| Literature DB >> 28625488 |
Zhe Zhao1, Liang Wang1, Wenling Gao1, Fei Hu1, Juen Zhang1, Yuqi Ren2, Rui Lin2, Qiru Feng3, Mingxiu Cheng4, Dapeng Ju5, Qingsheng Chi6, Dehua Wang6, Sen Song4, Minmin Luo7, Cheng Zhan8.
Abstract
Stress-induced hyperglycemia is a fundamental adaptive response that mobilizes energy stores in response to threats. Here, our examination of the contributions of the central catecholaminergic (CA) neuronal system to this adaptive response revealed that CA neurons in the ventrolateral medulla (VLM) control stress-induced hyperglycemia. Ablation of VLM CA neurons abolished the hyperglycemic response to both physical and psychological stress, whereas chemogenetic activation of these neurons was sufficient to induce hyperglycemia. We further found that CA neurons in the rostral VLM, but not those in the caudal VLM, cause hyperglycemia via descending projections to the spinal cord. Monosynaptic tracing experiments showed that VLM CA neurons receive direct inputs from multiple stress-responsive brain areas. Optogenetic studies identified an excitatory PVN-VLM circuit that induces hyperglycemia. This study establishes the central role of VLM CA neurons in stress-induced hyperglycemia and substantially expands our understanding of the central mechanism that controls glucose metabolism.Entities:
Keywords: catecholaminergic neurons; glucose metabolism; hypothalamic paraventricular nucleus-ventrolateral medulla pathway; stress; stress-induced hyperglycemia; ventrolateral medulla
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Year: 2017 PMID: 28625488 DOI: 10.1016/j.neuron.2017.05.031
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173