Szentirmai Eva, Kapás Levente, Sun Yuxiang, Smith Roy G, Krueger James M
Sleep and Performance Research Center, Department of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, Washington State University, Pullman, WA 99164, USA.
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):14069-74. doi: 10.1073/pnas.0903090106. Epub 2009 Aug 4.
Peptidergic mechanisms controlling feeding, metabolism, thermoregulation, and sleep overlap in the hypothalamus. Low ambient temperatures and food restriction induce hypothermic (torpor) bouts and characteristic metabolic and sleep changes in mice. We report that mice lacking the preproghrelin gene, but not those lacking the ghrelin receptor, have impaired abilities to manifest and integrate normal sleep and thermoregulatory responses to metabolic challenges. In response to fasting at 17 degrees C (a subthermoneutral ambient temperature), preproghrelin knockout mice enter hypothermic bouts associated with reduced sleep, culminating in a marked drop in body temperature to near-ambient levels. Prior treatment with obestatin, another preproghrelin gene product, attenuates the hypothermic response of preproghrelin knockout mice. Results suggest that obestatin is a component in the coordinated regulation of metabolism and sleep during torpor.
在下丘脑中,控制进食、新陈代谢、体温调节和睡眠的肽能机制相互重叠。低环境温度和食物限制会诱导小鼠出现低温(蛰伏)发作以及特征性的代谢和睡眠变化。我们报告称,缺乏前胃促生长素原基因的小鼠,但不包括缺乏胃促生长素受体的小鼠,在表现和整合对代谢挑战的正常睡眠及体温调节反应方面能力受损。在17摄氏度(低于热中性环境温度)下禁食时,前胃促生长素原基因敲除小鼠会进入与睡眠减少相关的低温发作,最终体温显著下降至接近环境温度水平。用另一种前胃促生长素原基因产物肥胖抑制素进行预先处理,可减弱前胃促生长素原基因敲除小鼠的低温反应。结果表明,肥胖抑制素是蛰伏期间新陈代谢和睡眠协调调节的一个组成部分。