Key result
Mild social defeat stress in mice induces cardiac fibrosis and increases plasma p-cresyl metabolites.
Why the study?
Psychosocial stress increases the risk of cardiovascular diseases, but its effects on systemic histopathology and gut-derived putrefactive metabolites remain to be observed.
Mild cardiac fibrosis occurs equally in sCSDS and control mice; hypothesis-generating and should not yet inform clinical practice.
Psychosocial stress precipitates mental illnesses, such as depression, and increases the risk of other health problems, including cardiovascular diseases. In this study, we observed the effects of psychosocial stress on the histopathological features of systemic organs and tissues in a mouse psychosocial stress model, namely the subchronic and mild social defeat stress (sCSDS) model. There were several pathological findings in the tissues of both sCSDS and control mice. Mild fibrosis of the heart was observed in sCSDS mice but not in control mice. Extramedullary hematopoiesis in the spleen and hemorrhage in the lungs were observed in both the control and sCSDS mice. Focal necrosis of the liver was seen only in control mice. Furthermore, putrefactive substances in the blood plasma were analyzed because these metabolites originating from intestinal fermentation might be linked to heart fibrosis. Among them, plasma p-cresyl glucuronide and p-cresyl sulfate concentrations significantly increased owing to subchronic social defeat stress, which might influence cardiac fibrosis in sCSDS mice. In conclusion, several pathological features such as increased cardiac fibrosis and elevated plasma putrefactive substances were found in sCSDS mice. Thus, sCSDS mice are a potential model for elucidating the pathophysiology of psychosocial stress and heart failure.
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Toyoda et al. (2023) studied Psychosocial stress. Subchronic and mild social defeat stress (sCSDS) vs. Control mice was evaluated on Cardiac fibrosis and plasma putrefactive metabolite concentrations. Subchronic and mild social defeat stress in male mice induced mild cardiac fibrosis and significantly increased plasma p-cresyl glucuronide and p-cresyl sulfate concentrations.
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