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选择性多巴胺摄取抑制剂GBR 12909:其对大鼠进食微观结构的影响。

The selective dopamine uptake inhibitor GBR 12909: its effects on the microstructure of feeding in rats.

作者信息

van der Hoek G A, Cooper S J

机构信息

Laboratory of Psychopharmacology, School of Psychology, University of Birmingham, UK.

出版信息

Pharmacol Biochem Behav. 1994 May;48(1):135-40. doi: 10.1016/0091-3057(94)90509-6.

Abstract

Previous experiments have investigated the anorectic effects of mazindol and cocaine, both of which can inhibit dopamine (DA) uptake into presynaptic terminals but do not do so selectively. GBR 12909, however, is an example of a potent and selective inhibitor of DA uptake and, therefore, the present study was concerned with investigating its possible effects on feeding behavior in nondeprived rats given access to a sweetened palatable diet. GBR 12909 (5-20 mg/kg, IP) was injected 2 h before a 60 min observation test. It produced a significant reduction in food intake, as a consequence of a reduction in the duration of feeding, without reducing the rate of eating. This anorectic profile is consistent with earlier findings for mazindol and cocaine. The other main behavioral effect of GBR 12909, observed in the present study, was to induce intense sniffing activity, but, unlike cocaine, it did not suppress grooming or induce hyperlocomotion. This selective behavioral effect of GBR 12909 indicates that sniffing can be isolated as one component of a broader array of components typically associated with DA-related stereotyped behavior.

摘要

以往的实验研究了吗茚酮和可卡因的厌食作用,这两种药物都能抑制多巴胺(DA)摄入突触前终末,但并非选择性地发挥作用。然而,GBR 12909是一种强效且选择性的DA摄取抑制剂,因此,本研究旨在探究其对可获取甜味可口食物的非饥饿大鼠进食行为的可能影响。在60分钟观察试验前2小时腹腔注射GBR 12909(5 - 20毫克/千克)。由于进食持续时间缩短,食物摄入量显著减少,但进食速度未降低。这种厌食特征与之前关于吗茚酮和可卡因的研究结果一致。在本研究中观察到的GBR 12909的另一个主要行为效应是诱发强烈的嗅探活动,但与可卡因不同的是,它不会抑制梳理行为或诱发运动亢进。GBR 12909的这种选择性行为效应表明,嗅探可作为通常与DA相关刻板行为的更广泛行为成分之一被分离出来。

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