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Input dependent modulation of olfactory bulb activity by HDB GABAergic projections

Basal forebrain modulation of central circuits is associated with active sensation, attention, and learning. While cholinergic modulations have been studied extensively the effect of non-cholinergic basal forebrain subpopulations on sensory processing remains largely unclear. Here, we directly compa...

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Autores principales: Böhm, Erik, Brunert, Daniela, Rothermel, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329849/
https://www.ncbi.nlm.nih.gov/pubmed/32612119
http://dx.doi.org/10.1038/s41598-020-67276-z
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author Böhm, Erik
Brunert, Daniela
Rothermel, Markus
author_facet Böhm, Erik
Brunert, Daniela
Rothermel, Markus
author_sort Böhm, Erik
collection PubMed
description Basal forebrain modulation of central circuits is associated with active sensation, attention, and learning. While cholinergic modulations have been studied extensively the effect of non-cholinergic basal forebrain subpopulations on sensory processing remains largely unclear. Here, we directly compare optogenetic manipulation effects of two major basal forebrain subpopulations on principal neuron activity in an early sensory processing area, i.e. mitral/tufted cells (MTCs) in the olfactory bulb. In contrast to cholinergic projections, which consistently increased MTC firing, activation of GABAergic fibers from basal forebrain to the olfactory bulb leads to differential modulation effects: while spontaneous MTC activity is mainly inhibited, odor-evoked firing is predominantly enhanced. Moreover, sniff-triggered averages revealed an enhancement of maximal sniff evoked firing amplitude and an inhibition of firing rates outside the maximal sniff phase. These findings demonstrate that GABAergic neuromodulation affects MTC firing in a bimodal, sensory-input dependent way, suggesting that GABAergic basal forebrain modulation could be an important factor in attention mediated filtering of sensory information to the brain.
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spelling pubmed-73298492020-07-06 Input dependent modulation of olfactory bulb activity by HDB GABAergic projections Böhm, Erik Brunert, Daniela Rothermel, Markus Sci Rep Article Basal forebrain modulation of central circuits is associated with active sensation, attention, and learning. While cholinergic modulations have been studied extensively the effect of non-cholinergic basal forebrain subpopulations on sensory processing remains largely unclear. Here, we directly compare optogenetic manipulation effects of two major basal forebrain subpopulations on principal neuron activity in an early sensory processing area, i.e. mitral/tufted cells (MTCs) in the olfactory bulb. In contrast to cholinergic projections, which consistently increased MTC firing, activation of GABAergic fibers from basal forebrain to the olfactory bulb leads to differential modulation effects: while spontaneous MTC activity is mainly inhibited, odor-evoked firing is predominantly enhanced. Moreover, sniff-triggered averages revealed an enhancement of maximal sniff evoked firing amplitude and an inhibition of firing rates outside the maximal sniff phase. These findings demonstrate that GABAergic neuromodulation affects MTC firing in a bimodal, sensory-input dependent way, suggesting that GABAergic basal forebrain modulation could be an important factor in attention mediated filtering of sensory information to the brain. Nature Publishing Group UK 2020-07-01 /pmc/articles/PMC7329849/ /pubmed/32612119 http://dx.doi.org/10.1038/s41598-020-67276-z Text en © The Author(s) 2020 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
Böhm, Erik
Brunert, Daniela
Rothermel, Markus
Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title_full Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title_fullStr Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title_full_unstemmed Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title_short Input dependent modulation of olfactory bulb activity by HDB GABAergic projections
title_sort input dependent modulation of olfactory bulb activity by hdb gabaergic projections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7329849/
https://www.ncbi.nlm.nih.gov/pubmed/32612119
http://dx.doi.org/10.1038/s41598-020-67276-z
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