Item type |
デフォルトアイテムタイプ_(フル)(1) |
公開日 |
2023-03-18 |
タイトル |
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タイトル |
Analgesic action of nicotine on tibial nerve transection (TNT)-induced mechanical allodynia through enhancement of the glycinergic inhibitory system in spinal cord |
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言語 |
en |
作成者 |
Abdin, Md. Joynal
Morioka, Norimitsu
Morita, Katsuya
Kitayama, Tomoya
Kitayama, Shigeo
Nakashima, Toshikatsu
Dohi, Toshihiro
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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権利情報 |
Copyright (c) 2006 Elsevier Ltd. |
主題 |
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主題Scheme |
Other |
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主題 |
nicotine |
主題 |
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主題Scheme |
Other |
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主題 |
nicotinic ACh receptor |
主題 |
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主題Scheme |
Other |
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主題 |
mechanical allodynia |
主題 |
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主題Scheme |
Other |
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主題 |
tibial nerve transection |
主題 |
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主題Scheme |
Other |
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主題 |
glycinergic system |
主題 |
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主題Scheme |
NDC |
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主題 |
490 |
内容記述 |
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内容記述 |
The activation of cholinergic pathways by nicotine elicits various physiological and pharmacological effects in mammals. For example, the stimulation of nicotinic acetylcholine receptors (nAChRs) leads to an antinociceptive effect. However, it remains to be elucidated which subtypes of nAChR are involved in the antinociceptive effect of nicotine on nerve injury-induced allodynia and the underlying cascades of the nAChR-mediated antiallodynic effect. In this study, we attempted to characterize the actions of nicotine at the spinal level against mechanical allodynia in an animal model of neuropathic pain, tibial nerve transection (TNT) in rats. It was found that the intrathecal injection of nicotine, RJR-2403, a selective 4 2 nAChR agonist, and choline, a selective 7 nAChR agonist, produced an antinociceptive effect on the TNT-induced allodynia. The actions of nicotine were almost completely suppressed by pretreatment with mecamylamine, a non-selective nicotinic antagonist, or dihydro- -erythroidine, a selective 4 2 nAChR antagonist, and partially reversed by pretreatment with methyllycaconitine, a selective 7 nAChR antagonist. Furthermore, pretreatment with strychnine, a glycine receptor antagonist, blocked the antinociception induced by nicotine, RJR-2403, and choline. On the other hand, the GABAA antagonist bicuculline did not reverse the antiallodynic effect of nicotine. Together, these results indicate that the 4 2 and 7 nAChR system, by enhancing the activities of glycinergic neurons at the spinal level, exerts a suppressive effect on the nociceptive transduction in neuropathic pain. |
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言語 |
en |
出版者 |
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出版者 |
Elsevier |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
AO |
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出版タイプResource |
http://purl.org/coar/version/c_b1a7d7d4d402bcce |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
10.1016/j.lfs.2006.08.011 |
関連情報 |
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識別子タイプ |
PMID |
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関連識別子 |
16950410 |
関連情報 |
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関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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関連識別子 |
http://dx.doi.org/10.1016/j.lfs.2006.08.011 |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
0024-3205 |
収録物識別子 |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AA00717011 |
開始ページ |
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開始ページ |
9 |
書誌情報 |
Life Sciences
Life Sciences
巻 80,
号 1,
p. 9-16,
発行日 2006-12-03
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旧ID |
17106 |