Department of Obstetrics and Gynaecology Mercy Perinatal Research Centre, Mercy Hospital for Women, University of Melbourne, Level 4/163 Studley Road, Heidelberg 3084, Victoria, Australia.
J Endocrinol. 2010 Jan;204(1):75-84. doi: 10.1677/JOE-09-0321. Epub 2009 Oct 15.
In response to oxidative stress, gestational diabetes mellitus (GDM) placenta releases less 8-isoprostane and tumour necrosis factor (TNF) alpha. The effect of oxidative stress on other cytokines and antioxidant gene expressions are unknown. The aim of this study is to further explore the antioxidant status and effect of oxidative stress in GDM tissue. Human placenta, omental and subcutaneous adipose tissue from women with and without GDM were exposed to hypoxanthine (HX)/xanthine oxidase (XO). Cytokine release was analysed by ELISA and cytokine and antioxidant gene expression by RT-PCR. Catalase (CAT) and glutathione reductase (GSR) mRNA expression was higher in GDM (n=18) compared with normal (n=23) placenta. There was no difference in glutathione peroxidase and superoxide dismutase mRNA expression. Antioxidant gene expression was unaltered between normal (n=18) and GDM (n=10) adipose tissue. HX/XO treatment significantly stimulated cytokine release (13/16 cytokines) and cytokine mRNA expression, and decreased antioxidant gene expression (CAT and GSR) in human placenta from normal pregnant women. In GDM placenta, HX/XO only significantly increased the release of 3/16 cytokines, while there was no effect on antioxidant gene expression. In normal and GDM adipose tissues, HX/XO increased proinflammatory cytokine and 8-isoprostane release, while there was no change in antioxidant gene expression. GDM placenta is characterised by increased antioxidant gene expression, and is less responsive to exogenous oxidative stress than tissues obtained from normal pregnant women. This may represent a protective or adaptive mechanism to prevent damage from further oxidative insult in utero as indicated by increased tissue antioxidant expression.
针对氧化应激,妊娠糖尿病(GDM)胎盘释放的 8-异前列腺素和肿瘤坏死因子(TNF)α减少。氧化应激对其他细胞因子和抗氧化基因表达的影响尚不清楚。本研究旨在进一步探讨 GDM 组织中的抗氧化状态和氧化应激的影响。将来自患有和不患有 GDM 的女性的人胎盘、网膜和皮下脂肪组织暴露于黄嘌呤(HX)/黄嘌呤氧化酶(XO)下。通过 ELISA 分析细胞因子释放,通过 RT-PCR 分析细胞因子和抗氧化基因表达。与正常(n=23)胎盘相比,GDM(n=18)胎盘中的过氧化氢酶(CAT)和谷胱甘肽还原酶(GSR)mRNA 表达更高。谷胱甘肽过氧化物酶和超氧化物歧化酶 mRNA 表达没有差异。正常(n=18)和 GDM(n=10)脂肪组织之间的抗氧化基因表达没有差异。HX/XO 处理显著刺激了来自正常妊娠妇女的胎盘的细胞因子释放(13/16 种细胞因子)和细胞因子 mRNA 表达,并降低了抗氧化基因表达(CAT 和 GSR)。在 GDM 胎盘,HX/XO 仅显著增加了 3/16 种细胞因子的释放,而对抗氧化基因表达没有影响。在正常和 GDM 脂肪组织中,HX/XO 增加了促炎细胞因子和 8-异前列腺素的释放,而抗氧化基因表达没有变化。GDM 胎盘的特征是抗氧化基因表达增加,并且对外源性氧化应激的反应性低于从正常孕妇获得的组织。这可能代表了一种保护或适应机制,以防止宫内进一步氧化损伤,如组织抗氧化表达增加所示。