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  1. 原著論文

Environmental enrichment increases radiation-induced apoptosis not spontaneous apotosis in mouse intestinal crypt cells

https://repo.qst.go.jp/records/2000363
https://repo.qst.go.jp/records/2000363
c4d6f51e-8321-489a-8d51-a8f34bc525ea
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2024-01-25
タイトル
タイトル Environmental enrichment increases radiation-induced apoptosis not spontaneous apotosis in mouse intestinal crypt cells
言語 en
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
著者 Yokomizo Shinya

× Yokomizo Shinya

Yokomizo Shinya

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Nishimura Mayumi

× Nishimura Mayumi

Nishimura Mayumi

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Morioka Takamitsu

× Morioka Takamitsu

Morioka Takamitsu

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Enzaka Utako

× Enzaka Utako

Enzaka Utako

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Tsuruoka Chizuru

× Tsuruoka Chizuru

Tsuruoka Chizuru

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Shang Yi

× Shang Yi

Shang Yi

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Nishimura Yukiko

× Nishimura Yukiko

Nishimura Yukiko

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Inoue Kazumasa

× Inoue Kazumasa

Inoue Kazumasa

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Fukushi Masahiro

× Fukushi Masahiro

Fukushi Masahiro

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Imaoka Tatsuhiko

× Imaoka Tatsuhiko

Imaoka Tatsuhiko

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Kakinuma Shizuko

× Kakinuma Shizuko

Kakinuma Shizuko

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Shimada Yoshiya

× Shimada Yoshiya

Shimada Yoshiya

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抄録
内容記述タイプ Abstract
内容記述 Background/aim: An enriched environment (EE) modifies apoptotic cell death and promotes cell proliferation in the central nervous system (CNS) in mice. However, few studies have examined the effects of an EE on apoptosis in non-CNS organs in model orgamisms. In addition, the intestinal tract is one of organs at high-risk of carcinogenesis after radiation exposure. Herein we evaluated the effects of an EE on spontaneous and radiation-induced apoptosis in intestinal crypt cells of mice.
Materials and methods: Juvenile (3-week-old) and adult (11-week-old) male B6C3F1 mice were housed in a standard environment or EE for 8 weeks and then were whole-body irradiated with 2 Gy X-rays. Apoptosis in the small intestine and colon was analyzed with antibody against cleaved caspase 3.
Results: The EE significantly reduced body weight; adipose tissue weight; and serum levels of total cholesterol, triglyceride, leptin, and insulin. Although EE did not change the spontaneous apoptotic index without irradiation, it significantly increased the index after irradiation in the colonic crypt. The apoptotic index in the small intestinal crypt showed similar patterns.
Conclusion: An EE enhances radiation-induced apoptosis of stem/progenitor cells in the small intestine and colon without affecting spontaneous apoptosis. An EE may thus reduce the risk of cancer in the intestinal tract after radiation exposure such as radiotherapy.
書誌情報 in vivo

巻 6, 号 2, p. 618-627, 発行日 2022-03
出版者
出版者 Stanford University Highwire Press
ISSN
収録物識別子タイプ ISSN
収録物識別子 0258-851X
DOI
識別子タイプ DOI
関連識別子 10.21873/invivo.12745
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