Tan Hock-Meng, Gundlach Andrew L, Morris Margaret J
Neuroendocrine Laboratory, Department of Pharmacology, The University of Melbourne, Vic. 3010, Australia.
Neuropeptides. 2005 Jun;39(3):333-6. doi: 10.1016/j.npep.2004.12.025. Epub 2005 Feb 16.
Galanin-like peptide (GALP) is a newly identified neuropeptide implicated in the regulation of metabolism and reproduction. GALP gene expression is decreased in the hypothalamus of genetically obese rodents, such as fa/fa rats and ob/ob mice, and central administration of GALP increases feeding in satiated rats. The effect of dietary obesity on GALP-induced feeding is unknown, so this study characterized the effects of central administration of GALP on feeding in a rat model of diet-induced obesity. Male Sprague-Dawley rats (n = 21) were randomly assigned to receive standard laboratory chow (12% fat as kcal) or high-fat cafeteria diet (35% fat) for 12 weeks before intracerebroventricular (icv) cannulae were implanted. Seven days later, rats received 0,0.2 or 0.3 nmol doses of GALP in randomized order at least 48 h apart. Food intake was measured at 0.5,1,2, 4 and 24 h post administration and body weight was measured at 24 h. Rats were maintained on their respective diets throughout the entire feeding experiment. Implementation of the high-fat diet led to significantly greater caloric intake (230%) and body weight (28%) compared to chow-fed control rats. GALP-induced feeding was rapid and maximal in both dietary groups at 30 min post injection. The 0.3 nmol dose of GALP led to significantly larger increases in caloric intake in high-fat fed rats than in chow-fed controls (35.4 +/- 3.7 and 22.1 +/- 1.3 kcal, respectively, at 30 min). It is not known if diet-induced obesity alters endogenous GALP levels, but our data suggest that adaptive responses in GALP signaling might occur during chronic overfeeding. One possible explanation is an increased sensitivity and/or number of specific GALP receptors, although actions of exogenous GALP may also represent pharmacological actions at galanin receptors.
甘丙肽样肽(GALP)是一种新发现的神经肽,参与新陈代谢和生殖的调节。在遗传性肥胖啮齿动物(如fa/fa大鼠和ob/ob小鼠)的下丘脑,GALP基因表达降低,而向饱足的大鼠中枢给予GALP会增加进食量。饮食性肥胖对GALP诱导进食的影响尚不清楚,因此本研究描述了向饮食诱导肥胖大鼠模型中枢给予GALP对进食的影响。雄性Sprague-Dawley大鼠(n = 21)在植入脑室内(icv)套管前12周被随机分配接受标准实验室饲料(12%的热量来自脂肪)或高脂自助饮食(35%的热量来自脂肪)。7天后,大鼠以随机顺序接受0、0.2或0.3 nmol剂量的GALP,每次给药间隔至少48小时。在给药后0.5、1、2、4和24小时测量食物摄入量,并在24小时测量体重。在整个喂养实验过程中,大鼠维持各自的饮食。与喂食对照大鼠相比,高脂饮食导致热量摄入显著增加(230%)和体重增加(28%)。在两个饮食组中,GALP诱导的进食在注射后30分钟迅速达到最大值。0.3 nmol剂量的GALP使高脂喂养大鼠的热量摄入增加显著大于喂食对照大鼠(分别在30分钟时为35.4±3.7和22.1±1.3千卡)。饮食诱导的肥胖是否会改变内源性GALP水平尚不清楚,但我们的数据表明,在长期过度喂养期间,GALP信号通路可能会发生适应性反应。一种可能的解释是特定GALP受体的敏感性和/或数量增加,尽管外源性GALP的作用也可能代表对甘丙肽受体的药理作用。