GH secretion in Prader-Labhard-Willi syndrome: somatotrope responsiveness to GHRH is enhanced by arginine but not by pyridostigmine

J Pediatr Endocrinol Metab. 1996 Nov-Dec;9(6):577-83. doi: 10.1515/jpem.1996.9.6.577.

Abstract

Low somatotrope responsiveness to secretagogues has been reported in patients affected by Prader-Labhard-Willi Syndrome (PLWS). In normal subjects, GH response to GHRH is known to be greatly potentiated to the same extent by pyridostigmine (PD) or arginine (ARG) which probably act via inhibition of hypothalamic somatostatin release. To clarify somatotrope responsiveness in 7 PLWS patients, we studied GH response to GHRH alone and to GHRH combined with PD or ARG. Eight normal short children were studied as controls (NC). GH response to GHRH in PLWS was lower than in NC (AUC: 615 +/- 205 micrograms/l.h, vs 1271 +/- 333 micrograms/l.h, p < 0.02). In NC, the GHRH-induced GH rise was potentiated to the same extent by PD or ARG. In contrast, in PLWS PD failed to increase the GH response to GHRH (AUC: 615 +/- 205 micrograms/l.h vs 621 +/- 176 micrograms/l.h, n.s.) which was enhanced by ARG (AUC: 615 +/- 205 micrograms/l.h vs 1633 +/- 425 micrograms/l.h, p < 0.02). However, the GH response to GHRH + ARG in PLWS was lower than in NC. In conclusion, our results demonstrate that in PLWS the low somatotrope responsiveness to GHRH is not enhanced by cholinergic potentiation while it is increased by arginine.

MeSH terms

  • Adolescent
  • Adult
  • Arginine / pharmacology
  • Body Weight
  • Drug Synergism
  • Female
  • Growth Hormone-Releasing Hormone / pharmacology*
  • Human Growth Hormone / metabolism*
  • Humans
  • Male
  • Pituitary Gland / drug effects*
  • Pituitary Gland / metabolism
  • Prader-Willi Syndrome / drug therapy
  • Prader-Willi Syndrome / physiopathology*
  • Pyridostigmine Bromide / pharmacology

Substances

  • Human Growth Hormone
  • Growth Hormone-Releasing Hormone
  • Arginine
  • Pyridostigmine Bromide