The Nitric Oxide Producing Reactions of Hydroxyurea

羟基脲的一氧化氮生成反应

• 批准号: 7152565
• 负责人: S BRUCE King
• 金额: $ 26.72万
• 依托单位: WAKE FOREST UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-09-10 至 2009-07-05
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7152565
• 关键词: Affect; African American; Biochemical; Blood Transfusion; Cells; Chemicals; Condition; Development; Enzyme Activation; Enzymes; Fetal Hemoglobin; Functional disorder; Goals; Hemoglobin; In Vitro; Kinetics; Mediating; Methods; Molecular; Nitric Oxide; Pain management; Patients; Pharmaceutical Preparations; Production; Proteins; Reaction; Research; Role; Sickle Cell; Sickle Cell Anemia; Site; Soluble Guanylate Cyclase; System; Techniques; Therapeutic; Tissues; Water; Work; base; chemical kinetics; chemical synthesis; design; hydroxyurea; in vivo; nitroxyl; oxidation; therapy development

DESCRIPTION (provided by applicant): Hydroxyurea represents a new treatment for sickle cell disease, a condition that affects 1 in 600 Americans of African descent. While the molecular mechanisms of how hydroxyurea beneficially affects sickle cell disease patients remain unknown, recent evidence indicates a role for nitric oxide (NO) in both the pathophysiology and treatment of sickle cell disease. The long-term goal of the proposed research is to thoroughly and clearly understand how the NO producing reactions of hydroxyurea contribute to the beneficial effects of hydroxyurea therapy. This goal is based upon the hypothesis that hydroxyurea-derived NO mediates the beneficial effects of hydroxyurea therapy in sickle cell disease. Product analysis, kinetic and spectroscopic studies will determine the mechanism of in vitro NO production from hydroxyurea, which should provide relevant information to the in vivo reaction. Similar studies applied to the incubation of hydroxyurea with various tissues and purified enzymes will reveal both the mechanism and site of in vivo NO formation from hydroxyurea. Specifically, these results will distinguish between hydrolytic and oxidative mechanisms of both in vitro and in vivo NO formation from hydroxyurea. In addition, the extent of the reaction of hydroxyurea-derived NO with the identified target proteins, soluble guanylate cyclase and cell-free hemoglobin, will be demonstrated by determining the extent of enzyme activation and the ultimate reaction products and kinetics of these reactions using spectroscopic methods and product analysis. These results will indicate the ability of hydroxyurea or hydroxyurea derived-NO to influence or react with these target proteins and provide evidence for a mechanism for the beneficial effects of hydroxyurea treatment. Unique hydroxyurea-based NO delivery systems and water-soluble nitroxyl donors will be prepared through chemical synthesis. The ability of these compounds to release NO will be determined using spectroscopic and cyclic voltammetric studies and these results will reveal the ability of these new systems to act as NO or nitroxyl donors. These new compounds will also be evaluated for their ability to stimulate soluble guanylate cyclase and react with cell free hemoglobin. Together, these results will provide important information regarding the mechanism of action of hydroxyurea that can be applied to the further development of superior sickle cell treatments.

描述（由申请人提供）：羟基脲是镰状细胞病的一种新疗法，该病影响600名非洲裔美国人中的1人。虽然羟基脲如何对镰状细胞病患者有益的分子机制尚不清楚，但最近的证据表明，一氧化氮（NO）在镰状细胞病的病理生理和治疗中都起着重要作用。本研究的长期目标是全面、清晰地了解羟基脲产生NO的反应如何促进羟基脲治疗的有益效果。这一目标是基于羟基脲衍生的NO介导羟基脲治疗镰状细胞病的有益作用的假设。产物分析、动力学和光谱研究将确定羟基脲在体外产生NO的机制，为体内反应提供相关信息。将类似的研究应用于羟基脲与各种组织和纯化酶的孵育，将揭示羟基脲在体内生成NO的机制和部位。具体来说，这些结果将区分体外和体内羟基脲形成NO的水解和氧化机制。此外，羟基脲衍生的NO与鉴定的靶蛋白、可溶性鸟苷酸环化酶和无细胞血红蛋白的反应程度，将通过使用光谱方法和产物分析来确定酶的激活程度、最终反应产物和这些反应的动力学来证明。这些结果将表明羟基脲或羟基脲衍生的no影响或与这些靶蛋白发生反应的能力，并为羟基脲处理的有益作用机制提供证据。通过化学合成制备独特的基于羟基脲的NO传递系统和水溶性硝基给体。这些化合物释放NO的能力将通过光谱和循环伏安研究来确定，这些结果将揭示这些新系统作为NO或硝基供体的能力。这些新化合物还将评估其刺激可溶性鸟苷酸环化酶和与无细胞血红蛋白反应的能力。总之，这些结果将为羟基脲的作用机制提供重要信息，可用于进一步开发优越的镰状细胞治疗方法。