April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Evaluation of AO-OCT and pv-OCT for detailed study of blood flow in mouse retinal capillaries and vessels
Author Affiliations & Notes
  • Azhar Zam
    UC Davis Eye-Pod, Dept. of Cell Biology and Human Anatomy, University of California Davis, Davis, CA
  • Pengfei Zhang
    UC Davis Eye-Pod, Dept. of Cell Biology and Human Anatomy, University of California Davis, Davis, CA
  • Yifan Jian
    BORG, School of Engineering Science, Simon Fraser University, Burnaby, BC, Canada
  • Marinko V Sarunic
    BORG, School of Engineering Science, Simon Fraser University, Burnaby, BC, Canada
  • Edward N Pugh
    UC Davis Eye-Pod, Dept. of Cell Biology and Human Anatomy, University of California Davis, Davis, CA
    Dept. of Physiology, University of California Davis, Davis, CA
  • Robert J Zawadzki
    UC Davis Eye-Pod, Dept. of Cell Biology and Human Anatomy, University of California Davis, Davis, CA
    VSRI, Dept. of Ophthalmology & Vision Science, University of California Davis, Davis, CA
  • Footnotes
    Commercial Relationships Azhar Zam, None; Pengfei Zhang, None; Yifan Jian, None; Marinko Sarunic, None; Edward Pugh, None; Robert Zawadzki, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 2090. doi:
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      Azhar Zam, Pengfei Zhang, Yifan Jian, Marinko V Sarunic, Edward N Pugh, Robert J Zawadzki; Evaluation of AO-OCT and pv-OCT for detailed study of blood flow in mouse retinal capillaries and vessels. Invest. Ophthalmol. Vis. Sci. 2014;55(13):2090.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: To evaluate feasibility of Adaptive Optics - Optical Coherence Tomography (AO-OCT) and phase variance optical coherence tomography (pv-OCT) for non-invasive and label-free visualization and quantification of retinal and choroidal blood flow in mice in-vivo.

Methods: Two high resolution retinal imaging modalities AO-OCT and pv-OCT have been used to investigate retinal vasculature in mice. Both systems use the same high-speed acquisition Fourier-Domain OCT (FD-OCT) engine (132nm @ 855 nm broadband light source (Superlum) and CMOS camera (Basler) operating at 125,000 A-scan/s). The AO-OCT system uses Adaptive Optics to achieve improved lateral resolution while pv-OCT allows visualization of capillary bed morphology through calculation of the variance of local contrast between consecutive images. Several pigmented Wild Type (c57BL/6) and albino (BALB/cJ) mice, both strains from Jackson Laboratory, have been used as the imaging targets. During the imaging, mice were anesthetized with 2-3% inhalational isoflurane anesthetic. Pupils were dilated and cyclopleged with Tropicamide and Phenylephrine.

Results: The two techniques offered complementary views of mouse retinal vasculature. pv-OCT offered fast mapping of capillary bed morphology while speckle tracking in the AO-OCT volumes allowed quantitative evaluation of flow speed within capillaries. Application of pv-OCT allowed for label- free mapping of retinal microvasculature that could be later used as reference for imaging areas of interest with AO-OCT. The absence of pigmentation in the albino mice resulted in much improved visualization of the choroidal vasculature.

Conclusions: Application of two distinct but related OCT imaging modalities enables a more comprehensive study and evaluation of retinal and choroidal vasculature. As evaluation of retinal and choroidal vasculature in vivo with standard Fluorescein Angiography is impractical due to contrast degradation by scleral scattering, the application of OCT based vasculature imaging methods provides a useful alternative for detailed study of the choroidal vasculature morphology and flow of albino strains.

Keywords: 552 imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • 688 retina • 452 choroid  
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