Chronic low dose islet amyloid polypeptide infusion reduces food intake, but does not influence glucose metabolism, in unrestrained conscious rats: Studies using a novel aortic catheterization technique

Urban Arnelo, Johan Permert, Jörgen Larsson, Roger D. Reidelberger, Catarina Arnelo, Thomas E. Adrian

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)

Abstract

Islet amyloid polypeptide (IAPP) is a 37-amino acid polypeptide coproduced with insulin in the β-cells of the pancreatic islets. The physiological effects of IAPP have not been established. Although effects on glucose metabolism are seen only at pharmacological doses both in vitro end in vivo, effects on food intake have been shown at near-physiological concentrations. The aim of the present study was to investigate the effects of similar elevations of circulating plasma IAPP levels on glucose metabolism in rats and to evaluate the function of a novel aortic catheterization technique. In a cross-over design, two sets of experiments in which conscious unrestrained rats received chronic lAPP infusions at 0 and 2 or 0 and 7 pmol/kg · min were performed. Peripheral glucose disposal was determined by means of the hyperinsulinemic euglycemic clamp technique. Chronic elevations of circulating IAPP at concentrations that reduced feed intake [43.5 ± 6.2 g (control) vs. 35.7 ± 8.2 g (IAPP; P < 0.01) and 84.0 ± 2.2 g (control) vs. 28.8 ± 1.4 g (IAPP; P = 0.07) for the 7 and 2 pmol/kg · min experiments, respectively] had no affect on the glucose metabolic rate [GMR; 18.5 ± 0.6 mmol/kg · h (control) vs. 18.7 ± 0.9 mmol/kg · h (IAPP) and 14.4 ± 0.7 mmol/kg · h (control) vs. 15.6 ± 0.7 mmol/kg · h (IAPP) for the 7 and 2 pmol/kg · min experiments, respectively]. Thus, effects on glucose metabolism are unlikely to explain the anorectic effect of IAPP.

Original languageEnglish
Pages (from-to)4081-4085
Number of pages5
JournalEndocrinology
Volume138
Issue number10
DOIs
Publication statusPublished - 1997
Externally publishedYes

ASJC Scopus subject areas

  • Endocrinology

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