Advertisement
J. Lipid Res.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


A more recent version of this article appeared on June 1, 2008

Papers In Press, published online ahead of print March 3, 2008
J. Lipid Res., doi:10.1194/jlr.M700486-JLR200
This Article
Right arrow Full Text (Accepted Manuscript)
Right arrow All Versions of this Article:
M700486-JLR200v1
49/6/1216    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 arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fezza, F.
Right arrow Articles by Maccarrone, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fezza, F.
Right arrow Articles by Maccarrone, M.
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 October 26, 2007
Revised on March 3, 2008
Accepted on March 3, 2008

Characterization of biotin-anandamide, a novel tool for the visualization of anandamide accumulation

Filomena Fezza, Sergio Oddi, Monia Di Tommaso, Chiara De Simone, Cinzia Rapino, Nicoletta Pasquariello, Enrico Dainese, Alessandro Finazzi-Agrò, and Mauro Maccarrone

Department of Biomedical Sciences, University of Teramo, Teramo

Corresponding Author: mmaccarrone{at}unite.it

Anandamide (arachidonoylethanolamide, AEA) acts as endogenous agonist of both cannabinoid and vanilloid receptors. During the last two decades, its metabolic pathways and biological activity have been extensively investigated and relatively well-characterized. In contrast, the effective nature and mechanism of AEA transport remain at present a controversial and still unsolved issue. Here we report the characterization of a biotinylated analogue of AEA (b-AEA), that has the same lipophylicity of the parent compound. In addition, by means of biochemical assays and fluorescence microscopy, we show that b-AEA is accumulated inside the cells in a way superimposable on that of AEA. Conversely, b-AEA does not interact nor interfere with the other components of the endocannabinoid system, i.e. type-1 and type-2 cannabinoid receptors, vanilloid receptor, AEA synthetase (NAPE-PLD) or AEA hydrolase (FAAH). Taken together, our data suggest that b-AEA could be a very useful probe for visualizing the accumulation and intracellular distribution of this endocannabinoid.


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?





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 2008 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement