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子痫前期中的胎盘肾素-血管紧张素系统与氧化应激。

The placental renin-angiotensin system and oxidative stress in pre-eclampsia.

机构信息

Division of Women's Health, King's College London, Women's Health Academic Centre, KHP, 10th Floor, North Wing, St. Thomas' Hospital, Westminster Bridge Road, London SE1 7EH, UK.

出版信息

Placenta. 2013 Feb;34(2):182-6. doi: 10.1016/j.placenta.2012.11.027. Epub 2012 Dec 14.

Abstract

UNLABELLED

There is an inverse correlation between human birthweight and umbilical venous angiotensin II (AngII) concentrations. Oxidative stress and increased pro-renin receptor (PRR) both enhance the cleavage of angiotensin I from angiotensinogen (AGT). Pre-eclampsia, a hypertensive disorder of pregnancy, manifests as high blood pressure and proteinuria, and is a state of increased oxidative stress.

HYPOTHESIS

Pre-eclampsia will be associated with increased placental expression of components of the renin-angiotensin system, which could result in reduced infant birthweight. Biopsies were taken 1 cm from the placental edge from 27 normotensive controls and 23 pre-eclamptic White European women. Immunohistochemistry was performed for AGT, PRR, glutathione peroxidase 3 (GPx3) and the AT1R and AT2R AngII receptors. Protein expression was semi-quantitatively assessed (H-score).

RESULTS

AT1R expression was significantly increased in pre-eclamptic placentae, and negatively correlated with birthweight (r = -0.529, P = 0.009). AT1R expression was also negatively correlated with GPx3 expression overall (r = -0.647; P = 0.005). AT2R expression positively correlated with AGT (r = 0.615, P = 0.002) in the pre-eclamptic placentae only.

CONCLUSIONS

The raised AT1R expression in pre-eclampsia, together with inadequate antioxidant protection, possibly through lower GPx activity, might enhance the vasoconstrictor effect of locally-generated AngII, contributing to the restricted fetal growth characteristic of pre-eclampsia. Conversely, the AT2R:AGT association within the pre-eclamptic placenta may provide a compensatory mechanism.

摘要

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人类出生体重与脐静脉血管紧张素 II(AngII)浓度呈反比关系。氧化应激和增加的前肾素受体(PRR)均增强血管紧张素原(AGT)从血管紧张素 I 的裂解。先兆子痫是一种妊娠高血压疾病,表现为高血压和蛋白尿,是氧化应激增加的状态。

假设

先兆子痫与肾素血管紧张素系统成分的胎盘表达增加有关,这可能导致婴儿出生体重降低。从 27 名正常血压对照组和 23 名白人欧洲先兆子痫妇女的胎盘边缘 1cm 处采集活检。进行免疫组织化学染色以检测 AGT、PRR、谷胱甘肽过氧化物酶 3(GPx3)以及 AT1R 和 AT2R AngII 受体。蛋白质表达进行半定量评估(H 评分)。

结果

在先兆子痫胎盘中,AT1R 表达显著增加,与出生体重呈负相关(r = -0.529,P = 0.009)。AT1R 表达与总体 GPx3 表达也呈负相关(r = -0.647;P = 0.005)。仅在先兆子痫胎盘中,AT2R 表达与 AGT 呈正相关(r = 0.615,P = 0.002)。

结论

先兆子痫中升高的 AT1R 表达,加上抗氧化保护不足,可能通过降低 GPx 活性,增强局部产生的 AngII 的血管收缩作用,导致先兆子痫特征性的胎儿生长受限。相反,在先兆子痫胎盘中 AT2R:AGT 之间的关联可能提供一种代偿机制。

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