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[阻断生物胺的神经元和非神经元摄取对三环类抗抑郁药肾上腺致敏作用的影响]

[Effect of blocking the neuronal and extraneuronal uptake of bioamines on the adrenosensitizing action of tricyclic antidepressants].

作者信息

Dolzhenko A T

出版信息

Biull Eksp Biol Med. 1976 May;81(5):556-8.

PMID:7328
Abstract

Tests conducted on isolated and denervated preparations of the rat seminal duct brought evidence that tricyclic antidepressants (melipromine, noverile and azaphen) when employed in low concentrations (1-10(-9) g/ml) produced an adrenosensitizing effect. Denervation with the subsequent block by desoxycorticosterone (1-10(-5) g/ml) of exteraneuronal amine uptake did not alter the position, shape and inclination of the "concentration-effect" noradrenaline curves received in the presence of noverile and cocaine. It is believed that there exists a predominance of the postsynaptic mechanism of the aminosensitizing action of tricyclic antidepressants on the smooth muscle organ.

摘要

对大鼠输精管的离体和去神经支配制剂进行的试验表明,三环类抗抑郁药(美立丙嗪、诺韦里尔和阿扎芬)在低浓度(1-10⁻⁹克/毫升)使用时会产生肾上腺致敏作用。去神经支配并随后用脱氧皮质酮(1-10⁻⁵克/毫升)阻断神经元外胺摄取,并没有改变在诺韦里尔和可卡因存在下获得的“浓度-效应”去甲肾上腺素曲线的位置、形状和斜率。据信,三环类抗抑郁药对平滑肌器官的氨基致敏作用的突触后机制占主导地位。

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