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Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus

The anti-oxidative stress effect of heme oxygenase-1 (HO-1) expression is being increasingly studied. However, few studies regarding HO-1 have been conducted in patients with gestational diabetes mellitus (GDM). In the present study, HO-1 expression was compared in peripheral blood mononuclear cells...

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Autores principales: XIN, GANG, DU, JUAN, WANG, YONG-TAO, LIANG, TING-TING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881034/
https://www.ncbi.nlm.nih.gov/pubmed/24396429
http://dx.doi.org/10.3892/etm.2013.1435
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author XIN, GANG
DU, JUAN
WANG, YONG-TAO
LIANG, TING-TING
author_facet XIN, GANG
DU, JUAN
WANG, YONG-TAO
LIANG, TING-TING
author_sort XIN, GANG
collection PubMed
description The anti-oxidative stress effect of heme oxygenase-1 (HO-1) expression is being increasingly studied. However, few studies regarding HO-1 have been conducted in patients with gestational diabetes mellitus (GDM). In the present study, HO-1 expression was compared in peripheral blood mononuclear cells at 24–28 weeks of pregnancy in patients with GDM and healthy females, to investigate the correlation between HO-1 and oxidative stress by calculation of MDA content in the peripheral blood serum (thiobarbituric acid method), tested ROS (flow cytometry method), HO-1mRNA (RT-PCR method), and HO-1 protein (western blotting method) of Mononuclear cells. The results show that the levels of serum malonaldehyde (MDA), reactive oxygen species (ROS), HO-1 mRNA and HO-1 protein expression in peripheral blood mononuclear cells were higher in the GDM group than in the control group. Correlation analysis showed that the expression levels of HO-1 protein were positively correlated with the HO-1 mRNA expression levels (r=0.680; P=0.000), and the levels of ROS (r=0.572; P=0.000) and MDA (r=0.614; P=0.000). HO-1 mRNA expression levels were found to positively correlate with the levels of MDA (r=0.451; P=0.010) and fasting plasma glucose (FPG; r=0.337; P=0.039). Partial correlation analysis demonstrated that, after removing the effects of body mass index, FPG and 2-h plasma glucose, HO-1 protein expression levels were positively correlated with the levels of HO-1 mRNA expression (r=0.611; P=0.005), ROS (r=0.526; P=0.021) and MDA (r=0.519; P=0.015). These findings indicate that pregnant females with GDM may be protected against oxidative injury due to the induction of adaptive and compensatory expression of HO-1 to guard against oxidative stress induced by high glucose levels.
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spelling pubmed-38810342014-01-06 Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus XIN, GANG DU, JUAN WANG, YONG-TAO LIANG, TING-TING Exp Ther Med Articles The anti-oxidative stress effect of heme oxygenase-1 (HO-1) expression is being increasingly studied. However, few studies regarding HO-1 have been conducted in patients with gestational diabetes mellitus (GDM). In the present study, HO-1 expression was compared in peripheral blood mononuclear cells at 24–28 weeks of pregnancy in patients with GDM and healthy females, to investigate the correlation between HO-1 and oxidative stress by calculation of MDA content in the peripheral blood serum (thiobarbituric acid method), tested ROS (flow cytometry method), HO-1mRNA (RT-PCR method), and HO-1 protein (western blotting method) of Mononuclear cells. The results show that the levels of serum malonaldehyde (MDA), reactive oxygen species (ROS), HO-1 mRNA and HO-1 protein expression in peripheral blood mononuclear cells were higher in the GDM group than in the control group. Correlation analysis showed that the expression levels of HO-1 protein were positively correlated with the HO-1 mRNA expression levels (r=0.680; P=0.000), and the levels of ROS (r=0.572; P=0.000) and MDA (r=0.614; P=0.000). HO-1 mRNA expression levels were found to positively correlate with the levels of MDA (r=0.451; P=0.010) and fasting plasma glucose (FPG; r=0.337; P=0.039). Partial correlation analysis demonstrated that, after removing the effects of body mass index, FPG and 2-h plasma glucose, HO-1 protein expression levels were positively correlated with the levels of HO-1 mRNA expression (r=0.611; P=0.005), ROS (r=0.526; P=0.021) and MDA (r=0.519; P=0.015). These findings indicate that pregnant females with GDM may be protected against oxidative injury due to the induction of adaptive and compensatory expression of HO-1 to guard against oxidative stress induced by high glucose levels. D.A. Spandidos 2014-02 2013-12-04 /pmc/articles/PMC3881034/ /pubmed/24396429 http://dx.doi.org/10.3892/etm.2013.1435 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
XIN, GANG
DU, JUAN
WANG, YONG-TAO
LIANG, TING-TING
Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title_full Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title_fullStr Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title_full_unstemmed Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title_short Effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
title_sort effect of oxidative stress on heme oxygenase-1 expression in patients with gestational diabetes mellitus
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3881034/
https://www.ncbi.nlm.nih.gov/pubmed/24396429
http://dx.doi.org/10.3892/etm.2013.1435
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