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首页> 外文期刊>American Journal of Physiology >Involvement of calcitonin gene-related peptide in control of human fetoplacental vascular tone.
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Involvement of calcitonin gene-related peptide in control of human fetoplacental vascular tone.

机译:降钙素基因相关肽参与控制人类胎盘血管张力。

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摘要

Calcitonin gene-related peptide (CGRP), one of the most potent endogenous vasodilators known, has been implicated in vascular adaptations and placental functions during pregnancy. The present study was designed to examine the existence of CGRP-A receptor components, the calcitonin receptor-like receptor (CRLR) and receptor activity-modifying protein 1 (RAMP1), in the human placenta and the vasoactivity of CGRP in the fetoplacental circulation. Immunofluorescent staining of the human placenta in term labor using polyclonal anti-CRLR and RAMP1 antibodies revealed that labeling specifically concentrated in the vascular endothelium and the underlying smooth muscle cells in the umbilical artery/vein, chorionic artery/vein, and stem villous vessels as well as in the trophoblast layer of the placental villi. In vitro isometric force measurement showed that CGRP dose dependently relaxes the umbilical artery/vein, chorionic artery/vein, and stem villous vessels. Furthermore, CGRP-induced relaxation of placentalvessels are inhibited by a CGRP receptor antagonist (CGRP8-37), ATP-sensitive potassium (KATP) channel blocker (glybenclamide), and cAMP-dependent protein kinase A inhibitor (Rp-cAMPS) and partially inhibited by a nitric oxide inhibitor (Nomega-nitro-l-arginine methyl ester). We propose that CGRP may play a role in the control of human fetoplacental vascular tone, and the vascular dilations in response to CGRP may involve activation of KATP channels, cAMP, and a nitric oxide pathway.
机译:降钙素基因相关肽(CGRP)是已知的最有效的内源性血管扩张剂之一,已与妊娠期间的血管适应和胎盘功能有关。本研究旨在检查人胎盘中CGRP-A受体成分,降钙素受体样受体(CRLR)和受体活性修饰蛋白1(RAMP1)的存在以及CGRP在胎儿胎盘循环中的血管活性。使用多克隆抗CRLR和RAMP1抗体对足月分娩的人胎盘进行的免疫荧光染色显示,标记特别集中在脐静脉/静脉,绒毛膜静脉/静脉以及干绒毛血管的血管内皮和基础平滑肌细胞中如胎盘绒毛的滋养层。体外等距力测量表明,CGRP剂量依赖性地松弛了脐动脉/静脉,绒毛膜动脉/静脉和茎绒毛血管。此外,CGRP诱导的胎盘血管松弛受到CGRP受体拮抗剂(CGRP8-37),ATP敏感性钾(KATP)通道阻滞剂(glybenclamide)和cAMP依赖性蛋白激酶A抑制剂(Rp-cAMPS)的抑制,并被部分抑制由一氧化氮抑制剂(Nomega-硝基-1-精氨酸甲酯)制成。我们建议CGRP可能在控制人类胎盘血管张力中发挥作用,并且响应CGRP的血管扩张可能涉及KATP通道,cAMP和一氧化氮途径的激活。

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