Defining renal S1P/sPRR/AT1R pathway in salt-sensitive hypertension

盐敏感性高血压肾 S1P/sPRR/AT1R 通路的定义

• 批准号: 9888044
• 负责人: Tianxin Yang
• 金额: --
• 依托单位: VA SALT LAKE CITY HEALTHCARE SYSTEM
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-10-01 至 2024-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9888044
• 关键词: Address; Antihypertensive Agents; Attenuated; Binding; Biological Markers; Biological Process; Blood Pressure; Cardiovascular Diseases; Chronic Kidney Failure; Data; Development; Enzymes; Equilibrium; Extracellular Domain; Fluid Balance; Generations; Goals; Hypertension; Inbred Dahl Rats; Injury to Kidney; Kidney; Mediating; Modeling; Pathogenesis; Pathway interactions; Peptide Hydrolases; Pharmacology; Production; Rattus; Receptor Inhibition; Receptor Signaling; Receptor, Angiotensin, Type 1; Regulation; Renal tubule structure; Renin; Renin-Angiotensin System; Renin-Angiotensin-Aldosterone System; Reporting; Role; Tertiary Protein Structure; Testing; Water; epithelial Na+ channel; human disease; hypertension treatment; inhibitor/antagonist; insight; member; neutralizing antibody; novel; receptor; salt sensitive; salt sensitive hypertension; site-1 protease

The important role of renin-angiotensin-aldosterone system in the pathogenesis of hypertension is highlighted by the wide use of its inhibitors for treatment of hypertension. The current proposal will address the role of renal site-1 protease/soluble (pro)renin receptor in pathogenesis of salt-sensitive hypertension. The proposal has the potential to advance our understanding of the fundamental mechanism of hypertension and also to identify a novel target for antihypertensive therapies.

肾素-血管紧张素-醛固酮系统在糖尿病发病机制中的重要作用 高血压的突出表现是其抑制剂广泛用于治疗高血压。 目前的提案将讨论肾脏位点 1 蛋白酶/可溶性肾素原 (pro) 的作用 盐敏感性高血压发病机制中的受体。该提案有可能 加深我们对高血压基本机制的认识， 确定抗高血压治疗的新靶点。