| Autor: |
Andolina D; Department of Psychology and Center 'Daniel Bovet,' Sapienza University, Rome, Italy.; IRCCS Fondazione Santa Lucia, Roma, Italy., Savi M; Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy., Ielpo D; Department of Psychology and Center 'Daniel Bovet,' Sapienza University, Rome, Italy., Barbetti M; Department of Chemistry, Life Sciences and Environmental Sustainability, Stress Physiology Lab, University of Parma, Parma, Italy., Bocchi L; Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy., Stilli D; Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parma, Italy., Ventura R; Department of Psychology and Center 'Daniel Bovet,' Sapienza University, Rome, Italy.; IRCCS Fondazione Santa Lucia, Roma, Italy., Lo Iacono L; Department of Psychology and Center 'Daniel Bovet,' Sapienza University, Rome, Italy.; IRCCS Fondazione Santa Lucia, Roma, Italy., Sgoifo A; Department of Chemistry, Life Sciences and Environmental Sustainability, Stress Physiology Lab, University of Parma, Parma, Italy., Carnevali L; Department of Chemistry, Life Sciences and Environmental Sustainability, Stress Physiology Lab, University of Parma, Parma, Italy. |
| Abstrakt: |
This study investigated epigenetic risk factors that may contribute to stress-related cardiac disease in a rodent model. Experiment 1 was designed to evaluate the expression of microRNA-34a (miR-34a), a known modulator of both stress responses and cardiac pathophysiology, in the heart of male adult rats exposed to a single or repeated episodes of social defeat stress. Moreover, RNA sequencing was conducted to identify transcriptomic profile changes in the heart of repeatedly stressed rats. Experiment 2 was designed to assess cardiac electromechanical changes induced by repeated social defeat stress that may predispose rats to cardiac dysfunction. Results indicated a larger cardiac miR-34a expression after repeated social defeat stress compared to a control condition. This molecular modification was associated with increased vulnerability to pharmacologically induced arrhythmias and signs of systolic left ventricular dysfunction. Gene expression analysis identified clusters of differentially expressed genes in the heart of repeatedly stressed rats that are mainly associated with morphological and functional properties of the mitochondria and may be directly regulated by miR-34a. These results suggest the presence of an association between miR-34a overexpression and signs of adverse electromechanical remodeling in the heart of rats exposed to repeated social defeat stress, and point to compromised mitochondria efficiency as a potential mediator of this link. This rat model may provide a useful tool for investigating the causal relationship between miR-34a expression, mitochondrial (dys)function, and cardiac alterations under stressful conditions, which could have important implications in the context of stress-related cardiac disease. |
