In vitro exhaustion of pancreatic β-cells

M. Hoenig, L. C. MacGregor, F. M. Matschinsky

Research output: Contribution to journalArticlepeer-review

Abstract

To learn more about possible limited β-cell secretory capacity and factors essential for insulin release, a perifusion system was applied that allowed the in vitro study of insulin secretion from isolated pancreatic islets for more than 6 h. Islets isolated from rats were stimulated with various glucose concentrations (7.5, 16.7 and 30 mM), α-ketoisocaproate (30 mM), and 30 mM glucose plus 1 mM 3-isobutyl-1-methylxanthine for several hours in Krebs-Ringer-bicarbonate buffer (KRB) or RPMI 1640. Islets showed 'exhaustion' with all stimulatory conditions used when KRB was the perifusion medium. This was not prevented by addition of amino acids, phosphate, myo-inositol or arachidonic acid. With RPMI 1640 as the basal medium, exhaustion was not seen at 7.5 mM but was readily approached at higher glucose concentrations. It is possible that the exhaustion phenomenon observed here is due to a depletion of a readily releasable insulin pool.

Original languageEnglish (US)
Pages (from-to)13/5
JournalAmerican Journal of Physiology - Endocrinology and Metabolism
Volume250
Issue number5
StatePublished - Jan 1 1986
Externally publishedYes

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Physiology (medical)

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