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Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats

Age-related changes to the balance between the pressure inside the eye (intraocular pressure, IOP) and the pressure inside the brain (intracranial pressure, ICP) can modify the risk of glaucoma. In this study, we consider whether the optic nerve in older rat eyes is more susceptible to acute IOP and...

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Autores principales: Zhao, Da, Nguyen, Christine T. O., He, Zheng, Wong, Vickie H. Y., van Koeverden, Anna K., Vingrys, Algis J., Bui, Bang V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811482/
https://www.ncbi.nlm.nih.gov/pubmed/29440700
http://dx.doi.org/10.1038/s41598-018-21203-5
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author Zhao, Da
Nguyen, Christine T. O.
He, Zheng
Wong, Vickie H. Y.
van Koeverden, Anna K.
Vingrys, Algis J.
Bui, Bang V.
author_facet Zhao, Da
Nguyen, Christine T. O.
He, Zheng
Wong, Vickie H. Y.
van Koeverden, Anna K.
Vingrys, Algis J.
Bui, Bang V.
author_sort Zhao, Da
collection PubMed
description Age-related changes to the balance between the pressure inside the eye (intraocular pressure, IOP) and the pressure inside the brain (intracranial pressure, ICP) can modify the risk of glaucoma. In this study, we consider whether the optic nerve in older rat eyes is more susceptible to acute IOP and ICP modification. We systematically manipulate both ICP and IOP and quantify their effects on ganglion cell function (electroretinography, ERG), optic nerve structure (optical coherence tomography, OCT) and retinal blood flow (Doppler OCT). We show that ganglion cell function in older eyes was more susceptible to a higher optic nerve pressure difference (ONPD = IOP – ICP). This age-related susceptibility could not be explained by poorer blood flow with elevated ONPD. Rather, as ONPD increased the retinal nerve fibre layer showed greater compression, and the retinal surface showed less deformation in older eyes. Our data suggest that age-related changes to connective tissues in and around the rat optic nerve make it less flexible, which may result in greater strain on ganglion cell axons. This may account for greater functional susceptibility to higher optic nerve pressure differences in older rat eyes. Further studies in a species with a well-developed lamina cribrosa are needed to determine the clinical importance of these observations.
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spelling pubmed-58114822018-02-16 Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats Zhao, Da Nguyen, Christine T. O. He, Zheng Wong, Vickie H. Y. van Koeverden, Anna K. Vingrys, Algis J. Bui, Bang V. Sci Rep Article Age-related changes to the balance between the pressure inside the eye (intraocular pressure, IOP) and the pressure inside the brain (intracranial pressure, ICP) can modify the risk of glaucoma. In this study, we consider whether the optic nerve in older rat eyes is more susceptible to acute IOP and ICP modification. We systematically manipulate both ICP and IOP and quantify their effects on ganglion cell function (electroretinography, ERG), optic nerve structure (optical coherence tomography, OCT) and retinal blood flow (Doppler OCT). We show that ganglion cell function in older eyes was more susceptible to a higher optic nerve pressure difference (ONPD = IOP – ICP). This age-related susceptibility could not be explained by poorer blood flow with elevated ONPD. Rather, as ONPD increased the retinal nerve fibre layer showed greater compression, and the retinal surface showed less deformation in older eyes. Our data suggest that age-related changes to connective tissues in and around the rat optic nerve make it less flexible, which may result in greater strain on ganglion cell axons. This may account for greater functional susceptibility to higher optic nerve pressure differences in older rat eyes. Further studies in a species with a well-developed lamina cribrosa are needed to determine the clinical importance of these observations. Nature Publishing Group UK 2018-02-13 /pmc/articles/PMC5811482/ /pubmed/29440700 http://dx.doi.org/10.1038/s41598-018-21203-5 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhao, Da
Nguyen, Christine T. O.
He, Zheng
Wong, Vickie H. Y.
van Koeverden, Anna K.
Vingrys, Algis J.
Bui, Bang V.
Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title_full Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title_fullStr Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title_full_unstemmed Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title_short Age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
title_sort age-related changes in the response of retinal structure, function and blood flow to pressure modification in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811482/
https://www.ncbi.nlm.nih.gov/pubmed/29440700
http://dx.doi.org/10.1038/s41598-018-21203-5
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