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Influence of enhanced antigenicity of renal vascular endothelium induced ischemia/reperfusion injury on the antigen antibody reaction in organ transplantation and the study of protective strategy for enhancedantigenicity

Influence of enhanced antigenicity of renal vascular endothelium induced ischemia/reperfusion injury on the antigen antibody reaction in organ transplantation and the study of protective strategy for enhancedantigenicity
肾血管内皮抗原性增强所致缺血/再灌注损伤对器官移植抗原抗体反应的影响及增强抗原性保护策略的研究
批准号:
15591668
负责人:
SATOH Shigeru
金额:
$1.73万
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
项目状态:
已结题
起止时间:
2003 至 2004

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中文摘要
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英文摘要
Several studies suggested that the vascular endothelial cells function as resident antigen presenting cells by presenting not only human leukocyte antigen but also costimulatory adhesionmoleculesB7 and these molecules expression was up-regulated both during acute rejection and after ischemia/reperfusion (I/R) injury. I/R injury may enhance allograft antigenicity in organ transplantation without antigen-antibody reaction. The present research studied the protective effects of resveratrol, a phenolic product anti-oxidant, on renal function and the expression of CD86 in rat kidneys with I/R injury.Wister rats were divided into four groups ; an I/R group, receiving right nephrectomy and 1-hour clamping of the left renalpedicle ; a Vehicle group, I/R plus 10% ethanol (0.1 ml/kg) by intra-peritoneum from day -1 through to 7; a Resveratrol group, I/S plus 4mg/kg resveratrol ; and a Shamgroup. Blood samples were obtained viathetailveinat-1,1,3,and 7days after the operation for the measurement … More of serum creatinine (Scr) levels. The expression of the CD86 protein was examined by immunofluorescence staining and quantitative level of CD86 messenger RNA (mRNA) was by real time reverse transcription polymerase chain reaction in the renal cortex at day 3. The presence of oxidative damage was assessed by determining the level of thiobarbituric acid reactive substance (TBARS) in renal homogenates.Scr levels of the Resveratrol group were significantly lower than those of the I/R and Vehicle groups on days 1 and 3 after the operation. The expression of CD86 protein in the glomerular endothelium was attenuated in the Resveratrol group compared to the I/R or Vehicle group. In the Resveratrol group, the CD86 mRNA levels was significantly lower than that in the I/R or Vehicle group, moreover, it was significantly lowerly about one fifth than that in the Shamgroup.Our results suggested that resveratrol markedly reduces renaldys function and at tenuates the mRNA and protein expression of CD86 following I/R injury. Less
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Effects of a phenolic compound, resveratrol, on the renal function and costimulatory adhesion molecule CD86 expression in rat kidneys with ischemia/reperfusion injury.
酚类化合物白藜芦醇对缺血/再灌注损伤大鼠肾脏肾功能和共刺激粘附分子 CD86 表达的影响。
DOI: 10.1679/aohc.68.41
发表时间: 2005
期刊: Archives of histology and cytology
影响因子: --
作者: [M. Saito*, S. Satoh, N. Kojima, H. Tada, Mitsuru Sato, Toshio Suzuki, H. Senoo, T. Habuchi]
通讯作者: T. Habuchi
Effects of a phenolic compound, resveratrol, on the renal function and costimulatory adhesion molecule CD86 expression in rat kidney with ischemia/reperfusion injury
酚类化合物白藜芦醇对缺血/再灌注损伤大鼠肾脏肾功能及共刺激粘附分子CD86表达的影响
DOI: --
发表时间: 2005
期刊: Archives of Histology and Cytology 68
影响因子: --
作者: [M Saito, S Satoh, N Kojima, H Tada, M Sato, T Suzuki, H Senoo, T Habuch]
通讯作者: T Habuch
Effects of phenolic compound, resveratrol, on the renal function and costimulatory adhesion molecule CD86 expression in rat kidneu with ischemia/reperfusion iniury
酚类化合物白藜芦醇对缺血/再灌注损伤大鼠肾功能及共刺激粘附分子CD86表达的影响
DOI: --
发表时间: 2005
期刊: Archives of Histology and Cytology 68
影响因子: --
作者: [M Saito, S Satoh, N Kojima, H Tada, M Sato, T Suzuki, H Senoo, T Habuch]
通讯作者: T Habuch
Analysis of the role of abscisic acid in the induction of ethylene biosynthesis in cut carnation flowers undergoing senescence
  • 批准号:
    24580050
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.49万
  • 财政年份:
    2012
  • 负责人:
    SATOH Shigeru
  • 依托单位:
Factors Increasing Interstitial Fibrosis and Its Reduction with Personalized Dosing of Immunosuppressive Drugs after Kidney Transplantation
  • 批准号:
    23592378
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.75万
  • 财政年份:
    2011
  • 负责人:
    SATOH Shigeru
  • 依托单位:
Community management for citizen participation and self-governing improvement in China
  • 批准号:
    23404025
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 资助金额:
    $8.82万
  • 财政年份:
    2011
  • 负责人:
    SATOH Shigeru
  • 依托单位:
Clinical and Genomic Risk Factors for Early Onset of Chronic Allograft Nephropathy
  • 批准号:
    20591894
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.0万
  • 财政年份:
    2008
  • 负责人:
    SATOH Shigeru
  • 依托单位:
国内基金
海外基金
缺氧诱导因子(HIF)-2α转录抑制树突状细胞CD36表达减轻肾脏缺血再灌注损伤的机制
  • 批准号:
    82370751
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    张明
  • 依托单位:
骨髓抑制再生单个核细胞移植通过调节线粒体功能在脑缺血再灌注损伤中的神经保护机制研究
  • 批准号:
    82371301
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    李轶
  • 依托单位:
TRIM21蛋白促进HIF1α的降解介导耳蜗血管纹缘细胞缺血再灌注致听力损伤的机制研究
  • 批准号:
    82371142
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    刘君
  • 依托单位:
肢体缺血后适应抑制肺泡巨噬细胞活化及防治肺缺血再灌注损伤机制的研究
  • 批准号:
    81070041
  • 项目类别:
    面上项目
  • 资助金额:
    32.0万元
  • 批准年份:
    2010
  • 负责人:
    甘辉立
  • 依托单位: