迟钝
雌激素
体温过低
内科学
温度调节
内分泌学
恒温
生物
休眠(计算)
化学
医学
算法
计算机科学
国家(计算机科学)
作者
Zhi Zhang,Fernando MCV Reis,Yanlin He,Jae W. Park,Johnathon Roy DiVittorio,Nilla Sivakumar,J. Edward Van Veen,Sandra Maesta‐Pereira,Michaël Shum,India Nichols,Megan G. Massa,Shawn Anderson,Ketema N. Paul,Marc Liesa,Olujimi A. Ajijola,Yong Xu,Avishek Adhikari,Stephanie M. Correa
标识
DOI:10.1038/s41467-020-20050-1
摘要
Abstract Homeotherms maintain a stable internal body temperature despite changing environments. During energy deficiency, some species can cease to defend their body temperature and enter a hypothermic and hypometabolic state known as torpor. Recent advances have revealed the medial preoptic area (MPA) as a key site for the regulation of torpor in mice. The MPA is estrogen-sensitive and estrogens also have potent effects on both temperature and metabolism. Here, we demonstrate that estrogen-sensitive neurons in the MPA can coordinate hypothermia and hypometabolism in mice. Selectively activating estrogen-sensitive MPA neurons was sufficient to drive a coordinated depression of metabolic rate and body temperature similar to torpor, as measured by body temperature, physical activity, indirect calorimetry, heart rate, and brain activity. Inducing torpor with a prolonged fast revealed larger and more variable calcium transients from estrogen-sensitive MPA neurons during bouts of hypothermia. Finally, whereas selective ablation of estrogen-sensitive MPA neurons demonstrated that these neurons are required for the full expression of fasting-induced torpor in both female and male mice, their effects on thermoregulation and torpor bout initiation exhibit differences across sex. Together, these findings suggest a role for estrogen-sensitive MPA neurons in directing the thermoregulatory and metabolic responses to energy deficiency.
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