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Activation of somatostatin receptor subtype 2 inhibits insulin secretion in the isolated perfused human pancreas.

  • F. Charles Brunicardi
  • , Azmi Atiya
  • , Stefan Moldovan
  • , Timothy C. Lee
  • , Shawn P. Fagan
  • , Robert M. Kleinman
  • , Thomas E. Adrian
  • , David H. Coy
  • , John H. Walsh
  • , William E. Fisher

Research output: Contribution to journalArticlepeer-review

Abstract

OBJECTIVES: Five distinct somatostatin receptors (SSTRs) have been cloned, characterized, and designated SSTRs 1-5. The role of these receptors in B-cell signaling has not been well characterized. METHODS: In the current study, the isolated perfused human pancreas model was used to determine the specific effect of 4 different somatostatin receptor agonists on insulin secretion. CONCLUSION: We demonstrated that the SSTR 2 agonist and octreotide significantly suppressed insulin secretion. Furthermore, even during the immunoneutralization of endogenous intrapancreatic somatostatin, the SSTR 2 agonist was able to reverse the effect of somatostatin immunoneutralization by suppressing insulin secretion. These results demonstrate that activation of SSTR 2 suppresses insulin secretion in the isolated perfused human pancreas.

Original languageEnglish
Pages (from-to)e84-89
JournalPancreas
Volume27
Issue number4
DOIs
Publication statusPublished - Nov 2003
Externally publishedYes

ASJC Scopus subject areas

  • Internal Medicine
  • Endocrinology, Diabetes and Metabolism
  • Hepatology
  • Endocrinology

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