Galassetti Pietro, Tate Donna, Neill Ray A, Richardson Antoinette, Leu Szu-Yun, Davis Stephen N
Division of Diabetes, Endocrinology & Metabolism, Vanderbilt Univ. School of Medicine, Nashville, TN 37232-6303, USA.
Am J Physiol Endocrinol Metab. 2006 Jun;290(6):E1109-17. doi: 10.1152/ajpendo.00244.2005. Epub 2006 Jan 10.
Hypoglycemia frequently occurs during or after exercise in intensively treated patients with type 1 diabetes mellitus (T1DM), but the underlying mechanisms are not clear. In both diabetic and nondiabetic subjects, moderate hypoglycemia blunts counterregulatory responses to subsequent exercise, but it is unknown whether milder levels of hypoglycemia can exert similar effects in a dose-dependent fashion. This study was designed to test the hypothesis that prior hypoglycemia of differing depths induces acute counterregulatory failure of proportionally greater magnitude during subsequent exercise in T1DM. Twenty-two T1DM patients (11 males/11 females, HbA1c 8.0 +/- 0.3%) were studied during 90 min of euglycemic cycling exercise after two 2-h periods of previous day euglycemia or hypoglycemia of 3.9, 3.3, or 2.8 mmol/l (HYPO-3.9, HYPO-3.3, HYPO-2.8, respectively). Patients' counterregulatory responses (circulating levels of neuroendocrine hormones, intermediary metabolites, substrate flux, tracer-determined glucose kinetics, and cardiovascular measurements) were assessed during exercise. Identical euglycemia and basal insulin levels were successfully maintained during all exercise studies, regardless of blood glucose levels during the previous day. After day 1 euglycemia, patients displayed normal counterregulatory responses to exercise. Conversely, when identical exercise was performed after day 1 hypoglycemia of increasing depth, a progressively greater blunting of glucagon, catecholamine, cortisol, endogenous glucose production, and lipolytic responses to exercise was observed. This was paralleled by a graduated increase in the amount of exogenous glucose needed to maintain euglycemia during exercise. Our results demonstrate that acute counterregulatory failure during prolonged, moderate-intensity exercise may be induced in a dose-dependent fashion by differing depths of antecedent hypoglycemia starting at only 3.9 mmol/l in patients with T1DM.
在强化治疗的1型糖尿病(T1DM)患者中,低血糖经常发生在运动期间或运动后,但其潜在机制尚不清楚。在糖尿病和非糖尿病受试者中,中度低血糖会减弱对随后运动的反调节反应,但尚不清楚较轻程度的低血糖是否能以剂量依赖的方式产生类似的效果。本研究旨在检验以下假设:在T1DM患者中,不同深度的先前低血糖会在随后的运动中诱发成比例更大程度的急性反调节功能衰竭。对22名T1DM患者(11名男性/11名女性,糖化血红蛋白8.0 +/- 0.3%)进行了研究,在前一天经历两个2小时的血糖正常期或血糖水平分别为3.9、3.3或2.8 mmol/l的低血糖期(分别为HYPO-3.9、HYPO-3.3、HYPO-2.8)后,进行90分钟的血糖正常的循环运动。在运动期间评估患者的反调节反应(神经内分泌激素的循环水平、中间代谢产物、底物通量、示踪剂测定的葡萄糖动力学和心血管测量)。在所有运动研究中,无论前一天的血糖水平如何,均成功维持相同的血糖正常水平和基础胰岛素水平。在第1天血糖正常后,患者对运动表现出正常的反调节反应。相反,当在第1天深度逐渐增加的低血糖后进行相同的运动时,观察到胰高血糖素、儿茶酚胺、皮质醇、内源性葡萄糖生成以及对运动的脂解反应逐渐受到更大程度的抑制。这与运动期间维持血糖正常所需的外源性葡萄糖量逐渐增加相平行。我们的结果表明,在T1DM患者中,仅从3.9 mmol/l开始的不同深度的先前低血糖可能以剂量依赖的方式诱发长时间中等强度运动期间的急性反调节功能衰竭。