首页> 外文期刊>Regulatory peptides. >Adrenomedullin inhibits angiotensin AT(1A) receptor expression and function in cardiac fibroblasts.
【24h】

Adrenomedullin inhibits angiotensin AT(1A) receptor expression and function in cardiac fibroblasts.

机译:肾上腺髓质素抑制心脏成纤维细胞中血管紧张素AT(1A)受体的表达和功能。

获取原文
获取原文并翻译 | 示例
           

摘要

Adrenomedullin (AM) is a multifunctional peptide hormone with wide-ranging actions related to cardiovascular homeostasis. AM receptors are highly expressed in the heart and AM has antihypertrophic and antiproliferative effects on cardiac myocytes and fibroblasts, respectively. We have investigated the interaction between AM and angiotensin II (Ang II) signalling in neonatal cardiac fibroblast cultures to determine whether the antagonistic effects of AM are mediated via the modulation of Ang II receptors. Cardiac fibroblasts exclusively expressed the Ang II type 1 receptor (AT(1)R) and binding to this site was downregulated by 35% following an 18-h incubation with 100 nM AM. Levels of AT(1A)R mRNA were dose-dependently lowered by AM, with a maximal 40-50% inhibition by 6 h. The decreases in both AT(1)R binding and AT(1A)R mRNA levels were mimicked by 8-Br-cAMP or forskolin, suggesting that the effects of AM were mediated via an elevation of cAMP. In cardiac fibroblasts pretreated with AM, the Ang II induction of collagen biosynthesis was attenuated, although basal collagen synthesis was unaffected. These data suggest that AM mediates the heterologous downregulation of AT(1)R expression via a relatively rapid decrease in AT(1A)R mRNA pools. This interaction may represent a relevant pathophysiological mechanism for modulating Ang II responsiveness in the diseased heart.
机译:肾上腺髓质素(AM)是一种多功能肽激素,具有与心血管稳态有关的广泛作用。 AM受体在心脏中高度表达,并且AM分别对心肌细胞和成纤维细胞具有抗肥大和抗增殖作用。我们研究了AM和新生心肌成纤维细胞培养物中血管紧张素II(Ang II)信号之间的相互作用,以确定AM的拮抗作用是否通过Ang II受体的调节介导。心脏成纤维细胞仅表达Ang II 1型受体(AT(1)R),与100 nM AM孵育18小时后,与该位点的结合被下调35%。 AM可以剂量依赖性地降低AT(1A)R mRNA的水平,到6 h抑制作用最大为40-50%。 AT(1)R结合和AT(1A)R mRNA水平的降低均被8-Br-cAMP或福司柯林模拟,表明AM的作用是通过cAMP的升高介导的。在AM预处理的心脏成纤维细胞中,尽管基础胶原合成不受影响,但Ang II对胶原生物合成的诱导作用减弱。这些数据表明AM通过AT(1A)R mRNA池的相对较快的减少来介导AT(1)R表达的异源下调。这种相互作用可能代表了在患病心脏中调节Ang II反应性的相关病理生理机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号