Department of Chemistry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, United States.
Center for Biotechnology, University of Nebraska-Lincoln, Lincoln, Nebraska 68588, United States.
ACS Chem Neurosci. 2023 Jul 19;14(14):2569-2581. doi: 10.1021/acschemneuro.3c00268. Epub 2023 Jul 3.
During the winter, hibernating mammals undergo extreme changes in physiology, which allow them to survive several months without access to food. These animals enter a state of torpor, which is characterized by decreased metabolism, near-freezing body temperatures, and a dramatically reduced heart rate. The neurochemical basis of this regulation is largely unknown. Based on prior evidence suggesting that the peptide-rich hypothalamus plays critical roles in hibernation, we hypothesized that changes in specific cell-cell signaling peptides (neuropeptides and peptide hormones) underlie physiological changes during torpor/arousal cycles. To test this hypothesis, we used a mass spectrometry-based peptidomics approach to examine seasonal changes of endogenous peptides that occur in the hypothalamus and pituitary of a model hibernating mammal, the thirteen-lined ground squirrel (). In the pituitary, we observed changes in several distinct peptide hormones as animals prepared for torpor in October, exited torpor in March, and progressed from spring (March) to fall (August). In the hypothalamus, we observed an overall increase in neuropeptides in October (pre-torpor), a decrease as the animal entered torpor, and an increase in a subset of neuropeptides during normothermic interbout arousals. Notable changes were observed for feeding regulatory peptides, opioid peptides, and several peptides without well-established functions. Overall, our study provides critical insight into changes in endogenous peptides in the hypothalamus and pituitary during mammalian hibernation that were not available from transcriptomic measurements. Understanding the molecular basis of the hibernation phenotype may pave the way for future efforts to employ hibernation-like strategies for organ preservation, combating obesity, and treatment of stroke.
在冬季,冬眠哺乳动物的生理机能会发生极端变化,使它们能够在几个月内不吃食物而存活。这些动物进入一种蛰伏状态,其特征是新陈代谢减缓、体温接近冰点,以及心率显著降低。这种调节的神经化学基础在很大程度上是未知的。基于先前的证据表明富含肽的下丘脑在冬眠中发挥关键作用,我们假设特定细胞-细胞信号肽(神经肽和肽激素)的变化是蛰伏/觉醒周期中生理变化的基础。为了验证这一假设,我们使用基于质谱的肽组学方法来检查在冬眠模型哺乳动物——十三线地松鼠()的下丘脑和垂体中发生的内源性肽的季节性变化。在垂体中,我们观察到几种不同的肽激素在动物为蛰伏做准备的 10 月、从蛰伏中苏醒的 3 月以及从春季(3 月)到秋季(8 月)的过程中发生了变化。在下丘脑中,我们观察到 10 月(蛰伏前)的神经肽总体增加,随着动物进入蛰伏而减少,并且在正常体温的间歇觉醒期间,一部分神经肽增加。观察到的变化显著的是与进食调节肽、阿片肽和几种功能尚未明确的肽有关。总的来说,我们的研究提供了在哺乳动物冬眠期间下丘脑和垂体内源性肽变化的关键见解,这些变化无法从转录组测量中获得。了解冬眠表型的分子基础可能为未来利用冬眠样策略进行器官保存、对抗肥胖和治疗中风铺平道路。