首页> 外文OA文献 >4-Hydroxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (PI-OH): a new potentiator of sympathomimetic amines on the rat anococcygeus muscle.
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4-Hydroxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (PI-OH): a new potentiator of sympathomimetic amines on the rat anococcygeus muscle.

机译:4-羟基-2-甲基-4-苯基-1,2,3,4-四氢异喹啉(PI-OH):一种新的拟交感神经胺增强剂,可刺激大鼠无球菌肌肉。

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摘要

1. The potentiating effects of racemic 4-hydroxy-2-methyl-4-phenyl-1,2,3,4-tetrahydroisoquinoline (PI-OH), cocaine, desipramine and nomifensine on the concentration-response curves of the rat anococcygeus muscle to noradrenaline (NA) and field stimulation were examined. 2. PI-OH and cocaine concentration-dependently potentiated the responses of anococcygeus muscle to NA and field stimulation, but the activity of PI-OH was stronger than that of cocaine on both responses. 3. At high concentrations the potentiating activities of desipramine and nomifensine were less, a fact that was explained by their postsynaptic inhibitory properties; the actions of nomifensine and desipramine as antagonists against NA were competitive and non-competitive, respectively. 4. It is concluded that PI-OH may be an ideal potentiator of the response to NA in adrenergically-innervated tissues because it has no side effects such as postsynaptic inhibition.
机译:1.外消旋4-羟基-2-甲基-4-苯基-1,2,3,4-四氢异喹啉(PI-OH),可卡因,地昔帕明和诺米芬对大鼠无球藻肌肉浓度-反应曲线的增强作用去甲肾上腺素(NA)和现场刺激进行了检查。 2. PI-OH和可卡因浓度依赖性地增强了珊瑚礁球菌对NA和野外刺激的反应,但PI-OH的活性均强于可卡因。 3.在高浓度下,地昔帕明和诺米芬的增强活性较低,这一事实可以通过其突触后抑制特性来解释。 Nomifensine和desipramine作为NA拮抗剂的作用分别是竞争性的和非竞争性的。 4.结论是,PI-OH可能是肾上腺能神经支配组织中对NA应答的理想增强剂,因为它没有诸如突触后抑制之类的副作用。

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