Homocysteine and Angiotensin II in Renovascular Remodeling

同型半胱氨酸和血管紧张素 II 在肾血管重塑中的作用

• 批准号: 8259720
• 负责人: Utpal Sen
• 金额: $ 37.44万
• 依托单位: UNIVERSITY OF LOUISVILLE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-05-01 至 2016-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8259720
• 关键词: 3-Mercaptopyruvate sulfurtransferase; Angiogenic Factor; Angiography; Angiostatins; Angiotensin II; Angiotensin Receptor; Animals; Anti-Inflammatory Agents; Anti-inflammatory; Attenuated; Barium; Barium Sulfate; Basement membrane; Blood Pressure; Blood Vessels; Blood flow; C10; CCL2 gene; Clinical Data; Collagen; Collagen Type IV; Control Animal; Cystathionine; Disease; Endostatins; Enzyme-Linked Immunosorbent Assay; Enzymes; Equilibrium; Extracellular Matrix; Extracellular Matrix Proteins; Fibrosis; Folic Acid; Functional disorder; Gel; Gelatinase A; Genetic; Glomerular Capillary; Glomerular Filtration Rate; Goals; Health; High Pressure Liquid Chromatography; Histology; Homocysteine; Homocystine; Hyperhomocysteinemia; Hypertension; Individual; Inflammation; Inflammatory; Infusion procedures; Injury; Intercellular adhesion molecule 1; Kidney; Lasers; Lead; Link; Lyase; MTHFR gene; Matrix Metalloproteinases; Measures; Mediating; Messenger RNA; Metabolism; Methylenetetrahydrofolate reductase (NADPH); Mitochondria; Modeling; Morbidity - disease rate; Mus; NADP; Outcomes Research; Oxidases; Oxidative Stress; Pathogenesis; Patients; Perfusion; Plasma; Pump; Reactive Oxygen Species; Renal Blood Flow; Renal function; Renovascular Hypertension; Research; Reverse Transcriptase Polymerase Chain Reaction; Risk; Risk Factors; Roentgen Rays; Role; Sclerosis; Stress; Testing; Therapeutic; Tissue Inhibitor of Metalloproteinase-1; Tissue Inhibitor of Metalloproteinases; Tissues; Vascular Cell Adhesion Molecule-1; Vascular Endothelial Growth Factors; Western Blotting; base; bevacizumab; density; drinking water; glomerulosclerosis; in vivo; inhibitor/antagonist; kidney vascular structure; mortality; mouse model; oxidation; podocyte; protein expression; research study; soft tissue; systolic hypertension

DESCRIPTION (provided by applicant): Although it is not clear whether hyperhomocysteinemia (HHcy), an elevated plasma homocysteine (Hcy) level, causes hypertension, recent clinical data suggest an association between systolic hypertension and HHcy. Both angiotensin II (Ang II) and Hcy decrease blood flow; however, the role of Hcy in Ang II mediated decrease in blood flow and vascular density is unclear. Interestingly, preliminary studies of this proposal suggest that Ang II increases plasma Hcy level in mice. Treatment of Ang II animals with folic acid (FA) decreases plasma Hcy and mitigates hypertension. Based on our preliminary studies, in this proposal, we hypothesize that HHcy decreases blood flow in part by decreasing vascular density, increasing oxidative, pro-inflammatory, pro-fibrotic and anti-angiogenic factors in Ang II mediated renovascular remodeling. FA treatment through Hcy clearance mechanism reduces plasma Hcy level that mitigates renal remodeling. The hypothesis will be tested by following their specific aims: (1) To determine whether the Hcy contributes to Ang II hypertension, in part, by inducing oxidative stress (Nox2, gp47phox, Nox4 and mtROS), exacerbating renal inflammation by inducing MCP-1, MIP-2, ICAM-1, VCAM-1, and if FA ameliorates these changes; (2) To determine whether the Hcy instigates Ang II hypertension and renovascular fibrosis, in part, by inducing collagen IV, MMP-2, -9, -13; TIMP-1,-2, -3, -4; and if FA mitigates this renovascular fibrosis; and (3) To determine whether the Hcy promotes Ang II hypertension and decreases renovascular blood flow, in part, by unbalancing of angiogenic (VEGF) and anti-angiogenic factors (angiostatin and endostatin), and if FA increases vascular density and blood flow. WT (C57BL/6J) mouse, genetic mouse model of HHcy (CBS) and mouse deficient with angiotensin receptor I (AT1R-/-) will be used in this study. In WT and CBS mice, hypertension will be created by infusing Ang II (1000 ng/kg/min for 4 weeks) through alzet mini pump. Control animals will receive only vehicle. In a separate group of animals FA (0.015g/L, in drinking water) will be introduced after 2 weeks of Ang II infusion and will be continued until the end of experiments (total 2 weeks). Appropriate FA controls will be used. AT1R-/- mice will be treated with or without Hcy (1.8 g/L for 4 weeks) to determine whether the effect of HHcy is AT1R dependent. Ambulatory blood pressure will be measured by DSI radiotelemetry (model TA11PA- C10). Plasma Hcy will be measured by HPLC. Vascular density will be measured by in vivo soft-tissue Barium sulfate-contrast X-ray angiography and renal cortical blood flow by moorFLPI full-filled laser perfusion imager. Renal function will be determined by measuring glomerular filtration rate (GFR). Histological kidney sections will be used to detect ROS, collagen, mesangial widening and podocyte injury. Plasma MCP-1, MIP-2, VCAM- 1 and ICAM-1 will be measured by ELISA. Tissue collagen, MMPs, TIMPs, Nox2, p47phox, Nox4, ICAM-1, VCAM-1 protein expressions will be measured by Western blot and immunostaining. MMPs activities will be measured by in gel zymography, TIMPs activity by reverse zymography, and mRNA abundance by Q-PCR. In addition to confirming the preliminary studies, the scope of the research will be extended to understand the implications of FA treatment in Ang II-induced hypertension to modulate pro-inflammatory, pro-fibrotic and anti- angiogenic factors. The results of this study will increase our understanding of role of Hcy in Ang II hypertension and renovascular remodeling. Additionally, the research outcome will provide the missing information of HHcy as a potential risk factor of renovascular fibrosis, which exacerbates hypertension, and will lead to develop or modify current therapeutic strategies of renovascular disease.

