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下丘脑外 GABA 能阿片促黑素原神经元调节 AgRP 神经元活性以控制摄食行为。

Extrahypothalamic GABAergic nociceptin-expressing neurons regulate AgRP neuron activity to control feeding behavior.

机构信息

Institute of Clinical Sciences, Faculty of Medicine, Imperial College, London, United Kingdom.

MRC London Institute of Medical Sciences, London, United Kingdom.

出版信息

J Clin Invest. 2020 Jan 2;130(1):126-142. doi: 10.1172/JCI130340.

Abstract

Arcuate nucleus agouti-related peptide (AgRP) neurons play a central role in feeding and are under complex regulation by both homeostatic hormonal and nutrient signals and hypothalamic neuronal pathways. Feeding may also be influenced by environmental cues, sensory inputs, and other behaviors, implying the involvement of higher brain regions. However, whether such pathways modulate feeding through direct synaptic control of AgRP neuron activity is unknown. Here, we show that nociceptin-expressing neurons in the anterior bed nuclei of the stria terminalis (aBNST) make direct GABAergic inputs onto AgRP neurons. We found that activation of these neurons inhibited AgRP neurons and feeding. The activity of these neurons increased upon food availability, and their ablation resulted in obesity. Furthermore, these neurons received afferent inputs from a range of upstream brain regions as well as hypothalamic nuclei. Therefore, aBNST GABAergic nociceptin neurons may act as a gateway to feeding behavior by connecting AgRP neurons to both homeostatic and nonhomeostatic neuronal inputs.

摘要

弓状核阿黑皮素原相关肽(AgRP)神经元在摄食中起核心作用,受到体内平衡激素和营养信号以及下丘脑神经元通路的复杂调节。摄食也可能受到环境线索、感觉输入和其他行为的影响,这意味着涉及到更高的脑区。然而,这些途径是否通过直接突触控制 AgRP 神经元的活动来调节摄食尚不清楚。在这里,我们显示终纹床核前部的阿片促黑素原(nociceptin)表达神经元对 AgRP 神经元有直接的 GABA 能输入。我们发现,这些神经元的激活抑制了 AgRP 神经元和摄食。这些神经元的活动在食物供应时增加,而它们的消融导致肥胖。此外,这些神经元还接收来自一系列上游脑区和下丘脑核的传入输入。因此,终纹床核前部 GABA 能阿片促黑素原神经元可能通过将 AgRP 神经元与体内平衡和非体内平衡的神经元输入连接起来,作为摄食行为的一个门户。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52f7/6934207/a55afd03ac2f/jci-130-130340-g036.jpg

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