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新型认知增强剂艾地苯醌在小鼠体内的精神药理学特征

Psychopharmacological profile of the new cognition enhancing agent exifone in the mouse.

作者信息

Porsolt R D, Lenègre A, Avril I, Lancrenon S, Stéru L, Doumont G

出版信息

Arzneimittelforschung. 1987 Apr;37(4):388-93.

PMID:2886129
Abstract

Hexahydro-2,3,4,3',4',5'-benzophenone (exifone, Adlone), a novel compound proposed for treating cognitive dysfunction in geriatric patients, was tested in a battery of standard psychopharmacological tests in the mouse. The results indicated that the compound was non-toxic and induced no signs of overt stimulation or sedation after acute administration of oral doses up to 1024 mg/kg. The compound was devoid of anxiolytic, anticonvulsant or classical neuroleptic activity and did not antagonize the effects of reserpine or a high dose of apomorphine, two tests indicative of classical antidepressant activity. On the other hand, exifone clearly decreased the duration of immobility in the tail suspension test and antagonized the hypothermia induced by a low dose of apomorphine. The compound shortened the duration of barbital induced sleep without affecting the duration of sleep induced by pentobarbital. The effects observed suggest that exifone is not devoid of psychotropic activity and might possess some properties of an atypical antidepressant.

摘要

六氢-2,3,4,3',4',5'-二苯甲酮(艾司酚酮,Adlone)是一种被提议用于治疗老年患者认知功能障碍的新型化合物,在一系列针对小鼠的标准精神药理学测试中进行了试验。结果表明,该化合物无毒,口服剂量高达1024mg/kg急性给药后未出现明显的兴奋或镇静迹象。该化合物没有抗焦虑、抗惊厥或经典抗精神病活性,并且在两项指示经典抗抑郁活性的测试中,它不拮抗利血平或高剂量阿扑吗啡的作用。另一方面,艾司酚酮在悬尾试验中明显缩短了不动时间,并拮抗了低剂量阿扑吗啡诱导的体温过低。该化合物缩短了巴比妥诱导的睡眠时间,而不影响戊巴比妥诱导的睡眠时间。观察到的这些效应表明,艾司酚酮并非没有精神活性,可能具有一些非典型抗抑郁药的特性。

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