Buccafusco J J, Graham J H, Aronstam R S
Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta 30912-3368.
Pharmacol Biochem Behav. 1988 Feb;29(2):309-13. doi: 10.1016/0091-3057(88)90161-x.
Atropine, a postsynaptic muscarinic antagonist, and clonidine, a presynaptic inhibitor of acetylcholine release, protect mice from the lethal effects of soman, a potent and irreversible cholinesterase inhibitor. The purpose of this study was to determine the effects of atropine (6 mg/kg) and clonidine (0.2 mg/kg) on soman-induced lethality and behavioral changes in the rat. Soman produced a dose-dependent increase in lethality over a narrow concentration range (50-200 micrograms/kg, SC). Soman produced time- and dose-dependent increases in tremor, salivation, hind limb extension, convulsions and chewing behaviors, as well as decreases in three normal stereotyped behaviors, sniffing, locomotion and rearing. Atropine and clonidine were equally effective at limiting soman-induced lethality and behavioral changes. The protective effects of clonidine and atropine were synergistic, even though clonidine antagonizes some of the stereotyped behaviors elicited by atropine. Simultaneous pretreatment with clonidine and atropine completely eliminated the lethality and behavioral changes produced by injection of 200 micrograms/kg soman.
阿托品是一种突触后毒蕈碱拮抗剂,可乐定是一种乙酰胆碱释放的突触前抑制剂,它们可保护小鼠免受强效不可逆胆碱酯酶抑制剂梭曼的致死作用。本研究的目的是确定阿托品(6毫克/千克)和可乐定(0.2毫克/千克)对梭曼诱导的大鼠致死率和行为变化的影响。在狭窄的浓度范围(50 - 200微克/千克,皮下注射)内,梭曼导致致死率呈剂量依赖性增加。梭曼产生了时间和剂量依赖性的震颤、流涎、后肢伸展、惊厥和咀嚼行为增加,以及三种正常刻板行为(嗅探、运动和站立)减少。阿托品和可乐定在限制梭曼诱导的致死率和行为变化方面同样有效。可乐定和阿托品的保护作用是协同的,尽管可乐定可拮抗阿托品引发的一些刻板行为。可乐定和阿托品同时预处理可完全消除注射200微克/千克梭曼所产生的致死率和行为变化。