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Section of Endocrinology and Metabolism, Department of Medicine, Tulane University Medical School (C.Y.B., G.A.R., D.D., C.M.B.) New Orleans, Louisiana 70112
the Division of Endocrinology and Metabolism, Department of Medicine, University of Virginia Health Sciences Center (S.S.P., M.O.T.) Charlottesville, Virginia 22908
Address requests for reprints to: Dr. C. Y. Bowers, Section of Endocrinology and Metabolism, Department of Medicine, Tulane University Medical School, New Orleans, Louisiana 70112.
The acute GH release stimulated by the synthetic hexapeptide, His-DTrp-Ala-Trp-DPhe-Lys-NH2 [GH releasing peptide (GHRP)], was determined in 18 normal men and compared with the effects of GH-releasing hormone, GHRH-(1–44)-NH2. Specificity of effect was assessed by measurement of serum PRL, LH, TSH, and cortisol. GHRP was administered at doses of 0.1, 0.3, and 1.0 µg/kg by iv bolus. GHRH at a dose of 1.0 µg/kg was administered alone and together with various does of GHRP.
No adverse clinical effects or laboratory abnormalities were observed in response to GHRP. A side-effect of mild facial flushing of 1- to 3-min duration occurred in 16 of the 18 subjects who received GHRH-(l–44)-NH2. Mean (±SEM) peak serum GH levels after injection ofplacebo and 0.1, 0.3, and 1.0 µg/kg GHRP were 1.2 ± 0.3, 7.6 ± 2.5, 16.5 ± 4.1, and 68.7 ± 15.5 µg/L, respectively. The submaximal dosages of 0.1 and 0.3 µg/kg GHRP plus 1 µg/kg GHRH stimulated GH release synergistically. Serum PRL and cortisol levels rose about 2-fold above basal levels only at the 1 µg/kg dose of GHRP, and there were no changes in serum LH and TSH over the first hour after administration of the peptide(s).
GHRP is a potent secretagogue of GH in normal men. Since GHRP and GHRH together stimulate GH release synergistically, these results suggest that GHRP and GHRH act independently. This supports our hypothesis that the GH-releasing activity of GHRP reflects a new physiological system in need of further characterization in animals and man.
* This work was supported in part by Grant DK-32632 and GCRC Grant RR-0847. Presented at the 71st Annual Meeting of The Endocrine Society, Seattle, WA, June 1989.
Received August 14, 1989.
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