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.

Related Concept Videos

Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
1.0K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
539
Mitral Regurgitation I: Introduction01:20

Mitral Regurgitation I: Introduction

Mitral regurgitation is characterized by the backward circulation of blood from the left ventricle to the left atrium during systole, a phase of the cardiac cycle when the heart contracts and pumps blood out of the chambers. This abnormal flow occurs primarily due to the dysfunction of the mitral valve or its supporting structures, which include the mitral leaflets, chordae tendineae, annulus, and papillary muscles.Etiology and Mechanisms:Primary Mitral Regurgitation: This type arises from...
645
Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
4.0K
Myocarditis I: Introduction01:21

Myocarditis I: Introduction

Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
460
Imbalances in Cardiac Output01:26

Imbalances in Cardiac Output

The heart's primary function is to pump blood throughout the body, maintaining a balance between blood sent out (cardiac output) and blood returning (venous return). If this balance is disrupted, it can result in congestive heart failure (CHF), a severe condition where the heart becomes an inefficient pump, leading to inadequate blood circulation.
CHF can occur due to the failure of either side of the heart. Left-side failure leads to pulmonary congestion—the right side continues to send...
3.3K