Inhibitory action of islet amyloid polypeptide and calcitonin gene-related peptide on release of insulin from the isolated perfused rat pancreas

Masafumi Kogire, Jin Ishizuka, James C. Thompson, George H. Greeley

Research output: Contribution to journalArticlepeer-review

58 Scopus citations

Abstract

Islet (or insulinoma) amyloid polypeptide (IAPP) is a 37-residue peptide recently purified from amyloid deposits in the pancreas of patients with type 2 diabetes and from amyloid deposits of a human insulinoma. IAPP immunoreactivity has been identified in islet B cells of diabetic and nondiabetic humans. IAPP is structurally similar to calcitonin gene-related peptide (CGRP). The purpose of this study was to examine the effects of IAPP and CGRP on glucose-and carbachol-stimulated release of insulin and pancreatic polypeptide (PP) from the isolated perfused rat pancreas. IAPP and CGRP, at 10-7M, failed to inhibit glucose-stimulated (16.7 mM) release of insulin. At the same concentration, however, IAPP significantly (p < 0.05) inhibited carbachol-stimulated (10-7M) release of insulin by 30%, and CGRP significantly inhibited carbachol-stimulated release of insulin by 33% when compared with the control group. IAPP also significantly decreased carbachol-stimulated release of PP. IAPP and CGRP, at 10-8M, did not inhibit carbachol-stimulated release of insulin and PP. These results suggest that IAPP and CGRP may have roles in the regulation of secretion of insulin. IAPP may inhibit secretion of insulin, at least in part, by blocking cholinergic mechanisms.

Original languageEnglish (US)
Pages (from-to)459-463
Number of pages5
JournalPancreas
Volume6
Issue number4
DOIs
StatePublished - Jul 1991
Externally publishedYes

Keywords

  • Calcitonin gene-related peptide
  • Carbachol
  • Glucose
  • Islet amyloid polypeptide
  • Isolated perfused rat pancreas
  • Release of insulin

ASJC Scopus subject areas

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

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