Glomerular endothelial dysfunction in progressive renal diseases and aging kidney and development the novel therapeutic strategy
进行性肾病和肾脏衰老中的肾小球内皮功能障碍及开发新的治疗策略
基本信息
- 批准号:15590867
- 负责人:
- 金额:$ 2.24万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:2003
- 资助国家:日本
- 起止时间:2003 至 2004
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Endothelial dysfunction is a well-established pathogenetic mechanism underlying the development of vascular and renal complications in the various forms of renal injuries and aging kidney as well. The aim of this study is to elucidate the pathogenetic mechanism of renal injury and explore the possible mechanism that could underlie endothelial dysfunction in the systemic vasculature in the progressive forms of renal injuries and senescent kidney. We hypothesized that an imbalance between reactive oxygen species (ROS) and nitric oxide (NO) in the vasculature is implicated in both renal injury and macrovascular dysfunction.We have successfully developed the novel method by which one could observe the generation of ROS and NO in situ. Briefly, under general anesthesia, The rat whole body was perfused by the infusion pump with 37℃ phosphate buffer saline (PBS) at a flow rate of 5ml/min. Once blood had been removed, the whole body was perfused with PBS containing 0.01mmol/L diaminorhodamine- … More 4M AM (DAR-4M AM), 0.05mmol/L dichlorodihydrofluorescin diaceate (DCFH-DA), 0.1mmol/L L-Arginine, and 2mmol/L CaCl2 for 10 minutes at a flow rate of 3ml/min. To remove the unreacted reagent and fix tissues, a postperfusion was added with 4% paraformaldehyde containing 0.2mmol/L Nw-nitro-L-arginine methyl ester hydrochloride (L-NAME ; Sigma-Aldrich Japan) for 30 minutes at a flow rate of 5ml/min. Fluorescent images of ROS and NO were obtained with a confocal laser-scanning microscopy TCS-NT (Leica-Microsystems, Tokyo, Japan). The wavelength was as follow ; DAR-4M AM, excitation at 560nm and emission at 575nm ; DCFH-DA, excitation at 490nm and emission at 530nm.We have discovered increased generation of ROS and deceased baioavailable NO in the renal tissue in the 5/6 nephrectomized rats. Accumulation of nitrotyrosine, a trace of nitrosative stress, was also increased in the renal vasculature and aorta We also found NADPH oxidase activity was implicated in the generation of ROS in this model. Angiotensin receptor blocker inhibited increased productions of ROS and NO, and significantly reduced nitrosative stress Less
内皮功能障碍是各种形式的肾损伤和衰老肾脏中血管和肾脏并发症发展的一个公认的发病机制。本研究的目的是阐明肾损伤的发病机制,并探讨在肾损伤和肾脏衰老的进展形式中全身血管内皮功能障碍的可能机制。我们假设血管中活性氧(ROS)和一氧化氮(NO)的失衡与肾损伤和大血管功能障碍有关,并成功地发展了原位观察ROS和NO生成的新方法。简单地说,在全身麻醉下,用37℃磷酸盐缓冲液(PBS)以5 ml/min的流速通过输液泵灌注大鼠全身。一旦去除血液,用含0.01mmol/L二氨基罗丹明- ...更多信息 上午4个月用DAR-4 M AM、0.05mmol/L DCFH-DA、0.1mmol/L L-精氨酸、2 mmol/L CaCl_2以3 ml/min的流速灌注10分钟,后灌注加入含0.2mmol/L N-硝基-L-精氨酸甲酯盐酸盐的4%多聚甲醛用共聚焦激光扫描显微镜TCS-NT(Leica-Microsystems,Tokyo,Japan)获得ROS和NO的荧光图像。DAR-4 M AM,激发波长560 nm,发射波长575 nm; DCFH-DA,激发波长490 nm,发射波长530 nm。在肾血管和主动脉中,硝基酪氨酸的积累也增加,这是亚硝化应激的痕迹。我们还发现,在该模型中,NADPH氧化酶活性与ROS的产生有关。血管紧张素受体阻断剂抑制ROS和NO的产生,并显着降低亚硝化应激
项目成果
期刊论文数量(34)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
NAD(P)H oxidase and uncoupled nitric oxide synthase are major sources of glomerular superoxide in rats with experimental diabetic nephropathy
- DOI:10.1152/ajprenal.00221.2004
- 发表时间:2005-06-01
- 期刊:
- 影响因子:4.2
- 作者:Satoh, M;Fujimoto, S;Kashihara, N
- 通讯作者:Kashihara, N
Implication of peritubular capillary loss and altered expression ovascular endothelial growth factor in IgA nephropathy.
IgA 肾病中管周毛细血管丢失和卵血管内皮生长因子表达改变的意义。
- DOI:
- 发表时间:2006
- 期刊:
- 影响因子:0
- 作者:Namikoshi T;Satoh M;et al
- 通讯作者:et al
A novel free radical scarenger, edarabone, protects against cisplatin-induced acute renal damage in vitro and in vivo.
