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Cav3.2 T-type calcium channels control acute itch in mice

Cav3.2 T-type calcium channels are important mediators of nociceptive signaling, but their roles in the transmission of itch remains poorly understood. Here we report a key involvement of these channels as key modulators of itch/pruritus-related behavior. We compared scratching behavior responses be...

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Autores principales: Gadotti, Vinicius M., Kreitinger, Joanna M., Wageling, Nicholas B., Budke, Dylan, Diaz, Philippe, Zamponi, Gerald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465799/
https://www.ncbi.nlm.nih.gov/pubmed/32873320
http://dx.doi.org/10.1186/s13041-020-00663-9
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author Gadotti, Vinicius M.
Kreitinger, Joanna M.
Wageling, Nicholas B.
Budke, Dylan
Diaz, Philippe
Zamponi, Gerald W.
author_facet Gadotti, Vinicius M.
Kreitinger, Joanna M.
Wageling, Nicholas B.
Budke, Dylan
Diaz, Philippe
Zamponi, Gerald W.
author_sort Gadotti, Vinicius M.
collection PubMed
description Cav3.2 T-type calcium channels are important mediators of nociceptive signaling, but their roles in the transmission of itch remains poorly understood. Here we report a key involvement of these channels as key modulators of itch/pruritus-related behavior. We compared scratching behavior responses between wild type and Cav3.2 null mice in models of histamine- or chloroquine-induced itch. We also evaluated the effect of the T-type calcium channel blocker DX332 in male and female wild-type mice injected with either histamine or chloroquine. Cav3.2 null mice exhibited decreased scratching responses during both histamine- and chloroquine-induced acute itch. DX332 co-injected with the pruritogens inhibited scratching responses of male and female mice treated with either histamine or chloroquine. Altogether, our data provide strong evidence that Cav3.2 T-type channels exert an important role in modulating histamine-dependent and -independent itch transmission in the primary sensory afferent pathway, and highlight these channels as potential pharmacological targets to treat pruritus.
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spelling pubmed-74657992020-09-03 Cav3.2 T-type calcium channels control acute itch in mice Gadotti, Vinicius M. Kreitinger, Joanna M. Wageling, Nicholas B. Budke, Dylan Diaz, Philippe Zamponi, Gerald W. Mol Brain Research Cav3.2 T-type calcium channels are important mediators of nociceptive signaling, but their roles in the transmission of itch remains poorly understood. Here we report a key involvement of these channels as key modulators of itch/pruritus-related behavior. We compared scratching behavior responses between wild type and Cav3.2 null mice in models of histamine- or chloroquine-induced itch. We also evaluated the effect of the T-type calcium channel blocker DX332 in male and female wild-type mice injected with either histamine or chloroquine. Cav3.2 null mice exhibited decreased scratching responses during both histamine- and chloroquine-induced acute itch. DX332 co-injected with the pruritogens inhibited scratching responses of male and female mice treated with either histamine or chloroquine. Altogether, our data provide strong evidence that Cav3.2 T-type channels exert an important role in modulating histamine-dependent and -independent itch transmission in the primary sensory afferent pathway, and highlight these channels as potential pharmacological targets to treat pruritus. BioMed Central 2020-09-01 /pmc/articles/PMC7465799/ /pubmed/32873320 http://dx.doi.org/10.1186/s13041-020-00663-9 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
Gadotti, Vinicius M.
Kreitinger, Joanna M.
Wageling, Nicholas B.
Budke, Dylan
Diaz, Philippe
Zamponi, Gerald W.
Cav3.2 T-type calcium channels control acute itch in mice
title Cav3.2 T-type calcium channels control acute itch in mice
title_full Cav3.2 T-type calcium channels control acute itch in mice
title_fullStr Cav3.2 T-type calcium channels control acute itch in mice
title_full_unstemmed Cav3.2 T-type calcium channels control acute itch in mice
title_short Cav3.2 T-type calcium channels control acute itch in mice
title_sort cav3.2 t-type calcium channels control acute itch in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465799/
https://www.ncbi.nlm.nih.gov/pubmed/32873320
http://dx.doi.org/10.1186/s13041-020-00663-9
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