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Plasma Epinephrine Contributes to the Development of Experimental Hypoglycemia-Associated Autonomic Failure.血浆肾上腺素有助于实验性低血糖相关自主神经衰竭的发展。
J Clin Endocrinol Metab. 2020 Nov 1;105(11):3416-27. doi: 10.1210/clinem/dgaa539.
2
Carvedilol prevents counterregulatory failure and impaired hypoglycaemia awareness in non-diabetic recurrently hypoglycaemic rats.卡维地洛可预防非糖尿病性反复发作性低血糖大鼠的拮抗反应衰竭和低血糖感知障碍。
Diabetologia. 2019 Apr;62(4):676-686. doi: 10.1007/s00125-018-4802-0. Epub 2019 Jan 9.
3
Norepinephrine stimulates glycogenolysis in astrocytes to fuel neurons with lactate.去甲肾上腺素刺激星形胶质细胞中的糖原分解,以产生乳酸为神经元供能。
PLoS Comput Biol. 2018 Aug 30;14(8):e1006392. doi: 10.1371/journal.pcbi.1006392. eCollection 2018 Aug.
4
Aerobic glycolysis during brain activation: adrenergic regulation and influence of norepinephrine on astrocytic metabolism.大脑激活过程中的有氧糖酵解:肾上腺素能调节及去甲肾上腺素对星形胶质细胞代谢的影响。
J Neurochem. 2016 Jul;138(1):14-52. doi: 10.1111/jnc.13630. Epub 2016 Jun 10.
5
A patient with acute liver failure and extreme hypoglycaemia with lactic acidosis who was not in a coma: causes and consequences of lactate-protected hypoglycaemia.一名患有急性肝衰竭、伴有乳酸酸中毒的严重低血糖且未昏迷的患者:乳酸保护型低血糖的病因及后果
Anaesth Intensive Care. 2014 Jul;42(4):507-11. doi: 10.1177/0310057X1404200413.
6
The rate of fall of blood glucose determines the necessity of forebrain-projecting catecholaminergic neurons for male rat sympathoadrenal responses.血糖下降率决定了投射到前脑的儿茶酚胺能神经元对于雄性大鼠交感肾上腺反应的必要性。
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7
Lactate-mediated glia-neuronal signalling in the mammalian brain.哺乳动物大脑中乳酸介导的神经胶质细胞-神经元信号传导
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8
Influence of VMH fuel sensing on hypoglycemic responses.VMH 对低血糖反应的燃料感应的影响。
Trends Endocrinol Metab. 2013 Dec;24(12):616-24. doi: 10.1016/j.tem.2013.08.005. Epub 2013 Sep 21.
9
Lactate-induced release of GABA in the ventromedial hypothalamus contributes to counterregulatory failure in recurrent hypoglycemia and diabetes.乳酸引起的腹内侧下丘脑 GABA 的释放有助于反复低血糖和糖尿病的代偿失败。
Diabetes. 2013 Dec;62(12):4239-46. doi: 10.2337/db13-0770. Epub 2013 Aug 12.
10
β2-Adrenergic receptor agonist administration promotes counter-regulatory responses and recovery from hypoglycaemia in rats.β2-肾上腺素能受体激动剂给药促进大鼠的代偿反应和低血糖恢复。
Diabetologia. 2013 Nov;56(11):2517-23. doi: 10.1007/s00125-013-3009-7. Epub 2013 Aug 10.

室旁核去甲肾上腺素能受体的反复激活抑制了对低血糖的反应。

Repeated Activation of Noradrenergic Receptors in the Ventromedial Hypothalamus Suppresses the Response to Hypoglycemia.

机构信息

Department of Endocrinology and Nephrology, Nordsjællands Hospital, Dyrehavevej, Denmark.

Department of Internal Medicine-Section of Endocrinology, Yale School of Medicine, New Haven, CT, USA.

出版信息

Endocrinology. 2021 Mar 1;162(3). doi: 10.1210/endocr/bqaa241.

DOI:10.1210/endocr/bqaa241
PMID:33367607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7814298/
Abstract

Activation of the adrenergic system in response to hypoglycemia is important for proper recovery from low glucose levels. However, it has been suggested that repeated adrenergic stimulation may also contribute to counterregulatory failure, but the underlying mechanisms are not known. The aim of this study was to establish whether repeated activation of noradrenergic receptors in the ventromedial hypothalamus (VMH) contributes to blunting of the counterregulatory response by enhancing local lactate production. The VMH of nondiabetic rats were infused with either artificial extracellular fluid, norepinephrine (NE), or salbutamol for 3 hours/day for 3 consecutive days before they underwent a hypoglycemic clamp with microdialysis to monitor changes in VMH lactate levels. Repeated exposure to NE or salbutamol suppressed both the glucagon and epinephrine responses to hypoglycemia compared to controls. Furthermore, antecedent NE and salbutamol treatments raised extracellular lactate levels in the VMH. To determine whether the elevated lactate levels were responsible for impairing the hormone response, we pharmacologically inhibited neuronal lactate transport in a subgroup of NE-treated rats during the clamp. Blocking neuronal lactate utilization improved the counterregulatory hormone responses in NE-treated animals, suggesting that repeated activation of VMH β2-adrenergic receptors increases local lactate levels which in turn, suppresses the counterregulatory hormone response to hypoglycemia.

摘要

低血糖时肾上腺素系统的激活对于从低葡萄糖水平中适当恢复是重要的。然而,已经有人提出,反复的肾上腺素刺激也可能导致代偿性衰竭,但潜在的机制尚不清楚。本研究的目的是确定在下丘脑腹内侧核(VMH)中重复激活去甲肾上腺素能受体是否通过增强局部乳酸产生而导致对激素反应的迟钝。在经历低血糖钳夹和微透析以监测 VMH 乳酸水平变化之前,将非糖尿病大鼠的 VMH 连续 3 天每天输注人工细胞外液、去甲肾上腺素(NE)或沙美特罗 3 小时。与对照组相比,反复暴露于 NE 或沙美特罗抑制了胰高血糖素和肾上腺素对低血糖的反应。此外,NE 和沙美特罗的先前处理提高了 VMH 中的细胞外乳酸水平。为了确定升高的乳酸水平是否会损害激素反应,我们在钳夹期间抑制了一部分 NE 处理的大鼠中的神经元乳酸转运,以确定是否升高的乳酸水平会损害激素反应。在 NE 处理的动物中,阻断神经元乳酸利用改善了激素反应,这表明 VMHβ2-肾上腺素受体的反复激活增加了局部乳酸水平,进而抑制了低血糖时的激素反应。