The PPARalpha-leukotriene B4 pathway to inflammation control.

Détails

ID Serval
serval:BIB_7762C6C15F29
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
The PPARalpha-leukotriene B4 pathway to inflammation control.
Périodique
Nature
Auteur⸱e⸱s
Devchand P.R., Keller H., Peters J.M., Vazquez M., Gonzalez F.J., Wahli W.
ISSN
0028-0836[print], 0028-0836[linking]
Statut éditorial
Publié
Date de publication
11/1996
Volume
384
Numéro
6604
Pages
39-43
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Inflammation is a local immune response to 'foreign' molecules, infection and injury. Leukotriene B4, a potent chemotactic agent that initiates, coordinates, sustains and amplifies the inflammatory response, is shown to be an activating ligand for the transcription factor PPARalpha. Because PPARalpha regulates the oxidative degradation of fatty acids and their derivatives, like this lipid mediator, a feedback mechanism is proposed that controls the duration of an inflammatory response and the clearance of leukotriene B4 in the liver. Thus PPARalpha offers a new route to the development of anti- or pro-inflammatory reagents.
Mots-clé
Adaptation, Physiological, Animals, Arachidonic Acid/metabolism, Cells, Cultured, Chloramphenicol O-Acetyltransferase/genetics, Fatty Acids/metabolism, Female, Gene Expression Regulation, Hela Cells, Humans, Inflammation/metabolism, Inflammation Mediators/metabolism, Leukotriene B4/metabolism, Ligands, Liver/metabolism, Male, Mice, Oxidation-Reduction, Plasmids, Pyrimidines/metabolism, Rats, Rats, Sprague-Dawley, Receptors, Cytoplasmic and Nuclear/metabolism, Time Factors, Transcription Factors/metabolism, Transfection
Pubmed
Web of science
Création de la notice
24/01/2008 17:04
Dernière modification de la notice
20/08/2019 15:34
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