In vivo imaging of murine vasodynamics analyzing different mouse strains by optical coherence tomography

Atheroscler Suppl. 2017 Nov:30:311-318. doi: 10.1016/j.atherosclerosissup.2017.05.023. Epub 2017 May 31.

Abstract

Background and aims: We tried to circumvent the limitations of standard organ chamber experiments using in vivo optical coherence tomography (OCT) to analyze the vascular function of small arteries in different mouse strains.

Methods: OCT images were acquired with a two-axis galvanometer scanner head. Time series (3 frames per second, 300 × 512 pixel per frame) of cross-sectional images were analyzed with image processing software measuring the time course of vessel lumen dynamics. Vascular function of murine saphenous artery of male C57BL/6 (wild-type) and hypercholesterolemic LDLR knockout (LDLR-/-) mice was analyzed at 6 weeks and after 14 weeks feeding a control or high-fat diet containing 21.2% butter fat and 2.1 mg/kg cholesterol. Vasoconstriction and vasodilation was analyzed by OCT in response to 80 mM K+ and 1 mM SNP.

Results: The OCT technique allowed determination of inner diameter, flow resistance, maximal velocity of diameter change and time to half-maximal diameter change in murine saphenous arteries of wild-type and LDLR-/- mice. LDLR-/- had impaired vasodilation and changes in vasodynamics after 14 weeks on control or high-fat diet, compared to wild-type mice. The diameter of the saphenous artery of LDLR-/- mice was reduced after vasoconstriction (38 ± 7 μm vs 12 ± 6 μm) and vasodilation (245 ± 8 μm vs 220 ± 10 μm) (P < 0.05 vs C57BL/6).

Conclusion: OCT was used as an innovative method to image vascular function of small arteries of wild-type and hypercholesterolemic LDLR-/- mice after high-fat diet. The method offers the ability to display differences in the vasodynamics at early stages of endothelial dysfunction in vivo.

Keywords: Atherosclerosis; Endothelial function; Hypercholesterolemia; Optical coherence tomography.

MeSH terms

  • Age Factors
  • Animals
  • Arteries / diagnostic imaging*
  • Arteries / metabolism
  • Arteries / physiopathology
  • Blood Flow Velocity
  • Diet, High-Fat
  • Disease Models, Animal
  • Genetic Predisposition to Disease
  • Hemodynamics*
  • Hypercholesterolemia / diagnostic imaging*
  • Hypercholesterolemia / genetics
  • Hypercholesterolemia / metabolism
  • Hypercholesterolemia / physiopathology
  • Image Processing, Computer-Assisted
  • Lower Extremity / blood supply*
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Receptors, LDL / deficiency
  • Receptors, LDL / genetics
  • Regional Blood Flow
  • Time Factors
  • Tomography, Optical Coherence*
  • Vascular Resistance
  • Vasoconstriction
  • Vasodilation

Substances

  • Receptors, LDL