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Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch

Itch and pain share similar mechanisms. It has been well documented that the anterior cingulate cortex (ACC) is important for pain-related perception. ACC has also been approved to be a potential pruritus-associated brain region. However, the mechanism of sensitization in pruriceptive neurons in the...

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Autores principales: Zhang, Ting-Ting, Shen, Feng-Yan, Ma, Li-Qing, Wen, Wen, Wang, Bin, Peng, Yuan-Zhi, Wang, Zhi-Ru, Zhao, Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966729/
https://www.ncbi.nlm.nih.gov/pubmed/27472923
http://dx.doi.org/10.1186/s13041-016-0251-1
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author Zhang, Ting-Ting
Shen, Feng-Yan
Ma, Li-Qing
Wen, Wen
Wang, Bin
Peng, Yuan-Zhi
Wang, Zhi-Ru
Zhao, Xuan
author_facet Zhang, Ting-Ting
Shen, Feng-Yan
Ma, Li-Qing
Wen, Wen
Wang, Bin
Peng, Yuan-Zhi
Wang, Zhi-Ru
Zhao, Xuan
author_sort Zhang, Ting-Ting
collection PubMed
description Itch and pain share similar mechanisms. It has been well documented that the anterior cingulate cortex (ACC) is important for pain-related perception. ACC has also been approved to be a potential pruritus-associated brain region. However, the mechanism of sensitization in pruriceptive neurons in the ACC is not clear. In current study, a chronic itch model was established by diphenylcyclopropenone (DCP) application. We found that both the frequency and amplitude of miniature excitatory postsynaptic currents in the ACC were enhanced after the formation of chronic itch. The paired-pulse ratio in ACC neurons recorded from the DCP group were smaller than those recorded in control group at the 50-ms interval. We also observe a significant increase in the AMPA/NMDA ratio in the DCP group. Moreover, an increased inward rectification of AMPARs in ACC pyramidal neurons was observed in the DCP group. Interestingly, the calculated ratio of silent synapses was significantly reduced in the DCP group compared with controls. Taken together, we conclude that a potentiation of synaptic transmission in the ACC can be induced by chronic itch, and unsilencing silent synapses, which probably involved recruitment of AMPARS, contributed to the potentiation of postsynaptic transmission.
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spelling pubmed-49667292016-07-30 Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch Zhang, Ting-Ting Shen, Feng-Yan Ma, Li-Qing Wen, Wen Wang, Bin Peng, Yuan-Zhi Wang, Zhi-Ru Zhao, Xuan Mol Brain Research Itch and pain share similar mechanisms. It has been well documented that the anterior cingulate cortex (ACC) is important for pain-related perception. ACC has also been approved to be a potential pruritus-associated brain region. However, the mechanism of sensitization in pruriceptive neurons in the ACC is not clear. In current study, a chronic itch model was established by diphenylcyclopropenone (DCP) application. We found that both the frequency and amplitude of miniature excitatory postsynaptic currents in the ACC were enhanced after the formation of chronic itch. The paired-pulse ratio in ACC neurons recorded from the DCP group were smaller than those recorded in control group at the 50-ms interval. We also observe a significant increase in the AMPA/NMDA ratio in the DCP group. Moreover, an increased inward rectification of AMPARs in ACC pyramidal neurons was observed in the DCP group. Interestingly, the calculated ratio of silent synapses was significantly reduced in the DCP group compared with controls. Taken together, we conclude that a potentiation of synaptic transmission in the ACC can be induced by chronic itch, and unsilencing silent synapses, which probably involved recruitment of AMPARS, contributed to the potentiation of postsynaptic transmission. BioMed Central 2016-07-29 /pmc/articles/PMC4966729/ /pubmed/27472923 http://dx.doi.org/10.1186/s13041-016-0251-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Research
Zhang, Ting-Ting
Shen, Feng-Yan
Ma, Li-Qing
Wen, Wen
Wang, Bin
Peng, Yuan-Zhi
Wang, Zhi-Ru
Zhao, Xuan
Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title_full Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title_fullStr Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title_full_unstemmed Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title_short Potentiation of synaptic transmission in Rat anterior cingulate cortex by chronic itch
title_sort potentiation of synaptic transmission in rat anterior cingulate cortex by chronic itch
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966729/
https://www.ncbi.nlm.nih.gov/pubmed/27472923
http://dx.doi.org/10.1186/s13041-016-0251-1
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