Impact of high-fat diet and vitamin D3 supplementation on aortic stenosis establishment in waved-2 epidermal growth factor receptor mutant mice

J Integr Med. 2019 Mar;17(2):107-114. doi: 10.1016/j.joim.2019.01.010. Epub 2019 Jan 30.

Abstract

Objective: The use of animal models of aortic stenosis (AS) remains essential to further elucidate its pathophysiology and to evaluate new therapeutic strategies. The waved-2 mouse AS model has been proposed; data have indicated that while aortic regurgitation (AR) is effectively induced, development of AS is rare. We aimed to evaluate the effect of high-fat diet (HFD) and vitamin D3 supplementation in this model.

Methods: HFD and subcutaneous vitamin D3 injections were initiated at the age of 6 weeks until the age of 6 (n = 16, 6-month treatment group) and 9 (n = 11, 9-month treatment group) months. Twelve waved-2 mice without supplementation were used as control. Echocardiography was performed at 3, 6 and 9 months. Blood serum analysis (calcium, 1,25(OH)2D3 and cholesterol), histology and immunohistochemistry (CD-31, CD-68 and osteopontin) were evaluated at the end of the experiment (6 or 9 months).

Results: Total cholesterol and 1,25(OH)2D3 were significantly increased relative to the control group. HFD and vitamin D3 supplementation did result in improvements to the model, since AS was only detected in 6 (15.3%) mice (2 in the 3 groups) and AR was developed in the remaining animals. Echocardiographic parameters, fibrosis, thickness, inflammation and valvular calcification, were not significantly different between the 6-month treatment and control groups. Similar results were also observed in the 9-month treatment group.

Conclusion: These results suggest that HFD and vitamin D3 supplementation have no effect in the waved-2 mouse model. This model essentially mimics AR and rarely AS. Further studies are needed to find a reliable animal model of AS.

Keywords: Aortic regurgitation; Aortic stenosis; Epidermal growth factor receptor; Experimental model; High-fat diet; Vitamin D(3).

MeSH terms

  • Animals
  • Aortic Valve Stenosis / drug therapy*
  • Aortic Valve Stenosis / etiology
  • Aortic Valve Stenosis / genetics
  • Aortic Valve Stenosis / metabolism
  • Cholecalciferol / administration & dosage*
  • Cholecalciferol / blood
  • Cholesterol / blood
  • Diet, High-Fat / adverse effects
  • Dietary Supplements / analysis
  • Disease Models, Animal
  • ErbB Receptors / genetics*
  • ErbB Receptors / metabolism
  • Female
  • Humans
  • Male
  • Mice

Substances

  • Cholecalciferol
  • Cholesterol
  • EGFR protein, mouse
  • ErbB Receptors