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子痫前期与人类脐带血管平滑肌细胞中神经元型一氧化氮合酶表达缺失有关。

Preeclampsia is associated with loss of neuronal nitric oxide synthase expression in vascular smooth muscle cells of the human umbilical cord.

作者信息

Schönfelder G, Fuhr N, Hadzidiakos D, John M, Hopp H, Paul M

机构信息

Institute of Clinical Pharmacology and Toxicology, Campus Benjamin Franklin, Charité-Universitätsmedizin Berlin, Berlin, Germany.

出版信息

Histopathology. 2004 Feb;44(2):116-28. doi: 10.1111/j.1365-2559.2004.01806.x.

Abstract

AIMS

Umbilical blood vessels are not innervated and regulation of blood flow to the placenta must depend on structural changes and the effect of vasoactive factors. Failure to achieve these adaptations may result in reduced fetoplacental perfusion. The purpose of this study was to determine whether neuronal nitric oxide synthase (nNOS) is expressed in human vascular smooth muscle cells (VSMCs) of the fetoplacental circulation. nNOS has been described as a non-endothelial NOS counterregulating vasoconstriction only in the VSMCs of animal models. Therefore, we investigated nNOS expression in the fetoplacental unit from preeclamptic and healthy pregnancies.

METHODS AND RESULTS

We investigated nNOS regulation by immunohistochemistry, Western blotting and reverse transcriptase-polymerase chain reaction analysis. nNOS activity was determined by measuring the conversion of L-3H-arginine to L-3H-citrulline. nNOS expression was revealed only in VSMCs of the human umbilical veins, but not in umbilical arteries. A more direct assessment of nNOS activity showed that a small, but consistent amount of nNOS is present in the denuded media of the umbilical vein. In VSMCs of the umbilical veins during preeclampsia a total loss of nNOS protein expression and a significant decrease in mRNA expression were seen.

CONCLUSIONS

Loss of nNOS expression is associated with preeclampsia. It may alter the regulation of blood flow in the fetal and maternal placental vasculature in preeclampsia. However, the impact of NO produced by nNOS on the vascular tone of umbilical veins remains to be elucidated.

摘要

目的

脐血管无神经支配,胎盘血流的调节必须依赖于结构变化和血管活性因子的作用。未能实现这些适应性变化可能导致胎儿-胎盘灌注减少。本研究的目的是确定神经元型一氧化氮合酶(nNOS)是否在胎儿-胎盘循环的人血管平滑肌细胞(VSMC)中表达。nNOS仅在动物模型的VSMC中被描述为一种非内皮型一氧化氮合酶,可对抗血管收缩。因此,我们研究了子痫前期和正常妊娠的胎儿-胎盘单位中nNOS的表达情况。

方法与结果

我们通过免疫组织化学、蛋白质印迹法和逆转录-聚合酶链反应分析来研究nNOS的调节情况。通过测量L-3H-精氨酸向L-3H-瓜氨酸的转化来测定nNOS活性。nNOS表达仅在人脐静脉的VSMC中被发现,而在脐动脉中未发现。对nNOS活性的更直接评估表明,脐静脉剥脱的中膜中存在少量但稳定的nNOS。在子痫前期患者的脐静脉VSMC中,nNOS蛋白表达完全丧失,mRNA表达显著降低。

结论

nNOS表达缺失与子痫前期有关。它可能改变子痫前期胎儿和母体胎盘血管系统中的血流调节。然而,nNOS产生的一氧化氮对脐静脉血管张力的影响仍有待阐明。

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