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  1. 医歯学総合研究科
  2. 医歯学総合研究科・学術誌論文

The Impact of Hypothermia on Emergence from Isoflurane Anesthesia in Orexin Neuron-Ablated Mice

http://hdl.handle.net/10232/21240
http://hdl.handle.net/10232/21240
fe687855-d095-4a17-a045-b9bd305f0209
名前 / ファイル ライセンス アクション
KUWAKI_AA-D-12-01092R2.pdf KUWAKI_AA-D-12-01092R2.pdf (444.9 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-06-16
タイトル
タイトル The Impact of Hypothermia on Emergence from Isoflurane Anesthesia in Orexin Neuron-Ablated Mice
タイトル言語 en
著者 黒木, 千晴

× 黒木, 千晴

WEKO 117173

en Kuroki, Chiharu

ja-Kana クロキ, チハル

ja 黒木, 千晴

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髙橋, 佳子

× 髙橋, 佳子

WEKO 117174

en Takahashi, Yoshiko

ja-Kana タカハシ, ヨシコ

ja 髙橋, 佳子

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大塚, 曜一郎

× 大塚, 曜一郎

WEKO 117175

en Ootsuka, Youichirou

ja-Kana オオツカ, ヨウイチロウ

ja 大塚, 曜一郎

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上村, 裕一

× 上村, 裕一

WEKO 117176

en Kanmura, Yuichi

ja-Kana カンムラ, ユウイチ

ja 上村, 裕一

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桑木, 共之

× 桑木, 共之

WEKO 117177

en Kuwaki, Tomoyuki

ja-Kana クワキ, トモユキ

ja 桑木, 共之

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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
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
要約
内容記述タイプ Other
内容記述 BACKGROUND: Orexin neurons regulate the sleep/wake cycle and are proposed to influence general anesthesia. In animal experiments, orexin neurons have been shown to drive emergence from general anesthesia. In human studies, however, the role of orexin neurons remains controversial, owing at least, in part, to the fact that orexin neurons are multifunctional. Orexin neurons regulate not only the sleep/wake cycle, but also body temperature. We hypothesized that orexin neurons do not directly regulate emergence from anesthesia, but instead affect emergence indirectly through thermoregulation because anesthesia-induced hypothermia can greatly influence emergence time. To test our hypothesis, we used simultaneous measurement of body temperature and locomotor activity.
METHODS: We used male orexin neuron-ablated (ORX-AB) mice and their corresponding wild-type (WT) littermates to investigate the role of orexin neurons in emergence. Body temperature was recorded using an intraperitoneally implanted telemetric probe, and locomotor activity was measured using an infrared motion sensor. Induction of anesthesia and emergence from anesthesia were defined behaviorally as loss and return, respectively, of body movement. Mice received general anesthesia with 1.5% isoflurane in 100% oxygen for 30 minutes under 3 conditions. In the first experiment, the anesthesia chamber was warmed (32[degrees]C), ensuring a constant body temperature of animals during anesthesia. In the second experiment, the anesthesia chamber was maintained at room temperature (25[degrees]C), allowing body temperature to fluctuate. In the third experiment in WT mice, the anesthesia chamber was cooled (23[degrees]C) so that their body temperature would decrease to the comparable value to that obtained in the ORX-AB mice during room temperature condition.
RESULTS: In the warmed condition, there were no significant differences between the ORX-AB and control mice with respect to body temperature, locomotor activity, induction time, or emergence time. In the room temperature condition, however, anesthesia-induced hypothermia was greater and longer lasting in ORX-AB mice than that in WT mice. Emergence time in ORX-AB mice was significantly prolonged from the warmed condition (14.2 +/- 0.8 vs 6.0 +/- 1.1 minutes) whereas that in WT mice was not different (7.4 +/- 0.8 vs 4.9 +/- 0.2 minutes). When body temperature was decreased by cooling in WT mice, emergence time was prolonged to 12.4 +/- 1.3 minutes. Induction time did not differ among temperature conditions or genotypes.
CONCLUSIONS: The effect of orexin deficiency to impair thermoregulation during general anesthesia is of sufficient magnitude that body temperature must be appropriately controlled when studying the role of orexin neurons in emergence from anesthesia.
内容記述言語 en
収録雑誌名 en : Anesthesia & Analgesia

巻 116, 号 5, p. 1001-1005, 発行日 2013-05-01
作成日
日付 2013-05-01
日付タイプ Issued
ISSN
収録物識別子タイプ PISSN
ISSN 00032999
NII書誌ID(雑誌)
収録物識別子タイプ NCID
NC ID AA00525156
PubMed Id
識別子タイプ PMID
PubMed Id 23477964
DOI
識別子タイプ DOI
DOI https://doi.org/10.1213/ANE.0b013e31828842f0
権利
権利情報の言語 en
権利情報 Lippincott, Williams & Wilkins
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
NDC
主題Scheme NDC
主題 493
公開者・出版者
出版者 Lippincott, Williams & Wilkins
出版者言語 en
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