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Dual‐labeled technique for human lipid metabolism studies using deuterated fatty acid isomers
Author(s) -
Emken E. A.,
Rohwedder W. K.,
Dutton H. J.,
Dougherty R.,
Iacono J. M.,
Mackin J.
Publication year - 1976
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/bf02532663
Subject(s) - chemistry , phospholipid , fatty acid , chromatography , metabolism , triolein , red blood cell , deuterium , biochemistry , physics , quantum mechanics , membrane , lipase , enzyme
Two deuterated fatty acids, elaidate‐ d 2 and oleate‐ d 4 , were fed simultaneously to a human subject as a mixture of trielaidin‐ d 6 and triolein‐ d 12 . Periodically, blood samples were drawn, and red blood cells were separated from the plasma. Red blood cells and plasma lipids were fractionated and analyzed by combined gas chromatography—multiple ion mass spectroscopy. Dual deuterium‐labeling allows rate and extent of fatty acid incorporation to be followed in various plasma and red cell neutral and phospholipid fractions. Maximum amount of deuterated fat varied from 4% in cholesterol ester to 64% in phosphatidyl ethanolamine. The highest levels of deuterated fat occurred in either 6‐, 8‐, or 12‐hr samples; generally, <1% labeled fatty acids could be detected in 72‐hr samples. Because the method is based on dual‐labeling, differences in the relative incorporation of both fatty acid isomers can be compared directly. Differences in rates of incorporation, rates of removal, and extent of incorporation of labeled fatty acids into blood plasma can also be determined reliably. Our experimental labeling of fats with deuterium permits for the first time the metabolism of two fatty acid isomers to be compared simultaneously in human subjects. This new method should be applicable to a variety of other lipid metabolic studies.