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PMID: 1898402 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Protection by acidotic pH against anoxia/reoxygenation injury to rat neonatal cardiac myocytes.

Biochemical and biophysical research communications ·Vol. 179 ·No. 2 ·1991-09-16 ·Pages 798-803

Bond JM, Herman B, Lemasters JJ

Abstract

We assessed the effect of acidosis on cell killing during anoxia and reoxygenation in cultured rat neonatal cardiac myocytes. After 4.5 hours of anoxia and glycolytic inhibition with 2-deoxyglucose, loss of viability was greater than 90% at pH 7.4. In contrast, at pH 6.2-7.0, viability was virtually unchanged. To model changes of pH and oxygenation during ischemia and reperfusion, myocytes were made anoxic at pH 6.2 for 4 hours, followed by reoxygenation at pH 7.4. Under these conditions, reoxygenation precipitated loss of viability to about half the cells. When pH was increased to 7.4 without reoxygenation, similar lethal injury occurred. No cell killing occurred after reoxygenation at pH 6.2. We conclude that acidosis protects against lethal anoxic injury, and that a rapid return from acidotic to physiologic pH contributes significantly to reperfusion injury to cardiac myocytes - a 'pH paradox'.

MeSH Terms
Acidosis/physiopathology Animals Cell Hypoxia/physiology Cell Survival Cells, Cultured Glycolysis Models, Biological Myocardial Reperfusion Injury/metabolism Myocardium/metabolism,pathology Oxygen Consumption Rats
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Bond J M
Department of Cell Biology & Anatomy, University of North Carolina, Chapel Hill 27599.
Herman B
Lemasters J J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1991-09-16
Pages
798-803
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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