J. Lipid Res.  Neurobiology of Lipids (ISSN1683-5506)
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 Yang, L. Y.
Right arrow Articles by Myher, J. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yang, L. Y.
Right arrow Articles by Myher, J. J.
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 36, 1046-1057, Copyright © 1995 by Lipid Research, Inc.


ARTICLES

Biosynthesis of chylomicron triacylglycerols by rats fed glyceryl or alkyl esters of menhaden oil fatty acids

LY Yang, a Kuksis and JJ Myher
Department of Biochemistry, University of Toronto, Canada.

We have previously shown great similarity in the distribution of fatty acids in the sn-1 and sn-3 positions of the chylomicron triacylglycerols (TG) from rats fed menhaden oil or its ethyl esters, and have proposed that the acylglycerol products of the phosphatidic acid (PA) pathway (ester feeding) are hydrolyzed to 2-monoacylglycerols (2-MG) prior to reconversion to TG via the 2-MG pathway (oil feeding) and secretion as chylomicrons. As the composition of the sn-2-position would also be retained if the TG were hydrolyzed only to the X-1,2- diacylglycerol (DG) stage before resynthesis, we have now retested the hypothesis by determining the molecular association and reverse isomer content of the sn-1,2- and sn-2,3-DG derived from the chylomicron TG and the PA resulting from the two feedings. The new data demonstrate a better than 90% homology among the molecular species of the PA from the oil and ester feeding, along with the characteristic association of the saturated acids with sn-1- and the unsaturated acids with sn-2- position. Due to increased proportion of unsaturated acids in the sn-1- position of the TG, there was only a 15-20% homology between the PA and the sn-1,2-DG moieties of the chylomicron TG from the oil and ester feeding. A lack of homology was also observed between the PA and free sn-1,2-DG, as well as between the free sn-1,2-DG and the sn-1,2-DG moieties of the chylomicron TG. On the basis of molecular association and the sn-1-/sn-3- reverse isomer content of the chylomicron TG a better than 90% homology was recognized between the chylomicron TG resulting from the oil and ester feeding. It is therefore concluded that hydrolysis to 2-MG followed by reesterification via the 2-MG pathway constitutes the most plausible mechanism for the transfer to chylomicrons of the TG arising from alkyl ester feeding.
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
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
V. Marcil, E. Delvin, E. Seidman, L. Poitras, M. Zoltowska, C. Garofalo, and E. Levy
Modulation of lipid synthesis, apolipoprotein biogenesis, and lipoprotein assembly by butyrate
Am J Physiol Gastrointest Liver Physiol, August 1, 2002; 283(2): G340 - G346.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.