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子痫前期和胎儿生长受限合并妊娠的胎盘组织中血管内皮生长因子的胎盘表达不支持分娩时胎盘存在缺氧情况。

Placental expression of vascular endothelial growth factor in placentae from pregnancies complicated by pre-eclampsia and intrauterine growth restriction does not support placental hypoxia at delivery.

作者信息

Lyall F, Young A, Boswell F, Kingdom J C, Greer I A

机构信息

Department of Obstetrics and Gynaecology, University of Glasgow, Royal Infirmary, UK.

出版信息

Placenta. 1997 May;18(4):269-76. doi: 10.1016/s0143-4004(97)80061-6.

Abstract

In view of the pathological placental features of pre-eclampsia and intrauterine growth restriction (IUGR), and the angiogenic effects of vascular endothelial growth factor (VEGF), the aim of this study was to determine the expression of VEGF in placentae from normal pregnancies and to compare the results with placentae from pregnancies complicated by pre-eclampsia and intrauterine growth restriction (IUGR). ELISA was used to measure circulating VEGF immunoreactivity in umbilical vein serum samples and immunohistochemistry was used to determine tissue expression of the protein. Since VEGF is known to be upregulated by hypoxia, the expression pattern of VEGF would provide further clues to the oxygen status in the placentae at the time of sampling, presently a subject under great debate. The geometric mean concentration of VEGF immunoreactivity in umbilical vein serum of normal pregnant women was 112.46 pg/ml, in women with pre-eclampsia 50.23 pg/ml and in IUGR alone 175.35 pg/ml. These values were not statistically different from each other. Immunolocalization of VEGF in normal term villous placenta was observed in the syncytiotrophoblast with less intense staining in stromal cells. No qualitative differences in localization of staining between the groups (normal pregnancies, pre-eclampsia, pre-eclampsia plus IUGR, and IUGR) was found. Intensity of staining in stromal cells was also similar in the groups studied. However, intensity of VEGF immunostaining in syncytiotrophoblast was significantly reduced in the three pathological groups (P < 0.02) compared with the control group. These results suggest that reduced VEGF may be responsible, at least in part, for the impaired vascular development which occurs in these conditions. Our results are therefore not consistent with villous placental hypoxia at the time of sample collection.

摘要

鉴于子痫前期和胎儿宫内生长受限(IUGR)的胎盘病理特征,以及血管内皮生长因子(VEGF)的血管生成作用,本研究的目的是确定正常妊娠胎盘组织中VEGF的表达,并将结果与子痫前期合并胎儿宫内生长受限(IUGR)妊娠的胎盘组织进行比较。采用酶联免疫吸附测定法(ELISA)检测脐静脉血清样本中循环VEGF免疫反应性,采用免疫组织化学法测定该蛋白的组织表达。由于已知VEGF会因缺氧而上调,VEGF的表达模式将为采样时胎盘的氧状态提供进一步线索,目前这是一个备受争议的问题。正常孕妇脐静脉血清中VEGF免疫反应性的几何平均浓度为112.46 pg/ml,子痫前期孕妇为50.23 pg/ml,单纯IUGR孕妇为175.35 pg/ml。这些值彼此之间无统计学差异。在足月绒毛膜胎盘中,VEGF的免疫定位在合体滋养层细胞中观察到,基质细胞中的染色较弱。未发现各组(正常妊娠、子痫前期、子痫前期合并IUGR和IUGR)之间染色定位的定性差异。在所研究的各组中,基质细胞中的染色强度也相似。然而,与对照组相比,三个病理组合体滋养层细胞中VEGF免疫染色强度显著降低(P < 0.02)。这些结果表明,VEGF降低可能至少部分导致了这些情况下发生的血管发育受损。因此,我们的结果与采样时绒毛膜胎盘缺氧不一致。

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