Key result
Voluntary wheel running mitigates diet-induced postpartum hemodynamic dysfunction by improving LV mechanics in mice.
Why the study?
Pregnancy and lactation increase cardiovascular demand and may unmask postpartum cardiac vulnerability under metabolic stress, but whether HFHS diet induces postpartum hemodynamic dysfunction with preserved EF and whether voluntary wheel running mitigates it is unclear.
Does voluntary wheel running mitigate postpartum hemodynamic dysfunction in female mice exposed to a high-fat/high-sucrose diet during pregnancy and lactation?
Does voluntary wheel running mitigate postpartum hemodynamic dysfunction in female mice exposed to a high-fat/high-sucrose diet during pregnancy and lactation?
Voluntary wheel running during pregnancy and lactation mitigates postpartum hemodynamic dysfunction and impaired ventricular-arterial coupling induced by a high-fat/high-sucrose diet in a murine model.
Answers are grounded in this paper and cite their sources.
Should not yet change clinical practice; hypothesis-generating for peripartum exercise to counter diet-induced hemodynamic dysfunction in women.
Pregnancy and lactation increase cardiovascular demand and may unmask postpartum cardiac vulnerability under metabolic stress. We tested whether exposure to a high-fat/high-sucrose (HFHS) diet from pre-mating through lactation induces postpartum hemodynamic dysfunction with preserved ejection fraction (EF) and whether voluntary wheel running mitigates these alterations. Virgin C57BL/6J female mice were assigned to control sedentary (CS), HFHS sedentary (HS), or HFHS with voluntary wheel running (HE) across the reproductive window. Left ventricular (LV) pressure–volume (P–V) analysis was performed 6–9 days after weaning at baseline and during dobutamine challenge to assess β-adrenergic reserve. Despite preserved EF, HS dams exhibited reduced end-diastolic volume (EDV) and impaired forward performance (lower stroke volume [SV], cardiac output [CO], and stroke work [SW]) accompanied by higher filling pressure, increased diastolic stiffness (end-diastolic elastance, E ed), impaired ventricular–arterial coupling (E es/E a), and reduced load-independent contractility (end-systolic elastance [E es]). Dobutamine increased chronotropic and inotropic indices across groups; however, HS remained lower than CS during dobutamine for SV and E es, indicating limited capacity to augment performance under stress. In contrast, wheel running improved intrinsic contractility and maintained E es/E a at rest and during dobutamine without differences in body or heart weight. These findings indicate that HFHS exposure across pregnancy and lactation is associated with postpartum hemodynamic dysfunction characterized by preserved EF with impaired filling, increased diastolic stiffness, and reduced reserve; voluntary wheel running across this window mitigates key abnormalities in systolic mechanics and ventricular–arterial coupling.
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Chung et al. (2026) studied this question. Voluntary wheel running during pregnancy and lactation mitigates diet-induced postpartum hemodynamic dysfunction by improving systolic mechanics and ventricular-arterial coupling in mice.
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