Heller S R, Cryer P E
Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Diabetes. 1991 Feb;40(2):223-6. doi: 10.2337/diab.40.2.223.
To test the hypothesis that hypoglycemia itself causes reduced neuroendocrine and symptomatic responses to subsequent hypoglycemia, we measured those responses during clamped hypoglycemia (2.8 mM) on consecutive mornings on two occasions, with interval afternoon (1400-1600) hypoglycemia (3 mM) on one occasion and interval afternoon euglycemia (5 mM) on the other, in nine nondiabetic humans. None of the measured responses were reduced by interval euglycemia. In contrast, plasma epinephrine (P less than 0.005), glucagon (P less than 0.005), pancreatic polypeptide (P less than 0.01), cortisol (P less than 0.02), and total (P less than 0.001), neurogenic (P less than 0.001) and neuroglycopenic (P less than 0.05) symptom responses to morning hypoglycemia were reduced after interval afternoon hypoglycemia. Thus, a single episode of hypoglycemia caused a generalized reduction of the neuroendocrine and symptomatic responses to subsequent hypoglycemia, a finding that may be important to the pathogenesis of iatrogenic hypoglycemia in insulin-dependent diabetes mellitus.
为了验证低血糖本身会导致对后续低血糖的神经内分泌反应和症状反应减弱这一假设,我们在九名非糖尿病患者中,于连续两个早晨的钳夹性低血糖(2.8 mM)期间测量了这些反应,其中一次在下午(14:00 - 16:00)进行间隔性低血糖(3 mM),另一次在下午进行间隔性血糖正常(5 mM)。间隔性血糖正常并未使任何测量的反应减弱。相比之下,在下午间隔性低血糖后,对早晨低血糖的血浆肾上腺素(P < 0.005)、胰高血糖素(P < 0.005)、胰多肽(P < 0.01)、皮质醇(P < 0.02)以及总的(P < 0.001)、神经源性(P < 0.001)和神经低血糖性(P < 0.05)症状反应均减弱。因此,单次低血糖发作会导致对后续低血糖的神经内分泌和症状反应普遍减弱,这一发现可能对胰岛素依赖型糖尿病医源性低血糖的发病机制具有重要意义。