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  1. Public
  2. 研究紀要
  3. ACTA MEDICA KINDAI UNIVERSITY
  4. 20(4)1995

Enhancement of fentanyl, clonidine and serotonin antinociceptive effects by diltiazem in spinal cord of rats

https://kindai.repo.nii.ac.jp/records/2003135
https://kindai.repo.nii.ac.jp/records/2003135
67359d39-a258-4e0e-897e-7515fed898fd
名前 / ファイル ライセンス アクション
AA0050842X-19951200-0311.pdf AA0050842X-19951200-0311.pdf (1.5 MB)
アイテムタイプ 紀要論文 / departmental bulletin paper(1)
公開日 2025-07-09
タイトル
タイトル Enhancement of fentanyl, clonidine and serotonin antinociceptive effects by diltiazem in spinal cord of rats
言語 en
作成者 Tsuchiya, Norio

× Tsuchiya, Norio

en Tsuchiya, Norio
Kinki University

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言語
言語 eng
キーワード
主題 fentanyl, Clonidine, 5-HT, calcium-channel blocker, spinal dorsal horn neuron, nociceptive response, naloxone, yohimbine, methysergide
内容記述
内容記述タイプ Abstract
内容記述 Intracellular and extracellular movement of calcium ions regulate neuronal excitability and releases of neurotransmitters in the central nervous system (CNS). The current study was designed to investigate the antinociceptive effects of intrathecal (i.t.) co-administrations of fentanyl (μ-agonists), clonidine (α2-adrenergic agonist) or 5-HT (serotonergic agonist) with diltiazem (a calcium-channel blocker) in rats. Antinociceptive effects were assessed with the tail-flick test. Although higher i.t. doses of fentanyl, clonidine or 5-HT respectively produced a significant antinociceptive effect, lower i.t. doses did not affect the noxious response. When similarly treated, diltiazem alone (100, 200 μg) failed to suppress the nociceptive effects. However, concomitant administrations of antinociceptively inactive doses of fentanyl (1.0 μg), clonidine (2.5 μg) or 5-HT (25 μg) with diltiazem (200 μg) elicited significant suppressions on the thermonociceptive response accordingly. Furthermore, suppressive effects induced by subanalgesic doses of fentanyl, clonidine, or 5-HT, and diltiazem were significantly blocked by naloxone (μ-antagonist), yohimbine (α2-adrenergic antagonist) and methysergide (serotonergic antagonist) respectively. Therefore, it is considered that diltiazem may significantly enhance the antinociceptive effect of each agent. These findings suggest that the calcium channel plays an important role in the antinociceptive effects in the spinal cord of rats.
言語 en
出版者
出版者 The Kinki University Medical Association
言語 en
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 departmental bulletin paper
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 03866092
開始ページ
開始ページ 311
終了ページ
終了ページ 323
書誌情報 en : ACTA MEDICA KINKI UNIVERSITY

巻 20, 号 4, p. 311-323, 発行日 1995-12
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