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Physiology of Somatostatin

This chapter appears in the following book:

Somatostatin Analogs in Diagnostics and Therapy

Edited by: Marek Pawlikowski
ISBN: 978-1-58706-223-0
» Get more information about this book at landesbioscience.com «

Chapter authors:
Marek Pawlikowski

Somatostatin (SST) was originally discovered as a hypothalamic peptide which inhibits growth hormone (GH) secretion from the pituitary gland. It appears in two molecular forms, composed from 14 or 28 amino-acid residues. Moreover, another family of peptides, called cortistatins (CST), was described. CST are encoded by a different gene, but they share partly the structure of SST and bind to SST receptors. The further studies revealed that SST is expressed not only in the hypothalamus, but is widely distributed in central and peripheral nervous systems as well as in nonneural peripheral tissues, mainly in the gut. SST is now known to exert the large spectrum of functions, mostly of inhibitory nature. It inhibits the secretion of hormones, like GH and thyrotropin (TSH), neuro-enterohormones like gastrin, cholecystokinin, vasoactive intestinal peptide (VIP), gastric inhibitory polypeptide (GIP), motilin, secretin, pancreatic polypeptide and glucagon-like peptides (GLP), and exocrine secretions. SST modulates the functions of nervous and immune systems and exerts a direct antiproliferative effects on cell and tissue growth. Because of a very short half-life time (approx. 60 seconds) the therapeutic application of exogenous SST is limited. To pass by this obstacle, the long-acting analogs of SST were synthesized.

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Additional chapters from this book:

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