Key result
Pregnancy-induced cardiac volume overload caused an initial passive deformation of the mitral valve, followed by a cell-mediated remodelling phase that restored homeostatic tissue-level behaviour.
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Valvular remodelling during volume overload is actively mediated by average MVIC deformations over weeks, suggesting serial and parallel additions of fibrillar material restore homeostatic stress.
Little is known about how valvular tissues grow and remodel in response to altered loading. In this work, we used the pregnancy state to represent a non-pathological cardiac volume overload that distends the mitral valve (MV), using both extant and new experimental data and a modified form of our MV structural constitutive model. We determined that there was an initial period of permanent set-like deformation where no remodelling occurs, followed by a remodelling phase that resulted in near-complete restoration of homeostatic tissue-level behaviour. In addition, we observed that changes in the underlying MV interstitial cell (MVIC) geometry closely paralleled the tissue-level remodelling events, undergoing an initial passive perturbation followed by a gradual recovery to the pre-pregnant state. Collectively, these results suggest that valvular remodelling is actively mediated by average MVIC deformations (i.e. not cycle to cycle, but over a period of weeks). Moreover, tissue-level remodelling is likely to be accomplished by serial and parallel additions of fibrillar material to restore the mean homeostatic fibre stress and MVIC geometries. This finding has significant implications in efforts to understand and predict MV growth and remodelling following such events as myocardial infarction and surgical repair, which also place the valve under altered loading conditions.
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Rego et al. (2016) studied Cardiac volume overload (pregnancy state). Pregnancy state (cardiac volume overload) vs. Pre-pregnant state was evaluated on Mitral valve leaflet remodelling and interstitial cell geometry changes. Pregnancy-induced cardiac volume overload caused an initial passive deformation of the mitral valve, followed by a cell-mediated remodelling phase that restored homeostatic tissue-level behaviour.
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