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新型化学实体GET73的抗酒精和抗焦虑特性

Anti-Alcohol and Anxiolytic Properties of a New Chemical Entity, GET73.

作者信息

Loche Antonella, Simonetti Francesco, Lobina Carla, Carai Mauro A M, Colombo Giancarlo, Castelli M Paola, Barone Domenico, Cacciaglia Roberto

机构信息

Laboratorio CT srl Sanremo, Italy.

出版信息

Front Psychiatry. 2012 Feb 14;3:8. doi: 10.3389/fpsyt.2012.00008. eCollection 2012.

Abstract

N-[(4-trifluoromethyl)benzyl]4-methoxybutyramide (GET73) is a newly synthesized compound structurally related to the clinically used, alcohol-substituting agent, gamma-hydroxybutyric acid (GHB). The present study was designed to assess whether GET73 may share with GHB the capacity to reduce alcohol intake in rats. Additionally, the effect of treatment with GET73 on anxiety-related behaviors and cognitive tasks in rats was investigated. A series of in vitro binding assays investigated the capacity of GET73 to bind to the GHB binding site and multiple other receptors. GET73 (10(-9)-10(-3) M) failed to inhibit [(3)H]GHB binding at both high- and low-affinity GHB recognition sites in rat cortical membranes. GET73 displayed minimal, if any, binding at dopamine, serotonin, GABA, and glutamate receptors in membranes from different rat brain areas. Acute treatment with low-to-moderate, non-sedative doses of GET73 (5-50 mg/kg, i.g. or i.p.) (a) reduced alcohol intake and suppressed "alcohol deprivation effect" (a model of alcohol relapse) in selectively bred, Sardinian alcohol-preferring (sP) rats, (b) exerted anxiolytic effects in Sprague-Dawley (SD) and sP rats exposed to the Elevated Plus Maze test, and (c) tended to induce promnestic effects in SD rats exposed to a modified water version of the Hebb-Williams maze test. Although the mechanism of GET73 action is currently unknown, the results of the present study suggest that GET73 has a multifaceted pharmacological profile, including the capacity to reduce alcohol drinking and anxiety-related behaviors in rats.

摘要

N-[(4-三氟甲基)苄基]4-甲氧基丁酰胺(GET73)是一种新合成的化合物,其结构与临床使用的酒精替代剂γ-羟基丁酸(GHB)相关。本研究旨在评估GET73是否与GHB一样具有减少大鼠酒精摄入量的能力。此外,还研究了GET73治疗对大鼠焦虑相关行为和认知任务的影响。一系列体外结合试验研究了GET73与GHB结合位点及其他多种受体结合的能力。GET73(10^(-9)-10^(-3) M)在大鼠皮质膜的高亲和力和低亲和力GHB识别位点均未能抑制[³H]GHB结合。GET73在来自不同大鼠脑区的膜中,对多巴胺、5-羟色胺、γ-氨基丁酸和谷氨酸受体的结合作用极小(若有结合)。用低至中等剂量、无镇静作用的GET73(5-50 mg/kg,灌胃或腹腔注射)进行急性治疗,(a)减少了选择性培育的撒丁岛嗜酒(sP)大鼠的酒精摄入量,并抑制了“酒精剥夺效应”(酒精复发模型),(b)在接受高架十字迷宫试验的Sprague-Dawley(SD)大鼠和sP大鼠中发挥了抗焦虑作用,(c)在接受改良水版Hebbe-Williams迷宫试验的SD大鼠中倾向于诱导记忆增强作用。尽管GET73的作用机制目前尚不清楚,但本研究结果表明,GET73具有多方面的药理学特性,包括减少大鼠酒精饮用量和与焦虑相关行为的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/576b/3278888/f1839ab02f19/fpsyt-03-00008-g001.jpg

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