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Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes
PURPOSE: The purpose of this study was to test the hypothesis that the superficial, intermediate, and deep retinal vascular plexus show different responses to intraocular pressure (IOP) elevation. METHODS: Anesthetized adult Long Evans rats (n = 14) were imaged using optical coherence tomography ang...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325622/ https://www.ncbi.nlm.nih.gov/pubmed/32031574 http://dx.doi.org/10.1167/iovs.61.2.2 |
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author | Zhao, Da He, Zheng Wang, Lin Fortune, Brad Lim, Jeremiah K H. Wong, Vickie H Y. Nguyen, Christine T O. Bui, Bang V. |
author_facet | Zhao, Da He, Zheng Wang, Lin Fortune, Brad Lim, Jeremiah K H. Wong, Vickie H Y. Nguyen, Christine T O. Bui, Bang V. |
author_sort | Zhao, Da |
collection | PubMed |
description | PURPOSE: The purpose of this study was to test the hypothesis that the superficial, intermediate, and deep retinal vascular plexus show different responses to intraocular pressure (IOP) elevation. METHODS: Anesthetized adult Long Evans rats (n = 14) were imaged using optical coherence tomography angiography (OCTA; Spectralis) at baseline (IOP 10 mm Hg) and in follow-up mode to examine the vasculature during IOP elevation (10 to 110 mm Hg, 10 mm Hg steps, each step 3 minutes). A 20° × 10° field was imaged. Vessel density within a 2D projection image was determined (%) for the superficial vascular complex (SVC), intermediate capillary plexus (ICP), and deep capillary plexus (DCP). Comparisons were made between layers using 2-way repeated measures ANOVA (layer versus IOP) following normalization to baseline (% relative to 10 mm Hg). RESULTS: The three vascular layers responded differently to IOP elevation. For IOPs between 40 and 60 mm Hg, DCP and ICP capillaries were significantly more resistant to IOP elevation than those in the SVC. When IOP was elevated above 70 mm Hg, all layers showed reduced vessel density. IOP induced change in SVC vessel density closely followed reductions in thickness of the inner retinal layers (nerve fiber, ganglion cell, and inner plexiform layer). This close relationship between reductions in tissue thickness and vessel density was less apparent for the ICP and DCP. CONCLUSIONS: These data show that the intermediate and deep vascular plexus in the rat retina have a greater capacity for autoregulation against mild IOP elevation but are more affected at high IOP. |
format | Online Article Text |
id | pubmed-7325622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73256222020-07-07 Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes Zhao, Da He, Zheng Wang, Lin Fortune, Brad Lim, Jeremiah K H. Wong, Vickie H Y. Nguyen, Christine T O. Bui, Bang V. Invest Ophthalmol Vis Sci Glaucoma PURPOSE: The purpose of this study was to test the hypothesis that the superficial, intermediate, and deep retinal vascular plexus show different responses to intraocular pressure (IOP) elevation. METHODS: Anesthetized adult Long Evans rats (n = 14) were imaged using optical coherence tomography angiography (OCTA; Spectralis) at baseline (IOP 10 mm Hg) and in follow-up mode to examine the vasculature during IOP elevation (10 to 110 mm Hg, 10 mm Hg steps, each step 3 minutes). A 20° × 10° field was imaged. Vessel density within a 2D projection image was determined (%) for the superficial vascular complex (SVC), intermediate capillary plexus (ICP), and deep capillary plexus (DCP). Comparisons were made between layers using 2-way repeated measures ANOVA (layer versus IOP) following normalization to baseline (% relative to 10 mm Hg). RESULTS: The three vascular layers responded differently to IOP elevation. For IOPs between 40 and 60 mm Hg, DCP and ICP capillaries were significantly more resistant to IOP elevation than those in the SVC. When IOP was elevated above 70 mm Hg, all layers showed reduced vessel density. IOP induced change in SVC vessel density closely followed reductions in thickness of the inner retinal layers (nerve fiber, ganglion cell, and inner plexiform layer). This close relationship between reductions in tissue thickness and vessel density was less apparent for the ICP and DCP. CONCLUSIONS: These data show that the intermediate and deep vascular plexus in the rat retina have a greater capacity for autoregulation against mild IOP elevation but are more affected at high IOP. The Association for Research in Vision and Ophthalmology 2020-02-07 2020-02 /pmc/articles/PMC7325622/ /pubmed/32031574 http://dx.doi.org/10.1167/iovs.61.2.2 Text en Copyright 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Glaucoma Zhao, Da He, Zheng Wang, Lin Fortune, Brad Lim, Jeremiah K H. Wong, Vickie H Y. Nguyen, Christine T O. Bui, Bang V. Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title | Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title_full | Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title_fullStr | Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title_full_unstemmed | Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title_short | Response of the Trilaminar Retinal Vessel Network to Intraocular Pressure Elevation in Rat Eyes |
title_sort | response of the trilaminar retinal vessel network to intraocular pressure elevation in rat eyes |
topic | Glaucoma |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325622/ https://www.ncbi.nlm.nih.gov/pubmed/32031574 http://dx.doi.org/10.1167/iovs.61.2.2 |
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