Pathological Changes and Metabolic Adaptation in the Myocardium of Rats in Response to Chronic Variable Mild Stress.
Marta OstrowskaMariola HerbetKamil PawłowskiAgnieszka KorgaEwa PoleszakJarosław DudkaPublished in: International journal of molecular sciences (2024)
Chronic variable mild stress (CVS) in rats is a well-established paradigm for inducing depressive-like behaviors and has been utilized extensively to explore potential therapeutic interventions for depression. While the behavioral and neurobiological effects of CVS have been extensively studied, its impact on myocardial function remains largely unexplored. To induce the CVS model, rats were exposed to various stressors over 40 days. Behavioral assessments confirmed depressive-like behavior. Biochemical analyses revealed alterations in myocardial metabolism, including changes in NAD+ and NADP+, and NADPH concentrations. Free amino acid analysis indicated disturbances in myocardial amino acid metabolism. Evaluation of oxidative DNA damage demonstrated an increased number of abasic sites in the DNA of rats exposed to CVS. Molecular analysis showed significant changes in gene expression associated with glucose metabolism, oxidative stress, and cardiac remodeling pathways. Histological staining revealed minor morphological changes in the myocardium of CVS-exposed rats, including increased acidophilicity of cells, collagen deposition surrounding blood vessels, and glycogen accumulation. This study provides novel insights into the impact of chronic stress on myocardial function and metabolism, highlighting potential mechanisms linking depression and cardiovascular diseases. Understanding these mechanisms may aid in the development of targeted therapeutic strategies to mitigate the adverse cardiovascular effects of depression.
Keyphrases
- left ventricular
- dna damage
- oxidative stress
- gene expression
- amino acid
- depressive symptoms
- stress induced
- cardiovascular disease
- induced apoptosis
- physical activity
- dna methylation
- emergency department
- single cell
- metabolic syndrome
- risk assessment
- heat stress
- cardiovascular risk factors
- cancer therapy
- dna repair
- data analysis
- atrial fibrillation
- nucleic acid
- heat shock