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米安色林及经典α-肾上腺素能受体阻断药对可乐定某些心血管和行为效应的拮抗作用。

Antagonism by mianserin and classical alpha-adrenoceptor blocking drugs of some cardiovascular and behavioral effects of clonidine.

作者信息

Robson R D, Antonaccio M J, Saelens J K, Liebman J

出版信息

Eur J Pharmacol. 1978 Feb 15;47(4):431-42. doi: 10.1016/0014-2999(78)90124-3.

Abstract

Antagonism of pressor responses to sympathetic outflow stimulation and alpha-adrenoceptor agonists in pithed spontaneously hypertensive rats was used to estimate postsynaptic alpha-adrenoceptor blocking activity of mianserin, phentolamine, phenoxybenzamine, piperoxan and yohimbine. Estimation of presynaptic alpha-adrenoceptor blocking activity of these drugs was obtained by studying their ability to antagonize clonidine-induced suppression of positive chronotropic responses to sympathetic outflow stimulation. In this manner, evidence was obtained that mianserin causes selective presynaptic alpha-adrenoceptor blockade. Mianserin, piperoxan and yohimbine antagonized clonidine-induced avoidance blockade or hypotension in spontaneously hypertensive rats, but methysergide, phenoxybenzamine and phentolamine were ineffective. These results suggest that mianserin may antagonize the central effects of clonidine by blockade of noradrenergic presynaptic or autoreceptors and possibly explain the antidepressant effect of mianserin as due to indirect activation of central noradrenergic neurons.

摘要

在脊髓横断的自发性高血压大鼠中,通过拮抗对交感神经传出刺激和α-肾上腺素能受体激动剂的升压反应,来评估米安色林、酚妥拉明、酚苄明、哌罗克生和育亨宾的突触后α-肾上腺素能受体阻断活性。通过研究这些药物拮抗可乐定诱导的对交感神经传出刺激的正性变时反应抑制的能力,来评估它们的突触前α-肾上腺素能受体阻断活性。通过这种方式,获得了证据表明米安色林引起选择性突触前α-肾上腺素能受体阻断。米安色林、哌罗克生和育亨宾拮抗了可乐定诱导的自发性高血压大鼠的回避阻断或低血压,但美西麦角、酚苄明和酚妥拉明无效。这些结果表明,米安色林可能通过阻断去甲肾上腺素能突触前或自身受体来拮抗可乐定的中枢效应,并可能解释米安色林的抗抑郁作用是由于间接激活中枢去甲肾上腺素能神经元。

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