发明名称 Stresscopins and their Uses
摘要 The invention provides novel nucleic acids and polypeptides, referred to herein as stresscopin 1 and stresscopin 2, which preferentially activate the CRH-R2 receptor over the R1 receptor. Stresscopins, analogs and mimetics, and related CRH-R2 agonists suppress food intake and heat-induced edema; but do not induce substantial release of ACTH. Stresscopin also finds use in the recovery phase of stress responses, as an anti-inflammatory agent, as a hypotensive agent, as a cardioprotective agent, and in the treatment of psychiatric and anxiolytic disorders. Stresscopin nucleic acid compositions find use in identifying homologous or related proteins and the DNA sequences encoding such proteins; in producing compositions that modulate the expression or function of the protein; and in studying associated physiological pathways.
申请公布号 US2015307571(A1) 申请公布日期 2015.10.29
申请号 US201514793575 申请日期 2015.07.07
申请人 The Board of Trustees of the Leland Stanford Junior University 发明人 Hsu Sheau Yu;Hsueh Aaron J.W.
分类号 C07K14/47 主分类号 C07K14/47
代理机构 代理人
主权项 1. A method of treating a metabolic disease comprising administering to a subject in need thereof, a vector comprising a nucleic acid molecule encoding the polypeptide as set forth in SEQ ID NO:5 or 6 or sequences having at least 90% identity to SEQ ID NO:5 or 6.
地址 Stanford CA US