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下丘脑中恢复体重的饥饿突触放大器。

A synaptic amplifier of hunger for regaining body weight in the hypothalamus.

机构信息

Synaptic Transmission in Energy Homeostasis Group, Max Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931 Cologne, Germany.

Synaptic Transmission in Energy Homeostasis Group, Max Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931 Cologne, Germany; Department of Neuronal Control of Metabolism, Max Planck Institute for Metabolism Research, Cologne, Germany.

出版信息

Cell Metab. 2023 May 2;35(5):770-785.e5. doi: 10.1016/j.cmet.2023.03.002. Epub 2023 Mar 24.

Abstract

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 (PVH) neurons in long-term body weight control. Silencing PVH 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.

摘要

限制热量摄入能有效减轻体重,但大多数节食者无法长期坚持热量不足,最终体重会反弹。控制饥饿的下丘脑回路对体重起着关键作用;然而,体重减轻如何塑造这些回路以促使进食,直到体重反弹,目前仍不清楚。在这里,我们研究了突触可塑性在促进饥饿的 AgRP 神经元的离散兴奋性传入中的作用。我们揭示了来自室旁下丘脑促甲状腺素释放(PVH)神经元的活动依赖性、显著持久的突触活动放大在长期体重控制中的重要作用。沉默 PVH 神经元会抑制对 AgRP 神经元兴奋性输入的增强,并减少伴随的体重反弹。该通路的短暂刺激足以持久地增强这种谷氨酸能饥饿突触,并触发一种 NMDA 受体依赖性的体重增加,这种增加会持久存在。这种活动依赖性突触放大器的鉴定为对抗体重反弹提供了一个以前未被认识到的靶点。

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