Novel Aspects of the Cardiac Renin-Angiotensin System

心脏肾素-血管紧张素系统的新方面

• 批准号: 7915547
• 负责人: KENNETH Melvin BAKER
• 金额: $ 31.5万
• 依托单位: TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-17 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7915547
• 关键词: AGTR2 gene; Adult; Affect; Affinity; Affinity Chromatography; Anabolism; Angiotensin II; Angiotensin Receptor; Angiotensin-Converting Enzyme Inhibitors; Angiotensinogen; Animal Model; Antibodies; Apoptosis; Binding; Binding Proteins; Binding Sites; Biological; Blood Vessels; Cardiac; Cardiac Myocytes; Cardiovascular system; Catheterization; Cell Nucleus; Cells; Characteristics; Chinese Hamster Ovary Cell; Chymase; Clinical; Clinical Trials; Co-Immunoprecipitations; Column Chromatography; Complications of Diabetes Mellitus; Cytoplasm; Data; Development; Diabetes Mellitus; Disease; Echocardiography; Endocrine; Event; Fibroblasts; Fibrosis; Figs - dietary; Functional disorder; Gene Components; Gene Expression; Gene Proteins; Genetic; Glucose; Glycolysis; Heart; Heart Diseases; Heart Hypertrophy; Hexosamines; Homeostasis; Human; Hyperglycemia; In Vitro; Inactive Renin; Intervention; Kidney; Knockout Mice; Label; Lead; Left; Life; Mass Spectrum Analysis; Measurement; Mediating; Meta-Analysis; Metabolic; Mus; Muscle Cells; Neonatal; Nuclear; Oxidative Stress; Pathology; Pathway interactions; Patients; Peptides; Peptidyl-Dipeptidase A; Phosphorylation; Prevention; Probability; Protein Biosynthesis Pathway; Protein Glycosylation; Proteins; Radiolabeled; Rattus; Regulation; Relative (related person); Renin; Renin-Angiotensin System; Reporting; Research; Role; Sepharose; Smooth Muscle Myocytes; Sodium Chloride; Source; Sp1 Transcription Factor; Specificity; Streptozocin; Structure; System; TP53 gene; Testing; Time; Ventricular; Water; analog; autocrine; base; diabetic; diabetic cardiomyopathy; diabetic patient; diabetic rat; extracellular; glycosylation; in vivo; inhibitor/antagonist; kidney vascular structure; mesangial cell; non-diabetic; novel; novel strategies; paracrine; promoter; protein expression; public health relevance; radiotracer; receptor; research study; transcription factor

DESCRIPTION (provided by applicant): The renin angiotensin system (RAS) has a central role in cardiovascular homeostasis and development of renal, vascular, and cardiac pathologies. The effects of angiotensin II (Ang II) are primarily mediated by binding to AT1 receptor in an endocrine and/or autocrine/paracrine manner. We and others have recently identified a novel, intracrine or intracellular, mode of Ang II-mediated actions that do not require Ang II-AT1 interaction. We reported that cardiac myocytes synthesize high levels of Ang II intracellularly, which redistributes to cytoplasm and nucleus, without affecting extracellular levels, in high glucose conditions. Intracellular Ang II (iAng II) synthesis in high glucose conditions is chymase, not angiotensin converting enzyme (ACE) dependent. Intracellular synthesis of Ang II is completely blocked by a renin inhibitor. We have also observed activation of the intracellular RAS in cardiac fibroblasts. Significantly, iAng II levels, cardiac myocyte apoptosis, oxidative stress, and cardiac fibrosis are markedly increased in the heart of diabetic rats, which are normalized by renin inhibition, not by ACE or AT1 inhibition. These observations suggest a significant role of iAng II in diabetic cardiomyopathy, with the implications that AT1 receptor antagonists and ACE inhibitors would be ineffective in blocking iAng II effects. The cellular mechanisms that lead to intracellular expression of RAS components and Ang II synthesis, in high glucose conditions, and the mechanism of iAng II actions are not known. We have reported that iAng II causes cardiac hypertrophy; however, the relative significance of iAng II versus extracellular Ang II in pathophysiological conditions is not known. In this proposal, we will test the hypothesis that metabolic changes, induced by high glucose, result in intracellular synthesis of Ang II, which has a significant role in development of diabetic cardiomyopathy, through interaction with novel intracellular proteins. We will use cardiac myocytes and fibroblasts, both neonatal and adult, to identify hyperglycemia-induced cellular events, such as the hexosamine biosynthesis pathway, protein O-glycosylation and oxidative stress, on regulation of the intracellular RAS, by pharmacological and genetic approaches. We will identify and characterize novel iAng II interacting proteins, using affinity binding and mass spectrometry approaches. AT1 receptor deficient mice will be utilized to determine the specific role of iAng II in diabetic cardiac dysfunction. The proposed studies will identify novel mechanisms of Ang II actions in the heart and provide for new strategies in clinical interventions for diabetic cardiomyopathy. PUBLIC HEALTH RELEVANCE: This research will focus on the development of novel strategies for the treatment of patients with diabetes. Blockade of the intracellular renin-angiotensin system, may provide substantial benefit for the prevention/treatment of diabetic cardiomyopathy, compared to standard therapy with angiotensin receptor blockers and angiotensin converting enzyme inhibitors.

