WEKO3
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The Keap1-Nrf2 pathway plays a central role in such mechanisms against oxidative and xenobiotic damage. Nrf2, as a transcription factor, activates a series of genes including NQO1 and HO-1.\nAs the mechanism of acute kidney injury (AKI) due to rhabdomyolysis, renal tubule injury due to oxidative stress is the major component of the pathology. Therefore, in rhabdomyolysisinduced AKI, reno-protective effect of Nrf2 activation is expected. In the present study, the role of Nrf2 activation in rhabdomyolysis-induced AKI was investigated. In vitro, human proximal tubular epithelial cells (hPTECs) were used to determine the significance of Nrf2 for hemin stimulation. Hemin stimulation revealed elevation of Nrf2-related antioxidant gene group and cytotoxicity. Nrf2 knockdown (KD) with Nrf2-siRNA suppressed the rise of the expression of the antioxidant genes against hemin stimulation, and the cell damage was significantly exacerbated. A model of rhabdomyolysis by glycerol intramuscular injection was also prepared in vivo using wild type mice (WT) and Nrf2-deficient mice (Nrf2 KO). These mice were of the C57BL/6J background. We divided them into four groups: (1) WT/Cont, (2) WT/rhabdomyolysis (RM), (3) Nrf2 KO/Cont, and (4) Nrf2 KO/RM. Renal dysfunction and macrophage infiltration occurred more often in the WT/RM than in the WT/Cont, and it significantly worsened in the Nrf2 KO/RM group compared to the WT/RM. The expression of the antioxidant gene group was suppressed more in the Nrf2 KO/RM group compared with the WT/RM.\nThese results indicate that Nrf2 activation exerts reno-protective effect in rhabdomyolysisinduced AKI. Nrf2 activation may be a new therapeutic target for rhabdomyolysis-induced AKI."}]}, "item_10001_textarea_6": {"attribute_name": "抄録(日)", "attribute_value_mlt": [{"subitem_textarea_language": "ja", "subitem_textarea_value": "生体は親電子性物質,活性酸素種によって生成される酸化ストレスから生体を保護する応答システムを有している.Keap1(Kelch-like ECH-associated protein 1) -Nrf2(NF-E2 related factor2)システムがこの応答機構において重要な役割を果たす.核内移行したNrf2は転写因子として,NQO1,HO-1などの抗酸化遺伝子群の発現を制御する. 横紋筋融解症による急性腎障害(AKI: Acute Kidney Injury)の機序として,酸化ストレスが尿細管障害に大きく関与する.それ故,横紋筋融解症誘発性AKI においてもNrf2活性化による腎保護効果が期待される.横紋筋融解症誘発性AKI におけるNrf2活性化の意義と治療標的としての可能性を検討した.ヒト近位尿細管上皮細胞(hPTECs)を用いhemin 刺激に対するNrf2活性化の意義を検討した.hemin 刺激によりhPTECs におけるNrf2関連抗酸化遺伝子群の上昇,細胞障害を認めた.Nrf2-siRNA によるNrf2ノックダウン(KD)を行うことでhemin 刺激に対する抗酸化遺伝子群の発現上昇は抑制され,細胞障害が有意に増悪した.野生型マウス (WT),Nrf2欠損マウス(Nrf2KO)を用い,グリセロール筋注による横紋筋融解症モデルを作成した.(1)WT/Cont,(2)WT/ 横紋筋融解症(RM),(3)Nrf2KO/Cont,(4)Nrf2KO/RM の4群で比較検討した.結果は,WT/Cont に比べWT/RM 群で腎機能障害,尿細管障害,マクロファージ浸潤を認め,Nrf2KO/RM 群で有意に増悪した.抗酸化遺伝子群の発現はNrf2KO/RM 群で低下していた. 横紋筋融解症誘発性AKI において,Nrf2活性化が腎保護効果を有する事が示された.横紋筋融解症によるAKI に対して,Nrf2活性化が新たな治療標的となり得ることが明らかとなった. 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マウス横紋筋融解症誘発性急性腎障害モデルにおけるNrf2活性化の意義の検討
https://kwmed.repo.nii.ac.jp/records/1887
https://kwmed.repo.nii.ac.jp/records/1887db1ba412-b8bd-4b02-ace5-ef9a51af8be8
名前 / ファイル | ライセンス | アクション |
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PDF (2.1 MB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2018-03-01 | |||||
タイトル | ||||||
言語 | ja | |||||
タイトル | マウス横紋筋融解症誘発性急性腎障害モデルにおけるNrf2活性化の意義の検討 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | The role of Nrf2 activation in mouse rhabdomyolysis-induced acute kidney injury model | |||||
言語 | ||||||
言語 | jpn | |||||
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 |
内田, 篤志
× 内田, 篤志× 長洲, 一× 城所, 研吾× 十川, 裕史× 板野, 精之× 春名, 克祐× 佐藤, 稔× 佐々木, 環× 柏原, 直樹× UCHIDA, Atsushi× NAGASU, Hajime× KIDOKORO, Kengo× SOGAWA, Yuji× ITANO, Seiji× HARUNA, Yoshisuke× SATOH, Minoru× SASAKI, Tamaki× KASHIHARA, Naoki |
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著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(日) | ||||||
ja | ||||||
川崎医科大学腎臓・高血圧内科学 | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
著者所属(英) | ||||||
en | ||||||
