Suppr超能文献

抗胆碱能抗帕金森病药物对梭曼中毒大鼠纹状体神经递质水平的影响

Effects of anticholinergic-antiparkinsonian drugs on striatal neurotransmitter levels of rats intoxicated with soman.

作者信息

Shih T M, Capacio B R, Cook L A

机构信息

Pharmacology Division, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010-5425.

出版信息

Pharmacol Biochem Behav. 1993 Mar;44(3):615-22. doi: 10.1016/0091-3057(93)90176-t.

Abstract

Antimuscarinic drugs possessing antiparkinson activity that were effective in preventing convulsions induced by the organophosphorus cholinesterase (ChE) inhibitor soman were studied for their effects on spinal cord ChE activity and striatal levels of acetylcholine (ACh) and catecholamines in soman-intoxicated rats. Either biperiden (BPR) or trihexyphenidyl (THP) was administered to rats at an anticonvulsant dose (0.125 mg/kg, IM) in the presence or absence of soman (100 micrograms/kg, SC). The time course (up to 2 h) for ChE activity and levels of ACh and catecholamines were measured after soman, BPR, THP, soman and BPR, or soman and THP treatment. Soman rapidly inhibited ChE activity (65-75%; 15-120 min) and increased ACh levels (35%; at 30 min). It did not affect norepinephrine or dopamine (DA), but elevated at later time points (60-120 min) levels of the DA metabolites, 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), thus indicating increased DA turnover. BPR and THP alone reduced striatal ACh level from control, but did not affect any other neurochemical parameters studied. THP and BPR each reversed the effects of soman on DOPAC and HVA levels, but neither affected ChE activity nor ACh level induced by soman. Thus, our findings suggest that the anticonvulsant effects of BPR and THP in soman poisoning may be attributed to their earlier reported muscarinic receptor blocking properties.

摘要

研究了具有抗帕金森活性且能有效预防有机磷胆碱酯酶(ChE)抑制剂梭曼诱发惊厥的抗毒蕈碱药物对梭曼中毒大鼠脊髓ChE活性以及纹状体中乙酰胆碱(ACh)和儿茶酚胺水平的影响。在有或无梭曼(100微克/千克,皮下注射)存在的情况下,以抗惊厥剂量(0.125毫克/千克,肌肉注射)给大鼠注射比哌立登(BPR)或苯海索(THP)。在给予梭曼、BPR、THP、梭曼和BPR或梭曼和THP处理后,测量ChE活性以及ACh和儿茶酚胺水平的时间进程(长达2小时)。梭曼迅速抑制ChE活性(65 - 75%;15 - 120分钟)并增加ACh水平(35%;在30分钟时)。它不影响去甲肾上腺素或多巴胺(DA),但在后期时间点(60 - 120分钟)升高了DA代谢产物3,4 - 二羟基苯乙酸(DOPAC)和高香草酸(HVA)的水平,从而表明DA周转增加。单独使用BPR和THP可使纹状体ACh水平低于对照,但不影响所研究的任何其他神经化学参数。THP和BPR各自逆转了梭曼对DOPAC和HVA水平的影响,但两者均不影响梭曼诱导的ChE活性或ACh水平。因此,我们的研究结果表明,BPR和THP在梭曼中毒中的抗惊厥作用可能归因于它们先前报道的毒蕈碱受体阻断特性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验