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    • 62. 发明申请
    • INHIBITION OF WET TYPE AGE RELATED MACULAR DEGENERATION (AMD) BY ADIPONECTIN OR ACRP 30
    • 通过ADIPONECTIN或ACRP 30抑制湿型年龄相关的微粒变性(AMD)
    • WO2006104964A2
    • 2006-10-05
    • PCT/US2006/011008
    • 2006-03-22
    • UNIVERSITY OF LOUISVILLE RESEARCH FOUNDATION, INC.BORA, Puran S.BORA, Nalini S.KAPLAN, Henry J.
    • BORA, Puran S.BORA, Nalini S.KAPLAN, Henry J.
    • A61K38/17
    • A61K38/2264
    • The present invention provides new methods of treating wet type of age related macular degeneration by administering adiponectin (APN) or a functional fragment derived therefrom. One of the pathological complications of age related macular degeneration (AMD) is choroidal angiogenesis or choroidal neovascularization (CNV). The inventors discovered that the level of APN expression is significantly lower in the choroids of the laser-induced mouse model of choroidal angiogenesis or choroidal neovascularization (CNV) than that of the control mice and that administration of recombinant adiponectin (rAPN) or a peptide derived from the globular domain of the intact APN protein to the mouse model of CNV reduced the size of CNV significantly. These studies are the first to demonstrate the inhibitory effect of adiponectin on choroidal angiogenesis and thus provide the basis for treating a condition or disease involving angiogenesis, particularly age related macular degeneration, with administration of adiponectin.
    • 本发明提供了通过施用脂联素(APN)或其衍生的功能性片段治疗湿性年龄相关性黄斑变性的新方法。 年龄相关性黄斑变性(AMD)的病理并发症之一是脉络膜血管生成或脉络膜新生血管形成(CNV)。 发明人发现激光诱导的脉络膜血管生成或脉络膜新血管形成(CNV)小鼠模型的脉络膜的APN表达水平显着低于对照小鼠,并且施用重组脂联素(rAPN)或肽衍生物 从完整的APN蛋白的球状结构域到CNV的小鼠模型显着降低了CNV的大小。 这些研究首先证明脂联素对脉络膜血管生成的抑制作用,从而提供了通过给予脂联素治疗涉及血管生成,特别是年龄相关性黄斑变性的病症或疾病的基础。