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  1. 広島大学の刊行物
  2. Hiroshima Journal of Medical Sciences
  3. 39巻4号

Effects of in vivo Pretreatment with Various Barbiturates on Anaerobic Halothane Metabolism in Rat Liver Microsomes

https://hiroshima.repo.nii.ac.jp/records/2013268
https://hiroshima.repo.nii.ac.jp/records/2013268
446bdb14-7b29-44eb-978a-9eb6111c05e7
名前 / ファイル ライセンス アクション
HiroshimaJMedSci_39_125.pdf HiroshimaJMedSci_39_125.pdf (478.3 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 Effects of in vivo Pretreatment with Various Barbiturates on Anaerobic Halothane Metabolism in Rat Liver Microsomes
言語 en
作成者 Taira, Yutaka

× Taira, Yutaka

en Taira, Yutaka

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Fujii, Kohyu

× Fujii, Kohyu

en Fujii, Kohyu

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Kikuchi, Hirosato

× Kikuchi, Hirosato

en Kikuchi, Hirosato

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Yuge, Osafumi

× Yuge, Osafumi

en Yuge, Osafumi

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Morio, Michio

× Morio, Michio

en Morio, Michio

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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 Anesthetics; halothane, barbiturates.
主題
主題Scheme Other
主題 Biotransformation; dehalogenation, induction.
主題
主題Scheme Other
主題 Microsomes; rat, liver.
主題
主題Scheme NDC
主題 490
内容記述
内容記述 The effects of in vivo pretreatment with phenobarbital (PB), thiopental (TP), thiamylal (TA), pentobarbital (PT), and secobarbital (SB) on hepatic microsomal enzymes, and the effects on anaerobic halothane dehalogenation, aminopyrine N-demethylation, and aniline hydroxylation in the microsomes were studied in male Wistar rats. Three hundred twenty μmol/kg (0.1ml) of PB, TP, TA, PT, SB, or 0.1ml of 0.9% saline were administered daily, intramuscularly, for periods of one day up to ten days. Daily administration of PB, TP, TA, or PT induced cytochrome P-450, NADPH-cytochrome P-450 reductase and/or cytochrome b5. However, administration of SB did not induce these enzymes. The potency of these enzyme inductions ranged in descending order as follows: PB, TP, TA, and PT. After five days of daily administration of PB, TP, or TA, the production of the anaerobic halothane metabolite, CDFE, increased to 187%, 134%, and 130% of the control, respectively. The production of another halothane metabolite, CTFE, likewise increased to 197%, 168%, and 163%. However, pretreatment with PT or SB had no effect on anaerobic halothane dehalogenation. Aminopyrine N-demethylation also increased after five days of daily administration of PB, TP, and TA. However, aniline hydroxylation decreased after five days of daily administration of TA. Other barbiturates had no effect on aniline hydroxylation. In this study we showed that whereas PT and SB did not enhance anaerobic halothane dehalogenation, PB, TP and TA did. We conclude that not only PB, and also TP and TA, may be enhancing factors in halothane hepatotoxicity. We recommend that, if barbiturates are necessary, SB and PT be used in the preadministration of halothane anesthesia.
言語 en
内容記述
内容記述タイプ Other
内容記述 This study was supported in part by a Research Grant from the Japanese Ministry of Education, Science and Culture.
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
関連情報
識別子タイプ PMID
関連識別子 2086563
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 125
書誌情報 Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences

巻 39, 号 4, p. 125-130, 発行日 1990-12
旧ID 38089
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