Publication:
International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature.

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Date

2018

Authors

Günther, Thomas
Tulipano, Giovanni
Dournaud, Pascal
Bousquet, Corinne
Csaba, Zsolt
Kreienkamp, Hans-Jürgen
Lupp, Amelie
Korbonits, Márta
Castaño, Justo P
Wester, Hans-Jürgen

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American Society for Pharmacology and Experimental Therapeutics
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Abstract

Somatostatin, also known as somatotropin-release inhibitory factor, is a cyclopeptide that exerts potent inhibitory actions on hormone secretion and neuronal excitability. Its physiologic functions are mediated by five G protein-coupled receptors (GPCRs) called somatostatin receptor (SST)1-5. These five receptors share common structural features and signaling mechanisms but differ in their cellular and subcellular localization and mode of regulation. SST2 and SST5 receptors have evolved as primary targets for pharmacological treatment of pituitary adenomas and neuroendocrine tumors. In addition, SST2 is a prototypical GPCR for the development of peptide-based radiopharmaceuticals for diagnostic and therapeutic interventions. This review article summarizes findings published in the last 25 years on the physiology, pharmacology, and clinical applications related to SSTs. We also discuss potential future developments and propose a new nomenclature.

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MeSH Terms

Protein conformation
Protein transport
Receptors, somatostatin
Signal transduction
Terminology as topic

DeCS Terms

Conformación proteica
Receptores de somatostatina
Terminología como asunto
Transducción de señal
Transporte de proteínas

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Keywords

Animals, Gene expression regulation, Humans, Ligands

Citation

Günther T, Tulipano G, Dournaud P, Bousquet C, Csaba Z, Kreienkamp HJ, et al. International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature. Pharmacol Rev. 2018 Oct;70(4):763-835