Estrogen-sensitive medial preoptic area neurons coordinate torpor in mice.
Zhi ZhangFernando M C V ReisYanlin HeJae W ParkJohnathon R DiVittorioNilla SivakumarJ Edward Van VeenSandra Maesta-PereiraMichael ShumIndia S NicholsMegan G MassaShawn AndersonKetema PaulMarc LiesaOlujimi A AjijolaYong XuAvishek AdhikariStephanie M CorreaPublished in: Nature communications (2020)
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.
Keyphrases
- spinal cord
- estrogen receptor
- heart rate
- physical activity
- cardiac arrest
- blood pressure
- heart rate variability
- high fat diet induced
- brain injury
- type diabetes
- poor prognosis
- metabolic syndrome
- spinal cord injury
- sleep quality
- adipose tissue
- depressive symptoms
- weight loss
- replacement therapy
- atrial fibrillation
- stress induced
- genetic diversity