Department of Biology, University of Minnesota Duluth, Duluth, Minnesota, United States of America.
PLoS One. 2013;8(1):e53574. doi: 10.1371/journal.pone.0053574. Epub 2013 Jan 2.
Hibernation is a natural adaptation that allows certain mammals to survive physiological extremes that are lethal to humans. Near freezing body temperatures, heart rates of 3-10 beats per minute, absence of food consumption, and depressed metabolism are characteristic of hibernation torpor bouts that are periodically interrupted by brief interbout arousals (IBAs). The molecular basis of torpor induction is unknown, however starved mice overexpressing the metabolic hormone fibroblast growth factor 21 (FGF21) promote fat utilization, reduce body temperature, and readily enter torpor-all hallmarks of mammalian hibernation. In this study we cloned FGF21 from the naturally hibernating thirteen-lined ground squirrel (Ictidomys tridecemlineatus) and found that levels of FGF21 mRNA in liver and FGF21 protein in serum are elevated during hibernation torpor bouts and significantly elevated during IBAs compared to summer active animals. The effects of artificially elevating circulating FGF21 concentrations 50 to 100-fold via adenoviral-mediated overexpression were examined at three different times of the year. This is the first time that a transgenic approach has been used in a natural hibernator to examine mechanistic aspects of hibernation. Surgically implanted transmitters measured various metrics of the hibernation phenotype over a 7-day period including changes in motor activity, heart rate and core body temperature. In April fed-state animals, FGF21 overexpression decreased blood insulin and free fatty acid concentrations, effects similar to those seen in obese mice. However, elevated FGF21 concentrations did not cause torpor in these fed-state animals nor did they cause torpor or affect metabolic parameters in fasted-state animals in March/April, August or October. We conclude that FGF21 is strongly regulated during torpor and IBA but that its overexpression is not sufficient to cause torpor in naturally hibernating ground squirrels.
冬眠是一种自然适应,使某些哺乳动物能够在对人类致命的生理极限中生存。接近冻结的体温、每分钟 3-10 次的心率、禁食和代谢抑制是冬眠性昏睡发作的特征,这些发作会被短暂的苏醒期(IBAs)周期性打断。诱导昏睡的分子基础尚不清楚,然而,饥饿的过表达代谢激素成纤维细胞生长因子 21(FGF21)的老鼠会促进脂肪利用、降低体温并轻易进入昏睡状态——所有这些都是哺乳动物冬眠的标志。在这项研究中,我们从自然冬眠的十三线地松鼠(Ictidomys tridecemlineatus)中克隆了 FGF21,发现肝脏中的 FGF21 mRNA 水平和血清中的 FGF21 蛋白在冬眠性昏睡发作期间升高,与夏季活跃的动物相比,在苏醒期升高更为显著。通过腺病毒介导的过表达,人为地将循环 FGF21 浓度提高 50 到 100 倍,在一年中的三个不同时间进行了检查。这是首次在自然冬眠动物中使用转基因方法来检查冬眠的机制方面。植入的发射器在 7 天的时间内测量了冬眠表型的各种指标,包括运动活动、心率和核心体温的变化。在 4 月的喂食状态动物中,FGF21 过表达降低了血液胰岛素和游离脂肪酸浓度,这与肥胖老鼠中的变化相似。然而,在这些喂食状态的动物中,升高的 FGF21 浓度并没有导致昏睡,也没有在 3 月/4 月、8 月或 10 月的禁食状态动物中导致昏睡或影响代谢参数。我们得出结论,FGF21 在冬眠和苏醒期受到强烈调节,但过表达不足以在自然冬眠的地松鼠中引起昏睡。