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    • 8. 发明专利
    • Medicinal composition for angiogenic therapy
    • 药物治疗用药物组合物
    • JP2012025759A
    • 2012-02-09
    • JP2011190400
    • 2011-09-01
    • Anges Mg IncRyuichi MorishitaアンジェスMg株式会社竜一 森下
    • MORISHITA RYUICHIKOIKE HIROMITANABE TADASHIAOKI MOTOKUNI
    • A61K45/00A61K48/00A61P7/02A61P9/10A61P9/14A61P43/00
    • PROBLEM TO BE SOLVED: To provide a new medicinal composition for angiogenic therapy.SOLUTION: The present invention discloses the medicinal composition for the angiogenic therapy containing, as effective components, at least one kind selected from the group comprising substances having a vasodilation effect and/or a platelet aggregation restraining effect, and substances generating the substances, and a gene encoding an angiogenesis factor. an enhancement agent for an angiogenic effect by a gene of encoding the angiogenesis factor, containing, as the effective components, at least one kind selected from the group comprising the substances having the vasodilation effect and/or the platelet aggregation restraining effect, and the substances generating the substances, an angiogenic medicine containing a prostacyclin synthetase gene as an active component, the medicinal composition for the angiogenic therapy containing an ets-1 gene and other gene encoding the angiogenesis factor as effective components, an enhancement agent for the angiogenic effect by the other gene encoding the angiogenesis factor, containing the ets-1 gene as the effective component, and an angiogenic medicine containing the ets-1 gene as an effective component.
    • 要解决的问题:提供用于血管生成治疗的新药物组合物。 解决方案:本发明公开了用于血管生成治疗的药物组合物,其含有选自包含具有血管舒张作用和/或血小板聚集抑制作用的物质的组中的至少一种作为有效成分,以及产生该物质的物质 ,以及编码血管生成因子的基因。 包含编码血管生成因子的基因的血管生成作用的增强剂,其含有选自包含具有血管舒张作用和/或血小板聚集抑制作用的物质的组中的至少一种作为有效成分,以及所述物质 生成含有前列环素合成酶基因作为活性成分的血管生成药物,含有ets-1基因的血管发生疗法的药物组合物和编码血管生成因子的其他基因作为有效成分,作为血管生成作用的增效剂 含有ets-1基因作为有效成分的编码血管生成因子的其他基因,以及含有ets-1基因作为有效成分的血管生成药。 版权所有(C)2012,JPO&INPIT
    • 9. 发明专利
    • Inflammatory disease-treating agent
    • 炎症性疾病治疗剂
    • JP2005120069A
    • 2005-05-12
    • JP2004049299
    • 2004-02-25
    • Anges Mg IncアンジェスMg株式会社
    • HATAE TOSHIHISAYOKOYAMA CHIEISHITANABE TADASHI
    • A61K45/00A61K31/00A61K31/557A61K31/5585A61K31/7088A61K38/00A61K48/00A61P29/00C12N9/90
    • A61K31/00A61K31/557A61K48/005C12N9/90
    • PROBLEM TO BE SOLVED: To provide an elucidation of a target gene of a PGI2-PPARδ transmission system and a new inflammatory disease-treating agent by taking the PGI2-PPARδ transmission system as the target.
      SOLUTION: This target of the PG (prostaglandin) I2-PPAR (peroxisome proliferator-activated receptor) δ transmission system is found to be an IL (interleukin)-13 gene by a microarray analysis. The association of a PGI2-PPARδ-IL-13 pathway with cellular adhesion is examined, and a fact that the production of the IL-13 mediated by the PPARδ inhibits the adhesion of monocytes with endothelium cells markedly is elucidated. The association between the PGI2-PPARδ-IL-13 pathway and COX (cyclooxygenase)-2 is examined, and it is found that the IL-13 production mediated by PGI2/PPARδ inhibits the expression of the COX-2. It is known that the monocyte-endothelium cell adhesion and COX-2 are related to the inflammation. Therefore, it is possible to use a cell adhesion inhibitor or COX-2 inhibitor by taking the PGI2-PPARδ-IL-13 pathway as the target can be utilized as an anti-inflammatory agent.
      COPYRIGHT: (C)2005,JPO&NCIPI
    • 待解决的问题:以PGI2-PPARδ传输系统为目标,提供PGI2-PPARδ传递系统的靶基因和新的炎性疾病治疗剂的阐释。 解决方案:通过微阵列分析发现PG(前列腺素)I2-PPAR(过氧化物酶体增殖物激活受体)δ传递系统的该靶标是IL(白细胞介素)-13基因。 检测PGI2-PPARδ-IL-13途径与细胞粘附的关联,并且阐明了由PPARδ介导的IL-13的产生抑制单核细胞与内皮细胞粘附的事实。 检测PGI2-PPARδ-IL-13途径与COX(环氧合酶)-2之间的关联,发现由PGI2 /PPARδ介导的IL-13产生抑制COX-2的表达。 已知单核细胞 - 内皮细胞粘附和COX-2与炎症有关。 因此,可以通过以PGI2-PPARδ-IL-13途径作为靶,可以使用细胞粘附抑制剂或COX-2抑制剂作为抗炎剂。 版权所有(C)2005,JPO&NCIPI