Human Hypertension and P450 Co-Hydroxylases and Epoxygenases

人类高血压与 P450 辅羟化酶和环氧合酶

• 批准号: 8111792
• 负责人: Nancy Brown
• 金额: $ 30.21万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8111792
• 关键词: Acids; Address; Affect; African American; Agonist; Aldosterone; Alkane 1-monooxygenase; Alleles; Amiloride; Androgens; Animal Model; Animals; Antihypertensive Agents; Arachidonic Acids; Asians; Attenuated; Biological Markers; Blood Pressure; Blood Vessels; Body Fluids; CYP4A11 gene; Cardiovascular system; Caucasians; Caucasoid Race; Cerebrum; Cessation of life; Clinical Research; Complications of Diabetes Mellitus; Congestive Heart Failure; Cytochrome P450; Cytosine; Data; Development; Diabetes Mellitus; Disease; Diuretics; Early Diagnosis; Eicosanoids; End stage renal failure; Enzymes; Epithelial; Excretory function; Experimental Models; Functional disorder; Future; Gender; Gene Structure; Genes; Genetic; Genetic Polymorphism; Genetic Variation; Genotype; Ghana; Goals; Health; Homologous Gene; Human; Hydroxyeicosatetraenoic Acids; Hydroxylation; Hypertension; Individual; Injury; Insulin Resistance; Intervention; Kidney; Kidney Diseases; Knock-out; Knockout Mice; Lead; Ligands; Medical; Metabolic; Metabolic syndrome; Mixed Function Oxygenases; Molecular; Morbidity - disease rate; Mus; Myocardial Infarction; Natriuresis; Nephrosclerosis; Organ; Peroxisome Proliferator-Activated Receptors; Phenotype; Physiological; Plasma; Play; Population Study; Prevalence; Production; Protein Isoforms; Proteins; Proteinuria; Renal Hypertension; Renin; Rodent; Rodent Model; Role; Serine; Site; Sodium; Sodium Channel; Sodium Chloride; Stroke; Testing; Thymidine; Tubular formation; United States; Urine; Variant; Vasoconstrictor Agents; Vasodilation; Vasodilator Agents; base; blood pressure regulation; clinical Diagnosis; genetic epidemiology; hemodynamics; human disease; improved; inhibitor/antagonist; insight; insulin sensitivity; interdisciplinary approach; kidney vascular structure; loss of function; men; mortality; novel strategies; prevent; receptor; renal tubular transport; response; salt intake; socioeconomics; urinary; vasoconstriction

The kidney plays a key role in the control of body fluid volume and composition, and tubular and/or hemodynamic dysfunction are common features of diseases such as hypertension and diabetes. The renal P450 arachidonic acid (AA) monooxygenase biosynthesizes hydroxy- and epoxy-AA derivatives that are known to modulate tubular transport and vascular reactivity. Animal models of P450 gene dysfunction confirmed the physiological importance of these enzymes, characterized their pathophysiological roles, and provided insights into the mechanism of action of their metabolites. Studies of the pathophysiological roles of human P450s identified associations between P450 gene variants with hypertension, the progression of renal disease, and with components of metabolic syndrome. This application proposes to build upon these studies and to address: a) mechanisms by which the P450-eicosanoids regulate renal tubular transport and vascular reactivity, b) the role of P450s in human hypertension and renal complications of diabetes, and c) the molecular basis of these pathophysiological roles. To achieve these goals, we developed a multidisciplinary approach for studies of P450-isoform specific phenotypes at the cellular, organ and whole animal levels, the analysis of associations between alterations in human P450 gene structure/expression and disease, and for clinical studies of their metabolic and functional consequences. Cyp2c and Cyp4a knockout mice will be used to study gene-dependent changes in: a) renal EET and/or 20-HETE synthase expression, b) tubular transport and/or vascular reactivity, and c) systemic blood pressure and the progression of renal disease. Associations between CYP2C8/2C9 or CYP4A11 genotypes with blood pressure, insulin sensitivity, and urine and plasma EET and 20-HETE levels will be explored to define pathophysiological correlations between variant alleles, AA epoxidation/hydroxylation, and individual responses to changes in dietary salt intake, the administration of diuretics, or peroxisomal proliferator activated receptor (alpha) ligands. Our long term goals are to provide a molecular understanding of role(s) of P450 eicosanoids in renal physiological, their mechanism and site of action, and relevance to human disease. These are needed for the development of meaningful approaches for: a) the unequivocal definition of human pathophysiological significance, and b) future pharmacological targeting, and clinical diagnosis and intervention.

肾脏在控制体液体积和组成中起关键作用，并且肾小管和/或肾间质也起关键作用。 血液动力学功能障碍是诸如高血压和糖尿病等疾病的共同特征。肾 P450花生四烯酸（AA）单加氧酶生物合成羟基和环氧AA衍生物， 已知调节肾小管转运和血管反应性。P450基因功能障碍的动物模型 证实了这些酶的生理重要性，表征了它们的病理生理作用， 提供了对其代谢物作用机制的见解。研究的病理生理作用， 人类P450发现了P450基因变异与高血压， 肾脏疾病，并伴有代谢综合征的组成部分。本应用程序建议在这些基础上构建 研究和解决：a）P450-类花生酸调节肾小管转运的机制， 血管反应性，B）P450在人类高血压和糖尿病肾脏并发症中的作用，以及c） 这些病理生理作用的分子基础。为了实现这些目标，我们开发了一个多学科的 细胞、器官和整体动物中P450亚型特异性表型的研究方法 水平，分析人类P450基因结构/表达的改变与 疾病，并用于其代谢和功能后果的临床研究。Cyp 2c和Cyp 4a敲除 小鼠将用于研究以下方面的基因依赖性变化：a）肾EET和/或20-HETE合酶表达， B）肾小管转运和/或血管反应性，和c）全身血压和肾损害的进展， 疾病CYP 2C 8/2C 9或CYP 4A 11基因型与血压、胰岛素敏感性、 将探讨尿液和血浆EET和20-HETE水平，以确定病理生理学相关性 变异等位基因、AA环氧化/羟基化与个体对膳食盐变化的反应之间的关系 摄入、利尿剂或过氧化物酶体增殖物激活受体（α）配体的施用。我们 长期目标是从分子水平了解P450类花生酸在肾脏疾病中的作用， 生理学、其作用机制和位点以及与人类疾病的相关性。这些都需要 发展有意义的方法：a）人类病理生理学的明确定义 意义，和B）未来药理学靶向，以及临床诊断和干预。