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抗高血压药物甲基多巴、拉贝洛尔、肼屈嗪和可乐定在体外可改善滋养层细胞与内皮细胞网络的相互作用。

Antihypertensive drugs methyldopa, labetalol, hydralazine, and clonidine improve trophoblast interaction with endothelial cellular networks in vitro.

作者信息

Xu Bei, Charlton Francesca, Makris Angela, Hennessy Annemarie

机构信息

aSchool of Medicine, University of Western Sydney, Penrith bRenal Unit, Liverpool Hospital, Liverpool cVascular Immunology Research Laboratory, The Heart Research Institute, University of Sydney, Newtown, New South Wales, Australia.

出版信息

J Hypertens. 2014 May;32(5):1075-83; discussion 1083. doi: 10.1097/HJH.0000000000000134.

Abstract

OBJECTIVES

The interaction between trophoblasts and maternal endothelium is important for placental vascular modeling. Failure of uterine spiral artery transformation is linked to the etiopathology of preeclampsia. Antihypertensive medications used to control hypertension in early pregnancy can alter placental and circulating cytokines. This study investigated whether selected antihypertensive drugs can modulate the interaction between trophoblast and endothelial cells.

METHODS

Human uterine myometrial microvascular endothelial cells were preincubated with (or without) low-dose tumor necrosis factor-α (TNF-α; 0.5 ng/ml) or TNF-α and soluble fms-like tyrosine kinase 1 (sFlt-1; 100 ng/ml). Red fluorescent-labeled endothelial cells were then cultured on Matrigel. After appearance of endothelial cellular networks, green fluorescent-labeled HTR-8/SVneo trophoblast cells were cocultured in the presence of pharmacological doses of methyldopa, labetalol, hydralazine, and clonidine. Images were captured after 24 h and drug effects on HTR-8/SVneo cell integration were quantified by Image Analysis software. The conditioned medium was collected to measure sFlt-1, vascular endothelial growth factor (VEGF), placental growth factor, interleukin-10, and interleukin-6 by ELISA.

RESULTS

Methyldopa, labetalol, hydralazine, and clonidine increased trophoblast integration into TNF-α-preincubated endothelial cellular networks. In conditioned medium, sFlt-1 was reduced by methyldopa, hydralazine, and clonidine alone. VEGF was increased by methyldopa. A decrease in placental growth factor was seen by methyldopa and also in nontreated endothelial cell coculture of the other three drugs.

CONCLUSION

Some antihypertensive drugs used in pregnancy may improve the cellular interaction between trophoblast and endothelial cells exposed to TNF-α. Methyldopa, hydralazine, and clonidine reduced sFlt-1 concentration in culture medium, whereas labetalol increased trophoblast integration independently of sFlt-1. Methyldopa increased VEGF concentration. Some pregnancy-related antihypertensives may affect placental vascularization.

摘要

目的

滋养层细胞与母体内皮细胞之间的相互作用对胎盘血管形成至关重要。子宫螺旋动脉转化失败与子痫前期的病因病理相关。用于控制孕早期高血压的抗高血压药物可改变胎盘和循环中的细胞因子。本研究调查了某些抗高血压药物是否能调节滋养层细胞与内皮细胞之间的相互作用。

方法

将人子宫肌层微血管内皮细胞预先与(或不与)低剂量肿瘤坏死因子-α(TNF-α;0.5纳克/毫升)或TNF-α和可溶性fms样酪氨酸激酶1(sFlt-1;100纳克/毫升)共同孵育。然后将红色荧光标记的内皮细胞接种于基质胶上培养。在内皮细胞网络形成后,将绿色荧光标记的HTR-8/SVneo滋养层细胞在给予药理剂量的甲基多巴、拉贝洛尔、肼屈嗪和可乐定的情况下共培养。24小时后采集图像,并用图像分析软件对药物对HTR-8/SVneo细胞整合的影响进行定量分析。收集条件培养基,通过酶联免疫吸附测定法检测sFlt-1、血管内皮生长因子(VEGF)、胎盘生长因子、白细胞介素-10和白细胞介素-6。

结果

甲基多巴、拉贝洛尔、肼屈嗪和可乐定可增加滋养层细胞融入预先与TNF-α孵育的内皮细胞网络。在条件培养基中,单独使用甲基多巴、肼屈嗪和可乐定可降低sFlt-1水平。甲基多巴可增加VEGF水平。甲基多巴以及其他三种药物在未处理的内皮细胞共培养中均可使胎盘生长因子水平降低。

结论

孕期使用的某些抗高血压药物可能改善暴露于TNF-α的滋养层细胞与内皮细胞之间的细胞相互作用。甲基多巴、肼屈嗪和可乐定可降低培养基中sFlt-1的浓度,而拉贝洛尔可独立于sFlt-1增加滋养层细胞的整合。甲基多巴可增加VEGF浓度。一些与妊娠相关的抗高血压药物可能影响胎盘血管形成。

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