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METHODS AND COMPOSITIONS FOR THERAPEUTIC MODULATION OF ALDOSTERONE LEVELS IN HEART DISEASE

机译:疾病中醛固酮水平的治疗性调制方法和组合物

摘要

The disclosure describes the contribution of elevated levels of circulating alsosterone to heart disease and other hyperaldosteronic conditions. Since activation of beta-arrestin I (beta.arr-1) by the Angiotensin II (AngII) type 1 receptor (AT1R) mediates AngII-induced aldosterone production, beta-arrestin I (beta.arr-1) is a therapeutic target for heart disease. Specifically, the disclosure provides a beta.arr-1 protein fragment comprising the C-terminus of beta.arr-1 (beta.arr1ct; 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 beta-arrestin (beta.arr-1). 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 beta.arr-1 activity and aldosterone production.
机译:本公开描述了循环中的甾酮水平升高对心脏病和其他醛固酮过多病症的贡献。由于血管紧张素II(AngII)1型受体(AT1R)对β-arrestinI(β.arr-1)的激活介导了AngII诱导的醛固酮的产生,因此β-arrestinI(β.arr-1)是治疗的靶点心脏病。具体地,本公开提供了包含β.arr-1的C-末端的β.arr-1蛋白片段(β.arr1ct; SEQ ID NO:3),包含该蛋白片段的组合物,以及使用该蛋白片段以用于通过抑制β-arrestin(β.arr-1)来降低心脏病和其他醛固酮过多症中醛固酮水平的升高。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β.arr-1活性和醛固酮产生的方法。

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