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下丘脑腹内侧核的不同神经元投射介导血糖和行为效应。

Distinct Neuronal Projections From the Hypothalamic Ventromedial Nucleus Mediate Glycemic and Behavioral Effects.

机构信息

UW Medicine Diabetes Institute, Department of Medicine, University of Washington, Seattle, WA.

School of Medicine, Creighton University, Omaha, NE.

出版信息

Diabetes. 2018 Dec;67(12):2518-2529. doi: 10.2337/db18-0380. Epub 2018 Sep 26.

DOI:10.2337/db18-0380
PMID:30257978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6245222/
Abstract

The hypothalamic ventromedial nucleus (VMN) is implicated both in autonomic control of blood glucose and in behaviors including fear and aggression, but whether these divergent effects involve the same or distinct neuronal subsets and their projections is unknown. To address this question, we used an optogenetic approach to selectively activate the subset of VMN neurons that express neuronal nitric oxide synthase 1 (VMN neurons) implicated in glucose counterregulation. We found that photoactivation of these neurons elicits ) robust hyperglycemia achieved by activation of counterregulatory responses usually reserved for the physiological response to hypoglycemia and ) defensive immobility behavior. Moreover, we show that the glucagon, but not corticosterone, response to insulin-induced hypoglycemia is blunted by photoinhibition of the same neurons. To investigate the neurocircuitry by which VMN neurons mediate these effects, and to determine whether these diverse effects are dissociable from one another, we activated downstream VMN projections in either the anterior bed nucleus of the stria terminalis (aBNST) or the periaqueductal gray (PAG). Whereas glycemic responses are fully recapitulated by activation of VMN projections to the aBNST, freezing immobility occurred only upon activation of VMN terminals in the PAG. These findings support previous evidence of a VMN→aBNST neurocircuit involved in glucose counterregulation and demonstrate that activation of VMN neuronal projections supplying the PAG robustly elicits defensive behaviors.

摘要

下丘脑腹内侧核(VMN)既参与自主控制血糖,也参与包括恐惧和攻击在内的行为,但这些不同的效应是否涉及相同或不同的神经元亚群及其投射尚不清楚。为了解决这个问题,我们使用光遗传学方法选择性地激活参与葡萄糖代偿的神经元一氧化氮合酶 1(VMN 神经元)。我们发现,这些神经元的光激活会引起)强烈的高血糖,这是通过激活通常保留用于对低血糖的生理反应的代偿反应来实现的,和)防御性不动行为。此外,我们还表明,通过对相同神经元进行光抑制,胰岛素诱导的低血糖引起的胰高血糖素反应而不是皮质酮反应减弱。为了研究 VMN 神经元介导这些效应的神经回路,并确定这些不同的效应是否彼此分离,我们激活了 VMN 投射到终纹床核前区(aBNST)或中脑导水管周围灰质(PAG)的下游投射。虽然激活 VMN 投射到 aBNST 可以完全再现血糖反应,但只有在激活 PAG 中的 VMN 末梢时才会发生冻结不动。这些发现支持了先前关于参与葡萄糖代偿的 VMN→aBNST 神经回路的证据,并表明激活供应 PAG 的 VMN 神经元投射会强烈引发防御行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/c2bbaf5106af/db180380f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/86f8d48b7120/db180380f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/abf09a29a9eb/db180380f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/6e10c95a2643/db180380f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/015d2913b81e/db180380f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/cf53035e1ffc/db180380f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/c2bbaf5106af/db180380f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/86f8d48b7120/db180380f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/abf09a29a9eb/db180380f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/6e10c95a2643/db180380f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/015d2913b81e/db180380f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/cf53035e1ffc/db180380f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/821e/6245222/c2bbaf5106af/db180380f6.jpg

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