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首页> 外文期刊>Japanese Journal of Pharmacology >COMPARATIVE EFFECTS OF IMIPRAMINE AND PROPRANOLOL ON THE TRANSMEMBRANE POTENTIALS OF THE ISOLATED RABBIT'S ATRIA
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COMPARATIVE EFFECTS OF IMIPRAMINE AND PROPRANOLOL ON THE TRANSMEMBRANE POTENTIALS OF THE ISOLATED RABBIT'S ATRIA

机译:丙咪嗪和普萘洛尔对离体兔纹状体膜跨膜电位的比较作用

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摘要

References(21) Cited-By(17) It has already been established that imipramine clinically available as an antidepressant potentiates the pressor response to noradrenaline (1-4), but depresses the same responses to tyramine, amphetamine and phenetylamine (3, 5, 6). The mechanism of the potentiation or the depression has been discussed to derive from the interference with the uptake of catecholamine into the binding site as cocaine (7-10) or from the change in the sensitiveness of effector organs caused by a depletion of the endogeneous catecholamine in a similar manner to reserpine. Furthermore, there is another possibility that imipramine potentiates the pressor response due to its adrenergic β-blocking mechanism. In the present experiments the effects of imipramine, propranolol and pronethalol on the adrenergic mechanism of the isolated rabbit's atria were comparatively investigated. The parameter used was the transmembrane potentials recorded from the right atrium and the S-A node. Responses of the potentials to the test compounds as well as the effects of the test compounds on the responses of the potentials to noradrenaline, adrenaline and isopropylnoradrenaline were observed.
机译:参考文献(21)Cited-By(17)已确定临床上可用的丙咪嗪作为抗抑郁药可增强对去甲肾上腺素(1-4)的升压反应,但会抑制对酪胺,苯丙胺和苯乙胺的相同反应(3,5, 6)。已经讨论了增强或抑制的机制是由于干扰儿茶酚胺作为可卡因进入结合位点而受到干扰(7-10),或者是由于内源性儿茶酚胺的消​​耗而引起的效应器官敏感性的变化。与利血平相似。此外,由于其肾上腺素的β-阻断机制,丙咪嗪有可能增强加压反应。在本实验中,比较研究了丙咪嗪,普萘洛尔和普萘洛尔对离体兔心房肾上腺素能机制的影响。使用的参数是从右心房和S-A节点记录的跨膜电位。观察到电势对测试化合物的响应以及测试化合物对电势对去甲肾上腺素,肾上腺素和异丙基去甲肾上腺素的响应的影响。

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