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,...

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Main Authors: Frédéric Huppé-Gourgues, Karim Jegouic, Elvire Vaucher
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-03-01
Series:Frontiers in Neural Circuits
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fncir.2018.00019/full
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author Frédéric Huppé-Gourgues
Frédéric Huppé-Gourgues
Karim Jegouic
Elvire Vaucher
author_facet Frédéric Huppé-Gourgues
Frédéric Huppé-Gourgues
Karim Jegouic
Elvire Vaucher
author_sort Frédéric Huppé-Gourgues
collection DOAJ
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.
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spelling doaj.art-05efcb9e3c224fdf917eea6dacb815f92022-12-22T03:54:21ZengFrontiers Media S.A.Frontiers in Neural Circuits1662-51102018-03-011210.3389/fncir.2018.00019330908Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the RatFrédéric Huppé-Gourgues0Frédéric Huppé-Gourgues1Karim Jegouic2Elvire Vaucher3Laboratoire de Neurobiologie de la Cognition Visuelle, École d’Optométrie, Université de Montréal, Montreal, QC, CanadaÉcole de Psychologie, Université de Moncton, Moncton, NB, CanadaLaboratoire de Neurobiologie de la Cognition Visuelle, École d’Optométrie, Université de Montréal, Montreal, QC, CanadaLaboratoire de Neurobiologie de la Cognition Visuelle, École d’Optométrie, Université de Montréal, Montreal, QC, CanadaAcetylcholine 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.http://journal.frontiersin.org/article/10.3389/fncir.2018.00019/fullcholera toxin Bvisual cortexdiagonal band of Brocaacetylcholinetopographic mapsLong–Evans rat
spellingShingle Frédéric Huppé-Gourgues
Frédéric Huppé-Gourgues
Karim Jegouic
Elvire Vaucher
Topographic Organization of Cholinergic Innervation From the Basal Forebrain to the Visual Cortex in the Rat
Frontiers in Neural Circuits
cholera toxin B
visual cortex
diagonal band of Broca
acetylcholine
topographic maps
Long–Evans 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 cholera toxin B
visual cortex
diagonal band of Broca
acetylcholine
topographic maps
Long–Evans rat
url http://journal.frontiersin.org/article/10.3389/fncir.2018.00019/full
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