Laboratory of Behavioral Neurobiology, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
Alcohol. 2009 Dec;43(8):571-80. doi: 10.1016/j.alcohol.2009.09.025.
Evidence suggests that the orexigenic peptide, galanin (GAL), in the hypothalamic paraventricular nucleus (PVN) has a role in stimulating the consumption of ethanol, in addition to a high-fat diet. This possibility was further examined in mutant mice that overexpress the GAL gene. Two sets of GAL-overexpressors (GALOE) compared with wild-type (WT) controls, maintained on laboratory chow and water, were trained to voluntarily drink increasing concentrations of ethanol, from 3 to 15%. In the GALOE versus WT mice, the results revealed the following: (1) a 35-40% increase in ethanol intake and ethanol preference, which was evident only at the highest (15%) ethanol concentration, in male but not female mice, and was seen with comparisons to littermate and nonlittermate WT controls, (2) a significantly larger, 60-75% increase in ethanol intake and ethanol preference after a day of food deprivation, again only in male GALOE mice, (3) no change in consumption of sucrose or quinine solutions in preference tests, and (4) a 55% increase in consumption of a fat-rich diet during a 2-h test period, in both male and female GALOE mice. These results obtained with overexpression of the GAL gene provide strong support for a physiological role of this peptide in stimulating the consumption of ethanol and a fat-rich diet. They reveal gender differences in the behavioral phenotype, which may reflect GAL's functional relationship to reproductive hormones in the stimulation of consummatory behavior.
有证据表明,下丘脑室旁核(PVN)中的食欲肽甘丙肽(GAL)除了促进高脂肪饮食外,还在刺激乙醇消耗方面发挥作用。这种可能性在过表达 GAL 基因的突变小鼠中进一步得到了研究。两组 GAL 过表达(GALOE)小鼠与野生型(WT)对照小鼠(用实验室饲料和水饲养)进行了自愿饮用不同浓度乙醇(从 3%到 15%)的训练。GALOE 与 WT 小鼠的结果显示:(1)在雄性而非雌性小鼠中,乙醇摄入量和乙醇偏好增加了 35-40%,这仅在最高(15%)乙醇浓度下明显,与同窝和非同窝 WT 对照小鼠的比较一致;(2)在禁食一天后,雄性 GALOE 小鼠的乙醇摄入量和乙醇偏好显著增加了 60-75%;(3)在偏好测试中,蔗糖或奎宁溶液的消耗量没有变化;(4)在 2 小时测试期间,雄性和雌性 GALOE 小鼠对高脂肪饮食的消耗量增加了 55%。这些通过 GAL 基因过表达获得的结果为该肽刺激乙醇和高脂肪饮食消耗的生理作用提供了有力支持。它们揭示了行为表型中的性别差异,这可能反映了 GAL 与生殖激素在促进摄食行为方面的功能关系。