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  1. 学術雑誌論文
  2. 小城 勝相

Effect of celecoxib, a selective cyclooxygenase-2 inhibitor on carbon tetrachloride intoxication in rats.

https://ouj.repo.nii.ac.jp/records/8171
https://ouj.repo.nii.ac.jp/records/8171
87987d46-b191-488e-be36-09d2eac1ce92
名前 / ファイル ライセンス アクション
Celecox.pdf Effect of celecoxib, a selective cyclooxygenase-2... (55.2 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-07-22
タイトル
タイトル Effect of celecoxib, a selective cyclooxygenase-2 inhibitor on carbon tetrachloride intoxication in rats.
タイトル
タイトル Effect of celecoxib, a selective cyclooxygenase-2 inhibitor on carbon tetrachloride intoxication in rats.
言語 en
言語
言語 eng
キーワード
言語 en
主題Scheme Other
主題 Alanine Transaminase
キーワード
言語 en
主題Scheme Other
主題 Animals
キーワード
言語 en
主題Scheme Other
主題 Antioxidants
キーワード
言語 en
主題Scheme Other
主題 Ascorbic Acid
キーワード
言語 en
主題Scheme Other
主題 Aspartate Aminotransferases
キーワード
言語 en
主題Scheme Other
主題 Carbon Tetrachloride Poisoning
キーワード
言語 en
主題Scheme Other
主題 Ceramides
キーワード
言語 en
主題Scheme Other
主題 Cyclooxygenase 2 Inhibitors
キーワード
言語 en
主題Scheme Other
主題 Drug-Induced Liver Injury
キーワード
言語 en
主題Scheme Other
主題 Liver
キーワード
言語 en
主題Scheme Other
主題 Male
キーワード
言語 en
主題Scheme Other
主題 Necrosis
キーワード
言語 en
主題Scheme Other
主題 Oxidative Stress
キーワード
言語 en
主題Scheme Other
主題 Pyrazoles
キーワード
言語 en
主題Scheme Other
主題 Rats
キーワード
言語 en
主題Scheme Other
主題 Rats, Wistar
キーワード
言語 en
主題Scheme Other
主題 Sulfonamides
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 Washino, Yukiko

× Washino, Yukiko

WEKO 10149

Washino, Yukiko

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Koga, Eriko

× Koga, Eriko

WEKO 10150

Koga, Eriko

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Kitamura, Yuko

× Kitamura, Yuko

WEKO 10151

Kitamura, Yuko

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Kamikawa, Chiaki

× Kamikawa, Chiaki

WEKO 10152

Kamikawa, Chiaki

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Kobayashi, Keiko

× Kobayashi, Keiko

WEKO 10153

Kobayashi, Keiko

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Nakagawa, Tomoka

× Nakagawa, Tomoka

WEKO 10154

Nakagawa, Tomoka

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Nakazaki, Chihiro

× Nakazaki, Chihiro

WEKO 10155

Nakazaki, Chihiro

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Ichi, Ikuyo

× Ichi, Ikuyo

WEKO 10156

Ichi, Ikuyo

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Kojo, Shosuke

× Kojo, Shosuke

WEKO 10157

Kojo, Shosuke

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抄録
内容記述タイプ Abstract
内容記述 CCl(4) (0.5 ml/kg as CCl(4)) was orally administered to rats. Twelve hours after administration of CCl(4), plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, indicators of liver necrosis, were significantly higher than those in the control group showing that active liver necrosis took place. At the same time the level of liver vitamin C was decreased significantly compared to that in the control group. Oral administration of 100 mg/kg each of celecoxib 3 and 8 h after CCl(4) treatment did not change plasma ALT and AST and liver vitamin C levels 12 h after CCl(4) treatment, but 24 h after CCl(4) treatment, significantly decreased plasma ALT and AST levels and elevated liver vitamin C level. These finding suggested that celecoxib effectively ameliorated the necrotic action and the oxidative stress induced by CCl(4) in the second phase. Although the plasma levels of all ceramide species were significantly increased 24 h after CCl(4) intoxication, treatment with celecoxib significantly reduced the total ceramide concentration in plasma. These results indicated that celecoxib significantly ameliorated the toxicity of CCl(4) in the second phase.
内容記述
内容記述タイプ Other
内容記述 CCl(4) (0.5 ml/kg as CCl(4)) was orally administered to rats. Twelve hours after administration of CCl(4), plasma alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, indicators of liver necrosis, were significantly higher than those in the control group showing that active liver necrosis took place. At the same time the level of liver vitamin C was decreased significantly compared to that in the control group. Oral administration of 100 mg/kg each of celecoxib 3 and 8 h after CCl(4) treatment did not change plasma ALT and AST and liver vitamin C levels 12 h after CCl(4) treatment, but 24 h after CCl(4) treatment, significantly decreased plasma ALT and AST levels and elevated liver vitamin C level. These finding suggested that celecoxib effectively ameliorated the necrotic action and the oxidative stress induced by CCl(4) in the second phase. Although the plasma levels of all ceramide species were significantly increased 24 h after CCl(4) intoxication, treatment with celecoxib significantly reduced the total ceramide concentration in plasma. These results indicated that celecoxib significantly ameliorated the toxicity of CCl(4) in the second phase.
書誌情報 en : Biological & pharmaceutical bulletin

巻 33, 号 4, p. 707-709, 発行日 2010-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-5215
PubMed番号
識別子タイプ PMID
関連識別子 20410610
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