JAXA Repository / AIREX 未来へ続く、宙(そら)への英知

このアイテムに関連するファイルはありません。

タイトルAltered I(sub f) channel gene expression in mouse hearts after myocardial infarction
その他のタイトル心筋梗塞後のマウス心臓におけるI(sub f)チャネルの遺伝子発現変化
著者(日)竹村 春起; 丹羽 統子; 北條 真弓; Lee, Jong-Kook; 安井 健二; 上田 裕一; 児玉 逸雄
著者(英)Takemura, Haruki; Niwa, Noriko; Hojo, Mayumi; Lee, Jong-Kook; Yasui, Kenji; Ueda, Yuichi; Kodama, Itsuo
著者所属(日)名古屋大学 大学院医学研究科; 名古屋大学環境医学研究所 器官系機能調節部門 循環器分野; 名古屋大学環境医学研究所 器官系機能調節部門 循環器分野; 名古屋大学環境医学研究所 器官系機能調節部門 循環器分野; 名古屋大学環境医学研究所 器官系機能調節部門 循環器分野; 名古屋大学 大学院医学研究科; 名古屋大学環境医学研究所 器官系機能調節部門 循環器分野
著者所属(英)Nagoya University Graduate School of Medicine; Research Institute of Environmental Medicine, Nagoya University Department of Circulation, Division of Regulation of Organ Function; Research Institute of Environmental Medicine, Nagoya University Department of Circulation, Division of Regulation of Organ Function; Research Institute of Environmental Medicine, Nagoya University Department of Circulation, Division of Regulation of Organ Function; Research Institute of Environmental Medicine, Nagoya University Department of Circulation, Division of Regulation of Organ Function; Nagoya University Graduate School of Medicine; Research Institute of Environmental Medicine, Nagoya University Department of Circulation, Division of Regulation of Organ Function
発行日2002-12
刊行物名Environmental Medicine
Environmental Medicine
46
1/2
開始ページ89
終了ページ91
刊行年月日2002-12
言語eng
抄録I(sub f) channels play a key role in the pacemaker activity of sinus node in adult heart. Four subtypes of (HCN1-4), which encode I(sub f) channel, have been identified. In the present study, quantitatively estimated was the expression of HCN1-4 mRNA in mouse ventricular myocardium 4 weeks after myocardial infarction (MI) by a real time PCR. In sham-operated control mice, HCN2 mRNA was expressed most abundantly (915.2 +/- 225.0 molecules/10(exp 5) GAPDH molecules) in the ventricle. The expressions of mRNAs for HCN1, HCN3 and HCN4 were less abundant (15.2 +/- 5.0, 9.7 +/- 1.1, 48.2 +/- 25.3 molecules/10(exp 5) GAPDH molecules, respectively). In mice after MI, HCN2 mRNA increased significantly by 2.7 fold compared to controls. There was no significant difference of HCN1, HCN3 and HCN4 mRNA between two groups. There is an upregulation of HCN2 mRNA in compensated hypertrophied muscle in MI. This might be responsible for an enhancement of abnormal automaticity in the hearts after MI.
キーワードpacemaker; mouse; I(sub f) channel; gene expression; myocardial infarction; PCR; HCN2 mRNA; heart failure; hypertrophy; ペースメーカー; マウス; I(sub f)チャネル; 遺伝子発現; 心筋梗塞; PCR; HCN2 mRNA; 心不全; 肥大
資料種別Technical Report
ISSN0287-0517
SHI-NOAA0045052023
URIhttps://repository.exst.jaxa.jp/dspace/handle/a-is/46910


このリポジトリに保管されているアイテムは、他に指定されている場合を除き、著作権により保護されています。