Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging

Callosal connections form elaborate patterns that bear close association with striate and extrastriate visual areas. Although it is known that retinal input is required for normal callosal development, there is little information regarding the period during which the retina is critically needed and...

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Main Authors: Jaime F. Olavarria, Andrew S. Bock, Lindsey A. Leigland, Christopher D. Kroenke
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2012/250196
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author Jaime F. Olavarria
Andrew S. Bock
Lindsey A. Leigland
Christopher D. Kroenke
author_facet Jaime F. Olavarria
Andrew S. Bock
Lindsey A. Leigland
Christopher D. Kroenke
author_sort Jaime F. Olavarria
collection DOAJ
description Callosal connections form elaborate patterns that bear close association with striate and extrastriate visual areas. Although it is known that retinal input is required for normal callosal development, there is little information regarding the period during which the retina is critically needed and whether this period correlates with the same developmental stage across species. Here we review the timing of this critical period, identified in rodents and ferrets by the effects that timed enucleations have on mature callosal connections, and compare it to other developmental milestones in these species. Subsequently, we compare these events to diffusion tensor imaging (DTI) measurements of water diffusion anisotropy within developing cerebral cortex. We observed that the relationship between the timing of the critical period and the DTI-characterized developmental trajectory is strikingly similar in rodents and ferrets, which opens the possibility of using cortical DTI trajectories for predicting the critical period in species, such as humans, in which this period likely occurs prenatally. Last, we discuss the potential of utilizing DTI to distinguish normal from abnormal cerebral cortical development, both within the context of aberrant connectivity induced by early retinal deafferentation, and more generally as a potential tool for detecting abnormalities associated with neurodevelopmental disorders.
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spelling doaj-art-12e681c9dd224cb1b2bbeb9013bfb5bd2025-02-03T01:23:27ZengWileyNeural Plasticity2090-59041687-54432012-01-01201210.1155/2012/250196250196Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor ImagingJaime F. Olavarria0Andrew S. Bock1Lindsey A. Leigland2Christopher D. Kroenke3Department of Psychology, Behavioral Neuroscience Program, University of Washington, Box 351525, Seattle, WA 98195-1525, USADepartment of Psychology, Behavioral Neuroscience Program, University of Washington, Box 351525, Seattle, WA 98195-1525, USAAdvanced Imaging Research Center and Department of Behavioral Neuroscience, Oregon Health and Science University, Mail Code L457, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USAAdvanced Imaging Research Center and Department of Behavioral Neuroscience, Oregon Health and Science University, Mail Code L457, 3181 SW Sam Jackson Park Road, Portland, OR 97239, USACallosal connections form elaborate patterns that bear close association with striate and extrastriate visual areas. Although it is known that retinal input is required for normal callosal development, there is little information regarding the period during which the retina is critically needed and whether this period correlates with the same developmental stage across species. Here we review the timing of this critical period, identified in rodents and ferrets by the effects that timed enucleations have on mature callosal connections, and compare it to other developmental milestones in these species. Subsequently, we compare these events to diffusion tensor imaging (DTI) measurements of water diffusion anisotropy within developing cerebral cortex. We observed that the relationship between the timing of the critical period and the DTI-characterized developmental trajectory is strikingly similar in rodents and ferrets, which opens the possibility of using cortical DTI trajectories for predicting the critical period in species, such as humans, in which this period likely occurs prenatally. Last, we discuss the potential of utilizing DTI to distinguish normal from abnormal cerebral cortical development, both within the context of aberrant connectivity induced by early retinal deafferentation, and more generally as a potential tool for detecting abnormalities associated with neurodevelopmental disorders.http://dx.doi.org/10.1155/2012/250196
spellingShingle Jaime F. Olavarria
Andrew S. Bock
Lindsey A. Leigland
Christopher D. Kroenke
Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
Neural Plasticity
title Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
title_full Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
title_fullStr Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
title_full_unstemmed Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
title_short Deafferentation-Induced Plasticity of Visual Callosal Connections: Predicting Critical Periods and Analyzing Cortical Abnormalities Using Diffusion Tensor Imaging
title_sort deafferentation induced plasticity of visual callosal connections predicting critical periods and analyzing cortical abnormalities using diffusion tensor imaging
url http://dx.doi.org/10.1155/2012/250196
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