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药物(CRL 40028)诱发多动的一种可能的α-肾上腺素能机制。

A possibe alpha-adrenergic mechanism for drug (CRL 40028)-induced hyperactivity.

作者信息

Duteil J, Rambert F A, Pessonnier J, Gombert R, Assous E

出版信息

Eur J Pharmacol. 1979 Oct 26;59(1-2):121-3. doi: 10.1016/0014-2999(79)90033-5.

Abstract

CRL 40028 (benzhydryl sulfinyl acetohydroxamic acid)-induced stimulation in mice, measured as an increase in locomotor activity was studied following an intraperitoneal injection of drugs known to block alpha-adrenergic receptors. Phenoxybenzamine (20 mg/kg), prazosin (0.5-1 mg/kg) and yohimbine (2 mg/kg) prevented the development of CRL 40028-induced hyperactivity. These results suggest that stimulation of an alpha-adrenergic postsynaptic receptor is of importance for the stimulant effect of CRL 40028.

摘要

在小鼠腹腔注射已知可阻断α-肾上腺素能受体的药物后,研究了CRL 40028(二苯甲基亚磺酰乙酰氧肟酸)诱导的刺激作用,该刺激作用以运动活性增加来衡量。酚苄明(20毫克/千克)、哌唑嗪(0.5 - 1毫克/千克)和育亨宾(2毫克/千克)可阻止CRL 40028诱导的多动的发展。这些结果表明,刺激α-肾上腺素能突触后受体对CRL 40028的刺激作用很重要。

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