依达拉邦是一种新型自由基清除剂,可在体外和体内预防顺铂诱导的急性肾损伤。
- DOI:
- 发表时间:2003
- 期刊:
- 影响因子:0
- 作者:Satoh M;Kashihara N;et al
- 通讯作者:et al
A novel free radical scavenger, edarabone, protects against cisplatin-induced acute renal damage in vitro and in vivo
- DOI:10.1124/jpet.102.047522
- 发表时间:2003-06-01
- 期刊:
- 影响因子:3.5
- 作者:Satoh, M;Kashihara, N;Makino, H
- 通讯作者:Makino, H
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
KASHIHARA Naoki其他文献
KASHIHARA Naoki的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('KASHIHARA Naoki', 18)}}的其他基金
Development of the novel in vivo bio-imaging technique to visualize microcirculation of pancreatic islet and its application to elucidate the pathogenesis of diabetes
开发新型体内生物成像技术来可视化胰岛微循环及其在阐明糖尿病发病机制中的应用
- 批准号:
25560215 - 财政年份:2013
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Challenging Exploratory Research
Investigation on the mechanisms of association of chronic kidney disease(CKD) and cardiovascular diseases.
慢性肾脏病(CKD)与心血管疾病的关联机制研究。
- 批准号:
21591047 - 财政年份:2009
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Chronic kidney disease (CKD) as a risk factor for cardiovascular diseases: investigation on pathogenesis and development of therapeutic strategy
慢性肾脏病(CKD)作为心血管疾病的危险因素:发病机制的研究和治疗策略的制定
- 批准号:
19590969 - 财政年份:2007
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Implication of reactive oxygen species, nitric oxide, and their imbalance in the pathogenesis of chronic kidney disease
活性氧、一氧化氮及其失衡在慢性肾脏病发病机制中的意义
- 批准号:
17590852 - 财政年份:2005
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Possible implication of oxidative damages of mitochondria and mitochondrial DNA in the progressive renal injuries
线粒体和线粒体 DNA 氧化损伤在进行性肾损伤中的可能意义
- 批准号:
13671130 - 财政年份:2001
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Activation mechanism of NF-kB and development of therapeutic strategy through its regulation.
NF-kB 的激活机制以及通过其调节制定治疗策略。
- 批准号:
11671061 - 财政年份:1999
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The role of NF-kB in the pathogenesis of glomerulonephritis and therapeutic strategy through its regulation.
NF-kB 在肾小球肾炎发病机制中的作用及其调节的治疗策略。
- 批准号:
09671167 - 财政年份:1997
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Phenotypic change of mesangial cells in the glomerulosclerosis
肾小球硬化症中系膜细胞的表型变化
- 批准号:
05670955 - 财政年份:1993
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
相似海外基金
Exhaled Nitric Oxide and Oxidative Stress in Pulmonary Arterial Hypertention Asso
肺动脉高压症中的呼出一氧化氮和氧化应激
- 批准号:
7755378 - 财政年份:2009
- 资助金额:
$ 2.24万 - 项目类别:
Exhaled Nitric Oxide and Oxidative Stress in Pulmonary Arterial Hypertention Asso
肺动脉高压症中的呼出一氧化氮和氧化应激
- 批准号:
7622953 - 财政年份:2009
- 资助金额:
$ 2.24万 - 项目类别:
Exhaled Nitric Oxide and Oxidative Stress in Pulmonary Arterial Hypertention Asso
肺动脉高压症中的呼出一氧化氮和氧化应激
- 批准号:
8009484 - 财政年份:2009
- 资助金额:
$ 2.24万 - 项目类别:
The change of an oxidative stress marker induced by photo aging at the time of nitric oxide synthase defect
一氧化氮合酶缺陷时光老化诱导的氧化应激标志物的变化
- 批准号:
19890264 - 财政年份:2007
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Young Scientists (Start-up)
Obesity, Nitric Oxide, Oxidative Stress, and Salt Sensitivity
肥胖、一氧化氮、氧化应激和盐敏感性
- 批准号:
7515959 - 财政年份:2007
- 资助金额:
$ 2.24万 - 项目类别:
URINARY MARKERS OF OXIDATIVE STRESS AND NITRIC OXIDE METABOLISM IN INFANTS
婴儿氧化应激和一氧化氮代谢的尿液标志物
- 批准号:
7207792 - 财政年份:2005
- 资助金额:
$ 2.24万 - 项目类别:
Oxidative Stress and Nitric Oxide in Aged Myocardium
老化心肌中的氧化应激和一氧化氮
- 批准号:
6780704 - 财政年份:2004
- 资助金额:
$ 2.24万 - 项目类别:
Oxidative Stress and Nitric Oxide in Aged Myocardium
老化心肌中的氧化应激和一氧化氮
- 批准号:
6949896 - 财政年份:2004
- 资助金额:
$ 2.24万 - 项目类别:
Urinary markers of oxidative stress and nitric oxide metabolism in infants
婴儿氧化应激和一氧化氮代谢的尿液标志物
- 批准号:
7041898 - 财政年份:2004
- 资助金额:
$ 2.24万 - 项目类别:
A intervention study for improvement of decreased nitric oxide levels and oxidative stress in arsenosis patients in China
改善中国砷中毒患者一氧化氮水平下降和氧化应激的干预研究
- 批准号:
15406004 - 财政年份:2003
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (B)