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PMID: 8067419 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Ratiometric methodology for NAD(P)H measurement in the perfused rat heart using surface fluorescence.

The American journal of physiology ·Vol. 267 ·No. 2 Pt 2 ·1994-08-00 ·Pages H636-44

Scott DA, Grotyohann LW, Cheung JY, Scaduto RC

Abstract

The surface fluorescence of the isolated perfused rat heart has been evaluated for the purpose of NAD(P)H quantitation. With the use of excitation at 340, 380, 415, and 430 nm with emission detection at 500 +/- 20 nm, the intensities at 340 and 380 nm excitation were found to be linearly related during NAD(P)H oxidation/reduction induced by changes in substrate availability. Changes in cardiac NAD(P)H caused similar changes at 340 and 380 nm excitation, but those at 340 nm were of greater magnitude. Isolated cardiac mitochondria exhibited essentially identical optical properties during changes in NAD(P)H content induced by changes in substrate availability and by NAD(H) oxidation/reduction caused by coupled phosphorylation of ADP. The changes in redox status of both isolated mitochondria and the intact perfused heart can be expressed by a 340/380 excitation fluorescence ratio because of these relationships. This value assumed a minimum and maximum value under conditions of complete oxidation and reduction, respectively. Use of this ratio in the perfused heart avoids the artifacts caused by cardiac motion and tissue stretch. Removal of motion artifacts with an excitation ratio could only be accomplished if the measurements at 340 and 380 nm were estimated at the same point in the cardiac cycle. A method of cardiac waveform reconstruction and signal averaging is described to obtain these data from sequential measurements. With these techniques, the reduction of cardiac NAD(P)H can be expressed as a percentage of the range obtained between minimum and maximum reduction. The described technique is of general utility in the assessment of cardiac bioenergetics.

MeSH Terms
Animals Artifacts Calcium/pharmacology Cardiac Pacing, Artificial Diacetyl/analogs & derivatives,pharmacology Fluorescence Heart/drug effects,physiology In Vitro Techniques Mitochondria, Heart/metabolism Motion Myocardial Contraction Myocardium/metabolism NADP/metabolism Oscillometry Oxidation-Reduction/drug effects Perfusion Rats
Chemicals
diacetylmonoxime NADP Diacetyl Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Scott D A
Department of Cellular and Molecular Physiology, Milton S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.
Grotyohann L W
Cheung J Y
Scaduto R C
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1994-08-00
Pages
H636-44
Language
English
Region
United States
NLM ID
0370511
Subset
IM
Grants
NHLBI NIH HHS · HL-43215 · United States
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