Volume 51, Issue 6 pp. 1279-1282
Note

Lactate isotopomer analysis by 1H NMR spectroscopy: Consideration of long-range nuclear spin–spin interactions

Steven G. Lloyd

Steven G. Lloyd

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama

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Huadong Zeng

Huadong Zeng

Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama

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PeiPei Wang

PeiPei Wang

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama

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John C. Chatham

Corresponding Author

John C. Chatham

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama

Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama

Department of Physiology and Biophysics and Clinical Nutrition Research Center, University of Alabama at Birmingham, Birmingham, Alabama

Division of Cardiovascular Disease, Department of Medicine, University of Alabama at Birmingham, McCallum Building 684, 1530 Third Avenue South, Birmingham, AL 35294-0005===Search for more papers by this author
First published: 24 May 2004
Citations: 28

Abstract

Lactate is a key metabolite and its rates of cellular uptake and release, its production rates from glucose and glycogen, and its interconversion rate with pyruvate are important determinants of cellular energy production. If lactate precursors such as pyruvate and glucose are labeled appropriately with 13C, 1H NMR spectroscopy provides a means of quantifying lactate production from each source and allows measurement of all these rates within a single experiment. However, due to the multiplicities of the resonance lines (from nuclear spin–spin couplings) in lactate 13C isotopomers, the 1H NMR spectra were found to be more complex than expected, requiring determination of all spin–spin interactions in this anion. All such values were determined for lactate and its precursor pyruvate. The method was then applied to simultaneously measure the rates of exogenous lactate uptake and rates of release of glucose-, glycogen-, and pyruvate-derived lactate in the isolated perfused rat heart. Magn Reson Med 51:1279–1282, 2004. © 2004 Wiley-Liss, Inc.

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