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Unless otherwise stated all data on this page refer to the human proteins. Gene information is provided for human (Hs), mouse (Mm) and rat (Rn).
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Somatostatin (somatotropin release inhibiting factor) is an abundant neuropeptide, which acts on five subtypes of somatostatin receptor (SST1-SST5; nomenclature as agreed by the NC-IUPHAR Subcommittee on Somatostatin Receptors [9]). Activation of these receptors produces a wide range of physiological effects throughout the body including the inhibition of secretion of many hormones. Endogenous ligands for these receptors are somatostatin-14 (SRIF-14 (SST, P61278)) and somatostatin-28 (SRIF-28 (SST, P61278)). Cortistatin-14 has also been suggested to be an endogenous ligand for somatostatin receptors [5].
SST1 receptor C Show summary »« Hide summary More detailed page
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SST2 receptor C Show summary »« Hide summary More detailed page
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SST3 receptor C Show summary »« Hide summary More detailed page
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SST4 receptor C Show summary »« Hide summary More detailed page
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SST5 receptor C Show summary »« Hide summary More detailed page
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* Key recommended reading is highlighted with an asterisk
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* Günther T, Tulipano G, Dournaud P, Bousquet C, Csaba Z, Kreienkamp HJ, Lupp A, Korbonits M, Castaño JP, Wester HJ et al.. (2018) International Union of Basic and Clinical Pharmacology. CV. Somatostatin Receptors: Structure, Function, Ligands, and New Nomenclature. Pharmacol Rev, 70 (4): 763-835. [PMID:30232095]
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Subcommittee members:
Stefan Schulz (Chairperson)
Corinne Bosquet
Justo P. Castaño
Zsolt Csaba
Pascal Dournaud
Hans-Jürgen Kreienkamp
Amelie Lupp
Shlomo Melmed
Giovanni Tulipano
Hans-Jürgen Wester |
Other contributors:
Micheal Culler
Jacques Epelbaum
Wasyl Feniuk
Anthony Harmar
Rebecca Hills
Leo Hofland
Daniel Hoyer (Past chairperson)
Patrick P. A. Humphrey
Wolfgang Meyerhof
Anne-Marie O'Carroll
Yogesh C. Patel
Terry Reisine
Jean-Claude Reubi
Marcus Schindler
Herbert Schmid
Agnes Schonbrunn
John E. Taylor
Annamaria Vezzani |
Database page citation (select format):
Concise Guide to PHARMACOLOGY citation:
Alexander SPH, Christopoulos A, Davenport AP, Kelly E, Mathie AA, Peters JA, Veale EL, Armstrong JF, Faccenda E, Harding SD, Davies JA et al. (2023) The Concise Guide to PHARMACOLOGY 2023/24: G protein-coupled receptors. Br J Pharmacol. 180 Suppl 2:S23-S144.
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License
[125I]Tyr11-SRIF-14, [125I]LTT-SRIF-28, [125I]CGP 23996 and [125I]Tyr10-CST14 may be used to label somatostatin receptors nonselectively. A number of nonpeptide subtype-selective agonists have been synthesised [17]. Octreotide and lanreotide are being used in the treatment of SST2-expressing neuroendocrine tumors and pasireotide for SST5-expressing neuroendocrine tumors. A novel peptide somatostatin analogue, veldoreotide (COR-005), has affinity for SST2, SST4 and SST5 receptors and is a potent inhibitor of GH secretion [16,19].