Effects of ghrelin and other neuropeptides (CART, MCH, orexin A and B, and GLP-1) on the release of insulin from isolated rat islets

Pancreas. 2003 Aug;27(2):161-6. doi: 10.1097/00006676-200308000-00009.

Abstract

Background and aims: Ghrelin, a neuropeptide containing 28 amino acids, shows a reciprocal diurnal plasma fluctuation to that of plasma insulin. The aim of this study is to clarify the dose and glucose-dependency of ghrelin on the insulin secretion and to compare its effect with that of other neuropeptides-GLP-1, CART (55-102), CART (55-76), CART (62-76), MCH, orexin A, and B.

Materials and methods: Rat islets were incubated with 1 pmol/l-1 micromol/l of ghrelin, CART fragments, MCH, orexin A or B, or GLP-1 (n = 16-32) in the presence of 16.7 mmol/l glucose. Ghrelin (10 nmol/l) was added to islets at glucose concentrations of 3.3, 6.6, 16.7 and 25 mmol/l, respectively (n = 28-32). Also, INS-1E cells were incubated with ghrelin (1 nmol/l) in the presence of glucose (3.3, 6.6, 16.7, and 25 mmol/l). In addition, we measured the mRNA expression of the ghrelin receptor using RT-PCR.

Results: Ghrelin inhibited insulin secretion from islets and INS-1E cells in a dose- and glucose-dependent manner. Neither 10 pmol/l-1 micromol/l of CART fragments, MCH, orexin A, nor orexin B changed the insulin secretion at 16.7 mmol/l glucose, while GLP-1, as expected, stimulated the insulin release from rat islets. Interestingly, ghrelin receptors were expressed both in islets, INS-1E, MIN 6 and alpha cell Tca-9 lines.

Conclusions: Ghrelin inhibits the insulin secretion in vitro in a dose- and glucose-dependent manner. Beta cells contain ghrelin receptors. CART fragments did not affect the insulin secretion. Ghrelin may play a physiological role for the regulation of insulin secretion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / pharmacology
  • Cell Line
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects
  • Ghrelin
  • Glucagon / pharmacology
  • Glucagon-Like Peptide 1
  • Glucose / pharmacology
  • Hypothalamic Hormones / pharmacology
  • In Vitro Techniques
  • Insulin / metabolism*
  • Insulin Secretion
  • Intracellular Signaling Peptides and Proteins*
  • Islets of Langerhans / cytology
  • Islets of Langerhans / drug effects*
  • Islets of Langerhans / metabolism
  • Melanins / pharmacology
  • Nerve Tissue Proteins
  • Neuropeptides / pharmacology*
  • Orexin Receptors
  • Orexins
  • Peptide Fragments / pharmacology
  • Peptide Hormones / pharmacology*
  • Pituitary Hormones / pharmacology
  • Protein Precursors / pharmacology
  • RNA, Messenger / drug effects
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, Ghrelin
  • Receptors, Neuropeptide
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Carrier Proteins
  • Ghrelin
  • Hypothalamic Hormones
  • Insulin
  • Intracellular Signaling Peptides and Proteins
  • Melanins
  • Nerve Tissue Proteins
  • Neuropeptides
  • Orexin Receptors
  • Orexins
  • Peptide Fragments
  • Peptide Hormones
  • Pituitary Hormones
  • Protein Precursors
  • RNA, Messenger
  • Receptors, G-Protein-Coupled
  • Receptors, Ghrelin
  • Receptors, Neuropeptide
  • cocaine- and amphetamine-regulated transcript protein (55-102)
  • melanin-concentrating hormone
  • Glucagon-Like Peptide 1
  • Glucagon
  • Glucose