Department of Integrative Physiology, Nagoya University Graduate School of Medicine, Nagoya, 466-8550, Japan.
PRESTO, Japan Science and Technology Agency, Kawaguchi, Saitama, 332-0012, Japan.
Bioessays. 2018 Aug;40(8):e1700252. doi: 10.1002/bies.201700252. Epub 2018 Jun 4.
The recent discovery of the medullary circuit driving "hunger responses" - reduced thermogenesis and promoted feeding - has greatly expanded our knowledge on the central neural networks for energy homeostasis. However, how hypothalamic hunger and satiety signals generated under fasted and fed conditions, respectively, control the medullary autonomic and somatic motor mechanisms remains unknown. Here, in reviewing this field, we propose two hypothalamomedullary neural pathways for hunger and satiety signaling. To trigger hunger signaling, neuropeptide Y activates a group of neurons in the paraventricular hypothalamic nucleus (PVH), which then stimulate an excitatory pathway to the medullary circuit to drive the hunger responses. In contrast, melanocortin-mediated satiety signaling activates a distinct group of PVH neurons, which then stimulate a putatively inhibitory pathway to the medullary circuit to counteract the hunger signaling. The medullary circuit likely contains inhibitory and excitatory premotor neurons whose alternate phasic activation generates the coordinated masticatory motor rhythms to promote feeding.
最近发现的驱动“饥饿反应”的髓质回路——减少产热和促进进食——极大地扩展了我们对能量平衡的中枢神经网络的认识。然而,在空腹和进食条件下分别产生的下丘脑饥饿和饱腹感信号如何控制髓质自主和躯体运动机制尚不清楚。在这里,在回顾这一领域时,我们提出了两条用于饥饿和饱腹感信号的下丘脑-髓质神经通路。为了触发饥饿信号,神经肽 Y 激活下丘脑室旁核 (PVH) 中的一组神经元,然后刺激兴奋通路到髓质回路以驱动饥饿反应。相比之下,黑素细胞激素介导的饱腹感信号激活了 PVH 中的另一组神经元,然后刺激到髓质回路的可能抑制性通路来抵消饥饿信号。髓质回路可能包含抑制性和兴奋性的前置运动神经元,它们的交替相位激活产生协调的咀嚼运动节律以促进进食。