Female obese ZSF1 rats developed diastolic dysfunction, cardiac hypertrophy, and fibrosis comparable in severity to obese males, establishing them as a relevant model for HFpEF.
Female obese ZSF1 rats develop diastolic dysfunction and cardiac remodeling similar to males, establishing them as a suitable preclinical model for HFpEF with multiple comorbidities.
Heart failure with a preserved ejection fraction (HFpEF) is associated with multiple comorbidities, such as old age, hypertension, type 2 diabetes and obesity and is more prevalent in females. Although the male obese ZSF1 rat has been proposed as a suitable model to study the development of diastolic dysfunction and early HFpEF, studies in female animals have not been performed yet. Therefore, we aimed to characterize the cardiac phenotype in female obese ZSF1 rats and their lean counterparts. Additionally, we aimed to investigate whether differences exist in disease progression in obese male and female ZSF1 rats. Therefore, male and female ZSF1 rats, lean as well as obese (N = 6-9/subgroup), were used. Every two weeks, from 12 to 26 weeks of age, systolic blood pressure and echocardiographic measurements were performed, and venous blood was sampled. Female obese ZSF1 rats, as compared to female lean ZSF1 rats, developed diastolic dysfunction with cardiac hypertrophy and fibrosis in the presence of severe dyslipidemia, increased plasma growth differentiation factor 15 and mild hypertension, and preservation of systolic function. Although obese female ZSF1 rats did not develop hyperglycemia, their diastolic dysfunction was as severe as in the obese males. Taken together, the results from the present study suggest that the female obese ZSF1 rat is a relevant animal model for HFpEF with multiple comorbidities, suitable for investigating novel therapeutic interventions.
Nguyen et al. (Wed,) conducted a other in Heart failure with preserved ejection fraction (HFpEF) (n=31). Obesity (obese ZSF1 phenotype) vs. Lean ZSF1 rats was evaluated on Diastolic dysfunction and cardiac remodeling. Female obese ZSF1 rats developed diastolic dysfunction, cardiac hypertrophy, and fibrosis comparable in severity to obese males, establishing them as a relevant model for HFpEF.
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