J. Lipid Res.  Neurobiology of Lipids (ISSN1683-5506)
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


A more recent version of this article appeared on September 1, 2005

Papers In Press, published online ahead of print June 1, 2005
J. Lipid Res., doi:10.1194/jlr.M500128-JLR200
This Article
Right arrow Full Text (Accepted Manuscript)
Right arrow All Versions of this Article:
M500128-JLR200v1
46/9/1974    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Lin, Y. H.
Right arrow Articles by Salem ., N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lin, Y. H.
Right arrow Articles by Salem ., N., Jr
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Submitted on April 4, 2005
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

Yu Hong Lin, Robert J. Pawlosky, and Norman Salem . Jr

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.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Lipid Res.Home page
S. Gagne, S. Crane, Z. Huang, C. S. Li, K. P. Bateman, and J.-F. Levesque
Rapid measurement of deuterium-labeled long-chain fatty acids in plasma by HPLC-ESI-MS
J. Lipid Res., January 1, 2007; 48(1): 252 - 259.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
Y. H. Lin and N. Salem Jr.
In vivo conversion of 18- and 20-C essential fatty acids in rats using the multiple simultaneous stable isotope method
J. Lipid Res., September 1, 2005; 46(9): 1962 - 1973.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 2005 by the American Society for Biochemistry and Molecular Biology.