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阿扑吗啡和N-正丙基去甲阿扑吗啡诱导大鼠阴茎勃起的研究

Penile erection induced by apomorphine and N-n-propyl-norapomorphine in rats.

作者信息

Benassi-Benelli A, Ferrari F, Quarantotti B P

出版信息

Arch Int Pharmacodyn Ther. 1979 Dec;242(2):241-7.

PMID:44457
Abstract

The intraperitoneal injection of apomorphine (APO) or N-n-propyl-norapomorphine (NPA) to adult male rats markedly increases the incidence of episodes of penile erection (PE). The effect is dose related for a dose range of APO from 25 to 500 microgram kg-1 and NPA from 1.25 to 50 microgram kg-1. Higher doses are progressively less effective until 1 and 5 mg kg-1 of APO and NPA, respectively, suppress even the natural occurrence of PE. APO differs from NPA not only on a potency basis but also in that doses of APO which elicit stereotypy no longer evoke PE, while a wide range of doses of NPA (12.5 to 500 microgram kg-1) produces simultaneously strong PE activation and stereotypy. The sexual stimulant response to APO and NPA is prevented by haloperidol (0.3 mg kg-1) and sulpiride (50 mg kg-1) but is not affected by domperidone (3 mg kg-1), an inhibitor of extracerebral dopamine receptors.

摘要

向成年雄性大鼠腹腔注射阿扑吗啡(APO)或N - 正丙基去甲阿扑吗啡(NPA)可显著增加阴茎勃起(PE)发作的发生率。对于APO剂量范围为25至500微克/千克以及NPA剂量范围为1.25至50微克/千克,该效应呈剂量相关。更高剂量的效果逐渐降低,直至分别为1毫克/千克和5毫克/千克的APO和NPA甚至抑制PE的自然发生。APO与NPA的不同不仅在于效力,还在于引发刻板行为的APO剂量不再诱发PE,而广泛剂量的NPA(12.5至500微克/千克)同时产生强烈的PE激活和刻板行为。氟哌啶醇(0.3毫克/千克)和舒必利(50毫克/千克)可阻止对APO和NPA的性刺激反应,但不受多潘立酮(3毫克/千克)影响,多潘立酮是一种脑外多巴胺受体抑制剂。

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