Evidence of extensive atherosclerosis, coronary artery disease and myocardial infarction in the ApoE-/-:Ins2+/Akita mouse fed a western diet

Atherosclerosis. 2018 Aug:275:88-96. doi: 10.1016/j.atherosclerosis.2018.05.044. Epub 2018 May 23.

Abstract

Background and aims: Diabetic patients with no history of cardiac infarction have a prevalence of coronary atherosclerosis and a risk of heart attack equivalent to euglycemic patients who have coronary atherosclerosis and have suffered a prior myocardial infarction. Although several murine models of diabetes have been established, none of these show indications of cardiac events. In an attempt to establish a diabetic mouse model with coronary atherosclerosis and myocardial injury, we have fed hyperglycemic ApoE-/-:Ins2+/Akita mice a western diet to enhance the dyslipidemic phenotype.

Methods: Five-week-old ApoE-/-:Ins2+/Akita mice and ApoE-/- controls were fed a diet, 0.15% cholesterol and 21% anhydrous milk lipids, until 25 weeks of age. Changes in lifespan, clinical and metabolic parameters were evaluated as well as atherosclerosis and heart injury.

Results: In comparison to male ApoE-/-, male ApoE-/-:Ins2+/Akita mice presented with chronic hyperglycemia (30.8 ± 1.2 mM vs. 9.3 ± 0.5 mM) accompanied by extremely high levels of total plasma cholesterol (49.3 ± 6.3 mM vs. 30.1 ± 1.5 mM) and triglycerides (11.6 ± 1.7 mM vs. 2.36 ± 0.18 mM). These mice have atherosclerosis at multiple vascular sites, including aortic sinus, ascending and descending aorta, brachiocephalic artery and coronary arteries. In addition, myocardial infarcts and a significant reduction of the lifespan (close to 20% of survival vs. other groups) were observed. Distinctively, both strains of female mice presented a parallel increase in plasma lipids, atherosclerosis, and no effects on mortality.

Conclusions: We have established a diabetic mouse model, the western-diet-fed male ApoE-/-:Ins2+/Akita mouse, with profound cardiovascular disease involving extensive atherosclerosis, coronary artery disease and myocardial infarct resulting in shortened lifespan.

Keywords: Atherosclerosis; Coronary artery disease; Diabetes mellitus; Dyslipidemia; Ischemia; Myocardial infarction.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / blood
  • Atherosclerosis / etiology*
  • Atherosclerosis / genetics
  • Atherosclerosis / pathology
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Coronary Artery Disease / blood
  • Coronary Artery Disease / etiology*
  • Coronary Artery Disease / genetics
  • Coronary Artery Disease / pathology
  • Coronary Vessels / metabolism
  • Coronary Vessels / pathology*
  • Diabetes Mellitus* / blood
  • Diabetes Mellitus* / genetics
  • Diet, Western*
  • Disease Models, Animal
  • Dyslipidemias / blood
  • Dyslipidemias / etiology*
  • Dyslipidemias / genetics
  • Female
  • Insulin / genetics
  • Lipids / blood
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout, ApoE
  • Myocardial Infarction / blood
  • Myocardial Infarction / etiology*
  • Myocardial Infarction / genetics
  • Myocardial Infarction / pathology
  • Myocardium / metabolism
  • Myocardium / pathology*
  • Plaque, Atherosclerotic*
  • Prognosis
  • Sex Factors
  • Time Factors

Substances

  • Biomarkers
  • Blood Glucose
  • Ins2 protein, mouse
  • Insulin
  • Lipids

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