دورية أكاديمية

Bisphenol A Regulates Sodium Ramp Currents in Mouse Dorsal Root Ganglion Neurons and Increases Nociception

التفاصيل البيبلوغرافية
العنوان: Bisphenol A Regulates Sodium Ramp Currents in Mouse Dorsal Root Ganglion Neurons and Increases Nociception
المؤلفون: Soriano, Sergi, Gil-Rivera, Minerva, Marroquí, Laura, Alonso Magdalena, Paloma, Fuentes, Esther, Gustafsson, Jan-Ake, Nadal, Ángel, Martinez-Pinna, Juan
المساهمون: Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología, Fisiología Neuroendocrina (FINE)
بيانات النشر: Springer Nature
سنة النشر: 2019
المجموعة: RUA - Repositorio Institucional de la Universidad de Alicante
مصطلحات موضوعية: Bisphenol A, Nociception, Sodium channels, Dorsal root ganglion, Fisiología
الوصف: 17β-Estradiol mediates the sensitivity to pain and is involved in sex differences in nociception. The widespread environmental disrupting chemical bisphenol A (BPA) has estrogenic activity, but its implications in pain are mostly unknown. Here we show that treatment of male mice with BPA (50 µg/kg/day) during 8 days, decreases the latency to pain behavior in response to heat, suggesting increased pain sensitivity. We demonstrate that incubation of dissociated dorsal root ganglia (DRG) nociceptors with 1 nM BPA increases the frequency of action potential firing. SCN9A encodes the voltage-gated sodium channel Nav1.7, which is present in DRG nociceptors and is essential in pain signaling. Nav1.7 and other voltage-gated sodium channels in mouse DRG are considered threshold channels because they produce ramp currents, amplifying small depolarizations and enhancing electrical activity. BPA increased Nav-mediated ramp currents elicited with slow depolarizations. Experiments using pharmacological tools as well as DRG from ERβ−/− mice indicate that this BPA effect involves ERα and phosphoinositide 3-kinase. The mRNA expression and biophysical properties other than ramp currents of Nav channels, were unchanged by BPA. Our data suggest that BPA at environmentally relevant doses affects the ability to detect noxious stimuli and therefore should be considered when studying the etiology of pain conditions. ; The authors’ laboratories are funded by the Ministerio de Economía, Industria y Competitividad, Agencia Estatal de Investigación (AEI) and Fondo Europeo de Desarrollo Regional (FEDER), BFU2017-86579-R (A.N.) and Generalitat Valenciana, PROMETEOII/2015/016 (A.N.). CIBERDEM is an initiative of the Instituto de Salud Carlos III. J.-A. G. was supported by a fellowship from the A. Welch Foundation (Grant E-0004).
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 2045-2322
العلاقة: https://doi.org/10.1038/s41598-019-46769-6Test; info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/BFU2017-86579-R; Scientific Reports. 2019, 9: 10306. doi:10.1038/s41598-019-46769-6; http://hdl.handle.net/10045/94727Test
DOI: 10.1038/s41598-019-46769-6
الإتاحة: https://doi.org/10.1038/s41598-019-46769-6Test
http://hdl.handle.net/10045/94727Test
حقوق: © The Author(s) 2019. Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0Test/. ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.3513407E
قاعدة البيانات: BASE
الوصف
تدمد:20452322
DOI:10.1038/s41598-019-46769-6