Transition from compensated hypertrophy to systolic heart failure in the spontaneously hypertensive rat: Structure, function, and transcript analysis

被引:29
|
作者
Brooks, Wesley W. [1 ,2 ]
Shen, Steven S. [3 ]
Conrad, Chester H. [1 ,2 ]
Goldstein, Ronald H. [1 ,2 ]
Bing, Oscar H. L. [1 ,2 ]
机构
[1] VA Boston Healthcare Syst, Boston, MA 02130 USA
[2] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Clin & Translat Sci Inst, Boston, MA 02118 USA
关键词
Heart failure; Hypertension; Cardiac hypertrophy; Gene expression microarray; CARDIAC GENE-EXPRESSION; CONVERTING ENZYME-INHIBITION; LEFT-VENTRICULAR HYPERTROPHY; TUMOR-NECROSIS-FACTOR; UP-REGULATION; MYOCARDIAL FIBROSIS; MICROARRAY ANALYSIS; FAILING MYOCARDIUM; DOWN-REGULATION; PROFILES;
D O I
10.1016/j.ygeno.2009.12.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Gene expression, determined by micro-array analysis, and left ventricular (LV) remodeling associated with the transition to systolic heart failure (HF) were examined in the spontaneously hypertensive rat (SHR). By combining transcript and gene set enrichment analysis (GSEA) of the LV with assessment of function and structure in age-matched SHR with and without HF, we aimed to better understand the molecular events underlying the onset of hypertensive HF. Failing hearts demonstrated depressed LV ejection fraction, systolic blood pressure, and LV papillary muscle force while LV end-diastolic and systolic volume and ventricular mass increased. 1431 transcripts were differentially expressed between failing and non-failing animals. GSEA identified multiple enriched gene sets, including those involving inflammation, oxidative stress, cell degradation and cell death, as well as TGF-beta and insulin signaling pathways. Our findings support the concept that these pathways and mechanisms may contribute to deterioration of cardiac function and remodeling associated with hypertensive HF. Published by Elsevier Inc.
引用
收藏
页码:84 / 92
页数:9
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