Korim Willian S, Llewellyn-Smith Ida J, Verberne Anthony J M
Clinical Pharmacology and Therapeutics Unit (W.S.K., A.J.M.V.), Department of Medicine Austin Health, University of Melbourne, Heidelberg, Victoria 3084, Australia; Florey Institute of Neuroscience and Mental Health (W.S.K.), University of Melbourne, Parkville, Victoria 3052, Australia; and Cardiovascular Medicine (I.J.L.-S.), Human Physiology and Centre for Neuroscience, School of Medicine, Flinders University, Bedford Park, South Australia 5042, Australia.
Endocrinology. 2016 Feb;157(2):810-9. doi: 10.1210/en.2015-1712. Epub 2015 Dec 11.
Iatrogenic hypoglycemia in response to insulin treatment is commonly experienced by patients with type 1 diabetes and can be life threatening. The body releases epinephrine in an attempt to counterregulate hypoglycemia, but the neural mechanisms underlying this phenomenon remain to be elucidated. Orexin neurons in the perifornical hypothalamus (PeH) project to the rostral ventrolateral medulla (RVLM) and are likely to be involved in epinephrine secretion during hypoglycemia. In anesthetized rats, we report that hypoglycemia increases the sympathetic preganglionic discharge to the adrenal gland by activating PeH orexin neurons that project to the RVLM (PeH-RVLM). Electrophysiological characterization shows that the majority of identified PeH-RVLM neurons, including a subpopulation of orexin neurons, are activated in response to hypoglycemia or glucoprivation. Furthermore, the excitatory input from the PeH is mediated by orexin type 2 receptors in the RVLM. These results suggest that activation of orexin PeH-RVLM neurons and orexin type 2 receptors in the RVLM facilitates epinephrine release by increasing sympathetic drive to adrenal chromaffin cells during hypoglycemia.
1型糖尿病患者在接受胰岛素治疗时常常会发生医源性低血糖,这可能会危及生命。身体会释放肾上腺素以试图对抗低血糖,但这一现象背后的神经机制仍有待阐明。穹窿周下丘脑(PeH)中的食欲素神经元投射到延髓头端腹外侧区(RVLM),并且可能参与低血糖期间的肾上腺素分泌。在麻醉大鼠中,我们报告低血糖通过激活投射到RVLM的PeH食欲素神经元(PeH-RVLM)增加了肾上腺的交感神经节前放电。电生理学特征表明,大多数已鉴定的PeH-RVLM神经元,包括食欲素神经元的一个亚群,在低血糖或糖剥夺反应中被激活。此外,来自PeH的兴奋性输入由RVLM中的2型食欲素受体介导。这些结果表明,低血糖期间,激活PeH-RVLM食欲素神经元和RVLM中的2型食欲素受体,通过增加对肾上腺嗜铬细胞的交感神经驱动,促进肾上腺素释放。