首页> 外国专利> Compositions comprising β-arrestin 1 and methods of use thereof for therapeutic modulation of aldosterone levels in heart disease

Compositions comprising β-arrestin 1 and methods of use thereof for therapeutic modulation of aldosterone levels in heart disease

机译:包含β-arrestin1的组合物及其在心脏病中治疗性调节醛固酮水平的使用方法

摘要

The invention concerns the contribution of elevated levels of circulating alsosterone to heart disease and other hyperaldosteronic conditions. Since activation of β-arrestin 1(βarr1) by the Angiotensin II (AngII) type 1 receptor (AT1R) mediates AngII-induced aldosterone production, β-arrestin 1(βarr1) is a therapeutic target for heart disease. The invention provides a βarr1 protein fragment comprising the C-terminus of βarr1 (βarr1ct; SEQ ID NO:3), compositions containing this protein fragment, and methods of using this protein fragment to reduce elevated levels of aldosterone in heart disease and other hyperaldosteronic conditions by inhibition of β-arrestin 1(βarr1). These compositions and methods are of therapeutic benefit in chronic heart failure and progression to heart failure after myocardial infarction (MI). Additionally, the invention provides an AngII peptide analog (SEQ ID NO:4), compositions containing this analog, and methods of using this analog for stimulation of βarr1 activity and aldosterone production.
机译:本发明涉及升高水平的循环甾烷酮对心脏病和其他醛固酮过多症的贡献。由于血管紧张素II(AngII)1型受体(AT 1 R)对β-arrestin1(βarr1)的激活介导了AngII诱导的醛固酮生成,因此β-arrestin1(βarr1)是治疗靶点用于心脏病。本发明提供了包含βarr1的C-末端的βarr1蛋白片段(βarr1ct; SEQ ID NO:3),包含该蛋白片段的组合物,以及在心脏病和其他醛固酮增多性疾病中使用该蛋白片段降低醛固酮水平升高的方法。通过抑制β-arrestin1(βarr1)。这些组合物和方法在慢性心力衰竭和心肌梗塞(MI)后发展为心力衰竭中具有治疗益处。另外,本发明提供了AngII肽类似物(SEQ ID NO:4),包含该类似物的组合物,以及使用该类似物刺激βarr1活性和醛固酮产生的方法。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

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