Journal of Cellular and Molecular Medicine · 2019 · 71 citations · 8 references
MedicineCardiologyPharmacologyEpigeneticsMolecular PharmacologyTranscriptional RegulationCardiovascular DiseaseCardiovascular Molecular PhysiologyCardiovascular PharmacologyHypertension PharmacotherapyHypertensive Heart DiseaseCardiac Fibrosis ModulationHistone AcetylationHistone Acetyltransferase InhibitionHistone-lysine AcetylationHypertensive CardiomyopathyLeft Ventricular Diastolic DysfunctionMurine ModelsMyofibroblast Differentiation
Epigenetic dysregulation plays a crucial role in cardiovascular diseases. Previously, we reported that acetyltransferase p300 (ATp300) inhibitor L002 prevents hypertension-induced cardiac hypertrophy and fibrosis in a murine model. In this short communication, we show that treatment of hypertensive mice with ATp300-specific small molecule inhibitor L002 or C646 reverses hypertension-induced left ventricular hypertrophy, cardiac fibrosis and diastolic dysfunction, without reducing elevated blood pressures. Biochemically, treatment with L002 and C646 also reverse hypertension-induced histone acetylation and myofibroblast differentiation in murine ventricles. Our results confirm and extend the role of ATp300, a major epigenetic regulator, in the pathobiology of cardiac hypertrophy and fibrosis. Most importantly, we identify the efficacies of ATp300 inhibitors C646 and L002 in reversing hypertension-induced cardiac hypertrophy and fibrosis, and discover new anti-hypertrophic and anti-fibrotic candidates.
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