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
基本信息
- 批准号:06557146
- 负责人:
- 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
- 起止时间:1994 至 1995
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
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.
成人呼吸窘迫综合征(ARDS)可作为多种疾病(包括败血症)的并发症发生,但尚不可能确定哪些高危患者会发生严重疾病。我们已经建立了一种比以前更快速和简单的方法来测量血清锰超氧化物歧化酶水平,并研究了在血液中连续测量的六种标志物预测脓毒症患者ARDS发展的能力。(发生ARDS前6- 24 h),6例继发ARDS患者血清锰超氧化物歧化酶浓度和过氧化氢酶活性均高于未发生ARDS的患者,酶预测脓毒症患者ARDS的发展与同时评估血清乳酸脱氢酶活性和因子VIII浓度具有相同的敏感性、特异性和有效性。相比之下,血清谷胱甘肽过氧化物酶活性和α Pi-弹性蛋白酶复合物的浓度并没有显着差异,在最初诊断的脓毒症的患者之间,谁没有随后发展的ARDS,并没有有效的预测ADRS.Measurement锰超氧化物歧化酶的发展,除了其他标志物,应有助于识别患者的最高风险的ARDS,并允许前瞻性治疗。
项目成果
期刊论文数量(24)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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。”
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
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)。
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
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)。
- DOI:
- 发表时间:
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- 影响因子:0
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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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- 发表时间:
- 期刊:
- 影响因子:0
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M.Asahi: "Inactivation of Glutathione Peroxidase by Nitric Oxide : Implication for Cytotoxicity." J.Biol.Chem.270. 21035-21039 (1995)
M.Asahi:“一氧化氮使谷胱甘肽过氧化物酶失活:对细胞毒性的影响。”
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- 影响因子:0
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TANIGUCHI Naoyuki其他文献
TANIGUCHI Naoyuki的其他文献
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{{ truncateString('TANIGUCHI Naoyuki', 18)}}的其他基金
Biological Regulation of GlcNAc cycle
GlcNAc 循环的生物调节
- 批准号:
20249018 - 财政年份:2008
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Integrated analyses of biological functions of sugar chains : Glycomics
糖链生物学功能的综合分析:糖组学
- 批准号:
13854010 - 财政年份:2001
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Scientific Research (S)
Redox regulation by glutathione and the roles of reactive oxygen and nitrogen species
谷胱甘肽的氧化还原调节以及活性氧和氮的作用
- 批准号:
10044286 - 财政年份:1998
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Regulation of Cellular Activity by Reactive Oxygen
活性氧对细胞活性的调节
- 批准号:
08408028 - 财政年份:1996
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Remodeling of cell surface oligosaccharides by introduction of glycogenes and its application
糖原引入对细胞表面寡糖的重塑及其应用
- 批准号:
08557015 - 财政年份:1996
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Significance of sugar moiery of recombinant glycoproteins
重组糖蛋白糖部分的意义
- 批准号:
07044263 - 财政年份:1995
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for international Scientific Research
Site-specific fragmentation of superoxide dismutase and DNA damage
超氧化物歧化酶的位点特异性断裂和 DNA 损伤
- 批准号:
06454166 - 财政年份:1994
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
The post-translational modification of proteins
蛋白质的翻译后修饰
- 批准号:
03304028 - 财政年份:1991
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Co-operative Research (A)
Enzyme immunoassay of human Mn-superoxide dismutase and its clinical application : Monitoring for myocardial injury.
人锰超氧化物歧化酶的酶联免疫分析及其临床应用:心肌损伤的监测。
- 批准号:
02557097 - 财政年份:1990
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
Inactivation of Cu,Zn-superoxide dismutase due to glycation
糖化导致铜、锌超氧化物歧化酶失活
- 批准号:
63480501 - 财政年份:1988
- 资助金额:
$ 5.31万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
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锰超氧化物歧化酶 (MnSOD) 对 RA 滑膜成纤维细胞线粒体活性氧化物质和凋亡细胞死亡的影响
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19592175 - 财政年份:2007
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