calpastatin and Cardiomegaly

calpastatin has been researched along with Cardiomegaly* in 2 studies

Other Studies

2 other study(ies) available for calpastatin and Cardiomegaly

ArticleYear
Targeted inhibition of calpain in mitochondria alleviates oxidative stress-induced myocardial injury.
    Acta pharmacologica Sinica, 2021, Volume: 42, Issue:6

    The protein levels and activities of calpain-1 and calpain-2 are increased in cardiac mitochondria under pathological conditions including ischemia, diabetes, and sepsis, and transgenic overexpression of mitochondrial-targeted calpain-1 induces dilated heart failure, which underscores an important role of increased calpain in mitochondria in mediating myocardial injury. However, it remains to be determined whether selective inhibition of calpain in mitochondria protects the heart under pathological conditions. In this study, we generated transgenic mice overexpressing mitochondrial-targeted calpastatin in cardiomyocytes. Their hearts were isolated and subjected to global ischemia/reperfusion. Hyperglycemia was induced in the transgenic mice by injections of STZ. We showed that transgenic calpastatin was expressed exclusively in mitochondria isolated from their hearts but not from other organs including skeletal muscle and lung tissues. Transgenic overexpression of mitochondrial-targeted calpastatin significantly attenuated mitochondrial oxidative stress and cell death induced by global ischemia/reperfusion in isolated hearts, and ameliorated mitochondrial oxidative stress, cell death, myocardial remodeling and dysfunction in STZ-treated transgenic mice. The protective effects of mitochondrial-targeted calpastatin were correlated with increased ATP5A1 protein expression and ATP synthase activity in isolated hearts subjected to global ischemia/reperfusion and hearts of STZ-treated transgenic mice. In cultured rat myoblast H9c2 cells, overexpression of mitochondrial-targeted calpastatin maintained the protein levels of ATP5A1 and ATP synthase activity, prevented mitochondrial ROS production and decreased cell death following hypoxia/reoxygenation, whereas upregulation of ATP5A1 or scavenging of mitochondrial ROS by mito-TEMPO abrogated mitochondrial ROS production and decreased cell death. These results confirm the role of calpain in myocardial injury, suggesting that selective inhibition of calpain in myocardial mitochondria by mitochondrial-targeted calpastatin is an effective strategy for alleviating myocardial injury and dysfunction in cardiac pathologies.

    Topics: Animals; Apoptosis; Calcium-Binding Proteins; Calpain; Cardiomegaly; Diabetes Mellitus, Experimental; Fibrosis; Male; Mice, Transgenic; Mitochondria, Heart; Mitochondrial Proton-Translocating ATPases; Myocytes, Cardiac; Oxidative Stress; Reactive Oxygen Species

2021
Taurine attenuates isoproterenol-induced H9c2 cardiomyocytes hypertrophy by improving antioxidative ability and inhibiting calpain-1-mediated apoptosis.
    Molecular and cellular biochemistry, 2020, Volume: 469, Issue:1-2

    Pathological cardiac hypertrophy is ultimately accompanied by cardiomyocyte apoptosis. Apoptosis mainly related to calpain-1-mediated apoptotic pathways. Studies had proved that taurine can maintain heart health through antioxidation and antiapoptotic functions, but the effect of taurine on cardiac hypertrophy is still unclear. This study aimed to determine whether taurine could inhibit calpain-1-mediated mitochondria-dependent apoptotic pathways in isoproterenol (ISO)-induced hypertrophic cardiomyocytes. We found that taurine could inhibit the increase in cell surface area and reduce the protein expression levels of the hypertrophic markers atrial natriuretic peptide, brain natriuretic polypeptide, and β-myosin heavy chain. Taurine also reduced ROS, intracellular Ca

    Topics: Animals; Apoptosis; Apoptotic Protease-Activating Factor 1; Atrial Natriuretic Factor; bcl-2-Associated X Protein; Calcium; Calcium-Binding Proteins; Calpain; Cardiomegaly; Caspase 3; Caspase 9; Cell Line; Cytochromes c; Isoproterenol; Membrane Potential, Mitochondrial; Mitochondria; Myocytes, Cardiac; Natriuretic Peptide, Brain; Natriuretic Peptides; Oxidative Stress; Proto-Oncogene Proteins c-bcl-2; Rats; Taurine; Ventricular Myosins

2020