Pulsatile growth hormone secretion in normal man during a continuous 24-hour infusion of human growth hormone releasing factor (1-40). Evidence for intermittent somatostatin secretion

• Published in: The Journal of clinical investigation Vol. 75; no. 5; pp. 1584 - 1590
• Main Authors: Vance, M L, Kaiser, D L, Evans, W S, Furlanetto, R, Vale, W, Rivier, J, Thorner, M O
• Format: Journal Article
• Language: English
• Published: Ann Arbor, MI American Society for Clinical Investigation 01.05.1985
• Subjects: Acromegaly - metabolism; Adult; Biological and medical sciences; Drug Interactions; Fundamental and applied biological sciences. Psychology; Growth Hormone - secretion; Growth Hormone-Releasing Hormone - administration & dosage; Hormones and neuropeptides. Regulation; Humans; Hypothalamus. Hypophysis. Epiphysis. Urophysis; Infusions, Parenteral; Insulin-Like Growth Factor I; Male; Middle Aged; Peptide Fragments - administration & dosage; Somatomedins - blood; Somatostatin - secretion; Time Factors; Vertebrates: endocrinology; Human; Protein hormone; Secretion curve; STH; Peptide hormone; Hormonal regulation; Somatostatin; Neuropeptide; Biological activity; STH-RH
• DOI: 10.1172/JCI111864
• ISSN: 0021-9738

Growth hormone (GH) secretory patterns were studied in a patient with ectopic growth hormone releasing factor (GRF) secretion and in normal men given continuous infusions of human growth hormone releasing factor (1-40)-OH (hGRF-40). In the patient with ectopic GRF secretion, GH secretion was pulsatile despite continuously elevated immunoreactive GRF levels. To determine if pulsatile GH secretion is maintained in normal subjects, we administered to six healthy young men vehicle or hGRF-40, 2 ng/kg per min, for 24 h and gave a supramaximal intravenous bolus dose of hGRF-40, 3.3 micrograms/kg, after 23.5 h of infusion. hGRF-40 infusion resulted in greater GH secretion than did vehicle infusion and pulsatile GH secretion was maintained throughout hGRF-40 infusion. During the 23.5 h of vehicle infusion, total GH secretion (microgram; mean +/- SEM) was 634 +/- 151 compared with 1,576 +/- 284 during hGRF-40 infusion (P = 0.042). The GH response to the intravenous bolus of hGRF-40 was greater after vehicle infusion than after hGRF-40 infusion; 877 +/- 170 and 386 +/- 125 micrograms of GH was secreted after the bolus on vehicle and hGRF-40 days, respectively (P = 0.015). The total amount of GH secreted during the 25.5 h of the two study days was not different; 1,504 +/- 260 and 1,952 +/- 383 micrograms were secreted during vehicle and hGRF-40 days, respectively (P = 0.36). Not only was pulsatile GH secretion maintained during hGRF-40 infusion, but there was augmentation of naturally occurring GH pulses, which is in contrast to the effect of gonadotropin-releasing hormone on gonadotropin secretion. We suggest that GH pulses are a result of GRF secretion that is associated with a diminution or withdrawal of somatostatin secretion.