Effect of angiotensin-converting enzyme inhibition on pituitary hormone responses to insulin-induced hypoglycemia in humans

Lori M. Winer, Agostino Molteni, Mark E Molitch*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Renin, angiotensin-II, and angiotensin-converting enzyme (ACE) have been found in the hypothalamus and pituitary in rats, and renin, angiotensinogen, and ACE have been found in human pituitary lactotrophs. To determine the physiological relevance of the renin-angiotensin system in the pituitary hormone response to stress in humans, we created significant inhibition of ACE by administering a clinically used dose (10 mg) of enalapril (E) 4 h before measuring the stress hormone responses to insulin-induced hypoglycemia. Eight fasting lean healthy males (aged 20-35 yr) were given either placebo (P) or E (10 mg, orally) in two studies separated by at least 5 days in a blinded study design. Glucose, ACTH, cortisol, PRL, and GH levels were measured before E or P and at 20-min intervals beginning 20 min before insulin administration. ACE levels were similar at baseline (E, 21.6 ± 2.7; P, 22.4 ± 2.4 mU/mL/min), but were significantly lower at the time of insulin injection with E treatment (E, 2.9 ± 0 5; P, 20.9 ± 2.5 mU/mL/min; P < 0.001). The mean of the total area under the curve of PRL secretion was significantly lower for the E group (E, 3767.2 ± 710.7; P, 4554.9 ± 650.1 μg/L·min; P < 0.05). Although the mean peak PRL levels were lower for the E group, this did not reach statistical significance (E, 53.0 ± 9.7; P, 64.4 ± 9.4 μg/L; 0.05 < P < 0.10). These differences in PRL responses appeared to be due primarily to substantial decreases in PRL responses with E in three of the eight subjects. No significant differences were found with ACTH, cortisol, or GH for basal levels, peak levels, or areas under the curve.

Original languageEnglish (US)
Pages (from-to)256-259
Number of pages4
JournalJournal of Clinical Endocrinology and Metabolism
Volume71
Issue number1
DOIs
StatePublished - Jan 1 1990

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

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