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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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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. |
format | Online Article Text |
id | pubmed-4966729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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