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Progressive impairment of atrial myocyte function during left ventricular hypertrophy and heart failure
- Source :
- Journal of Molecular and Cellular Cardiology. 114:253-263
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Hypertensive heart disease (HHD) can cause left ventricular (LV) hypertrophy and heart failure (HF). It is unclear, though, which factors may contribute to the transition from compensated LV hypertrophy to HF in HHD. We hypothesized that maladaptive atrial remodeling with impaired atrial myocyte function would occur in advanced HHD and may be associated with the emergence of HF. Experiments were performed on atrial myocytes and tissue from old (15-25months) normotensive Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR) with advanced HHD. Based on the absence or presence of elevated lung weight, a sign of lung congestion and heart failure, SHR were divided into a non-failing (SHR-NF) and failing (SHR-HF) group. Compared with WKY, SHR exhibited elevated blood pressure, LV hypertrophy and left atrial (LA) hypertrophy with increased LA expression of markers of hypertrophy and fibrosis. SHR-HF were distinguished from SHR-NF by aggravated hypertrophy and fibrosis. SHR-HF atrial myocytes exhibited reduced contractility and impaired SR Ca2+ handling. Moreover, in SHR the expression and phosphorylation of SR Ca2+-regulating proteins (SERCA2a, calsequestrin, RyR2 and phospholamban) showed negative correlation with increasing lung weight. Increasing stimulation frequency (1-2-4Hz) of atrial myocytes caused a progressive increase in arrhythmogenic Ca2+ release (including alternans), which was observed most frequently in SHR-HF. Thus, in old SHR with advanced HHD there is profound structural and functional atrial remodeling. The occurrence of HF in SHR is associated with LA and RA hypertrophy, increased atrial fibrosis, impaired atrial myocyte contractility and SR Ca2+ handling and increased propensity for arrhythmogenic Ca2+ release. Therefore, functional remodeling intrinsic to atrial myocytes may contribute to the transition from compensated LV hypertrophy to HF in advanced HHD and an increased propensity of atrial arrhythmias in HF.
- Subjects :
- Male
Sarcomeres
0301 basic medicine
medicine.medical_specialty
030204 cardiovascular system & hematology
Left ventricular hypertrophy
Rats, Inbred WKY
Ryanodine receptor 2
Muscle hypertrophy
Contractility
03 medical and health sciences
0302 clinical medicine
Rats, Inbred SHR
Internal medicine
medicine
Animals
Myocytes, Cardiac
Calcium Signaling
Heart Atria
cardiovascular diseases
Phosphorylation
Atrium (heart)
Molecular Biology
Heart Failure
business.industry
Arrhythmias, Cardiac
musculoskeletal system
medicine.disease
Myocardial Contraction
Hypertensive heart disease
Phospholamban
030104 developmental biology
medicine.anatomical_structure
Heart failure
Hypertension
cardiovascular system
Cardiology
Calcium
Hypertrophy, Left Ventricular
Cardiology and Cardiovascular Medicine
business
circulatory and respiratory physiology
Subjects
Details
- ISSN :
- 00222828
- Volume :
- 114
- Database :
- OpenAIRE
- Journal :
- Journal of Molecular and Cellular Cardiology
- Accession number :
- edsair.doi.dedup.....e694ebabe27674196a4449885440b676
- Full Text :
- https://doi.org/10.1016/j.yjmcc.2017.11.020