Hyperlipidemia and atherosclerotic lesion development in Ldlr-deficient mice on a long-term high-fat diet

PLoS One. 2012;7(4):e35835. doi: 10.1371/journal.pone.0035835. Epub 2012 Apr 25.

Abstract

Background: Mice deficient in the LDL receptor (Ldlr(-/-) mice) have been widely used as a model to mimic human atherosclerosis. However, the time-course of atherosclerotic lesion development and distribution of lesions at specific time-points are yet to be established. The current study sought to determine the progression and distribution of lesions in Ldlr(-/-) mice.

Methodology/principal findings: Ldlr-deficient mice fed regular chow or a high-fat (HF) diet for 0.5 to 12 months were analyzed for atherosclerotic lesions with en face and cross-sectional imaging. Mice displayed significant individual differences in lesion development when fed a chow diet, whereas those on a HF diet developed lesions in a time-dependent and site-selective manner. Specifically, mice subjected to the HF diet showed slight atherosclerotic lesions distributed exclusively in the aortic roots or innominate artery before 3 months. Lesions extended to the thoracic aorta at 6 months and abdominal aorta at 9 months. Cross-sectional analysis revealed the presence of advanced lesions in the aortic sinus after 3 months in the group on the HF diet and in the innominate artery at 6 to 9 months. The HF diet additionally resulted in increased total cholesterol, LDL, glucose, and HBA1c levels, along with the complication of obesity.

Conclusions/significance: Ldlr-deficient mice on the HF diet tend to develop site-selective and size-specific atherosclerotic lesions over time. The current study should provide information on diet induction or drug intervention times and facilitate estimation of the appropriate locations of atherosclerotic lesions in Ldlr(-/-) mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta, Thoracic / pathology*
  • Atherosclerosis / blood
  • Atherosclerosis / etiology
  • Atherosclerosis / pathology*
  • Blood Glucose / analysis
  • Brachiocephalic Trunk / pathology*
  • Cholesterol / blood
  • Diet, High-Fat / adverse effects*
  • Disease Progression
  • Glycated Hemoglobin / analysis
  • Humans
  • Hyperlipidemias / blood
  • Hyperlipidemias / etiology
  • Hyperlipidemias / pathology*
  • Lipoproteins, LDL / blood
  • Male
  • Mice
  • Mice, Knockout
  • Obesity / blood
  • Obesity / etiology
  • Obesity / pathology*
  • Receptors, LDL / deficiency*
  • Receptors, LDL / genetics
  • Time
  • Triglycerides / blood

Substances

  • Blood Glucose
  • Glycated Hemoglobin A
  • Lipoproteins, LDL
  • Receptors, LDL
  • Triglycerides
  • Cholesterol