Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons

This study was conducted to determine whether Nav1.8 contributes to the release and/or synthesis of substance P (SP) in adult mice dorsal root ganglion (DRG) neurons. The SP released from cultured DRG neurons of Nav1.8 knock-out mice exposed to either capsaicin or KCl was significantly lower than th...

Full description

Bibliographic Details
Main Authors: He-Bin Tang, Eri Shiba, Yu-Sang Li, Norimitsu Morioka, Tai-Xing Zheng, Nobukuni Ogata, Yoshihiro Nakata
Format: Article
Language:English
Published: Elsevier 2008-01-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861319313544
id doaj-06f793a37dce46e19c360f949c13f59d
record_format Article
spelling doaj-06f793a37dce46e19c360f949c13f59d2020-11-25T02:31:05ZengElsevierJournal of Pharmacological Sciences1347-86132008-01-011082190197Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion NeuronsHe-Bin Tang0Eri Shiba1Yu-Sang Li2Norimitsu Morioka3Tai-Xing Zheng4Nobukuni Ogata5Yoshihiro Nakata6Department of Pharmacology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8553, JapanDepartment of Pharmacology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8553, JapanDepartments of Pathology and Kasumi 1-2-3, Minami-ku, Hiroshima 734-8551, JapanDepartment of Pharmacology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8553, JapanNeurophysiology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8551, Japan.Neurophysiology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8551, Japan.Department of Pharmacology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima 734-8553, Japan; Corresponding author. ynakata@hiroshima-u.ac.jpThis study was conducted to determine whether Nav1.8 contributes to the release and/or synthesis of substance P (SP) in adult mice dorsal root ganglion (DRG) neurons. The SP released from cultured DRG neurons of Nav1.8 knock-out mice exposed to either capsaicin or KCl was significantly lower than that from wild-type (C57BL/6) mice based on a radioimmunoassay. The SP level of L6 DRG in Nav1.8 knock-out mice was also lower than that in wild-type mice. After chronic constriction injury (CCI) of the sciatic nerve, the level of SP decreased in the L6 ipsilateral DRG of wild-type but not Nav1.8 knock-out mice. The preprotachykinin-A (PPT-A) mRNAs in L4 –6 DRGs of Nav1.8 knock-out mice also fell to half their normally abundant levels of expression. There were significant increases in Nav1.8 expression of the L6 contralateral DRG from wild-type mice and in the percentage of neurons expressing neurokinin-1 receptor in the cytosol of L6 DRGs from wild-type or Nav1.8 knock-out mice. These findings suggest that Nav1.8 is involved in the regulation of the release and synthesis of SP in the DRG neurons of wild-type mice. Keywords:: dorsal root ganglion (DRG), chronic constriction injury (CCI), Nav1.8 knock-out mice, preprotachykinin-A (PPT-A) mRNA, substance P (SP)http://www.sciencedirect.com/science/article/pii/S1347861319313544
collection DOAJ
language English
format Article
sources DOAJ
author He-Bin Tang
Eri Shiba
Yu-Sang Li
Norimitsu Morioka
Tai-Xing Zheng
Nobukuni Ogata
Yoshihiro Nakata
spellingShingle He-Bin Tang
Eri Shiba
Yu-Sang Li
Norimitsu Morioka
Tai-Xing Zheng
Nobukuni Ogata
Yoshihiro Nakata
Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
Journal of Pharmacological Sciences
author_facet He-Bin Tang
Eri Shiba
Yu-Sang Li
Norimitsu Morioka
Tai-Xing Zheng
Nobukuni Ogata
Yoshihiro Nakata
author_sort He-Bin Tang
title Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
title_short Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
title_full Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
title_fullStr Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
title_full_unstemmed Involvement of Voltage-Gated Sodium Channel NaV1.8 in the Regulation of the Release and Synthesis of Substance P in Adult Mouse Dorsal Root Ganglion Neurons
title_sort involvement of voltage-gated sodium channel nav1.8 in the regulation of the release and synthesis of substance p in adult mouse dorsal root ganglion neurons
publisher Elsevier
series Journal of Pharmacological Sciences
issn 1347-8613
publishDate 2008-01-01
description This study was conducted to determine whether Nav1.8 contributes to the release and/or synthesis of substance P (SP) in adult mice dorsal root ganglion (DRG) neurons. The SP released from cultured DRG neurons of Nav1.8 knock-out mice exposed to either capsaicin or KCl was significantly lower than that from wild-type (C57BL/6) mice based on a radioimmunoassay. The SP level of L6 DRG in Nav1.8 knock-out mice was also lower than that in wild-type mice. After chronic constriction injury (CCI) of the sciatic nerve, the level of SP decreased in the L6 ipsilateral DRG of wild-type but not Nav1.8 knock-out mice. The preprotachykinin-A (PPT-A) mRNAs in L4 –6 DRGs of Nav1.8 knock-out mice also fell to half their normally abundant levels of expression. There were significant increases in Nav1.8 expression of the L6 contralateral DRG from wild-type mice and in the percentage of neurons expressing neurokinin-1 receptor in the cytosol of L6 DRGs from wild-type or Nav1.8 knock-out mice. These findings suggest that Nav1.8 is involved in the regulation of the release and synthesis of SP in the DRG neurons of wild-type mice. Keywords:: dorsal root ganglion (DRG), chronic constriction injury (CCI), Nav1.8 knock-out mice, preprotachykinin-A (PPT-A) mRNA, substance P (SP)
url http://www.sciencedirect.com/science/article/pii/S1347861319313544
work_keys_str_mv AT hebintang involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT erishiba involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT yusangli involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT norimitsumorioka involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT taixingzheng involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT nobukuniogata involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
AT yoshihironakata involvementofvoltagegatedsodiumchannelnav18intheregulationofthereleaseandsynthesisofsubstancepinadultmousedorsalrootganglionneurons
_version_ 1724825300769964032