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Papers In Press, published online ahead of print June 1, 2005
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LMBB, NIAAA, NIH, Bethesda, MD 20892-9410
Corresponding Author: nsalem{at}niaaa.nih.gov
This study reports methods for the quantitative determination of stable isotope labeled essential fatty acids (EFA) as well as an experiment where deuterium labeled linoleic and a-linolenic acids were compared to those labeled with carbon-13 in rat plasma in vivo. Standard curves were constructed in order to compensate for concentration and plasma matrix effects. It was observed that endogenous pools of fatty acids had a greater suppressing effect on the measurements of 13C-U-labeled EFAs relative to those labeled with 2H5. Using these methods, the in vivo metabolism of orally administered deuterated-linolenate, 13C-U-labeled linolenate, deuterated-linoleate and 13C-U-labeled linoleate was compared in adult rats (n = 11). There were no significant differences in the concentrations of the 2H vs. 13C isotopomers of 18:2n-6, 18:3n-3, 20:4n-6 and 22:6n-3 in rat plasma samples at 24 h after dosing. jlr Thus, there appears to be little isotope effect for 2H5 vs. 13C-U-labeled EFA when the data are calculated using the conventional standard curves and corrected for endogenous fatty acid pool size and matrix effects.
Revised on May 18, 2005
Accepted on May 19, 2005
Simultaneous quantitative determination of deuterium- and carbon-13-labeled essential fatty acids in rat plasma
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