Showing posts with label PPAR-delta. Show all posts
Showing posts with label PPAR-delta. Show all posts

Thursday, February 11, 2010

Protein Important for Mitochondrial Biogenesis Cooperates With HO-1 To Increase Stress Resistance In Endothelial Cells

ConclusionWe have identified an important relationship between PPARdelta, PGC1alpha, and haem oxygenase-1, demonstrating that haem oxygenase-1 induction plays an important role in cytoprotective actions of PPARdelta ligands in vascular endothelium. In light of the protective effects of haem oxygenase-1 against atherogenesis, we suggest that PPARdelta represents a potentially important therapeutic target in the vasculature.

CiteULike: PPARdelta and PGC1alpha act cooperatively to induce haem oxygenase-1 and enhance vascular endothelial cell resistance to stress: "Ali, F., Ali, N. S., Bauer, A., Boyle, J. J., Hamdulay, S. S., Haskard, D. O., Randi, A. M., and Mason, J. C. (2010). Ppardelta and pgc1alpha act cooperatively to induce haem oxygenase-1 and enhance vascular endothelial cell resistance to stress. Cardiovasc Res, 85(4):701-710."

Thursday, December 10, 2009

Increased hepatic oxidative metabolism distinguishes the action of Peroxisome Proliferator-Activated Receptor delta from Peroxisome Proliferator-Activated Receptor gamma in the Ob/Ob mouse

Increased hepatic oxidative metabolism distinguishes the action of Peroxisome Proliferator-Activated Receptor delta from Peroxisome Proliferator-Activated Receptor gamma in the Ob/Ob mouse: "URL: Increased hepatic oxidative metabolism distinguishes the action of Peroxisome Proliferator-Activated Receptor delta from Peroxisome Proliferator-Activated Receptor gamma in the Ob/Ob mouse


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Sunday, October 18, 2009

New study identifies cellular mechanism that causes lupuslike symptoms in mice

New study identifies cellular mechanism that causes lupuslike symptoms in mice

Macrophages, the scavenger cells of the body's immune system, are responsible for disposing of dying cells. Stanford University School of Medicine researchers have identified one pathway in this important process in mice that, if disrupted, causes a lupuslike autoimmune disease.