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Development and practical use of predictive methods of adult respiratory distress syndrome in patients with sepsis

Development and practical use of predictive methods of adult respiratory distress syndrome in patients with sepsis
脓毒症患者成人呼吸窘迫综合征预测方法的开发和实践应用
批准号:
06557146
负责人:
TANIGUCHI Naoyuki
金额:
$5.31万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

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中文摘要
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英文摘要
Adult respiratory distress syndrome (ARDS) can develop as a complication of various disorders, including sepsis, but it has not been possible to identify which of the patients at risk will develop serious disorfer. We have established a more rapid and easy method to measure serum levels of manganese superoxide dismutase than before and investigated the ability of six markers, measured sequentially in blood, to predict development of ARDS in patients with sepsis.At the initial diagnosis of sepsis (6-24h before the development of ARDS), serum manganese superoxide dismutase concentration and catalase activity were higher in the 6 patients who subsequently developed ARDS than in patients who did not develop ARDS.These changes in antioxidant enzymes predicted the development of ARDS in septic patients with the same sensitivity, specificity, and efficiency as simultaneous assessments of serum lactate dehydrogenase activity and factor VIII concentration. By contrast, serum glutathione peroxidase activity and alpha Pi-elastase complex concentration did not differ at the initial diagnosis of sepsis between patients who did and did not subsequently develop ARDS,and were not as effective in predicting the development of ARDS.Measurement of manganese superoxide dismutase, in addition to the other markers, should facilitate identification of patients at highest risk of ARDS and allow prospective treatment.
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S.Goto: "Augment of transport for cisplatin-glutathione adduct in cisplatin-resistant cancer cells." Cancer Res.55. 4297-4301 (1995)
S.Goto:“增强顺铂-谷胱甘肽加合物在顺铂耐药癌细胞中的转运。”
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Y.Kayanoki: "Suppression of antioxidative enzyme expression by transforming growthfactor-β1 in rat hepatocytes." J.Biol.Chem.269. 15488-15492 (1994)
Y. Kayanoki:“通过转化生长因子-β1 抑制大鼠肝细胞中的抗氧化酶表达。”J.Biol.Chem.269(1994)。
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Kayanoki Y.: "Suppression of antioxidative enzyme expression by transforming growth tactor-β1 in rat hepatocytes." J.Biol.Chem.269. 15488-15492 (1994)
Kayanoki Y.:“通过转化大鼠肝细胞中的生长因子-β1 来抑制抗氧化酶的表达。”J.Biol.Chem.269(1994)。
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Takahashi M.: "In Vivo Glycation of Aldehyde Reductase,a Major 3-Deoxyglucosone Reducing Enzyme:ldentification of Glycation Sites." Biochemistry. 34. 1443-1438 (199)
Takahashi M.:“醛还原酶的体内糖化,一种主要的 3-脱氧葡萄糖酮还原酶:糖化位点的识别。”
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20
    Biological Regulation of GlcNAc cycle
    Integrated analyses of biological functions of sugar chains : Glycomics
    • 批准号:
      13854010
    • 项目类别:
      Grant-in-Aid for Scientific Research (S)
    • 资助金额:
      $78.71万
    • 财政年份:
      2001
    • 负责人:
      TANIGUCHI Naoyuki
    • 依托单位:
    Redox regulation by glutathione and the roles of reactive oxygen and nitrogen species
    • 批准号:
      10044286
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $9.92万
    • 财政年份:
      1998
    • 负责人:
      TANIGUCHI Naoyuki
    • 依托单位:
    Regulation of Cellular Activity by Reactive Oxygen
    • 批准号:
      08408028
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $21.18万
    • 财政年份:
      1996
    • 负责人:
      TANIGUCHI Naoyuki
    • 依托单位:
    海外基金