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Nrf2 plays a critical role in the metabolic response during and after spaceflight
被引:0
|作者:
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
机构:
[1] Tohoku University,Department of Integrative Genomics, Tohoku Medical Megabank Organization
[2] Tohoku University Graduate School of Medicine,Department of Medical Biochemistry
[3] JEM Utilization Center,Department of Health Record Informatics, Tohoku Medical Megabank Organization
[4] Human Spaceflight Technology Directorate,Laboratory of Oncology, Pharmacy Practice and Sciences, Graduate School of Pharmaceutical Sciences
[5] JAXA,Advanced Research Center for Innovations in Next
[6] Tohoku University,GEneration Medicine (INGEM)
[7] Tohoku University,Center for Radioisotope Sciences
[8] Tohoku University,Division of Oxygen Biology
[9] Tohoku University Graduate School of Medicine,Department of Molecular Hematology
[10] Tohoku University Graduate School of Medicine,undefined
[11] Tohoku University Graduate School of Medicine,undefined
[12] Translational Research Program,undefined
[13] Fred Hutchinson Cancer Research Center,undefined
来源:
Communications Biology
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摘要:
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 Nrf2 knockout. We conducted metabolome analyses of plasma from wild-type and Nrf2 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 Nrf2 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 Nrf2 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.
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