Pintor A, Fortuna S, Nalepa I, Michalek H
Laboratory of Pharmacology, Istituto Superiore di Sanità, Rome, Italy.
Neurotoxicology. 1992 Spring;13(1):289-94.
The effects of acute and repeated treatments with an anticholinesterase (anti-ChE) compound, diisopropylfluorophosphate (DFP) on M1-acetylcholine receptor (M1-AChRs) density and on M1-mediated breakdown of inositol phospholipids were studied in the cerebral cortex of rats. The DFP doses induced an about 75% inhibition of cortical ChE 48 hr after the last treatment. The acute treatment did not change Bmax of M1-AChRs (measured as 3H-pirenzepine binding), while 1-week and 2-weeks treatments induced their significant down-regulation, by 14 and 29%, respectively. The responsiveness of M1-AChRs was measured in cortical prisms as accumulation of inositol phosphate (IP) following stimulation with a cholinergic agonist, carbachol (from 10 to 1000 microM). The IP accumulation (expressed as ratio stimulated/basal IP content) was lower in acute DFP rats than in controls at few carbachol concentrations, and after 2 weeks at most carbachol concentrations. This resulted in a significant increase of EC50. The data indicate the involvement of cortical phosphatidyl inositol system during intoxication by anti-ChE agents, namely a decreased efficiency of post-receptor mechanisms.
研究了抗胆碱酯酶(anti-ChE)化合物二异丙基氟磷酸酯(DFP)急性和重复给药对大鼠大脑皮质M1-乙酰胆碱受体(M1-AChRs)密度以及M1介导的肌醇磷脂分解的影响。在最后一次给药后48小时,DFP剂量诱导皮质胆碱酯酶抑制约75%。急性给药未改变M1-AChRs的Bmax(以3H-哌仑西平结合测定),而1周和2周给药分别诱导其显著下调14%和29%。在皮质棱柱体中,通过胆碱能激动剂卡巴胆碱(10至1000 microM)刺激后肌醇磷酸(IP)的积累来测量M1-AChRs的反应性。在少数卡巴胆碱浓度下,急性DFP处理大鼠的IP积累(以刺激/基础IP含量的比值表示)低于对照组,在2周后,大多数卡巴胆碱浓度下也是如此。这导致EC50显著增加。数据表明抗胆碱酯酶药物中毒期间皮质磷脂酰肌醇系统参与其中,即受体后机制效率降低。