Cardiorenal association
Cardiorenal association
批准号:
15390264
负责人:
ITO Sadayoshi
金额:
$9.54万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2004
中文摘要
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英文摘要
Close relation exists between the kidney function and cardiovascular morbidity/mortality. Inhibition of the renin-angiotensin system (RAS) and/or aldosterone improve outcome of patients with heart failure. It is suggested that in order to achieve cardiorenal protection, high doses of RAS inhibitors must be used. However, because of elevation of serum creatinine or potassium, many patients are often not treated with RAS blockers or high enough doses. This study aimed to clarify mechanisms that relate the kidney and heart. The means to prevent decline in renal function associated with RAS blockade were investigated.Non-genomic action of aldosterone : We studied a rapid non-genomic action of aldosterone in isolated microperfused rabbit afferent or efferent arterioles. Aldosterone induced vasoconstriction in both arterioles within 5 minutes, and the constriction was stronger in efferent arterioles. The constriction was not blocked with a mineralocorticoid receptor blocker but blocked with … More phospholipase C inhibitors. In addition, removal of the endothelium enhanced the constriction. Our studies suggest that aldosterone causes constriction of glomerular arterioles via nongenomic mechanisms.Effect of adenosine A1 receptor blocker (AAB) in Dahl salt sensitive rats (SSR) : Adenosine has unique actions in intrarenal hemodynamics. We studied the effect of AAB or furosemide (Fur) alone or in combination on top of enalapril (ENA) on blood pressure, renal function and histology in SSR. Phenotypic changes of mesangial and epithelial cells were also assessed with immunohistochemistry. Compared with vehicle group, urinary protein excretion and serum creatinine levels were lower in the ENA+FK, ENA+Fur and ENA+FK+Fur groups, and survival rate was 27, 71. 80 and 88%, respectively. Phenotypic changes, particularly those in epithelial cells, were least in the last group. We conclude that in SSR combination of FK, ENA and Fur inhibits macrophage infiltration, phenotypic changes in mesangial and epithelial cells, and thereby protects the kidney and improve survival rate. Less
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Successful Treatment of Severe Hypertension with the Combination of Angiotensin Converting Enzyme Inhibitor and Angiotensin II Receptor Blocker.
联合使用血管紧张素转换酶抑制剂和血管紧张素 II 受体阻滞剂成功治疗严重高血压。
DOI:
--
发表时间:
2003
期刊:
Hypertens Res 26
影响因子:
--
作者:
[Hattori N, Mizuno Y, Ando Y et al., Tanemoto M]
通讯作者:
Tanemoto M
Ishizuka T, Ito O, Ito S, et al.: "Regulation of Cytochrome P-450 4A Activity by Peroxisome Proliferator-Activated Receptors in the Rat Kidney"Hypertens Res. 26. 929-936 (2003)
Ishizuka T、Ito O、Ito S 等人:“大鼠肾脏中过氧化物酶体增殖物激活受体对细胞色素 P-450 4A 活性的调节”Hypertens Res。
DOI:
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发表时间:
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作者:
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DOI:
10.1007/s11010-005-9038-x
发表时间:
2006-03-01
期刊:
MOLECULAR AND CELLULAR BIOCHEMISTRY
影响因子:
4.3
作者:
[Ito, O, Nakamura, Y, Kohzuki, M]
通讯作者:
Kohzuki, M
Arima S, Ito S.: "The Mechanisms Underlying Altered Vascular Resistance of Glomerular Afferent and Efferent Arterioles in Diabetic Nephropathy"Nephrol Dial Transplant. 18. 1966-1969 (2003)
Arima S,Ito S.:“糖尿病肾病肾小球传入和传出小动脉血管阻力改变的机制”肾拨号移植。
DOI:
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发表时间:
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作者:
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通讯作者:
Suzuki T, Mikkaichi T, Ito S, et al.: "Isolation and Characterization of Novel Kidney-Specific Digoxin Transporters"Proc.Natl.Acad Sci U.S.A.. (in press). (2004)
Suzuki T、Mikkaichi T、Ito S 等人:“新型肾脏特异性地高辛转运蛋白的分离和表征”Proc.Natl.Acad Sci U.S.A.(正在出版)。
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共 39 条
Exploration of specific biomarkers for carbonyl stress inducible disease.
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批准号:24390211
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.65万
-
财政年份:2012
-
负责人:ITO Sadayoshi
-
依托单位:
Role of amine-carbonyl reaction as a novel mechanism for renal disease
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批准号:22659164
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项目类别:Grant-in-Aid for Challenging Exploratory Research
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资助金额:$2.07万
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财政年份:2010
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负责人:ITO Sadayoshi
-
依托单位:
Mechanisms of cardiovascular-renal connection on life-style diseases
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批准号:21390259
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$11.48万
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财政年份:2009
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负责人:ITO Sadayoshi
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依托单位:
Empire, Nation-state and Region in Modern Western World.
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批准号:15320103
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$10.18万
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财政年份:2003
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负责人:ITO Sadayoshi
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依托单位:
Mechanisms regulating glomerular hemodynamics
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批准号:12470208
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.96万
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财政年份:2000
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负责人:ITO Sadayoshi
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依托单位:
The Control of Glomerular hemodynamics and its significance in renal dysfunction and hypertension
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批准号:10470215
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$8.19万
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财政年份:1998
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负责人:ITO Sadayoshi
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依托单位:
Control of glomerular function by juxtaglomerular apparatus
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批准号:08044233
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$1.54万
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财政年份:1996
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负责人:ITO Sadayoshi
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依托单位:
Role of the juxtaglomerular apparatus in hypertension and progressive renal impairment
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批准号:08457283
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$5.38万
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财政年份:1996
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负责人:ITO Sadayoshi
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依托单位:
国内基金
海外基金
Renin-Angiotensin System在介导机械通气所致肺微血管内皮细胞功能障碍中的作用及其机制研究
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批准号:81372100
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项目类别:面上项目
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资助金额:70.0万元
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批准年份:2013
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负责人:毛燕飞
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依托单位:
骨化三醇降低IgA肾病患者尿蛋白的机制研究
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批准号:81100503
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项目类别:青年科学基金项目
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资助金额:22.0万元
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批准年份:2011
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负责人:刘立军
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依托单位: