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Synthesis of endogenous nitric oxide under low oxygen partial pressure

机译:低氧分压下内源性一氧化氮的合成

摘要

The present invention provides methods of promoting synthesis of nitric oxide or endothelium-derived relaxing factor (EDRF) in hypoxic mammalian tissues by administering at least one N-hydroxyguanidine compound that is a substrate of nitric oxide synthase, and, optionally, one or more vasoactive agents and/or thromboxane A2 receptor antagonists. The present invention also provides methods of promoting vasorelaxation and treating sexual dysfunctions in patients by administering at least one N-hydroxyguanidine compound that is a substrate for nitric oxide synthase, and, optionally, at least one vasoactive agent and/or thromboxane A2 receptor antagonist. The present invention also provides methods for treating clinical conditions resulting from hypoxic conditions such as pulmonary disease, cardiovascular disorders, circulatory hypoxia, specific organ hypoxia, localized hypoxia, edema, central nervous system disorders, memory loss, or arterial disease. The present invention also provides methods for treating clinical conditions resulting from an abnormally high level of arginase activity, such as, heart disease, systemic hypertension, pulmonary hypertension, sexual dysfunction, autoimmune disease, chronic renal failure and cerebral vasospasm. The present invention also provides methods for treating clinical conditions associated with a deficient nitric oxide pathway by administering at least one N-hydroxyguanidine compound and, optionally, one or more vasoactive agents and/or thromboxane A2 receptor antagonists. The present invention also provides pharmaceutical compositions comprising at least one N-hydroxyguanidine compound, and, optionally, one or more vasoactive agents and/or thromboxane A2 receptor antagonists.
机译:本发明提供了通过给予至少一种作为一氧化氮合酶底物的N-羟基胍化合物和任选地一种或多种血管活性剂来促进低氧哺乳动物组织中一氧化氮或内皮源性舒张因子(EDRF)的合成的方法。剂和/或血栓烷A2受体拮抗剂。本发明还提供了通过施用至少一种作为一氧化氮合酶底物的N-羟基胍化合物和任选地至少一种血管活性剂和/或血栓烷A 2受体拮抗剂来促进患者的血管舒张和治疗性功能障碍的方法。本发明还提供了用于治疗由缺氧状况引起的临床状况的方法,所述缺氧状况诸如肺部疾病,心血管疾病,循环性缺氧,特定器官缺氧,局部性缺氧,水肿,中枢神经系统疾病,记忆力减退或动脉疾病。本发明还提供了用于治疗由异常高水平的精氨酸酶活性引起的临床状况的方法,所述精氨酸酶活性的异常状况例如心脏病,全身性高血压,肺动脉高压,性功能障碍,自身免疫疾病,慢性肾衰竭和脑血管痉挛。本发明还提供了通过施用至少一种N-羟基胍化合物和任选地一种或多种血管活性剂和/或血栓烷A 2受体拮抗剂来治疗与一氧化氮途径不足相关的临床病症的方法。本发明还提供了包含至少一种N-羟基胍化合物,以及任选地一种或多种血管活性剂和/或血栓烷A2受体拮抗剂的药物组合物。

著录项

  • 公开/公告号JP2004500344A

    专利类型

  • 公开/公告日2004-01-08

    原文格式PDF

  • 申请/专利号JP20010534372

  • 申请日2000-10-26

  • 分类号A61K45/00;A61K31/155;A61K31/198;A61P9/00;A61P9/12;A61P11/00;A61P11/06;A61P11/08;A61P13/12;A61P15/00;A61P25/00;A61P25/08;A61P25/28;A61P37/02;A61P43/00;

  • 国家 JP

  • 入库时间 2022-08-21 23:23:38

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