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Updated: Jul 4, 2026

Quantification of Atherosclerosis in Mice
06:59

Quantification of Atherosclerosis in Mice

Published on: June 12, 2019

A practical approach to using mice in atherosclerosis research.

Stewart C Whitman1

  • 1The University of Ottawa Heart Institute, University of Ottawa, Ottawa, Ontario, Canada. swhitman@ottawaheart.ca

The Clinical Biochemist. Reviews
|June 3, 2008
PubMed
Summary

This review guides researchers on using mouse models for atherosclerosis studies. It details lesion types, formation timing, and analysis methods for apolipoprotein E deficient and LDL receptor deficient mice.

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Area of Science:

  • Cardiovascular Research
  • Animal Models
  • Atherosclerosis Research

Background:

  • Mice are widely used animal models for studying atherosclerosis.
  • Apolipoprotein E (apoE) deficient and low-density lipoprotein (LDL) receptor deficient mice are common models.
  • Researchers new to these models require guidance on experimental design and analysis.

Purpose of the Study:

  • To provide a practical guide for researchers using mouse models of atherosclerosis.
  • To detail the characteristics of lesions in apoE and LDL receptor deficient mice.
  • To outline methods for analyzing atherosclerotic lesions in these models.

Main Methods:

  • Review of current literature on mouse models of atherosclerosis.
  • Description of lesion types and their expected formation timelines.

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Last Updated: Jul 4, 2026

Quantification of Atherosclerosis in Mice
06:59

Quantification of Atherosclerosis in Mice

Published on: June 12, 2019

Isolation and Analysis of Aortic Arch and Root Lesions in an Atherosclerotic Mouse Model
07:49

Isolation and Analysis of Aortic Arch and Root Lesions in an Atherosclerotic Mouse Model

Published on: February 14, 2025

  • Summary of biochemical and morphometric analysis techniques.
  • Main Results:

    • ApoE and LDL receptor deficient mice develop distinct atherosclerotic lesion profiles.
    • Specific age ranges are associated with the development of different lesion types.
    • Standardized methods exist for lesion quantification and characterization.

    Conclusions:

    • Effective use of mouse models requires understanding lesion progression and analysis techniques.
    • ApoE and LDL receptor deficient mice offer valuable insights into atherosclerosis.
    • This review serves as a foundational resource for planning atherosclerosis experiments in mice.