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儿茶酚胺摄取抑制在逆转胍乙啶对肾上腺素能神经元的阻断作用中的重要性。

The importance of catecholamine uptake inhibition in the reversal of guanethidine blockade of adrenergic neurons.

作者信息

Lee C H, Strosberg A M, Warren L A

出版信息

Res Commun Chem Pathol Pharmacol. 1980 Oct;30(1):3-14.

PMID:7433767
Abstract

Adrenergic neuron blockade was induced by guanethidine in the pithed rat preparation. The pressor response to spinal electric stimulation was inhibited. The guanethidine blockade was reversed or prevented not only by tricyclic antidepressants but also by tripelennamine (an H1 antihistamine), tranylcypromine (a monoamine oxidase inhibitor) and viloxazine (a new antidepressant structurally unrelated to tricyclic antidepressants). Since these compounds all share neuronal uptake inhibitory activity, it seems that this property per se is sufficient to reverse/prevent the adrenergic neuron blockade induced by guanethdine.

摘要

在脊髓横断的大鼠制备物中,胍乙啶可诱导肾上腺素能神经元阻滞。对脊髓电刺激的升压反应受到抑制。不仅三环类抗抑郁药,而且曲吡那敏(一种H1抗组胺药)、反苯环丙胺(一种单胺氧化酶抑制剂)和维洛沙嗪(一种在结构上与三环类抗抑郁药无关的新型抗抑郁药)均可逆转或预防胍乙啶阻滞。由于这些化合物均具有神经元摄取抑制活性,因此似乎该特性本身就足以逆转/预防胍乙啶诱导的肾上腺素能神经元阻滞。

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