論文

2021年12月

Nrf2 plays a critical role in the metabolic response during and after spaceflight

Communications Biology
  • Akira Uruno
  • Daisuke Saigusa
  • Takafumi Suzuki
  • Akane Yumoto
  • Tomohiro Nakamura
  • Naomi Matsukawa
  • Takahiro Yamazaki
  • Ristumi Saito
  • Keiko Taguchi
  • Mikiko Suzuki
  • Norio Suzuki
  • Akihito Otsuki
  • Fumiki Katsuoka
  • Eiji Hishinuma
  • Risa Okada
  • Seizo Koshiba
  • Yoshihisa Tomioka
  • Ritsuko Shimizu
  • Masaki Shirakawa
  • Thomas W. Kensler
  • Dai Shiba
  • Masayuki Yamamoto
  • 全て表示

4
1
記述言語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s42003-021-02904-6
出版者・発行元
Springer Science and Business Media LLC

<title>Abstract</title>Space travel induces stresses that contribute to health problems, as well as inducing the expression of Nrf2 (NF-E2-related factor-2) target genes that mediate adaptive responses to oxidative and other stress responses. The volume of epididymal white adipose tissue (eWAT) in mice increases during spaceflight, a change that is attenuated by <italic>Nrf2</italic> knockout. We conducted metabolome analyses of plasma from wild-type and <italic>Nrf2</italic> knockout mice collected at pre-flight, in-flight and post-flight time points, as well as tissues collected post-flight to clarify the metabolic responses during and after spaceflight and the contribution of Nrf2 to these responses. Plasma glycerophospholipid and sphingolipid levels were elevated during spaceflight, whereas triacylglycerol levels were lower after spaceflight. In wild-type mouse eWAT, triacylglycerol levels were increased, but phosphatidylcholine levels were decreased, and these changes were attenuated in <italic>Nrf2</italic> knockout mice. Transcriptome analyses revealed marked changes in the expression of lipid-related genes in the liver and eWAT after spaceflight and the effects of <italic>Nrf2</italic> knockout on these changes. Based on these results, we concluded that space stress provokes significant responses in lipid metabolism during and after spaceflight; Nrf2 plays critical roles in these responses.

リンク情報
DOI
https://doi.org/10.1038/s42003-021-02904-6
URL
https://www.nature.com/articles/s42003-021-02904-6.pdf
URL
https://www.nature.com/articles/s42003-021-02904-6
ID情報
  • DOI : 10.1038/s42003-021-02904-6
  • eISSN : 2399-3642

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