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  1. 学術雑誌論文

Suppression of the Excitability of Nociceptive Secondary Sensory Neurons Following Systemic Administration of Astaxanthin in Rats

https://az.repo.nii.ac.jp/records/2000241
https://az.repo.nii.ac.jp/records/2000241
de7e7867-5bca-451a-a1ef-fe32f595feb0
名前 / ファイル ライセンス アクション
anesthres-01-00012.pdf anesthres-01-00012.pdf (2.5 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2024-12-24
タイトル
タイトル Suppression of the Excitability of Nociceptive Secondary Sensory Neurons Following Systemic Administration of Astaxanthin in Rats
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Chida, Risako

× Chida, Risako

en Chida, Risako

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Yamaguchi, Sana

× Yamaguchi, Sana

en Yamaguchi, Sana

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Utugi, Syogo

× Utugi, Syogo

en Utugi, Syogo

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Sashide, Yukito

× Sashide, Yukito

en Sashide, Yukito

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Takeda, Mamoru

× Takeda, Mamoru

en Takeda, Mamoru

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Abstract
内容記述タイプ Abstract
内容記述 Although astaxanthin (AST) has demonstrated a modulatory effect on voltage-gated Ca2+ (Cav) channels and excitatory glutamate neuronal transmission in vitro, particularly on the excitability of nociceptive sensory neurons, its action in vivo remains to be determined. This research sought to determine if an acute intravenous administration of AST in rats reduces the excitability of wide-dynamic range (WDR) spinal trigeminal nucleus caudalis (SpVc) neurons in response to nociceptive and non-nociceptive mechanical stimulation in vivo. In anesthetized rats, extracellular single-unit recordings were carried out on SpVc neurons following mechanical stimulation of the orofacial area. The average firing rate of SpVc WDR neurons in response to both gentle and painful mechanical stimuli significantly and dose-dependently decreased after the application of AST (1–5 mM, i.v.), and maximum suppression of discharge frequency for both non-noxious and nociceptive mechanical stimuli occurred within 10 min. These suppressive effects persisted for about 20 min. These results suggest that acute intravenous AST administration suppresses the SpVc nociceptive transmission, possibly by inhibiting Cav channels and excitatory glutamate neuronal transmission, implicating AST as a potential therapeutic agent for the treatment of trigeminal nociceptive pain without side effects.
言語 en
書誌情報 Anesthesia Research

巻 1, 号 2, p. 117-127, 発行日 2024-09-02
出版者
出版者 MDPI
DOI
識別子タイプ DOI
関連識別子 10.3390/anesthres1020012
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
査読
内容記述タイプ Other
内容記述 査読あり
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