We evaluated the recovery of blood glucose after insulin-induced hypoglycemia in six insulin-dependent diabetics (insulin-infused and initially euglycemic) and six normal controls after comparable reductions in plasma glucose. In contrast to controls, the recovery of plasma glucose was delayed in diabetics (2-h plasma glucose 80 ± 5 mg/dl and 58 ± 5 mg/dl, respectively, P < 0.01). This delay was due to the absence of a rebound in hepatic glucose output in the diabetics, whereas glucose output rose two- to threefold above baseline in normals. The impaired rebound in glucose output in diabetics could not be attributed to hyperinsulinemia. Rather, hypoglycemia-induced secretion of epinephrine and glucagon was reduced in thediabetics by 60–80% as compared with normals (P < 0.001). The diabetics did not suffer from overt neuropathy and plasma cortisol, growth hormone, and norepinephrine increased normally following hypoglycemia. The data suggest that prolonged hypoglycemia may frequently occur in tightly controlled type I diabetics because of impaired rebound in hepatic glucose release which in turn may be a consequence of reduced secretion of epinephrine and glucagon.
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Original contribution|
June 01 1983
Impaired Counterregulation of Hypoglycemia in Insulin-dependent Diabetes Mellitus
Jerry Kleinbaum;
Jerry Kleinbaum
Endocrinology Division, Department of Medicine, and the Diabetes Research and Training Center, Albert Einstein College of Medicine
Bronx, New York
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Harry Shamoon
Harry Shamoon
Endocrinology Division, Department of Medicine, and the Diabetes Research and Training Center, Albert Einstein College of Medicine
Bronx, New York
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Address reprint requests to Harry Shamoon, M.D., Albert Einstein College of Medicine, 1300 Morris Park Avenue, 501 Forch., Bronx, New York 10461.
Citation
Jerry Kleinbaum, Harry Shamoon; Impaired Counterregulation of Hypoglycemia in Insulin-dependent Diabetes Mellitus. Diabetes 1 June 1983; 32 (6): 493–498. https://doi.org/10.2337/diab.32.6.493
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