Basu Ananda, Yadav Yogesh, Carter Rickey E, Basu Rita
Division of Endocrinology, University of Virginia School of Medicine, Charlottesville, VA, US.
Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, US.
J Clin Endocrinol Metab. 2020 Jul 1;105(7):e2378-88. doi: 10.1210/clinem/dgaa241.
The effect of physiological changes in night-time cortisol and glucagon on endogenous glucose production (EGP) and nocturnal glycemia are unknown.
To determine the effects of changes in cortisol and glucagon on EGP during the night.
Two overnight protocols were conducted. In Protocol 1, endogenous cortisol was blocked with metyrapone and hydrocortisone infused either at constant (constant) or increasing (variable) rates to mimic basal or physiological nocturnal cortisol concentrations. In Protocol 2, endogenous glucagon was blocked with somatostatin and exogenous glucagon was infused at either basal or elevated rates to mimic nocturnal glucagon concentrations observed in nondiabetic (ND) and type 2 diabetes (T2D) individuals. EGP was measured using [3-3H] glucose and gluconeogenesis estimated with 2H2O in all studies.
Mayo Clinic Clinical Research Trials Unit, Rochester, MN, US.
In Protocol 1, 34 subjects (17 ND and 17 T2D) and in Protocol 2, 39 subjects (21 ND and 18 T2D) were studied.
Endogenous glucose production.
EGP, gluconeogenesis, and glycogenolysis were higher with variable than with constant cortisol at 7 am in T2D subjects. In contrast, nocturnal EGP did not differ in ND subjects between variable and constant cortisol. While elevated glucagon increased EGP, glycogenolysis, and gluconeogenesis in ND, the data in T2D subjects indicated that EGP and gluconeogenesis but not glycogenolysis were higher during the early part of the night.
Nocturnal hyperglucagonemia, but not physiological rise in cortisol, contributes to nocturnal hyperglycemia in T2D due to increased gluconeogenesis.
夜间皮质醇和胰高血糖素的生理变化对内源性葡萄糖生成(EGP)和夜间血糖的影响尚不清楚。
确定夜间皮质醇和胰高血糖素变化对EGP的影响。
进行了两个过夜方案。在方案1中,用甲吡酮阻断内源性皮质醇,并以恒定(恒定)或递增(可变)速率输注氢化可的松,以模拟基础或生理性夜间皮质醇浓度。在方案2中,用生长抑素阻断内源性胰高血糖素,并以基础或升高速率输注外源性胰高血糖素,以模拟在非糖尿病(ND)和2型糖尿病(T2D)个体中观察到的夜间胰高血糖素浓度。在所有研究中,使用[3-3H]葡萄糖测量EGP,并用2H2O估计糖异生。
美国明尼苏达州罗切斯特市梅奥诊所临床研究试验单位。
在方案1中,研究了34名受试者(17名ND和17名T2D),在方案2中,研究了39名受试者(21名ND和18名T2D)。
内源性葡萄糖生成。
在T2D受试者中,上午7点时,可变皮质醇组的EGP、糖异生和糖原分解高于恒定皮质醇组。相比之下