PMID: 6987657Jan 1, 1980Paper

Phe4]somatostatin: a potent, selective inhibitor of growth hormone release

Proceedings of the National Academy of Sciences of the United States of America
C A MeyersA V Schally

Abstract

[Phe4]Somatostatin was twice as active as somatostatin (SS) in suppressing rat growth hormone release in vitro but had only weak activity toward inhibition of insulin and glucagon release in vivo. The ability of this analogue to inhibit growth hormone release more actively than SS was confirmed in vivo by two separately designed bioassays. Further structure/activity studies of position 4 were carried out with [Glu4]SS, [Thr4]SS, and des-Lys4-SS, all of which had negligible inhibiting activity in the pituitary and pancreas. In this context the strikingly selective activity of [Phe4]SS suggests a fundamental difference in the SS receptors of pituitary and pancreas and the normal side-chain basicity of position 4 appears to be more important for action in pancreas than in pituitary. [Phe4]SS has properties that may be useful in the development of agents for the treatment of acromegaly or other disorders associated with increased growth hormone levels.

References

Jan 24, 1977·Biochemical and Biophysical Research Communications·C MeyersF Labrie
Mar 7, 1977·Biochemical and Biophysical Research Communications·D SarantakisE L Lien
Oct 15, 1973·Biochemical and Biophysical Research Communications·D H CoyA V Schally
Dec 20, 1976·Biochemical and Biophysical Research Communications·V M GarskyN H Grant

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Citations

Apr 1, 1983·The Journal of Clinical Investigation·L E RosenthalK Dharmsathaphorn
Jan 1, 1986·Scandinavian Journal of Gastroenterology. Supplement·M J Lewin
Aug 1, 1984·Journal of Endocrinological Investigation·C RedekoppR A Donald

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