J. Lipid Res. Acyl Labeled PIP's available August 1, 2008
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
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 Coots, R. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Coots, R. H.
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?

Journal of Lipid Research, Vol. 5, 473-476, July 1964
Copyright © 1964 by Lipid Research, Inc.

A comparison of the metabolism of cis, cis-linoleic, trans,trans-linoleic, and a mixture of cis,trans- and trans,cis-linoleic acids in the rat

Robert H. Coots

The Procter and Gamble Company, Miami Valley Laboratories, Cincinnati, Ohio

A comparison has been made of the metabolism of cis,cis-linoleic, trans,trans-linoleic, and a mixture of cis,trans- and trans,cis-linoleic acids in the rat. The data show that linoleic acid and its geometric isomers were well absorbed. These acids were readily oxidized to CO2 with no apparent difference in rate or extent of catabolism between the trans-isomers. However, the trans-isomers of linoleic acid were catabolized to CO2 to a somewhat greater extent than was cis,cis-linoleic acid. Although these differences were small, they are consistent with the fact that the geometric isomers have no essential fatty acid activity and, therefore, might conceivably be more available as an energy source than the cis,cis-isomer. The trans-linoleic acids, like the cis,cis-linoleic acid, were transported in the lymph mainly as glycerides. There were no major differences in the distribution of the various acids among the lymph lipid classes, indicating that the rat does not distinguish among the linoleic acid isomers as far as digestion and absorption are concerned. Linoleic acid and its trans-isomers were metabolized in an efficient and apparently normal manner.

Submitted on February 17, 1964
Accepted on April 1, 1964


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
L. Bretillon, J. M. Chardigny, J. L. Sébédio, J. P. Noël, C. M. Scrimgeour, C. E. Fernie, O. Loreau, P. Gachon, and B. Beaufrère
Isomerization increases the postprandial oxidation of linoleic acid but not {{alpha}}-linolenic acid in men
J. Lipid Res., June 1, 2001; 42(6): 995 - 997.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 1964 by the American Society for Biochemistry and Molecular Biology.