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Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders
Amniotic fluid contains numerous biomolecules derived from fetus and mother, thus providing precious information on pregnancy. Here, we evaluated oxidative stress of human amniotic fluid and measured the concentration of catalytic Fe(II). Amniotic fluid samples were collected with consent from a tot...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306665/ https://www.ncbi.nlm.nih.gov/pubmed/25678752 http://dx.doi.org/10.3164/jcbn.14-82 |
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author | Hattori, Yuka Mukaide, Takahiro Jiang, Li Kotani, Tomomi Tsuda, Hiroyuki Mano, Yukio Sumigama, Seiji Hirayama, Tasuku Nagasawa, Hideko Kikkawa, Fumitaka Toyokuni, Shinya |
author_facet | Hattori, Yuka Mukaide, Takahiro Jiang, Li Kotani, Tomomi Tsuda, Hiroyuki Mano, Yukio Sumigama, Seiji Hirayama, Tasuku Nagasawa, Hideko Kikkawa, Fumitaka Toyokuni, Shinya |
author_sort | Hattori, Yuka |
collection | PubMed |
description | Amniotic fluid contains numerous biomolecules derived from fetus and mother, thus providing precious information on pregnancy. Here, we evaluated oxidative stress of human amniotic fluid and measured the concentration of catalytic Fe(II). Amniotic fluid samples were collected with consent from a total of 89 subjects in Nagoya University Hospital, under necessary medical interventions: normal pregnancy at term, normal pregnancy at the 2nd trimester, preterm delivery with maternal disorders but without fetal disorders, congenital diaphragmatic hernia, fetal growth restriction, pregnancy-induced hypertension, gestational diabetes mellitus, Down syndrome and trisomy 18. Catalytic Fe(II) and oxidative stress markers (8-hydroxy-2'-deoxyguanosine, 8-OHdG; dityrosine) were determined with RhoNox-1 and specific antibodies, respectively, using plate assays. Levels of 8-OHdG and dityrosine were higher in the 3rd trimester compared with the 2nd trimester in normal subjects, and the abnormal groups generally showed lower levels than the controls, thus suggesting that they represent fetal metabolic activities. In contrast, catalytic Fe(II) was higher in the 2nd trimester than the 3rd trimester in the normal subjects, and overall the abnormal groups showed higher levels than the controls, suggesting that high catalytic Fe(II) at late gestation reflects fetal pathologic alterations. Notably, products of H(2)O(2) and catalytic Fe(II) remained almost constant in amniotic fluid. |
format | Online Article Text |
id | pubmed-4306665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-43066652015-02-12 Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders Hattori, Yuka Mukaide, Takahiro Jiang, Li Kotani, Tomomi Tsuda, Hiroyuki Mano, Yukio Sumigama, Seiji Hirayama, Tasuku Nagasawa, Hideko Kikkawa, Fumitaka Toyokuni, Shinya J Clin Biochem Nutr Original Article Amniotic fluid contains numerous biomolecules derived from fetus and mother, thus providing precious information on pregnancy. Here, we evaluated oxidative stress of human amniotic fluid and measured the concentration of catalytic Fe(II). Amniotic fluid samples were collected with consent from a total of 89 subjects in Nagoya University Hospital, under necessary medical interventions: normal pregnancy at term, normal pregnancy at the 2nd trimester, preterm delivery with maternal disorders but without fetal disorders, congenital diaphragmatic hernia, fetal growth restriction, pregnancy-induced hypertension, gestational diabetes mellitus, Down syndrome and trisomy 18. Catalytic Fe(II) and oxidative stress markers (8-hydroxy-2'-deoxyguanosine, 8-OHdG; dityrosine) were determined with RhoNox-1 and specific antibodies, respectively, using plate assays. Levels of 8-OHdG and dityrosine were higher in the 3rd trimester compared with the 2nd trimester in normal subjects, and the abnormal groups generally showed lower levels than the controls, thus suggesting that they represent fetal metabolic activities. In contrast, catalytic Fe(II) was higher in the 2nd trimester than the 3rd trimester in the normal subjects, and overall the abnormal groups showed higher levels than the controls, suggesting that high catalytic Fe(II) at late gestation reflects fetal pathologic alterations. Notably, products of H(2)O(2) and catalytic Fe(II) remained almost constant in amniotic fluid. the Society for Free Radical Research Japan 2015-01 2014-11-01 /pmc/articles/PMC4306665/ /pubmed/25678752 http://dx.doi.org/10.3164/jcbn.14-82 Text en Copyright © 2015 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hattori, Yuka Mukaide, Takahiro Jiang, Li Kotani, Tomomi Tsuda, Hiroyuki Mano, Yukio Sumigama, Seiji Hirayama, Tasuku Nagasawa, Hideko Kikkawa, Fumitaka Toyokuni, Shinya Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title | Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title_full | Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title_fullStr | Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title_full_unstemmed | Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title_short | Catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
title_sort | catalytic ferrous iron in amniotic fluid as a predictive marker of human maternal-fetal disorders |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4306665/ https://www.ncbi.nlm.nih.gov/pubmed/25678752 http://dx.doi.org/10.3164/jcbn.14-82 |
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