the magnitude of muscarinic receptor-mediated phosphoinositide hydrolysis was unchanged following short-term DFP treatment suggesting that a physiological desensitization in this response does not accompany acute down-regulation of [3H]NMS binding sites.

摘要

当使用毒蕈碱拮抗剂[3H]N-甲基东莨菪碱([3H]NMS)作为配体时,单次注射有机磷酸酯二异丙基氟磷酸酯(DFP)后18小时和24小时,小鼠脑毒蕈碱型乙酰胆碱受体密度分别降低了25%和27%。特异性[3H]NMS结合的下调是快速可逆的,在DFP给药后36小时达到对照水平。氨甲酰胆碱和哌仑西平对未处理和DFP处理小鼠脑匀浆中[3H]NMS或[3H]喹核醇基苯甲酸酯([3H]QNB)特异性结合的竞争表明,急性DFP处理后毒蕈碱受体密度的改变并未伴随着特定毒蕈碱受体结合构象的变化。此外,短期DFP处理后毒蕈碱受体介导的磷酸肌醇水解幅度未发生变化,这表明该反应中的生理性脱敏并不伴随[3H]NMS结合位点的急性下调。

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