描述(由申请人提供)：肾素血管紧张素系统(RAS)在心血管内稳态和肾脏、血管和心脏病理的发展中起着核心作用。血管紧张素II(Ang II)的作用主要通过与AT1受体的内分泌和/或自分泌/旁分泌方式介导。我们和其他人最近发现了一种新的Ang II介导的不需要Ang II-AT1相互作用的作用模式。我们报道在高糖条件下，心肌细胞在细胞内合成高水平的Ang II，Ang II重新分布到胞浆和胞核，而不影响细胞外水平。在高糖条件下，细胞内Ang II(Iang II)的合成依赖于糜酶，而不依赖于血管紧张素转换酶(ACE)。血管紧张素II的细胞内合成被肾素抑制剂完全阻断。我们还观察到心脏成纤维细胞内RAS的激活。值得注意的是，糖尿病大鼠心脏中Iang II水平、心肌细胞凋亡、氧化应激和心脏纤维化显著增加，这些都通过肾素抑制而不是ACE或AT1抑制来正常化。这些观察表明Iang II在糖尿病心肌病中起重要作用，AT1受体拮抗剂和ACE抑制剂在阻断Iang II效应方面无效。在高糖条件下，导致RAS组分的细胞内表达和Ang II合成的细胞机制以及Iang II的作用机制尚不清楚。我们已经报道了Iang II导致心肌肥厚；然而，Iang II和细胞外Ang II在病理生理条件下的相对意义尚不清楚。在这个提案中，我们将验证这样的假设，即高糖诱导的代谢变化导致细胞内Ang II的合成，Ang II通过与新的细胞内蛋白相互作用而在糖尿病心肌病的发展中发挥重要作用。我们将使用心肌细胞和成纤维细胞，包括新生儿和成人，以确定高血糖诱导的细胞事件，如氨基己糖生物合成途径，蛋白质O-糖基化和氧化应激，通过药理学和遗传学方法调节细胞内RAS。我们将使用亲和结合和质谱学方法鉴定和表征新的Iang II相互作用蛋白。AT1受体缺陷小鼠将被用来确定Iang II在糖尿病心脏功能障碍中的特定作用。这些拟议的研究将确定Ang II在心脏中的新作用机制，并为糖尿病心肌病的临床干预提供新的策略。公共卫生相关性：这项研究将侧重于开发治疗糖尿病患者的新策略。与血管紧张素受体阻滞剂和血管紧张素转换酶抑制剂的标准治疗相比，阻断细胞内肾素-血管紧张素系统可能为糖尿病心肌病的预防/治疗提供实质性的好处。