Home LiteratureArticle Details
PMID: 10909972 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Acute overexpression of lactate dehydrogenase-A perturbs beta-cell mitochondrial metabolism and insulin secretion.

Diabetes ·Vol. 49 ·No. 7 ·2000-07-00 ·Pages 1149-55

Ainscow EK, Zhao C, Rutter GA

Abstract

Islet beta-cells express low levels of lactate dehydrogenase and have high glycerol phosphate dehydrogenase activity. To determine whether this configuration favors oxidative glucose metabolism via mitochondria in the beta-cell and is important for beta-cell metabolic signal transduction, we have determined the effects on glucose metabolism and insulin secretion of acute overexpression of the skeletal muscle isoform of lactate dehydrogenase (LDH)-A. Monitored in single MIN6 beta-cells, LDH hyperexpression (achieved by intranuclear cDNA microinjection or adenoviral infection) diminished the response to glucose of both phases of increases in mitochondrial NAD(P)H, as well as increases in mitochondrial membrane potential, cytosolic free ATP, and cystolic free Ca2+. These effects were observed at all glucose concentrations, but were most pronounced at submaximal glucose levels. Correspondingly, adenoviral vector-mediated LDH-A overexpression reduced insulin secretion stimulated by 11 mmol/l glucose and the subsequent response to stimulation with 30 mmol/l glucose, but it was without significant effect when the concentration of glucose was raised acutely from 3 to 30 mmol/l. Thus, overexpression of LDH activity interferes with normal glucose metabolism and insulin secretion in the islet beta-cell type, and it may therefore be directly responsible for insulin secretory defects in some forms of type 2 diabetes. The results also reinforce the view that glucose-derived pyruvate metabolism in the mitochondrion is critical for glucose-stimulated insulin secretion in the beta-cell.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Cell Line DNA, Complementary Glucose/pharmacology Insulin/metabolism Insulin Secretion Intracellular Membranes/physiology Islets of Langerhans/drug effects,metabolism,physiology Isoenzymes Kinetics L-Lactate Dehydrogenase/genetics,metabolism Mitochondria/metabolism Muscle, Skeletal/enzymology NAD/metabolism NADP/metabolism RNA, Messenger/genetics Recombinant Proteins/metabolism Transcription, Genetic
Chemicals
DNA, Complementary Insulin Isoenzymes RNA, Messenger Recombinant Proteins NAD NADP Adenosine Triphosphate L-Lactate Dehydrogenase Glucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Ainscow E K
Department of Biochemistry, School of Medical Sciences, University Walk, University of Bristol, UK.
Zhao C
Rutter G A
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2000-07-00
Pages
1149-55
Language
English
Region
United States
NLM ID
0372763
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com