Department of Nephrology and Hypertension, Kawasaki Medical School | ||||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | 活性酸素種 | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | 尿細管障害 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | hemin | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | Reactive oxygen species | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | Tubular injury | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | Hemin | |||||
抄録(日) | ||||||
ja | ||||||
生体は親電子性物質,活性酸素種によって生成される酸化ストレスから生体を保護する応答システムを有している.Keap1(Kelch-like ECH-associated protein 1) -Nrf2(NF-E2 related factor2)システムがこの応答機構において重要な役割を果たす.核内移行したNrf2は転写因子として,NQO1,HO-1などの抗酸化遺伝子群の発現を制御する. 横紋筋融解症による急性腎障害(AKI: Acute Kidney Injury)の機序として,酸化ストレスが尿細管障害に大きく関与する.それ故,横紋筋融解症誘発性AKI においてもNrf2活性化による腎保護効果が期待される.横紋筋融解症誘発性AKI におけるNrf2活性化の意義と治療標的としての可能性を検討した.ヒト近位尿細管上皮細胞(hPTECs)を用いhemin 刺激に対するNrf2活性化の意義を検討した.hemin 刺激によりhPTECs におけるNrf2関連抗酸化遺伝子群の上昇,細胞障害を認めた.Nrf2-siRNA によるNrf2ノックダウン(KD)を行うことでhemin 刺激に対する抗酸化遺伝子群の発現上昇は抑制され,細胞障害が有意に増悪した.野生型マウス (WT),Nrf2欠損マウス(Nrf2KO)を用い,グリセロール筋注による横紋筋融解症モデルを作成した.(1)WT/Cont,(2)WT/ 横紋筋融解症(RM),(3)Nrf2KO/Cont,(4)Nrf2KO/RM の4群で比較検討した.結果は,WT/Cont に比べWT/RM 群で腎機能障害,尿細管障害,マクロファージ浸潤を認め,Nrf2KO/RM 群で有意に増悪した.抗酸化遺伝子群の発現はNrf2KO/RM 群で低下していた. 横紋筋融解症誘発性AKI において,Nrf2活性化が腎保護効果を有する事が示された.横紋筋融解症によるAKI に対して,Nrf2活性化が新たな治療標的となり得ることが明らかとなった. | ||||||
抄録(英) | ||||||
en | ||||||
Cells are equipped with cytoprotective systems against oxidative stress caused by reactive oxygen species and electrophilic stress. The Keap1-Nrf2 pathway plays a central role in such mechanisms against oxidative and xenobiotic damage. Nrf2, as a transcription factor, activates a series of genes including NQO1 and HO-1. As the mechanism of acute kidney injury (AKI) due to rhabdomyolysis, renal tubule injury due to oxidative stress is the major component of the pathology. Therefore, in rhabdomyolysisinduced AKI, reno-protective effect of Nrf2 activation is expected. In the present study, the role of Nrf2 activation in rhabdomyolysis-induced AKI was investigated. In vitro, human proximal tubular epithelial cells (hPTECs) were used to determine the significance of Nrf2 for hemin stimulation. Hemin stimulation revealed elevation of Nrf2-related antioxidant gene group and cytotoxicity. Nrf2 knockdown (KD) with Nrf2-siRNA suppressed the rise of the expression of the antioxidant genes against hemin stimulation, and the cell damage was significantly exacerbated. A model of rhabdomyolysis by glycerol intramuscular injection was also prepared in vivo using wild type mice (WT) and Nrf2-deficient mice (Nrf2 KO). These mice were of the C57BL/6J background. We divided them into four groups: (1) WT/Cont, (2) WT/rhabdomyolysis (RM), (3) Nrf2 KO/Cont, and (4) Nrf2 KO/RM. Renal dysfunction and macrophage infiltration occurred more often in the WT/RM than in the WT/Cont, and it significantly worsened in the Nrf2 KO/RM group compared to the WT/RM. The expression of the antioxidant gene group was suppressed more in the Nrf2 KO/RM group compared with the WT/RM. These results indicate that Nrf2 activation exerts reno-protective effect in rhabdomyolysisinduced AKI. Nrf2 activation may be a new therapeutic target for rhabdomyolysis-induced AKI. |
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書誌情報 |
ja : 川崎医学会誌 en : Kawasaki medical journal 巻 43, 号 2, p. 81-93, 発行日 2017 |
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出版者 | ||||||
言語 | ja | |||||
出版者 | 川崎医学会 | |||||
ISSN | ||||||
収録物識別子タイプ | PISSN | |||||
収録物識別子 | 0386-5924 | |||||
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収録物識別子タイプ | EISSN | |||||
収録物識別子 | 2758-089X | |||||
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収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00045593 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN12940574 | |||||
DOI | ||||||
関連タイプ | isIdenticalTo | |||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.11482/KMJ-J43(2)81 | |||||
記事種別(日) | ||||||
内容記述タイプ | Other | |||||
内容記述 | 原著論文 | |||||
言語 | ja | |||||
記事種別(英) | ||||||
内容記述タイプ | Other | |||||
内容記述 | Regular Article | |||||
言語 | en | |||||
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識別子タイプ | URI | |||||
関連識別子 | http://igakkai.kms-igakkai.com/wp/wp-content/uploads/2017/KMJ-J43(2)81.pdf | |||||
著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 |