亚慢性外消旋γ -乙烯基- gaba使Sprague Dawley和Zucker肥胖大鼠体重减轻。

Amy DeMarco, Reema M Dalal, Milan Kahanda, Uma Mullapudi, Jessica Pai, Crystie Hammel, Courtney N B Liebling, Vinal Patel, Jonathan D Brodie, Wynne K Schiffer, Stephen L Dewey, Stefanie D Aquilina
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引用次数: 5

摘要

鉴于肥胖症的日益流行,开发有效药物治疗的压力越来越大。在完成一项随机、双盲、安慰剂对照试验以及两项小型开放标签试验后,伽马乙烯基gaba (GVG)已被证明是安全有效的治疗可卡因和/或甲基苯丙胺依赖的药物。在这些发现的延伸中,本研究检验了GVG是否能在青春期和遗传性肥胖动物中产生体重减轻。具体来说,青春期的Sprague Dawley大鼠和青春期和成年的Zucker脂肪大鼠接受了不同剂量的GVG (75-300 mg/kg, i.p,外消旋),治疗期不超过连续14天。GVG在所有组中均以剂量依赖的方式产生显著的体重减轻。这些影响是明显的,因为观察到原始体重平均下降了12-20%。这些发现表明,GVG可能是一种有效的肥胖治疗方法。此外,这些结果发生在基因肥胖的动物身上,提供了一种可能性,即GVG甚至可以帮助控制由暴饮暴食引起的严重肥胖,暴饮暴食是一种涉及食物消费的紊乱,其模式类似于在可卡因和甲基苯丙胺依赖的受试者中观察到的强迫性药物寻求行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subchronic racemic gamma vinyl-GABA produces weight loss in Sprague Dawley and Zucker fatty rats.

Given the growing obesity epidemic, pressure to develop an effective pharmacologic treatment is mounting. Following the completion of a randomized, double-blind, placebo controlled trial as well as two small open label trials, gamma vinyl-GABA (GVG) has been shown to be safe and effective for treating cocaine and/or methamphetamine dependence. In an extension of these findings, the present study examined whether GVG could produce weight loss in adolescent as well as genetically obese animals. Specifically, adolescent Sprague Dawley and adolescent and adult Zucker fatty rats received GVG at various doses (75-300 mg/kg, i.p., racemic) for treatment periods lasting no longer than 14 consecutive days. GVG produced significant weight loss in a dose dependent fashion in all groups. These effects were marked, as average decreases of 12-20% of original body weight were observed. These findings suggest that GVG may be useful as a treatment for obesity. Further, that these results occurred in genetically obese animals offers the possibility that GVG may even help manage severe obesity resulting from binge-eating, a disorder involving food consumption in a pattern similar to the compulsive drug-seeking behavior observed in cocaine and methamphetamine dependent subjects.

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