Sandi C, Borrell J, Guaza C
Department of Psychobiology, Cajal Institute, Madrid, Spain.
Peptides. 1990 Jul-Aug;11(4):697-702. doi: 10.1016/0196-9781(90)90183-6.
The relationship between the opiate peptides Leu-enkephalin and [D-Ala2-Met5]enkephalinamide (DAME) and the initial expression and maintenance of ethanol preference was studied in male Wistar rats. Subcutaneous administration of both peptides prior to the first choice test between water and ethanol induced reductions on ethanol intake and subsequently on total fluid intake. Leu-enkephalin treatment also diminished ethanol preference in the day of treatment and in consecutive days. Neither Leu-enkephalin nor DAME treatments modified rats sucrose preference or intake. The results suggest that the enkephalins studied, when administered in the early phases of ethanol preference, interfere with the mechanisms involved in the propensity to drink ethanol.
在雄性Wistar大鼠中研究了阿片肽亮氨酸脑啡肽和[D-丙氨酸2-甲硫氨酸5]脑啡肽酰胺(DAME)与乙醇偏好的初始表达及维持之间的关系。在水和乙醇之间进行首次选择测试之前皮下注射这两种肽,会导致乙醇摄入量以及随后的总液体摄入量减少。亮氨酸脑啡肽处理在处理当天及随后连续几天也会降低乙醇偏好。亮氨酸脑啡肽和DAME处理均未改变大鼠的蔗糖偏好或摄入量。结果表明,所研究的脑啡肽在乙醇偏好形成的早期阶段给药时,会干扰与饮酒倾向相关的机制。