Horm Metab Res 1997; 29(4): 184-189
DOI: 10.1055/s-2007-979018
Originals Clinical

© Georg Thieme Verlag Stuttgart · New York

Immunoreactive Growth Hormone-Releasing Hormone (IR-GHRH) in the Feto-Placental Circulation and Differential Effects of L-Dopa, L-Arginine and Somatostatin-14 on the Plasma Levels of IR-GHRN in Normal Adults

H. Saito1 , 2 , E. Hosoi2 , 4 , R. Yamasaki2 , K. Kameyama2 , M. Irahara3 , Y. Ohno3 , S. Saito2
  • 1Department of Internal Medicine, Tokushima Teishin (Posts and Telecommunications) Hospital, Tokushima, Japan
  • 2The First Department of Internal Medicine, The University of Tokushima, Tokushima, Japan
  • 3Department of Obstetrics and Gynecology, School of Medicine, The University of Tokushima, Tokushima, Japan
  • 4Department of Medical Technology, School of Medical Sciences, The University of Tokushima, Tokushima, Japan
Further Information

Publication History

1995

1997

Publication Date:
23 April 2007 (online)

The relation of the physiological releases of growth hormone-releasing hormone (GHRH) and growth hormone (GH) into the circulation in various conditions was investigated using a sensitive and specific radioimmunoassay for plasma GHRH. The mean fasting plasma level of immunoreactive (IR)-GHRH in 72 normal adults was 10.3 ± 0.5 (mean ± SEM) pg/ml and there was no significant sex difference in the level. The concentrations of IR-GHRH in plasma from the umbilical artery and umbilical vein were 107.3 ± 20.5 pg/ml and 33.6 ± 3.8 pg/ml, respectively, and a marked arterio-venous gradient was observed in all 12 individuals examined. The plasma level of IR-GHRH in the maternal vein was significantly lower than that in the cord blood, but was similar to that in non-pregnant women. In normal adults, although there was no apparent fluctuation in the level of plasma IR-GHRH or of plasma GH during bed rest, a significant increase of plasma IR-GHRH was detected followed by, or synchronized with the surge of plasma GH after oral administration of L-dopa. In contrast, on L-arginine infusion, no proportional elevation of plasma IR-GHRH with increase in plasma GH was observed. During and after intravenous infusion of somatostatin, the circulating IR-GHRH level did not increase, but on stopping the infusion there was an immediate and marked rebound surge of GH. We conclude that 1) the elevated IR-GHRH in the cord blood plasma originates from the fetus and may have a primary role in enhancing secretion of GH which promotes growth in early human life, and 2) the participations of GHRH in the mechanisms of GH secretion seen after administrations of L-dopa, L-arginine and somatostatin are different.