下丘脑
谷氨酸的
兴奋性突触后电位
突触
长时程增强
生物
突触可塑性
神经传递
神经科学
内分泌学
内科学
医学
谷氨酸受体
抑制性突触后电位
受体
作者
Katarzyna Grzelka,Hannah Wilhelms,Stephan Dodt,Marie-Luise Dreisow,Joseph C. Madara,Samuel J. Walker,Chen Wu,Daqing Wang,Bradford B. Lowell,Henning Fenselau
出处
期刊:Cell Metabolism
[Elsevier]
日期:2023-05-01
卷期号:35 (5): 770-785.e5
被引量:22
标识
DOI:10.1016/j.cmet.2023.03.002
摘要
Restricting caloric intake effectively reduces body weight, but most dieters fail long-term adherence to caloric deficit and eventually regain lost weight. Hypothalamic circuits that control hunger drive critically determine body weight; yet, how weight loss sculpts these circuits to motivate food consumption until lost weight is regained remains unclear. Here, we probe the contribution of synaptic plasticity in discrete excitatory afferents on hunger-promoting AgRP neurons. We reveal a crucial role for activity-dependent, remarkably long-lasting amplification of synaptic activity originating from paraventricular hypothalamus thyrotropin-releasing (PVHTRH) neurons in long-term body weight control. Silencing PVHTRH neurons inhibits the potentiation of excitatory input to AgRP neurons and diminishes concomitant regain of lost weight. Brief stimulation of the pathway is sufficient to enduringly potentiate this glutamatergic hunger synapse and triggers an NMDAR-dependent gaining of body weight that enduringly persists. Identification of this activity-dependent synaptic amplifier provides a previously unrecognized target to combat regain of lost weight.
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