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单胺氧化酶A和单胺氧化酶B对犬隐静脉中去甲肾上腺素失活的影响。

Influence of MAO A and MAO B on the inactivation of noradrenaline in the saphenous vein of the dog.

作者信息

Caramona M M, Araújo D, Brandão F

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 Feb;328(4):401-6. doi: 10.1007/BF00692908.

Abstract

Specific inhibitors of MAO A (clorgyline 0.1 mumol/l) and of MAO B [(-)deprenyl 10 mumol/l] were used in dog saphenous vein strips in order to study the relative influence of the two types of MAO on: 1. Termination of contractile response to exogenous noradrenaline (NA); 2. Metabolism and accumulation of exogenous (3H)-NA; 3. Metabolism of 3H-NA released by electrical stimulation. To study the termination of contractile response to exogenous NA, the oil immersion technique was used to determine the time for half-relaxation. The experiments were performed on strips with or without treatment with cocaine 10 mumol/l (to inhibit neuronal uptake) plus U-0521 100 mumol/l (to inhibit catechol-O-methyl transferase) before and after exposure to MAO inhibitors. Clorgyline, but not (-)deprenyl enhanced significantly the time for half-relaxation of the strips, whether cocaine was present or not. To study the metabolism and accumulation of exogenous 3H-NA, the strips were incubated (with or without preincubation with cocaine) with 3H-NA 0.23 mumol/l and 2.3 mumol/l in the presence and in the absence of MAO inhibitors. The formation of deaminated metabolites was significantly reduced by clorgyline, but not by deprenyl. To study the metabolism of 3H-NA released by electrical stimulation, the strips were incubated with 3H-NA 1.4 mumol/l. In the presence of cocaine and U-0521, field stimulation was applied during two periods of 5 min (10 Hz, 100 V, 2 ms), in the absence or presence of MAO inhibitors. Under these experimental conditions clorgyline, but not deprenyl, abolished DOPEG formation, without affecting the other metabolites.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了研究单胺氧化酶(MAO)两种类型对以下方面的相对影响,在犬隐静脉条上使用了MAO A的特异性抑制剂(氯吉兰0.1微摩尔/升)和MAO B的特异性抑制剂[(-)司来吉兰10微摩尔/升]:1. 对外源性去甲肾上腺素(NA)收缩反应的终止;2. 外源性(3H)-NA的代谢和积累;3. 电刺激释放的3H-NA的代谢。为了研究对外源性NA收缩反应的终止,采用油浸技术确定半松弛时间。在暴露于MAO抑制剂之前和之后,对用或不用10微摩尔/升可卡因(抑制神经元摄取)加100微摩尔/升U-0521(抑制儿茶酚-O-甲基转移酶)处理的静脉条进行实验。无论是否存在可卡因,氯吉兰均显著延长静脉条的半松弛时间,但(-)司来吉兰则不然。为了研究外源性3H-NA的代谢和积累,在有和没有MAO抑制剂的情况下,将静脉条与0.23微摩尔/升和2.3微摩尔/升的3H-NA一起孵育(有或没有预先与可卡因孵育)。氯吉兰显著减少了脱氨基代谢产物的形成,但司来吉兰则不然。为了研究电刺激释放的3H-NA的代谢,将静脉条与1.4微摩尔/升的3H-NA一起孵育。在存在可卡因和U-0521的情况下,在5分钟的两个时间段(10赫兹,100伏,2毫秒)施加场刺激,分别在不存在或存在MAO抑制剂的情况下进行。在这些实验条件下,氯吉兰而非司来吉兰消除了DOPEG的形成,而不影响其他代谢产物。(摘要截短于第250个单词)

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