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  1. 広島大学の刊行物
  2. Hiroshima Journal of Medical Sciences
  3. 50巻3号

Propofol Relaxes Extrapulmonary Artery but not Intrapulmonary Artery through Nitric Oxide Pathway

https://hiroshima.repo.nii.ac.jp/records/2013506
https://hiroshima.repo.nii.ac.jp/records/2013506
0986b6e6-7007-4c3d-8867-ffc068fe73f5
名前 / ファイル ライセンス アクション
HiroshimaJMedSci_50_61.pdf HiroshimaJMedSci_50_61.pdf (462.0 KB)
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
タイトル Propofol Relaxes Extrapulmonary Artery but not Intrapulmonary Artery through Nitric Oxide Pathway
言語 en
作成者 Tanaka, Hiroyuki

× Tanaka, Hiroyuki

en Tanaka, Hiroyuki

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Yamanoue, Takao

× Yamanoue, Takao

en Yamanoue, Takao

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Kuroda, Masahiko

× Kuroda, Masahiko

en Kuroda, Masahiko

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Kawamoto, Masashi

× Kawamoto, Masashi

en Kawamoto, Masashi

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Yuge, Osafumi

× Yuge, Osafumi

en Yuge, Osafumi

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
主題
主題Scheme Other
主題 Propofol
主題
主題Scheme Other
主題 Pulmonary circulation
主題
主題Scheme Other
主題 Endothelium
主題
主題Scheme Other
主題 Nitric oxide
主題
主題Scheme NDC
主題 490
内容記述
内容記述 The object of this study was to compare vasorelaxing responses to propofol by the intrapulmonary artery (IPA) and the extrapulmonary artery (EPA), and to identify the mechanisms of action. Rat pulmonary arterial rings were isolated and suspended in organ chambers where isometric tension development was measured under optimal resting tension. All pulmonary arterial rings were pre-contracted with phenylephrine. Propofol (DiprivanTM) and the vehicle (10% IntralipidTM) were administered cumulatively in the presence or absence of Nω-nitro-L-arginine methyl ester (L-NAME). Sodium nitroprusside (SNP), a nitric oxide donor, was administered cumulatively. Propofol relaxed both EPA and IPA in a dose dependent manner (p<0.05), while the vehicle alone showed no effect. The vasorelaxing responses to propofol were significantly higher in EPA than IPA at higher concentrations (10-4 M and 10-4.5M) (p<0.05), and were decreased by L-NAME in EPA (p<0.05), though it had no effect in IPA. The concentration for SNP causing 50% relaxation was not significantly different between the two arteries. We concluded that the response of smooth muscle to nitric oxide was the same between EPA and IPA; however, the vasorelaxing mechanisms of propofol seemed to be different between them at higher doses, suggesting that a mechanism exists and operates through the nitric oxide pathway.
言語 en
内容記述
内容記述タイプ Other
内容記述 This study was supported by a Grant-in-Aid (No. 09771158) from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
出版者
出版者 Hiroshima University Medical Press
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 departmental bulletin paper
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0018-2052
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00664312
開始ページ
開始ページ 61
書誌情報 Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences

巻 50, 号 3, p. 61-64, 発行日 2001-09
旧ID 37687
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