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Isolation of Atrial Cardiomyocytes from a Rat Model of Metabolic Syndrome-related Heart Failure with Preserved Ejection Fraction
Published on: July 26, 2018
Progressive impairment of atrial myocyte function during left ventricular hypertrophy and heart failure
Florentina Pluteanu1, Yulia Nikonova2, Anna Holzapfel2
1Institute of Pharmacology and Clinical Pharmacy, Biochemical and Pharmacological Center (BPC) Marburg, University of Marburg, Karl-von-Frisch-Str. 1, D-35032 Marburg, Germany; Institute for Pharmacology and Toxicology, University of Münster, Domagkstr. 12, D-48149 Münster, Germany.
Insights
In hypertensive heart disease, atrial remodeling and impaired myocyte function contribute to heart failure progression. This study in rats reveals how these changes worsen heart failure and arrhythmias.
Area of Science:
- Cardiology
- Physiology
Background:
- Hypertensive heart disease (HHD) leads to left ventricular (LV) hypertrophy and heart failure (HF).
- Factors driving the transition from compensated LV hypertrophy to HF in HHD remain unclear.
- Maladaptive atrial remodeling and impaired atrial myocyte function are hypothesized to contribute to HF development in advanced HHD.
Purpose of the Study:
- To investigate the role of atrial remodeling and myocyte function in the progression of HHD to HF.
- To examine structural and functional changes in atrial myocytes and tissue in a rat model of advanced HHD.
Main Methods:
- Experiments utilized atrial myocytes and tissue from normotensive Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR) with advanced HHD.
- SHR were categorized into non-failing (SHR-NF) and failing (SHR-HF) groups based on lung weight.
- Evaluated blood pressure, LV and atrial hypertrophy, fibrosis, atrial myocyte contractility, SR Ca2+ handling, and arrhythmogenic Ca2+ release.
Main Results:
- SHR exhibited elevated blood pressure, LV hypertrophy, and left atrial (LA) hypertrophy with increased fibrosis compared to WKY.
- SHR-HF showed aggravated hypertrophy and fibrosis, reduced atrial myocyte contractility, and impaired SR Ca2+ handling.
- Increased stimulation frequency led to more arrhythmogenic Ca2+ release in SHR-HF, correlating negatively with SR Ca2+ regulating proteins and lung weight.
Conclusions:
- Advanced HHD in old SHR is characterized by significant structural and functional atrial remodeling.
- HF development in SHR is linked to atrial hypertrophy, fibrosis, impaired myocyte function, and altered Ca2+ handling.
- Atrial myocyte dysfunction may drive the transition to HF and increase arrhythmia susceptibility in HHD.
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.
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