Michel Signe, Becskei Csilla, Erguven Elif, Lutz Thomas A, Riediger Thomas
Institute of Veterinary Physiology, University of Zürich, Zürich, Switzerland.
Neuroendocrinology. 2007;86(2):124-35. doi: 10.1159/000107579. Epub 2007 Aug 16.
The pancreatic hormone amylin decreases food intake via activation of area postrema (AP) neurons. We investigated whether amylin's potency to reduce food intake and to induce c-Fos expression in the AP/nucleus of the solitary tract region is affected by the feeding conditions and specifically by the macronutrient composition of the diet. Whereas a low dose of amylin (5 microg/kg s.c.) induced very little c-Fos expression in ad libitum chow fed rats, it caused a strong c-Fos expression in 24-hour food-deprived rats and in rats that received a nutrient-deficient non-caloric mash (NCM; vanilla-flavoured cellulose) 24 h before injection. To reveal the contribution of single nutrients to the low c-Fos expression after chow feeding, amylin-induced c-Fos was analyzed after feeding NCM that was selectively supplemented with glucose, fat (lard), or protein (casein), matching the intake of these nutrients of chow-fed rats. While the rats fed NCM supplemented with glucose or fat displayed an equally strong amylin-induced activation as fasted rats or rats fed plain NCM, a significantly lower c-Fos expression was observed in rats fed a protein-supplemented NCM or a NCM containing all three nutrients. In line with this lower activation, the same dose of amylin failed to reduce food intake in NCM/protein-fed rats, while amylin caused a reduction in feeding when animals received NCM, NCM/glucose, or NCM/fat. Interestingly, amylin effectively reduced food intake in ad libitum chow fed rats despite the low level of amylin-induced c-Fos expression in the AP under these conditions. We conclude that the anorectic potential of amylin may be attenuated by diet-derived proteins, whereas this effect appears to be overridden when the amount of carbohydrates/fat is high relative to the protein content, such as, e.g., in standard chow.
胰腺激素胰淀素通过激活最后区(AP)神经元来减少食物摄入量。我们研究了胰淀素减少食物摄入量以及在AP/孤束核区域诱导c-Fos表达的能力是否受进食条件影响,特别是受饮食中常量营养素组成的影响。低剂量的胰淀素(5微克/千克,皮下注射)在自由进食普通饲料的大鼠中诱导的c-Fos表达很少,而在禁食24小时的大鼠以及在注射前24小时接受营养缺乏的无热量糊状物(NCM;香草味纤维素)的大鼠中,它会引起强烈的c-Fos表达。为了揭示单一营养素对普通饲料喂养后低c-Fos表达的作用,在喂食选择性补充了葡萄糖、脂肪(猪油)或蛋白质(酪蛋白)的NCM后,分析了胰淀素诱导的c-Fos,这些营养素的摄入量与普通饲料喂养大鼠的摄入量相匹配。虽然喂食补充了葡萄糖或脂肪的NCM的大鼠与禁食大鼠或喂食普通NCM的大鼠一样,显示出同样强烈的胰淀素诱导激活,但在喂食补充了蛋白质的NCM或含有所有三种营养素的NCM的大鼠中,观察到c-Fos表达明显较低。与这种较低的激活一致,相同剂量的胰淀素未能减少喂食NCM/蛋白质的大鼠的食物摄入量,而当动物接受NCM、NCM/葡萄糖或NCM/脂肪时,胰淀素会导致进食量减少。有趣的是,尽管在这些条件下AP中胰淀素诱导的c-Fos表达水平较低,但胰淀素在自由进食普通饲料的大鼠中仍有效减少了食物摄入量。我们得出结论,饮食中的蛋白质可能会减弱胰淀素的厌食潜力,而当碳水化合物/脂肪的量相对于蛋白质含量较高时,例如在标准普通饲料中,这种影响似乎会被抵消。