Literature DB >> 3926535

Nutrient insulin secretagogues decrease 45Ca2+ efflux from islet cells by a mechanism other than the inhibition of the Na+-Ca2+ countertransport.

J C Henquin, R de Miguel, M G Garrino, M Hermans, M Nenquin.   

Abstract

The mechanism whereby nutrient insulin secretagogues decrease 45Ca2+ efflux from islet cells is controversial. It was studied with mouse islets perifused with Ca2+-free solutions. In the presence of Na+, glucose and ketoisocaproate inhibited 45Ca2+ efflux by about 50%. Substitution of choline+ salts for Na+ salts decreased the efflux rate by 45%, but did not prevent glucose from decreasing it further. Ketoisocaproate also inhibited 45Ca2+ efflux, but less markedly than in an Na+ medium. Omission of Na+ decreased the efflux rate even when it was already lowered by glucose or ketoisocaproate. It is thus clear that nutrient insulin secretagogues decrease 45Ca2+ efflux from islet cells by a mechanism other than the inhibition of the Na+-Ca2+ countertransport, possibly by increasing sequestration of the ion in cellular organelles.

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Year:  1985        PMID: 3926535     DOI: 10.1016/0014-5793(85)81237-0

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

1.  Abnormal regulation of insulin secretion in the genetically obese (ob/ob) mouse.

Authors:  M Black; H M Heick; N Bégin-Heick
Journal:  Biochem J       Date:  1986-09-15       Impact factor: 3.857

2.  Cyclic adenosine monophosphate differently affects the response of mouse pancreatic beta-cells to various amino acids.

Authors:  J C Henquin; H P Meissner
Journal:  J Physiol       Date:  1986-12       Impact factor: 5.182

3.  Action potentials and insulin secretion: new insights into the role of Kv channels.

Authors:  D A Jacobson; L H Philipson
Journal:  Diabetes Obes Metab       Date:  2007-11       Impact factor: 6.577

  3 in total

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