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- Akiyama Shizuko
- Center for Perinatal Medicine, Tohoku University Hospital Department of Pediatrics, Tohoku University Hospital
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- Ohta Hidenobu
- Center for Perinatal Medicine, Tohoku University Hospital Department of Pediatrics, Tohoku University Hospital Department of Obstetrics and Gynecology, Tohoku University Hospital
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- Watanabe Shimpei
- Center for Perinatal Medicine, Tohoku University Hospital Department of Pediatrics, Tohoku University Hospital
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- Moriya Takahiro
- Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University
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- Hariu Aya
- Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University
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- Nakahata Norimichi
- Department of Cellular Signaling, Graduate School of Pharmaceutical Sciences, Tohoku University
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- Chisaka Hiroshi
- Center for Perinatal Medicine, Tohoku University Hospital Department of Obstetrics and Gynecology, Tohoku University Hospital
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- Matsuda Tadashi
- Center for Perinatal Medicine, Tohoku University Hospital Department of Pediatrics, Tohoku University Hospital
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- Kimura Yoshitaka
- Tohoku University Institute for International Advanced Research and Education
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- Tsuchiya Shigeru
- Department of Obstetrics and Gynecology, Tohoku University Hospital
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- Tei Hajime
- Kanazawa University Institute of Science and Engineering Faculty of Natural System
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- Okamura Kunihiro
- Center for Perinatal Medicine, Tohoku University Hospital Department of Obstetrics and Gynecology, Tohoku University Hospital
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- Yaegashi Nobuo
- Center for Perinatal Medicine, Tohoku University Hospital Department of Obstetrics and Gynecology, Tohoku University Hospital
この論文をさがす
抄録
Maternal circadian information has been reported to play an important role in fetal physiology and development. Hormones and nutrition have been mainly investigated as circadian cues from mother to fetus. However, the influences of circadian properties of the pregnant reproductive organs on fetuses have not been fully investigated. To gain an insight on the circadian functions of the reproductive organs, we examined molecular clocks in the pregnant rat uterus and placenta. By using a Period1-luciferase (Per1-luc) rat, whose tissues express luciferase corresponding to activation of Period1, a “key clock gene”, we examined the uterus clock during non-pregnancy, on embryonic day 12 (E12), and on E22 (the end of pregnancy) in a light-dark (LD) cycle and constant darkness (DD). By in situ hybridization we further explored Per1 mRNA rhythms in the placenta on E12 and E22. The uterus in vitro showed clear circadian Per1-luc rhythms both in and out of pregnancy, having peaks at around the time corresponding to dusk in LD. Likewise, in DD, the uterus in vitro had the same Per1-luc rhythms. The decidua in LD showed circadian Per1 mRNA rhythms, peaking during night 6 h after dusk, while the decidua in DD showed the same Per1 mRNA rhythms only on E22. In contrast, the labyrinth showed no circadian Per1 mRNA rhythms in LD or DD during pregnancy. These results suggest that the uterus and decidua, a maternally-originated tissue of the placenta, but not the labyrinth, a fetus-originated tissue of the placenta, can provide the fetus with circadian information.
収録刊行物
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- The Tohoku Journal of Experimental Medicine
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The Tohoku Journal of Experimental Medicine 221 (4), 287-298, 2010
東北ジャーナル刊行会
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詳細情報 詳細情報について
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- CRID
- 1390282679221481600
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- NII論文ID
- 130004459846
- 10027085356
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- NII書誌ID
- AA00863920
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- ISSN
- 13493329
- 00408727
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可