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- Title
Estrogen blunts neuroendocrine and metabolic responses to hypoglycemia.
- Authors
Sandoval, Darleen A.; Ertl, Andrew C.; Richardson, M. Antoinette; Tate, Donna B.; Davis, Stephen N.
- Abstract
This study tested the hypothesis that estrogen is the mechanism responsible for the sexual dimorphism present in the neuroendocrine and metabolic responses to hypoglycemia. Postmenopausal women receiving (E2; n = 8) or not receiving (NO E2; n = 9) estrogen replacement were compared with age- and BMI-matched male subjects (n = 8) during a single-step 2-h hyperinsulinemic-hypoglycemic clamp. Plasma insulin (599 +/- 28 pmol/l) and glucose (2.9 +/- 0.03 mmol/l) levels were similar among all groups during the glucose clamp. In response to hypoglycemia, epinephrine (2.8 +/- 0.6 vs. 5.8 +/- 0.8 and 4.4 +/- 0.5 nmol/l), glucagon (57 +/- 8 vs. 77 +/- 8 and 126 +/- 18 ng/l), and endogenous glucose production (2 +/- 2 vs. 10 +/- 2 and 6 +/- 3 micro mol x kg(-1) x min(-1)) were significantly lower in E2 vs. both NO E2 and male subjects (P < 0.05). These reduced counterregulatory responses resulted in significantly greater glucose infusion rates (16 +/- 2 vs. 6 +/- 2 and 6 +/- 3 micro mol x kg(-1) x min(-1); P < 0.01) in E2 vs. both NO E2 and male subjects. Pancreatic polypeptide was significantly lower (P < 0.05) in both the E2 and NO E2 groups compared with the male subjects (136 +/- 20 and 136 +/- 23 vs. 194 +/- 16 pmol/l). Last, glycerol (36 +/- 3 vs. 47 +/- 5 micro mol/l; P < 0.05), lactate (1.4 +/- 0.1 vs. 1.8 +/- 0.2 mmol/l; P < 0.05), and muscle sympathetic nerve activity (19 +/- 4 to 27 +/- 4 vs. 27 +/- 5 to 42 +/- 6 bursts/min; P < 0.05) responses to hypoglycemia were all significantly lower in E2 vs. NO E2 subjects. We conclude that estrogen appears to play a major role in the sexual dimorphism present in counterregulatory responses to hypoglycemia in healthy humans.
- Subjects
ESTROGEN; HYPOGLYCEMIA; NEUROENDOCRINOLOGY; SYMPATHETIC nervous system physiology; ADRENALINE; COMPARATIVE studies; ESTRADIOL; FATTY acids; GLUCAGON; HOMEOSTASIS; HORMONES; HYDROCORTISONE; HYPERINSULINISM; INSULIN; RESEARCH methodology; MEDICAL cooperation; METABOLISM; RESEARCH; SYMPATHETIC nervous system; THERAPEUTICS; EVALUATION research; HUMAN growth hormone; SKELETAL muscle; GLUCOSE clamp technique; INNERVATION
- Publication
Diabetes, 2003, Vol 52, Issue 7, p1749
- ISSN
0012-1797
- Publication type
journal article
- DOI
10.2337/diabetes.52.7.1749