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Microvasc Res ; 132: 104055, 2020 11.
Article in English | MEDLINE | ID: mdl-32777249

ABSTRACT

Optical coherence tomography angiography (OCT-A) allows in vivo, non-invasive, functional imaging of retinal perfusion. The purpose of this study was to determine the reliability of OCT-A in visualizing the complete retinal vasculature by comparing in vivo OCT-A images to matched ex vivo retinal tissue in mice. Adult female C57BL/6 mice were imaged to obtain OCT-A images of the superficial vascular complex, intermediate capillary plexus and deep capillary plexus. Z-stack fluorescence images of whole-mounted retinas, labeled for vascular endothelial cells by anti-isolectin immunohistochemistry and FITC-dextran perfusion, were generated. The OCT-A and fluorescence images were manually colocalized and vessel length measured for each of the techniques. Mean vessel length among all plexuses showed less than 13% difference between OCT-A and lectin immunohistochemistry and less than 4% difference between OCT-A and FITC-dextran perfusion. The strength of the correlation between OCT-A and lectin immunohistochemistry ranged from 0.46-0.95, while that between OCT-A and FITC-perfusion ranged from 0.67-0.88. OCT-A visualized retinal vasculature in vivo to a similar extent in matched ex vivo histology images. Our results show that OCT-A is a reliable method for acquiring in vivo images of retinal perfusion in mice, with the ability to differentiate each vascular plexus.


Subject(s)
Angiography , Capillaries/cytology , Capillaries/diagnostic imaging , Endothelial Cells/cytology , Microcirculation , Microscopy, Fluorescence , Perfusion Imaging , Retinal Vessels/cytology , Retinal Vessels/diagnostic imaging , Tomography, Optical Coherence , Animals , Female , Mice, Inbred C57BL , Predictive Value of Tests , Regional Blood Flow , Reproducibility of Results
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