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Cardiac PPARalpha expression in patients with dilated cardiomyopathy.

作者信息

Schupp Michael, Kintscher Ulrich, Fielitz Jens, Thomas Jennifer, Pregla Reinhard, Hetzer Roland, Unger Thomas, Regitz-Zagrosek Vera

机构信息

Center for Cardiovascular Research, CCR, Institute of Pharmacology and Toxicology, Charité-Universitätsmedizin Berlin, CCM, Hessischestr. 3-4, 10115 Berlin, Germany.

出版信息

Eur J Heart Fail. 2006 May;8(3):290-4. doi: 10.1016/j.ejheart.2005.09.003. Epub 2005 Nov 22.

Abstract

BACKGROUND

The peroxisome proliferator-activated receptor alpha (PPARalpha) is a central regulator of myocardial fatty acid (FA) metabolism implicated in the pathogenesis of heart failure.

AIMS

To characterize PPARalpha regulation in human dilated cardiomyopathy (DCM), we studied the expression of cardiac PPARalpha, cardiac carnitine palmitoyl-transferase I (CPT-1), a major PPARalpha target gene, and of the cardiac glucose transporter GLUT-4 in patients with DCM.

METHODS

Left ventricular biopsies were taken from patients with DCM (n=16) and control subjects (n=15), and mRNA expression was quantitated using real-time PCR (SYBR((R))Green) and protein expression was measured by Western immunoblotting.

RESULTS

Left ventricular PPARalpha mRNA levels were significantly increased in the DCM group compared to the control group (136+/-25.4% vs. control, p<0.01). Consistently, DCM patients had a significantly higher cardiac CPT-1 mRNA expression (147+/-51% vs. control, p<0.05) compared to the control group. Cardiac GLUT-4 expression was similar in both groups.

CONCLUSION

Elevated cardiac PPARalpha levels followed by an induction of cardiac CPT-1 expression may result in increased fatty acid metabolism for cardiac energy production in DCM, suggesting a specific cardiac metabolic program in human DCM compared to other types of cardiomyopathy.

摘要

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