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AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain

The corticostriatal circuit plays an important role in the regulation of reward- and aversion-types of behaviors. Specifically, the projection from the prelimbic cortex (PL) to the nucleus accumbens (NAc) has been shown to regulate sensory and affective aspects of pain in a number of rodent models....

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Autores principales: Zeng, Fei, Zhang, Qiaosheng, Liu, Yaling, Sun, Guanghao, Li, Anna, Talay, Robert S., Wang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923831/
https://www.ncbi.nlm.nih.gov/pubmed/33653395
http://dx.doi.org/10.1186/s13041-021-00757-y
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author Zeng, Fei
Zhang, Qiaosheng
Liu, Yaling
Sun, Guanghao
Li, Anna
Talay, Robert S.
Wang, Jing
author_facet Zeng, Fei
Zhang, Qiaosheng
Liu, Yaling
Sun, Guanghao
Li, Anna
Talay, Robert S.
Wang, Jing
author_sort Zeng, Fei
collection PubMed
description The corticostriatal circuit plays an important role in the regulation of reward- and aversion-types of behaviors. Specifically, the projection from the prelimbic cortex (PL) to the nucleus accumbens (NAc) has been shown to regulate sensory and affective aspects of pain in a number of rodent models. Previous studies have shown that enhancement of glutamate signaling through the NAc by AMPAkines, a class of agents that specifically potentiate the function of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, reduces acute and persistent pain. However, it is not known whether postsynaptic potentiation of the NAc with these agents can achieve the full anti-nociceptive effects of PL activation. Here we compared the impact of AMPAkine treatment in the NAc with optogenetic activation of the PL on pain behaviors in rats. We found that not only does AMPAkine treatment partially reconstitute the PL inhibition of sensory withdrawals, it fully occludes the effect of the PL on reducing the aversive component of pain. These results indicate that the NAc is likely one of the key targets for the PL, especially in the regulation of pain aversion. Furthermore, our results lend support for neuromodulation or pharmacological activation of the corticostriatal circuit as an important analgesic approach.
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spelling pubmed-79238312021-03-03 AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain Zeng, Fei Zhang, Qiaosheng Liu, Yaling Sun, Guanghao Li, Anna Talay, Robert S. Wang, Jing Mol Brain Research The corticostriatal circuit plays an important role in the regulation of reward- and aversion-types of behaviors. Specifically, the projection from the prelimbic cortex (PL) to the nucleus accumbens (NAc) has been shown to regulate sensory and affective aspects of pain in a number of rodent models. Previous studies have shown that enhancement of glutamate signaling through the NAc by AMPAkines, a class of agents that specifically potentiate the function of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, reduces acute and persistent pain. However, it is not known whether postsynaptic potentiation of the NAc with these agents can achieve the full anti-nociceptive effects of PL activation. Here we compared the impact of AMPAkine treatment in the NAc with optogenetic activation of the PL on pain behaviors in rats. We found that not only does AMPAkine treatment partially reconstitute the PL inhibition of sensory withdrawals, it fully occludes the effect of the PL on reducing the aversive component of pain. These results indicate that the NAc is likely one of the key targets for the PL, especially in the regulation of pain aversion. Furthermore, our results lend support for neuromodulation or pharmacological activation of the corticostriatal circuit as an important analgesic approach. BioMed Central 2021-03-02 /pmc/articles/PMC7923831/ /pubmed/33653395 http://dx.doi.org/10.1186/s13041-021-00757-y Text en © The Author(s) 2021 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
Zeng, Fei
Zhang, Qiaosheng
Liu, Yaling
Sun, Guanghao
Li, Anna
Talay, Robert S.
Wang, Jing
AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title_full AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title_fullStr AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title_full_unstemmed AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title_short AMPAkines potentiate the corticostriatal pathway to reduce acute and chronic pain
title_sort ampakines potentiate the corticostriatal pathway to reduce acute and chronic pain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923831/
https://www.ncbi.nlm.nih.gov/pubmed/33653395
http://dx.doi.org/10.1186/s13041-021-00757-y
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