Koska P, Dojcsák Kiss-Tóth E, Juhász Szalai A, Kovács G L, Barkai L, Rácz O, Fodor Bertalan
University of Miskolc Department of Nanobiotechnology and Regenerative Medicine, Faculty of Health Care Miskolc Hungary.
Acta Physiol Hung. 2013 Jun;100(2):133-9. doi: 10.1556/APhysiol.100.2013.2.1.
An important obstacle to achieve optimal glycaemic control in diabetics on intensive insulin therapy is the frequent occurrence of insulin induced hypoglycaemic events. In healthy subjects and in diabetics without autonomic neuropathy hypoglycaemia activates the sympathetic nervous system, resulting in epinephrine and glucagon release. Both hormones increase hepatic glucose production and this counterregulatory response is of key importance of glucose homeostasis. Recent research shed light on the fact that antecedent hypoglycaemic episodes play pivotal role in hypoglycaemia associated autonomic failure (HAAF). In this condition the sympatho-adrenal response to decreased blood glucose level is blunted. The existence of HAAF clearly indicates that the nervous system contributes to glucose homeostasis in a substantial manner. This review outlines the mechanisms of both peripheral and central neuronal glucose sensing and of neural pathways involved in the counterregulatory response.
在接受强化胰岛素治疗的糖尿病患者中,实现最佳血糖控制的一个重要障碍是胰岛素诱导的低血糖事件频繁发生。在健康受试者和无自主神经病变的糖尿病患者中,低血糖会激活交感神经系统,导致肾上腺素和胰高血糖素释放。这两种激素都会增加肝脏葡萄糖生成,这种反调节反应对葡萄糖稳态至关重要。最近的研究揭示了先前的低血糖发作在低血糖相关自主神经功能衰竭(HAAF)中起关键作用这一事实。在这种情况下,交感 - 肾上腺对血糖水平降低的反应减弱。HAAF的存在清楚地表明神经系统对葡萄糖稳态有重要贡献。本综述概述了外周和中枢神经元葡萄糖感知机制以及参与反调节反应的神经通路。