Wilson David F, Matschinsky Franz M
Perelman School of Medicine, Department of Biochemistry and Biophysics, University of Pennsylvania , Philadelphia, Pennsylvania.
J Appl Physiol (1985). 2019 Jun 1;126(6):1746-1755. doi: 10.1152/japplphysiol.00047.2019. Epub 2019 Apr 11.
In glucose homeostasis, glucose concentration is sensed by its metabolism through glucokinase (GCK) and oxidative phosphorylation. Because oxidative phosphorylation is an integral part of the sensory system, glucose sensing is necessarily dependent on oxygen pressure. Much of the dependence on oxygen is suppressed by location of glucose sensing cells in tissues with well-regulated blood flow. In healthy individuals the oxygen dependence is primarily observed in response to transient global hypoxia events such as during birth or transition to high altitude. The GCK sensing system is, however, used to control release of both insulin and glucagon, the preeminant hormonal regulators of blood glucose, as well as glucose sensitive neuronal activity. Suppression of oxygen delivery to glucose-sensing cells or interference with regulation of tissue blood flow by either local or systemic causes, stresses the glucose regulatory system. This is true whether the stress is imposed locally, such as by altered oxygen delivery to the pancreas, or globally, as in pulmonary insufficiency or exposure to high altitude. It may be expected that chronic application of this stress predisposes individuals to developing diabetes. Type 2 diabetes is a broad class of diseases characterized by disturbance of glucose homeostasis, i.e., having either hyperglycemia and/or decreased sensitivity to insulin. Given the role of oxidative phosphorylation in glucose sensing, tissue oxygen deprivation may predispose individuals to developing diabetes as well as contributing to the disease itself. This is particularly true in age-related diabetes because the incidence of vascular insufficiency increases markedly with increasing age. Glucose sensing requires glucose metabolism through glycolysis and oxidative phosphorylation. Dependence of the latter on oxygen concentration imposes an oxygen dependence on glucose sensing. We have used a validated computational model to quantify that dependence. Evidence is presented that tissue oxygenation plays an important role in predisposition of individuals to developing type 2 diabetes and in progression of the disease.
在葡萄糖稳态中,葡萄糖浓度通过其经由葡萄糖激酶(GCK)的代谢和氧化磷酸化来感知。由于氧化磷酸化是传感系统的一个组成部分,葡萄糖传感必然依赖于氧分压。葡萄糖传感细胞位于血流调节良好的组织中,这在很大程度上抑制了对氧的依赖性。在健康个体中,对氧的依赖性主要在诸如出生时或过渡到高海拔期间的短暂全身性缺氧事件中观察到。然而,GCK传感系统用于控制胰岛素和胰高血糖素的释放,胰岛素和胰高血糖素是血糖的主要激素调节因子,以及葡萄糖敏感神经元活动。向葡萄糖传感细胞的氧输送受到抑制或局部或全身原因对组织血流调节的干扰,都会给葡萄糖调节系统带来压力。无论这种压力是局部施加的,如胰腺氧输送改变,还是全身性的,如肺功能不全或暴露于高海拔,都是如此。可以预期,长期施加这种压力会使个体易患糖尿病。2型糖尿病是一大类以葡萄糖稳态紊乱为特征的疾病,即具有高血糖和/或对胰岛素敏感性降低。鉴于氧化磷酸化在葡萄糖传感中的作用,组织缺氧可能使个体易患糖尿病,并导致疾病本身。在与年龄相关的糖尿病中尤其如此,因为血管功能不全的发生率随着年龄的增加而显著增加。葡萄糖传感需要通过糖酵解和氧化磷酸化进行葡萄糖代谢。后者对氧浓度的依赖性使葡萄糖传感对氧产生依赖性。我们使用经过验证的计算模型来量化这种依赖性。有证据表明,组织氧合在个体易患2型糖尿病的倾向以及疾病进展中起重要作用。