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PMID: 9974390 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Role of NADH shuttle system in glucose-induced activation of mitochondrial metabolism and insulin secretion.

Science (New York, N.Y.) ·Vol. 283 ·No. 5404 ·1999-02-12 ·Pages 981-5

Eto K, Tsubamoto Y, Terauchi Y, Sugiyama T, Kishimoto T, Takahashi N, Yamauchi N, Kubota N, Murayama S, Aizawa T, Akanuma Y, Aizawa S, Kasai H, Yazaki Y, Kadowaki T

Abstract

Glucose metabolism in glycolysis and in mitochondria is pivotal to glucose-induced insulin secretion from pancreatic beta cells. One or more factors derived from glycolysis other than pyruvate appear to be required for the generation of mitochondrial signals that lead to insulin secretion. The electrons of the glycolysis-derived reduced form of nicotinamide adenine dinucleotide (NADH) are transferred to mitochondria through the NADH shuttle system. By abolishing the NADH shuttle function, glucose-induced increases in NADH autofluorescence, mitochondrial membrane potential, and adenosine triphosphate content were reduced and glucose-induced insulin secretion was abrogated. The NADH shuttle evidently couples glycolysis with activation of mitochondrial energy metabolism to trigger insulin secretion.

MeSH Terms
Adenosine Triphosphate/metabolism Amino Acid Sequence Aminooxyacetic Acid/pharmacology Animals Aspartate Aminotransferases/antagonists & inhibitors Calcium/metabolism Citric Acid Cycle Enzyme Inhibitors/pharmacology Female Gene Targeting Glucose/metabolism,pharmacology Glycerolphosphate Dehydrogenase/genetics,metabolism Glycolysis Insulin/metabolism Insulin Secretion Islets of Langerhans/metabolism Male Membrane Potentials Mice Mice, Inbred BALB C Mice, Inbred C57BL Mitochondria/metabolism Models, Biological Molecular Sequence Data NAD/metabolism Pyruvic Acid/metabolism
Chemicals
Enzyme Inhibitors Insulin NAD Aminooxyacetic Acid Pyruvic Acid Adenosine Triphosphate Glycerolphosphate Dehydrogenase Aspartate Aminotransferases Glucose Calcium
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Eto K
Department of Internal Medicine, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113, Japan. Tokyo,
Tsubamoto Y
Terauchi Y
Sugiyama T
Kishimoto T
Takahashi N
Yamauchi N
Kubota N
Murayama S
Aizawa T
Akanuma Y
Aizawa S
Kasai H
Yazaki Y
Kadowaki T
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1999-02-12
Pages
981-5
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Corrections
CommentIn
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