Clinical Science, Journal Year: 2024, Volume and Issue: 138(18), P. 1173 - 1177
Published: Sept. 1, 2024
Abstract Cardiac functional, morphological, and histological analysis, coupled with liquid chromatography mass spectrometry, of two transgenic mouse models cardiomyocyte-specific overexpression insulin-like growth factor 1 receptor (IGF1R) or a dominant-negative PI3K mutant (DCM-dnPI3K) revealed distinctive functional molecular profiles during physiological (driven by IGF1R overexpression) pathological dn-PI3K atrial remodeling. The current study confirmed previously reported findings, including ventricular dilatation enhanced systolic function no evidence arrhythmia in model, as well hypertrophy decreased intermittent fibrillation DCM-dnPI3K model. Novel findings obtained from the left (LA) characterization female mice that enlargement resulted increased myocyte size was associated preserved function, determined maintained LA ejection fraction (EF). proteomic profile (Tg) enriched for metabolic remodeling showed protein expression pattern similar to healthy human atria; on other hand, fibrosis normal impaired due reduced EF. both structural AF atria
Language: Английский