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Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma

Although elevated intraocular pressure (IOP) and age are major risk factors for glaucoma, their effects on glaucoma pathogenesis remain unclear. This study examined the onset and progression of glaucomatous changes to ocular anatomy and physiology, structural and physiological brain integrity, and v...

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Autores principales: Yang, Xiao-Ling, van der Merwe, Yolandi, Sims, Jeffrey, Parra, Carlos, Ho, Leon C., Schuman, Joel S., Wollstein, Gadi, Lathrop, Kira L., Chan, Kevin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854610/
https://www.ncbi.nlm.nih.gov/pubmed/29545576
http://dx.doi.org/10.1038/s41598-018-22850-4
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author Yang, Xiao-Ling
van der Merwe, Yolandi
Sims, Jeffrey
Parra, Carlos
Ho, Leon C.
Schuman, Joel S.
Wollstein, Gadi
Lathrop, Kira L.
Chan, Kevin C.
author_facet Yang, Xiao-Ling
van der Merwe, Yolandi
Sims, Jeffrey
Parra, Carlos
Ho, Leon C.
Schuman, Joel S.
Wollstein, Gadi
Lathrop, Kira L.
Chan, Kevin C.
author_sort Yang, Xiao-Ling
collection PubMed
description Although elevated intraocular pressure (IOP) and age are major risk factors for glaucoma, their effects on glaucoma pathogenesis remain unclear. This study examined the onset and progression of glaucomatous changes to ocular anatomy and physiology, structural and physiological brain integrity, and visuomotor behavior in the DBA/2J mice via non-invasive tonometry, multi-parametric magnetic resonance imaging (MRI) and optokinetic assessments from 5 to 12 months of age. Using T2-weighted MRI, diffusion tensor MRI, and manganese-enhanced MRI, increasing IOP elevation at 9 and 12 months old coincided with anterior chamber deepening, altered fractional anisotropy and radial diffusivity of the optic nerve and optic tract, as well as reduced anterograde manganese transport along the visual pathway respectively in the DBA/2J mice. Vitreous body elongation and visuomotor function deterioration were observed until 9 months old, whereas axial diffusivity only decreased at 12 months old in diffusion tensor MRI. Under the same experimental settings, C57BL/6J mice only showed modest age-related changes. Taken together, these results indicate that the anterior and posterior visual pathways of the DBA/2J mice exhibit differential susceptibility to glaucomatous neurodegeneration observable by in vivo multi-modal examinations.
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spelling pubmed-58546102018-03-22 Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma Yang, Xiao-Ling van der Merwe, Yolandi Sims, Jeffrey Parra, Carlos Ho, Leon C. Schuman, Joel S. Wollstein, Gadi Lathrop, Kira L. Chan, Kevin C. Sci Rep Article Although elevated intraocular pressure (IOP) and age are major risk factors for glaucoma, their effects on glaucoma pathogenesis remain unclear. This study examined the onset and progression of glaucomatous changes to ocular anatomy and physiology, structural and physiological brain integrity, and visuomotor behavior in the DBA/2J mice via non-invasive tonometry, multi-parametric magnetic resonance imaging (MRI) and optokinetic assessments from 5 to 12 months of age. Using T2-weighted MRI, diffusion tensor MRI, and manganese-enhanced MRI, increasing IOP elevation at 9 and 12 months old coincided with anterior chamber deepening, altered fractional anisotropy and radial diffusivity of the optic nerve and optic tract, as well as reduced anterograde manganese transport along the visual pathway respectively in the DBA/2J mice. Vitreous body elongation and visuomotor function deterioration were observed until 9 months old, whereas axial diffusivity only decreased at 12 months old in diffusion tensor MRI. Under the same experimental settings, C57BL/6J mice only showed modest age-related changes. Taken together, these results indicate that the anterior and posterior visual pathways of the DBA/2J mice exhibit differential susceptibility to glaucomatous neurodegeneration observable by in vivo multi-modal examinations. Nature Publishing Group UK 2018-03-15 /pmc/articles/PMC5854610/ /pubmed/29545576 http://dx.doi.org/10.1038/s41598-018-22850-4 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
Yang, Xiao-Ling
van der Merwe, Yolandi
Sims, Jeffrey
Parra, Carlos
Ho, Leon C.
Schuman, Joel S.
Wollstein, Gadi
Lathrop, Kira L.
Chan, Kevin C.
Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title_full Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title_fullStr Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title_full_unstemmed Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title_short Age-related Changes in Eye, Brain and Visuomotor Behavior in the DBA/2J Mouse Model of Chronic Glaucoma
title_sort age-related changes in eye, brain and visuomotor behavior in the dba/2j mouse model of chronic glaucoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5854610/
https://www.ncbi.nlm.nih.gov/pubmed/29545576
http://dx.doi.org/10.1038/s41598-018-22850-4
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