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Published on: August 30, 2022
Spontaneous Degenerative Aortic Valve Disease in New Zealand Obese Mice
Christiane Ott1,2, Kathleen Pappritz2,3, Niklas Hegemann2,4
1Department of Molecular Toxicology German Institute of Human Nutrition Potsdam-Rehbruecke Germany.
Abstract:
Background Degenerative aortic valve (AoV) disease and resulting aortic stenosis are major clinical health problems. Murine models of valve disease are rare, resulting in a translational knowledge gap on underlying mechanisms, functional consequences, and potential therapies. Naïve New Zealand obese (NZO) mice were recently found to have a dramatic decline of left ventricular (LV) function at early age. Therefore, we aimed to identify the underlying cause of reduced LV function in NZO mice. Methods and Results Cardiac function and pulmonary hemodynamics of NZO and age-matched C57BL/6J mice were monitored by serial echocardiographic examinations. AoVs in NZO mice demonstrated extensive thickening, asymmetric aortic leaflet formation, and cartilaginous transformation of the valvular stroma. Doppler echocardiography of the aorta revealed increased peak velocity profiles, holodiastolic flow reversal, and dilatation of the ascending aorta, consistent with aortic stenosis and regurgitation. Compensated LV hypertrophy deteriorated to decompensated LV failure and remodeling, as indicated by increased LV mass, interstitial fibrosis, and inflammatory cell infiltration. Elevated LV pressures in NZO mice were associated with lung congestion and cor pulmonale, evident as right ventricular dilatation, decreased right ventricular function, and increased mean right ventricular systolic pressure, indicative for the development of pulmonary hypertension and ultimately right ventricular failure. Conclusions NZO mice demonstrate as a novel murine model to spontaneously develop degenerative AoV disease, aortic stenosis, and the associated end organ damages of both ventricles and the lung. Closely mimicking the clinical scenario of degenerative AoV disease, the model may facilitate a better mechanistic understanding and testing of novel treatment strategies in degenerative AoV disease.
Insights
Naïve New Zealand obese mice spontaneously develop aortic valve disease and stenosis, leading to heart and lung failure. This new model mimics human degenerative aortic valve disease, aiding research into mechanisms and therapies.
Area of Science:
- Cardiovascular Biology
- Translational Medicine
- Murine Models
Background:
- Degenerative aortic valve (AoV) disease and aortic stenosis are significant clinical challenges.
- A lack of suitable murine models hinders understanding of AoV disease mechanisms and therapeutic development.
- Naïve New Zealand obese (NZO) mice exhibit early-onset left ventricular (LV) dysfunction.
Purpose of the Study:
- To investigate the cause of reduced LV function in NZO mice.
- To characterize the spontaneous development of AoV disease in NZO mice.
- To establish NZO mice as a novel model for degenerative AoV disease research.
Main Methods:
- Serial echocardiography to assess cardiac function and pulmonary hemodynamics in NZO and C57BL/6J mice.
- Detailed analysis of aortic valve morphology and aortic flow dynamics.
- Histopathological examination for LV remodeling, fibrosis, and inflammation.
Main Results:
- NZO mice exhibited thickened AoVs with abnormal leaflet formation and cartilaginous changes.
- Doppler echocardiography revealed aortic stenosis, regurgitation, and ascending aorta dilatation.
- Progressive LV hypertrophy, decompensation, fibrosis, inflammation, and pulmonary hypertension with right ventricular failure were observed.
Conclusions:
- NZO mice spontaneously develop degenerative AoV disease, mimicking human aortic stenosis.
- This model exhibits significant end-organ damage in both ventricles and the lungs.
- The NZO mouse model offers a valuable platform for mechanistic studies and testing therapies for degenerative AoV disease.

