Abstract
Targeted and regulated genetic manipulation, physiological intervention to introduce biomechanical stress and injury, sophisticated measurement of cardiac function in transgenic heart at whole organ and cellular level, and the molecular/biochemical/genomic analysis of signaling pathways in cardiomyocytes represent the most significant advances in recent years in this field. Such progress has helped make inroads into understanding the molecular mechanism of cardiac hypertrophy and heart failure. Delineating intracellular signaling pathways involved in the different aspects of cardiac hypertrophy and remodeling will have significant implications in drug development for heart failure.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
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Review
MeSH terms
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Angiotensin II / metabolism
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Animals
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Animals, Genetically Modified
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Antigens, CD / metabolism
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Calcineurin / metabolism
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Calcium-Calmodulin-Dependent Protein Kinases / metabolism
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Cardiomegaly / genetics
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Cardiomegaly / physiopathology*
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Cytokine Receptor gp130
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GTP-Binding Protein alpha Subunits, Gq-G11
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Heart Failure / genetics
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Heart Failure / metabolism
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Heart Failure / physiopathology
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Heterotrimeric GTP-Binding Proteins / metabolism
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Membrane Glycoproteins / metabolism
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Mitogen-Activated Protein Kinases / metabolism
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Monomeric GTP-Binding Proteins / metabolism
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Myocardial Contraction
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Protein Kinase C / metabolism
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Receptor Protein-Tyrosine Kinases / metabolism
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Receptors, Angiotensin / genetics
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Receptors, Angiotensin / metabolism
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Signal Transduction / genetics
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Signal Transduction / physiology*
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Transcription, Genetic
Substances
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Antigens, CD
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Membrane Glycoproteins
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Receptors, Angiotensin
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Angiotensin II
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Cytokine Receptor gp130
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Receptor Protein-Tyrosine Kinases
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Protein Kinase C
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Calcium-Calmodulin-Dependent Protein Kinases
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Mitogen-Activated Protein Kinases
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Calcineurin
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GTP-Binding Protein alpha Subunits, Gq-G11
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Heterotrimeric GTP-Binding Proteins
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Monomeric GTP-Binding Proteins