| Item type |
学術雑誌論文 / Journal Article(1) |
| 公開日 |
2024-07-20 |
| タイトル |
|
|
タイトル |
Dynamic change and preventive role of stress response via Keap1-Nrf2 during renal crystal formation |
|
言語 |
en |
| 言語 |
|
|
言語 |
eng |
| 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 |
Calcium oxalate |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Urolithiasis |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Antioxidants |
| 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 |
牛本 千春子
杉木 滋
國井 健司郎
井上 慎也
黒田 絵莉子
赤井 良子
岩脇 隆夫
宮澤 克人
|
| 著者(英) |
|
|
|
姓名 |
Chiharuko Ushimoto |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Shigeru Sugiki |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Kenshirou Kunii |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Shinya Inoue |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Eriko Kuroda |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Ryoko Akai |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Takao Iwawaki |
|
|
言語 |
en |
| 著者(英) |
|
|
|
姓名 |
Katsuhito Miyazawa |
|
|
言語 |
en |
| 抄録 |
|
|
内容記述タイプ |
Abstract |
|
内容記述 |
Oxidative stress is a major risk factor for calcium oxalate nephrolithiasis. Reports suggest that oxidative stress response is induced in animals and humans with kidney stones. Keap1, Nrf2, and HO-1 are known as oxidative stress mediators. However, the association between oxidative stress response and stone formation is unclear. In this study, we analyzed oxidative stress response from the acute to the crystal formation phase when crystal formation was applied to renal crystal mice model and bioimaging mice and investigated the effect on crystal formation. In renal tissues, after glyoxylate administration, HO-1 increased for up to 6 h and returned to baseline at 24 h. This was observed following each daily dose until five days after the crystallization phase; however, the range of increase was attenuated. The possibility that Nrf2 activity influenced the number of crystals was considered in the experiment. Crystal formation increased in Nrf2-deficient mice and could be reduced by Nrf2 activators. In conclusion, the oxidative stress response via the Keap1-Nrf2 pathway may contribute to crystal formation. Particularly, this pathway may be a prospective target for drug development to prevent and cure nephrolithiasis. |
|
言語 |
en |
| 書誌情報 |
en : Free Radic Biol Med
巻 207,
p. 120-132
|
| 出版者 |
|
|
出版者 |
Elsevier |
|
言語 |
en |
| DOI |
|
|
|
識別子タイプ |
DOI |
|
|
関連識別子 |
https://doi.org/10.1016/j.freeradbiomed.2023.07.013 |
| 著者版フラグ |
|
|
出版タイプ |
NA |
|
出版タイプResource |
http://purl.org/coar/version/c_be7fb7dd8ff6fe43 |