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Cyclo-glycyl-glutamine inhibits ethanol intake in P and Sprague-Dawley rats.

机译:环糖基-谷氨酰胺抑制P和Sprague-Dawley大鼠的乙醇摄入。

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摘要

Peptide inhibitors of ethanol consumption have shown promise. The purpose of this study was to test the cyclized form of the opioid-derived dipeptide, glycyl-L-glutamine to reduce ethanol consumption after either peripheral injections or site-specific injections into the nucleus accumbens (NAC) of high drinking and low drinking rats. Following I.P. cyclo-glycyl-glutamine (c-GQ), the data show a mean decrease in ethanol intake of 34.4% in P rats, and 39.4% in Sprague-Dawley rats at doses between 5 and 25mg/kg. The data show that peripherally administered c-GQ is effective in reducing ethanol consumption in both high (P) and low (SD) drinking strains of rats and suggests a therapeutic potential.
机译:乙醇消耗的肽抑制剂已显示出希望。这项研究的目的是测试高剂量和低剂量大鼠的伏隔核(NAC)周围注射或位点特异性注射后阿片样物质衍生的二肽,甘氨酰L-谷氨酰胺的环化形式以减少乙醇消耗。继I.P.环糖基-谷氨酰胺(c-GQ),数据显示,在5至25 mg / kg的剂量下,P大鼠的乙醇摄入量平均减少34.4%,Sprague-Dawley大鼠的乙醇摄入量平均减少39.4%。数据显示,在高(P)和低(SD)饮用品系的大鼠中,外周给予c-GQ可以有效减少乙醇消耗,并具有治疗潜力。

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