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Hydrogen-rich water ameliorates rat placental stress induced by water restriction

Dehydration is one of the intrauterine abnormalities that could lead to fetal growth retardation and to increase the risk of a variety of adult diseases later in life. This study were to determine the impact of hydrogen-rich water (HRW) supplementation on placental angiotensin II type 1 receptor and...

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Autores principales: Shi, Yun-Zhi, Jin, Song, Qin, Han, Jiang, Heng-Bo, Song, Guo-Hua, Qin, Shu-Cun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178645/
https://www.ncbi.nlm.nih.gov/pubmed/30319761
http://dx.doi.org/10.4103/2045-9912.241064
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author Shi, Yun-Zhi
Jin, Song
Qin, Han
Jiang, Heng-Bo
Song, Guo-Hua
Qin, Shu-Cun
author_facet Shi, Yun-Zhi
Jin, Song
Qin, Han
Jiang, Heng-Bo
Song, Guo-Hua
Qin, Shu-Cun
author_sort Shi, Yun-Zhi
collection PubMed
description Dehydration is one of the intrauterine abnormalities that could lead to fetal growth retardation and to increase the risk of a variety of adult diseases later in life. This study were to determine the impact of hydrogen-rich water (HRW) supplementation on placental angiotensin II type 1 receptor and placental oxidative stress induced by water restriction. Pregnant Wistar rat were randomly assigned to one of the three groups (n =12 per group). In control group, pure water and food were supplied ad libitum. Water restriction group and HRW group were respectively given pure water and HRW with free access to food, excepting only one hour was available for drinking from day 7 to day 17 of pregnancy. The placental damages and biomarkers of stress were detected by histopathology, immunohistochemistry and western blot, as well as serological test were performed. We demonstrated that maternal water restriction resulted in reduced urine volume and increased serum osmotic pressure, along with decreased fetus weight and crown-rump length. Although placental weight and the number of fetuses had no significant difference among groups, the placental efficiency significantly increased after the oral administration of HRW to the mothers. Meanwhile, the serological derivatives of reactive oxygen metabolites decreased, a significant improvement of placental microstructure with more developed junctional zone and denser labyrinth was manifested, the upregulated expression of angiotensin II type 1 receptor, nuclear factoκB, malondialdehyde, 8-hydroxydeoxyguanosine, p38, c-Jun N-terminal kinase and down-regulation of superoxide dismutase were revealed in the placenta. Collectively, HRW administration is able to effectively attenuate placental stress induced by water restriction.
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spelling pubmed-61786452018-10-12 Hydrogen-rich water ameliorates rat placental stress induced by water restriction Shi, Yun-Zhi Jin, Song Qin, Han Jiang, Heng-Bo Song, Guo-Hua Qin, Shu-Cun Med Gas Res Research Article Dehydration is one of the intrauterine abnormalities that could lead to fetal growth retardation and to increase the risk of a variety of adult diseases later in life. This study were to determine the impact of hydrogen-rich water (HRW) supplementation on placental angiotensin II type 1 receptor and placental oxidative stress induced by water restriction. Pregnant Wistar rat were randomly assigned to one of the three groups (n =12 per group). In control group, pure water and food were supplied ad libitum. Water restriction group and HRW group were respectively given pure water and HRW with free access to food, excepting only one hour was available for drinking from day 7 to day 17 of pregnancy. The placental damages and biomarkers of stress were detected by histopathology, immunohistochemistry and western blot, as well as serological test were performed. We demonstrated that maternal water restriction resulted in reduced urine volume and increased serum osmotic pressure, along with decreased fetus weight and crown-rump length. Although placental weight and the number of fetuses had no significant difference among groups, the placental efficiency significantly increased after the oral administration of HRW to the mothers. Meanwhile, the serological derivatives of reactive oxygen metabolites decreased, a significant improvement of placental microstructure with more developed junctional zone and denser labyrinth was manifested, the upregulated expression of angiotensin II type 1 receptor, nuclear factoκB, malondialdehyde, 8-hydroxydeoxyguanosine, p38, c-Jun N-terminal kinase and down-regulation of superoxide dismutase were revealed in the placenta. Collectively, HRW administration is able to effectively attenuate placental stress induced by water restriction. Medknow Publications & Media Pvt Ltd 2018-09-25 /pmc/articles/PMC6178645/ /pubmed/30319761 http://dx.doi.org/10.4103/2045-9912.241064 Text en Copyright: © 2018 Medical Gas Research http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Shi, Yun-Zhi
Jin, Song
Qin, Han
Jiang, Heng-Bo
Song, Guo-Hua
Qin, Shu-Cun
Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title_full Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title_fullStr Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title_full_unstemmed Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title_short Hydrogen-rich water ameliorates rat placental stress induced by water restriction
title_sort hydrogen-rich water ameliorates rat placental stress induced by water restriction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6178645/
https://www.ncbi.nlm.nih.gov/pubmed/30319761
http://dx.doi.org/10.4103/2045-9912.241064
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