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Correlation of spectral domain optical coherence tomography with histology and electron microscopy in the porcine retina. | LitMetric

Correlation of spectral domain optical coherence tomography with histology and electron microscopy in the porcine retina.

Exp Eye Res

Department of Medical Physiology, Texas A&M University Health Science Center, Temple, TX, USA; Department of Ophthalmology and Ophthalmic Vascular Research Program, Scott & White Eye Institute, Temple, TX, USA. Electronic address:

Published: December 2018

Spectral domain optical coherence tomography (SD-OCT) is used as a non-invasive tool for retinal morphological assessment in vivo. Information on the correlation of SD-OCT with retinal histology in the porcine retina, a model resembling the human retina, is limited. Herein, we correlated the hypo- and hyper-reflective bands on SD-OCT with histology of the lamellar architecture and cellular constituents of the porcine retina. SD-OCT images were acquired with the Heidelberg Spectralis HRA + OCT. Histological analysis was performed using epoxy resin embedded tissue and transmission electron microscopy. Photomicrographs from the histologic sections were linearly scaled to correct for tissue shrinkage and correlated with SD-OCT images. SD-OCT images correlated well with histomorphometric data. A hyper-reflective band in the mid-to-outer inner nuclear layer correlated with the presence of abundant mitochondria in horizontal cell processes and adjacent bipolar cells. A concentration of cone nuclei corresponded to a relative hypo-reflective band in the outer portion of the outer nuclear layer. The presence of 3 hyper-reflective bands in the outer retina corresponded to: 1) the external limiting membrane; 2) the cone and rod ellipsoid zones; and 3) the interdigitation zone of photoreceptor outer segments/retinal pigment epithelium (RPE) apical cell processes and the RPE. These correlative and normative SD-OCT data may be employed to characterize and assess the in vivo histologic changes in retinal vascular and degenerative diseases and the responses to novel therapeutic interventions in this large animal model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348113PMC
http://dx.doi.org/10.1016/j.exer.2018.08.003DOI Listing

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