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Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex

Anterior cingulate cortex (ACC) plays important roles in sensory perception including pain and itch. Neurons in the ACC receive various neuromodulatory inputs from subcortical structures, including locus coeruleus noradrenaline (LC-NA) neurons. Few studies have been reported about synaptic and behav...

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Autores principales: Koga, Kohei, Yamada, Akihiro, Song, Qian, Li, Xu-Hui, Chen, Qi-Yu, Liu, Ren-Hao, Ge, Jun, Zhan, Cheng, Furue, Hidemasa, Zhuo, Min, Chen, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098117/
https://www.ncbi.nlm.nih.gov/pubmed/32216807
http://dx.doi.org/10.1186/s13041-020-00586-5
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author Koga, Kohei
Yamada, Akihiro
Song, Qian
Li, Xu-Hui
Chen, Qi-Yu
Liu, Ren-Hao
Ge, Jun
Zhan, Cheng
Furue, Hidemasa
Zhuo, Min
Chen, Tao
author_facet Koga, Kohei
Yamada, Akihiro
Song, Qian
Li, Xu-Hui
Chen, Qi-Yu
Liu, Ren-Hao
Ge, Jun
Zhan, Cheng
Furue, Hidemasa
Zhuo, Min
Chen, Tao
author_sort Koga, Kohei
collection PubMed
description Anterior cingulate cortex (ACC) plays important roles in sensory perception including pain and itch. Neurons in the ACC receive various neuromodulatory inputs from subcortical structures, including locus coeruleus noradrenaline (LC-NA) neurons. Few studies have been reported about synaptic and behavioral functions of LC-NA projections to the ACC. Using viral-genetic method (AAV-DIO-eYFP) on DBH-cre mice, we found that LC-NA formed synaptic connections to ACC pyramidal cells but not interneurons. This is further supported by the electron microscopic study showing NAergic fibers contact the presynaptic inputs and post-synaptic areas of the pyramidal cells. NA application produced both pre- and post-synaptic potentiation effects in ACC excitatory transmission in vivo and in vitro. Activation of LC-NA projection to the ACC by optogenetic method produced enhancement of excitatory transmission in vitro and induced scratching and behavioral sensitization for mechanical stimulation. Our results demonstrate that LC-NA projections enhance or facilitate brain responses to pain and itch by potentiating glutamatergic synaptic transmissions in the ACC.
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spelling pubmed-70981172020-03-27 Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex Koga, Kohei Yamada, Akihiro Song, Qian Li, Xu-Hui Chen, Qi-Yu Liu, Ren-Hao Ge, Jun Zhan, Cheng Furue, Hidemasa Zhuo, Min Chen, Tao Mol Brain Research Anterior cingulate cortex (ACC) plays important roles in sensory perception including pain and itch. Neurons in the ACC receive various neuromodulatory inputs from subcortical structures, including locus coeruleus noradrenaline (LC-NA) neurons. Few studies have been reported about synaptic and behavioral functions of LC-NA projections to the ACC. Using viral-genetic method (AAV-DIO-eYFP) on DBH-cre mice, we found that LC-NA formed synaptic connections to ACC pyramidal cells but not interneurons. This is further supported by the electron microscopic study showing NAergic fibers contact the presynaptic inputs and post-synaptic areas of the pyramidal cells. NA application produced both pre- and post-synaptic potentiation effects in ACC excitatory transmission in vivo and in vitro. Activation of LC-NA projection to the ACC by optogenetic method produced enhancement of excitatory transmission in vitro and induced scratching and behavioral sensitization for mechanical stimulation. Our results demonstrate that LC-NA projections enhance or facilitate brain responses to pain and itch by potentiating glutamatergic synaptic transmissions in the ACC. BioMed Central 2020-03-26 /pmc/articles/PMC7098117/ /pubmed/32216807 http://dx.doi.org/10.1186/s13041-020-00586-5 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Koga, Kohei
Yamada, Akihiro
Song, Qian
Li, Xu-Hui
Chen, Qi-Yu
Liu, Ren-Hao
Ge, Jun
Zhan, Cheng
Furue, Hidemasa
Zhuo, Min
Chen, Tao
Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title_full Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title_fullStr Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title_full_unstemmed Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title_short Ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
title_sort ascending noradrenergic excitation from the locus coeruleus to the anterior cingulate cortex
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098117/
https://www.ncbi.nlm.nih.gov/pubmed/32216807
http://dx.doi.org/10.1186/s13041-020-00586-5
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