| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Endocrinology, Vol 125, 1711-1717, Copyright © 1989 by Endocrine Society
ARTICLES |
T Bick, MB Youdim and Z Hochberg
Department of Pharmacology, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
The secretory pattern of GH is pulsatile in both man and experimental animals. The present study was undertaken to investigate the effect of the endogenous pulsatility of serum GH on the dynamics of plasma membrane GH binding sites. In order to characterize somatogenic and total specific binding, male rats 45 days old were decapitated at 15- min intervals, and rat liver membranes were prepared. Binding studies were done in parallel with and without excess ovine PRL, 1 microgram/tube. Removal of endogenous ligand was performed by exposing the membranes to 3 M MgCl2. A composite picture of serum GH showed relatively good synchronization of the secretory episodes among the animals. Peak levels of the spontaneous secretion pulse of rat GH were followed by an immediate decrease in free somatogenic binding. Two hours later the binding activity returned to presecretion levels, essentially resetting the cell for another cycle. The kinetics of desaturated somatogenic binding were similar. The occupancy of liver GH somatogenic binding sites was maximal at the time of peak serum GH. High levels of the endogenous hormone caused an immediate sharp down- regulation of lactogenic desaturated binding. Up-regulation of the binding sites occurred about 90 min later. Scatchard analysis showed that binding activity of the membranes was a result of the altered number of binding sites, while the binding affinity remained fairly constant. Thus, the centrally regulated GH secretion in the male rat is complemented by appropriate dynamics of the GH receptor turnover, which in turn recognizes individual pulses and allows individual pulse- related responses to occur.
This article has been cited by other articles:
![]() |
M. Lampit and Z.'e. Hochberg Prevention of Growth Deceleration after Withdrawal of Growth Hormone Therapy in Idiopathic Short Stature J. Clin. Endocrinol. Metab., August 1, 2002; 87(8): 3573 - 3577. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Gebert, S.-H. Park, and D. J. Waxman Down-Regulation of Liver JAK2-STAT5b Signaling by the Female Plasma Pattern of Continuous Growth Hormone Stimulation Mol. Endocrinol., February 1, 1999; 13(2): 213 - 227. [Abstract] [Full Text] |
||||
![]() |
T. Amit, T. Bergman, F. Dastot, M. B. H. Youdim, S. Amselem, and Z.'e. Hochberg A Membrane-Fixed, Truncated Isoform of the Human Growth Hormone Receptor J. Clin. Endocrinol. Metab., November 1, 1997; 82(11): 3813 - 3817. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Pellegrini, M. T. Bluet-Pajot, F. Mounier, P. Bennett, C. Kordon, and J. Epelbaum Central Administration of a Growth Hormone (GH) Receptor mRNA Antisense Increases GH Pulsatility and Decreases Hypothalamic Somatostatin Expression in Rats J. Neurosci., December 15, 1996; 16(24): 8140 - 8148. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |