Feldman J M, Roche J M
Pharmacol Biochem Behav. 1976 Apr;4(4):447-53. doi: 10.1016/0091-3057(76)90062-9.
To determine if anaesthetic agents alter monoamine inactivation, we exposed tissue homogenates (liver, kidney and brain) from mice and rabbits to ether and chloroform vapors and carbon dioxide gas. These anaesthetic agents inhibited monoamine oxidase (MAO) activity against typtamine and serotonin. Concentrations of anaesthetic agents that are achieved in the plasma of man during general anaesthesia caused a 27% (ether) and 49% (chloroform) reduction in mouse liver MAO; higher concentrations caused a 95% inhibition mouse or rabbit liver MAO. Kinetic analysis with tryptamine as substrate indicate that ether and chloroform are noncompetitive, reversible MAO inhibitors that preferentially inhibit Type B MAO. Ether and chloroform cause noncompetitive inhibition of serotonin oxidation by mouse liver MAO and competitive inhibition of serotonin oxidation by mouse brain and kidney MAO. Ether or chloroform did not alter catechol-O-methyltransferase activity from tissues of mice. Isolated blood platelets (rabbit and human) were used as a model system for neuronal uptake. Ether caused an irreversible inhibition of serotonin uptake by platelets.
为了确定麻醉剂是否会改变单胺失活,我们将小鼠和兔子的组织匀浆(肝脏、肾脏和大脑)暴露于乙醚、氯仿蒸气和二氧化碳气体中。这些麻醉剂抑制了针对色胺和5-羟色胺的单胺氧化酶(MAO)活性。在全身麻醉期间人体血浆中达到的麻醉剂浓度,使小鼠肝脏MAO活性降低了27%(乙醚)和49%(氯仿);更高的浓度对小鼠或兔子肝脏MAO产生了95%的抑制作用。以色胺为底物的动力学分析表明,乙醚和氯仿是非竞争性、可逆的MAO抑制剂,它们优先抑制B型MAO。乙醚和氯仿对小鼠肝脏MAO氧化5-羟色胺产生非竞争性抑制,对小鼠大脑和肾脏MAO氧化5-羟色胺产生竞争性抑制。乙醚或氯仿不会改变小鼠组织中的儿茶酚-O-甲基转移酶活性。分离的血小板(兔子和人类)被用作神经元摄取的模型系统。乙醚对血小板摄取5-羟色胺产生不可逆抑制作用。