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Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging

During aging, human response times (RTs) to unisensory and crossmodal stimuli decrease. However, the elderly benefit more from crossmodal stimulus representations than younger people. The underlying short-latency multisensory integration process is mediated by direct crossmodal connections at the le...

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Autores principales: Henschke, Julia U., Ohl, Frank W., Budinger, Eike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840148/
https://www.ncbi.nlm.nih.gov/pubmed/29551970
http://dx.doi.org/10.3389/fnagi.2018.00052
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author Henschke, Julia U.
Ohl, Frank W.
Budinger, Eike
author_facet Henschke, Julia U.
Ohl, Frank W.
Budinger, Eike
author_sort Henschke, Julia U.
collection PubMed
description During aging, human response times (RTs) to unisensory and crossmodal stimuli decrease. However, the elderly benefit more from crossmodal stimulus representations than younger people. The underlying short-latency multisensory integration process is mediated by direct crossmodal connections at the level of primary sensory cortices. We investigate the age-related changes of these connections using a rodent model (Mongolian gerbil), retrograde tracer injections into the primary auditory (A1), somatosensory (S1), and visual cortex (V1), and immunohistochemistry for markers of apoptosis (Caspase-3), axonal plasticity (Growth associated protein 43, GAP 43), and a calcium-binding protein (Parvalbumin, PV). In adult animals, primary sensory cortices receive a substantial number of direct thalamic inputs from nuclei of their matched, but also from nuclei of non-matched sensory modalities. There are also direct intracortical connections among primary sensory cortices and connections with secondary sensory cortices of other modalities. In very old animals, the crossmodal connections strongly decrease in number or vanish entirely. This is likely due to a retraction of the projection neuron axonal branches rather than ongoing programmed cell death. The loss of crossmodal connections is also accompanied by changes in anatomical correlates of inhibition and excitation in the sensory thalamus and cortex. Together, the loss and restructuring of crossmodal connections during aging suggest a shift of multisensory processing from primary cortices towards other sensory brain areas in elderly individuals.
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spelling pubmed-58401482018-03-16 Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging Henschke, Julia U. Ohl, Frank W. Budinger, Eike Front Aging Neurosci Neuroscience During aging, human response times (RTs) to unisensory and crossmodal stimuli decrease. However, the elderly benefit more from crossmodal stimulus representations than younger people. The underlying short-latency multisensory integration process is mediated by direct crossmodal connections at the level of primary sensory cortices. We investigate the age-related changes of these connections using a rodent model (Mongolian gerbil), retrograde tracer injections into the primary auditory (A1), somatosensory (S1), and visual cortex (V1), and immunohistochemistry for markers of apoptosis (Caspase-3), axonal plasticity (Growth associated protein 43, GAP 43), and a calcium-binding protein (Parvalbumin, PV). In adult animals, primary sensory cortices receive a substantial number of direct thalamic inputs from nuclei of their matched, but also from nuclei of non-matched sensory modalities. There are also direct intracortical connections among primary sensory cortices and connections with secondary sensory cortices of other modalities. In very old animals, the crossmodal connections strongly decrease in number or vanish entirely. This is likely due to a retraction of the projection neuron axonal branches rather than ongoing programmed cell death. The loss of crossmodal connections is also accompanied by changes in anatomical correlates of inhibition and excitation in the sensory thalamus and cortex. Together, the loss and restructuring of crossmodal connections during aging suggest a shift of multisensory processing from primary cortices towards other sensory brain areas in elderly individuals. Frontiers Media S.A. 2018-03-02 /pmc/articles/PMC5840148/ /pubmed/29551970 http://dx.doi.org/10.3389/fnagi.2018.00052 Text en Copyright © 2018 Henschke, Ohl and Budinger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Henschke, Julia U.
Ohl, Frank W.
Budinger, Eike
Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title_full Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title_fullStr Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title_full_unstemmed Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title_short Crossmodal Connections of Primary Sensory Cortices Largely Vanish During Normal Aging
title_sort crossmodal connections of primary sensory cortices largely vanish during normal aging
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840148/
https://www.ncbi.nlm.nih.gov/pubmed/29551970
http://dx.doi.org/10.3389/fnagi.2018.00052
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