z-logo
open-access-imgOpen Access
Fenofibrate Inhibits Endothelin-1 Expression by Peroxisome Proliferator–Activated Receptor α–Dependent and Independent Mechanisms in Human Endothelial Cells
Author(s) -
Corine Glineur,
Barbara Gross,
Bernadette Neve,
Corinne Rommens,
Gerard T. Chew,
Françoise MartinNizard,
Fernando RodríguezPascual,
Santiago Lamas,
Gerald F. Watts,
Bart Staels
Publication year - 2013
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.112.300665
Subject(s) - fenofibrate , peroxisome proliferator activated receptor , peroxisome proliferator activated receptor gamma , peroxisome proliferator activated receptor alpha , endothelin 1 , endothelin receptor , microbiology and biotechnology , chemistry , peroxisome , receptor , cancer research , medicine , endocrinology , biology , nuclear receptor , transcription factor , biochemistry , gene
Dyslipidemia contributes to endothelial dysfunction in type 2 diabetes mellitus. Fenofibrate (FF), a ligand of the peroxisome proliferator-activated receptor-α (PPARα), has beneficial effects on microvascular complications. FF may act on the endothelium by regulating vasoactive factors, including endothelin-1 (ET-1). In vitro, FF decreases ET-1 expression in human microvascular endothelial cells. We investigated the molecular mechanisms involved in the effect of FF treatment on plasma levels of ET-1 in type 2 diabetes mellitus patients.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom