Dissociation between gene and protein expression of metabolic enzymes in a rodent model of heart failure

被引:33
作者
Morgan, Eric E.
Chandler, Margaret P.
Young, Martin E.
McElfresh, Tracy A.
Kung, Theodore A.
Rennison, Julie H.
Tserng, Kou-Yi
Hoit, Brian D.
Stanley, William C.
机构
[1] Case Western Reserve Univ, Sch Med, Dept Physiol & Biophys, Cleveland, OH 44106 USA
[2] Univ Texas, Hlth Sci Ctr, Brown Fdn Inst Mol Med, Houston, TX USA
[3] Vet Affairs Med Res Ctr, Cleveland, OH USA
[4] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[5] Univ Hosp Cleveland, Cleveland, OH 44106 USA
关键词
cardiac; ceramide; metabolism; PPAR alpha; RXR alpha;
D O I
10.1016/j.ejheart.2006.01.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Studies in advanced heart failure show down-regulation of fatty acid oxidation genes, possibly due to decreased expression of the nuclear transcription factors peroxisome proliferator activated receptor a (PPAR alpha) and retinoid X receptor alpha (RXR alpha). We assessed mRNA and protein expression of PPAR alpha and RXR alpha, and for several PPAR/RXR regulated metabolic proteins at 8 and 20 weeks following myocardial infarction induced by coronary artery ligation. Infarction resulted in heart failure, as indicated by reduced LV fractional shortening and increased end diastolic area compared to sham. There was a progressive increase in LV end systolic area, myocardial ceramide content and atrial natriuretic peptide mRNA, and a deterioration in LV fractional area of shortening from 8 to 20 weeks. Protein and mRNA expression of PPARa and RXR alpha were not different among groups. The mRNA for PPAR/RXR regulated genes (e.g. medium chain acyl-CoA dehydrogenase (MCAD)) was down-regulated at 8 and 20 weeks post-infarction; however, neither the protein expression nor activity of MCAD was reduced compared to sham. In conclusion, reduced mRNA expression of PPAR/RXR regulated genes is not dependent on reduced PPAR/RXR protein expression. (c) 2006 European Society of Cardiology. Published by Elsevier B.V All rights reserved.
引用
收藏
页码:687 / 693
页数:7
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