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Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat
Acetylcholine is an important neurotransmitter for the regulation of visual attention, plasticity, and perceptual learning. It is released in the visual cortex predominantly by cholinergic projections from the basal forebrain, where stimulation may produce potentiation of visual processes. However,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890115/ https://www.ncbi.nlm.nih.gov/pubmed/29662442 http://dx.doi.org/10.3389/fncir.2018.00019 |
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author | Huppé-Gourgues, Frédéric Jegouic, Karim Vaucher, Elvire |
author_facet | Huppé-Gourgues, Frédéric Jegouic, Karim Vaucher, Elvire |
author_sort | Huppé-Gourgues, Frédéric |
collection | PubMed |
description | Acetylcholine is an important neurotransmitter for the regulation of visual attention, plasticity, and perceptual learning. It is released in the visual cortex predominantly by cholinergic projections from the basal forebrain, where stimulation may produce potentiation of visual processes. However, little is known about the fine organization of these corticopetal projections, such as whether basal forebrain neurons projecting to the primary and secondary visual cortical areas (V1 and V2, respectively) are organized retinotopically. The aim of this study was to map these basal forebrain-V1/V2 projections. Microinjections of the fluorescent retrograde tracer cholera toxin b fragment in different sites within V1 and V2 in Long–Evans rats were performed. Retrogradely labeled cell bodies in the horizontal and vertical limbs of the diagonal band of Broca (HDB and VDB, respectively), nucleus basalis magnocellularis, and substantia innominata (SI), were mapped ex vivo with a computer-assisted microscope stage controlled by stereological software. Choline acetyltranferase immunohistochemistry was used to identify cholinergic cells. Our results showed a predominance of cholinergic projections coming from the HDB. These projections were not retinotopically organized but projections to V1 arised from neurons located in the anterior HDB/SI whereas projections to V2 arised from neurons located throughout the whole extent of HDB/SI. The absence of a clear topography of these projections suggests that BF activation can stimulate visual cortices broadly. |
format | Online Article Text |
id | pubmed-5890115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58901152018-04-16 Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat Huppé-Gourgues, Frédéric Jegouic, Karim Vaucher, Elvire Front Neural Circuits Neuroscience Acetylcholine is an important neurotransmitter for the regulation of visual attention, plasticity, and perceptual learning. It is released in the visual cortex predominantly by cholinergic projections from the basal forebrain, where stimulation may produce potentiation of visual processes. However, little is known about the fine organization of these corticopetal projections, such as whether basal forebrain neurons projecting to the primary and secondary visual cortical areas (V1 and V2, respectively) are organized retinotopically. The aim of this study was to map these basal forebrain-V1/V2 projections. Microinjections of the fluorescent retrograde tracer cholera toxin b fragment in different sites within V1 and V2 in Long–Evans rats were performed. Retrogradely labeled cell bodies in the horizontal and vertical limbs of the diagonal band of Broca (HDB and VDB, respectively), nucleus basalis magnocellularis, and substantia innominata (SI), were mapped ex vivo with a computer-assisted microscope stage controlled by stereological software. Choline acetyltranferase immunohistochemistry was used to identify cholinergic cells. Our results showed a predominance of cholinergic projections coming from the HDB. These projections were not retinotopically organized but projections to V1 arised from neurons located in the anterior HDB/SI whereas projections to V2 arised from neurons located throughout the whole extent of HDB/SI. The absence of a clear topography of these projections suggests that BF activation can stimulate visual cortices broadly. Frontiers Media S.A. 2018-03-08 /pmc/articles/PMC5890115/ /pubmed/29662442 http://dx.doi.org/10.3389/fncir.2018.00019 Text en Copyright © 2018 Huppé-Gourgues, Jegouic and Vaucher. 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 Huppé-Gourgues, Frédéric Jegouic, Karim Vaucher, Elvire Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title | Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title_full | Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title_fullStr | Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title_full_unstemmed | Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title_short | Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat |
title_sort | topographic organization of cholinergic innervation from the basal forebrain to the visual cortex in the rat |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890115/ https://www.ncbi.nlm.nih.gov/pubmed/29662442 http://dx.doi.org/10.3389/fncir.2018.00019 |
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