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 Thomas, C. E.
Right arrow Articles by Kalyanaraman, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Thomas, C. E.
Right arrow Articles by Kalyanaraman, B.
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 35, 610-619, Copyright © 1994 by Lipid Research, Inc.


ARTICLES

Nitrone spin trap lipophilicity as a determinant for inhibition of low density lipoprotein oxidation and activation of interleukin-1 beta release from human monocytes

CE Thomas, G Ku and B Kalyanaraman
Marion Merrell Dow Research Institute, Cincinnati, OH 45215.

One means by which oxidation of low density lipoproteins (LDL) may contribute to atherogenesis is by their ability to induce the release of interleukin-1 beta from monocytes. In the present study, the effect of the lipophilic nitrone spin trap alpha-phenyl-tert-butylnitrone (PBN) on lipoprotein oxidation and subsequent release of interleukin-1 beta was examined. The hydrophilic nitrone spin trap alpha-(4-pyridyl 1- oxide)-N-tert butylnitrone (POBN) was also studied to evaluate the importance of spin trap localization within the lipoprotein. PBN inhibited copper-induced modification of low density lipoproteins in a dose-dependent fashion as judged by measurement of thiobarbituric acid reactive substances, electrophoretic mobility, and fluorescence changes, while POBN was relatively ineffective. As demonstrated by electron spin resonance spectrometry, spectra of PBN adducts were highly immobilized, which reflects their presence within the LDL matrix. Experiments using chromium oxalate, a paramagnetic relaxing agent, revealed that the PBN adduct is composed of a mobile component (exposed to the LDL aqueous phase) and an immobilized component, localized in the lipid-protein interface or in the bulk lipid. Cholesteryl ester phospholipid dispersions in which only the core cholesteryl esters are subject to oxidation were also used to compare PBN and POBN. Again, PBN prevented the oxidation of the core lipids while POBN had little effect, further suggesting that PBN is capable of localization within the core of LDL. In agreement, attenuation of low density lipoprotein oxidation by PBN also decreased their ability to induce interleukin-1 beta release from human monocytes. Conversely, POBN had little effect on the release of interleukin-1 beta from cells incubated with copper-oxidized lipoproteins. These results suggest that the ability of a nitrone spin trap to prevent low density lipoprotein oxidation and its biologic effect(s) requires its incorporation into the particle.
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. Biol. Chem.Home page
C. E. Thomas, D. F. Ohlweiler, A. A. Carr, T. R. Nieduzak, D. A. Hay, G. Adams, R. Vaz, and R. C. Bernotas
Characterization of the Radical Trapping Activity of a Novel Series of Cyclic Nitrone Spin Traps
J. Biol. Chem., February 9, 1996; 271(6): 3097 - 3104.
[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 © 1994 by the American Society for Biochemistry and Molecular Biology.