Journal
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
Volume 298, Issue 6, Pages R1597-R1606Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00825.2009
Keywords
heart failure
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Funding
- Deutsche Forschungsgemeinschaft [DFG-GK-754II-III, FG-1054, Re662/6-1]
- Commission of the European Community [EUGeneHeart-LSHM-CT-2005-018833]
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Fliegner D, Schubert C, Penkalla A, Witt H, Kararigas G, Dworatzek E, Staub E, Martus P, Noppinger PR, Kintscher U, Gustafsson J angstrom, Regitz-Zagrosek V. Female sex and estrogen receptor-beta attenuate cardiac remodeling and apoptosis in pressure overload. Am J Physiol Regul Integr Comp Physiol 298: R1597-R1606, 2010. First published April 7, 2010; doi:10.1152/ajpregu.00825.2009.-We investigated sex differences and the role of estrogen receptor-beta (ER beta) on myocardial hypertrophy in a mouse model of pressure overload. We performed transverse aortic constriction (TAC) or sham surgery in male and female wild-type (WT) and ER beta knockout (ER beta(-/-)) mice. All mice were characterized by echocardiography and hemodynamic measurements and were killed 9 wk after surgery. Left ventricular (LV) samples were analyzed by microarray profiling, real-time RTPCR, and histology. After 9 wk, WT males showed more hypertrophy and heart failure signs than WT females. Notably, WT females developed a concentric form of hypertrophy, while males developed eccentric hypertrophy. ER beta deletion augmented the TAC-induced increase in cardiomyocyte diameter in both sexes. Gene expression profiling revealed that WT male hearts had a stronger induction of matrix-related genes and a stronger repression of mitochondrial genes than WT female hearts. ER beta(-/-) mice exhibited a different transcriptional response. ER beta(-/-)/TAC mice of both sexes exhibited induction of proapoptotic genes with a stronger expression in ER beta(-/-) males. Cardiac fibrosis was more pronounced in male WT/TAC than in female mice. This difference was abolished in ER beta(-/-) mice. The number of apoptotic nuclei was increased in both sexes of ER beta(-/-)/TAC mice, most prominent in males. Female sex offers protection against ventricular chamber dilation in the TAC model. Both female sex and ER beta attenuate the development of fibrosis and apoptosis, thus slowing the progression to heart failure.
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