描述（由申请人提供）：虽然尚不清楚高同型半胱氨酸血症（HHcy），即血浆同型半胱氨酸（Hcy）水平升高是否会导致高血压，但最近的临床数据表明收缩期高血压与HHcy之间存在关联。血管紧张素II （Ang II）和Hcy均可减少血流量；然而，Hcy在Ang II介导的血流量和血管密度下降中的作用尚不清楚。有趣的是，这项提议的初步研究表明，Ang II增加了小鼠血浆Hcy水平。用叶酸（FA）治疗Ang II型动物可降低血浆Hcy并减轻高血压。根据我们的初步研究，在本提案中，我们假设HHcy在一定程度上通过降低血管密度，增加Ang II介导的肾血管重构中的氧化、促炎、促纤维化和抗血管生成因子来减少血流量。FA治疗通过Hcy清除机制降低血浆Hcy水平，减轻肾脏重构。该假设将通过以下具体目标进行验证：(1)确定Hcy是否通过诱导氧化应激（Nox2, gp47phox， Nox4和mtROS），通过诱导MCP-1， MIP-2, ICAM-1， VCAM-1加剧肾脏炎症，以及FA是否改善这些变化来促进Ang II型高血压；(2)确定Hcy是否部分通过诱导IV型胶原、MMP-2、-9、-13诱导Ang II型高血压和肾血管纤维化；Timp-1,-2, -3, -4；如果FA减轻了肾血管纤维化；(3)确定Hcy是否通过血管生成因子（VEGF）和抗血管生成因子（血管抑制素和内皮抑制素）失衡而促进Ang II型高血压并减少肾血管血流，以及FA是否增加血管密度和血流。本研究将采用WT （C57BL/6J）小鼠、HHcy （CBS）遗传小鼠模型和血管紧张素受体I （AT1R-/-）缺陷小鼠。在WT和CBS小鼠中，通过alzet小泵灌注Ang II （1000 ng/kg/min，持续4周）引起高血压。对照动物只接受载具。在另一组动物中，在Ang II输注2周后加入FA （0.015g/L，饮用水中），并持续到实验结束（共2周）。将使用适当的FA控制。将AT1R-/-小鼠分别给予或不给予Hcy （1.8 g/L，持续4周），以确定Hcy的作用是否依赖于AT1R。动态血压由DSI无线遥测仪（TA11PA- C10型）测量。采用高效液相色谱法测定血浆Hcy。血管密度通过体内软组织硫酸钡对比x线血管造影测量，肾皮质血流通过moorFLPI全填充激光灌注成像仪测量。肾功能将通过测量肾小球滤过率（GFR）来确定。肾组织切片将用于检测ROS、胶原、系膜增宽和足细胞损伤。ELISA检测血浆MCP-1、MIP-2、VCAM- 1和ICAM-1。Western blot和免疫染色检测组织胶原蛋白、MMPs、TIMPs、Nox2、p47phox、Nox4、ICAM-1、VCAM-1蛋白的表达。用凝胶酶谱法测定MMPs活性，用反向酶谱法测定TIMPs活性，用Q-PCR测定mRNA丰度。除了确认初步研究外，研究的范围将扩大到了解FA治疗在Ang ii诱导的高血压中调节促炎、促纤维化和抗血管生成因子的意义。本研究结果将增加我们对Hcy在II型高血压和肾血管重构中的作用的理解。此外，该研究结果将提供HHcy作为肾血管性纤维化的潜在危险因素的缺失信息，这将导致开发或修改当前肾血管性疾病的治疗策略。