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Parabrachial neuron types categorically encode thermoregulation variables during heat defense

Heat defense is crucial for survival and fitness. Transmission of thermosensory signals into hypothalamic thermoregulation centers represents a key layer of regulation in heat defense. Yet, how these signals are transmitted into the hypothalamus remains poorly understood. Here, we reveal that latera...

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Detalles Bibliográficos
Autores principales: Yang, Wen Z., Du, Xiaosa, Zhang, Wen, Gao, Cuicui, Xie, Hengchang, Xiao, Yan, Jia, Xiaoning, Liu, Jiashu, Xu, Jianhui, Fu, Xin, Tu, Hongqing, Fu, Xiaoyu, Ni, Xinyan, He, Miao, Yang, Jiajun, Wang, Hong, Yang, Haitao, Xu, Xiao-hong, Shen, Wei L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7467693/
https://www.ncbi.nlm.nih.gov/pubmed/32917598
http://dx.doi.org/10.1126/sciadv.abb9414
Descripción
Sumario:Heat defense is crucial for survival and fitness. Transmission of thermosensory signals into hypothalamic thermoregulation centers represents a key layer of regulation in heat defense. Yet, how these signals are transmitted into the hypothalamus remains poorly understood. Here, we reveal that lateral parabrachial nucleus (LPB) glutamatergic prodynorphin and cholecystokinin neuron populations are progressively recruited to defend elevated body temperature. These two nonoverlapping neuron types form circuits with downstream preoptic hypothalamic neurons to inhibit the thermogenesis of brown adipose tissues (BATs) and activate tail vasodilation, respectively. Both circuits are activated by warmth and can limit fever development. The prodynorphin circuit is further required for regulating energy expenditure and body weight homeostasis. Thus, these findings establish that the genetic and functional specificity of heat defense neurons occurs as early as in the LPB and uncover categorical neuron types for encoding two heat defense variables, inhibition of BAT thermogenesis and activation of vasodilation.