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Division of Endocrinology, Diabetes and Metabolism, General Clinical Research Center, and Diabetes Research and Training Center, Washington University School of Medicine, St. Louis, Missouri 63110
We tested the
hypothesis that increased endogenous cortisol secretion reduces
autonomic neuroendocrine and neurogenic symptom responses to subsequent
hypoglycemia. Twelve healthy young adults were studied on two separate
occasions, once after infusions of a pharmacological dose of
-(1-24)-ACTH (100 µg/h) from 0930 to 1200 and
1330 to 1600, which raised plasma cortisol levels to ~45 µg/dl on
day 1, and once after saline infusions on day 1. Hyperinsulinemic (2.0 mU · kg
1 · min
1) stepped
hypoglycemic clamps (90, 75, 65, 55, and 45 mg/dl glucose steps) were
performed on the morning of day 2 on both occasions. These
markedly elevated antecedent endogenous cortisol levels reduced the
adrenomedullary (P = 0.004, final plasma epinephrine levels of 489 ± 64 vs. 816 ± 113 pg/ml), sympathetic neural
(P = 0.0022, final plasma norepinephrine levels of
244 ± 15 vs. 342 ± 22 pg/ml), parasympathetic neural
(P = 0.0434, final plasma pancreatic polypeptide levels
of 312 ± 37 vs. 424 ± 56 pg/ml), and neurogenic (autonomic)
symptom (P = 0.0097, final symptom score of 7.1 ± 1.5 vs. 10.6 ± 1.6) responses to subsequent hypoglycemia. Growth
hormone, but not glucagon or cortisol, responses were also reduced. The
findings that increased endogenous cortisol secretion reduces autonomic
neuroendocrine and neurogenic symptom responses to subsequent
hypoglycemia are potentially relevant to cortisol mediation of
hypoglycemia-associated autonomic failure, and thus a vicious cycle of
recurrent iatrogenic hypoglycemia, in people with diabetes mellitus.
epinephrine; norepinephrine; glucagon; diabetes; hypoglycemia-associated autonomic failure
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