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Burn injury differentially alters whole-blood and organ glutathione synthesis rates: An experimental model

烧伤差异改变全血及脏器谷胱甘肽合成速率的实验模型

作     者:Zhe-Wei Fei Vernon R. Young Xiao-Ming Lu Andrew B. Rhodes Ronald G.Tompkins Alan J. Fischman Yong-Ming Yu 

作者机构:Shriners Burns Hospital and Burn & Trauma Service Massachusetts General Hospital Harvard Medical School Boston MA 02114 Shriners Burns Hospital and Burn & Trauma Service Massachusetts General Hospital Harvard Medical School Boston MA 02114 Laboratory of Human Nutrition Massachusetts Institute of Technology Cambridge MA 02142 USA 

出 版 物:《Burns & Trauma》 (烧伤与创伤(英文))

年 卷 期:2013年第1卷第2期

页      面:87-94页

学科分类:0831[工学-生物医学工程(可授工学、理学、医学学位)] 1002[医学-临床医学] 081704[工学-应用化学] 1001[医学-基础医学(可授医学、理学学位)] 07[理学] 1011[医学-护理学(可授医学、理学学位)] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学] 0836[工学-生物工程] 

基  金:NIH grants GM 02700  DK 15856  P-30-DK-40561  and grants from the Shriners Burns Hospital 84070 

主  题:Burn injury glutathione glutathione concentration synthesis rate whole blood 

摘      要:Previous studies from our laboratories revealed a reduced rate of whole-blood (WB) glutathione (GSH) synthesis in severely burned patients. To determine whether WB GSH metabolism is an indicator of the status of GSH metabolism in one or more of the major organs, we used a burn rabbit model to determine GSH concentrations and rates of synthesis in WB, liver, lungs, kidney, and skeletal muscle. L-[1-13C]-cysteine was infused intravenously for 6 h in rabbits at 3 days post-burn and in sham burn controls. WB and organ 13C-enrichment of cysteine and GSH was determined by gas chromatography/mass spectrometry. Plasma cysteine metabolic flux was increased significantly (P 0.01) following burn injury. WB, liver, and lung GSH concentrations (P = 0.054, P 0.05, and P 0.05, respectively) and fractional rates of GSH synthesis (P 0.05, P 0.01, and P 0.05, respectively) were reduced at 3 days post-burn. Kidney was unaffected. There also appears to be an increased rate of GSH transport out of the liver after burn injury. Hence, there is a differential impact of burn injury on tissue and organ GSH status, with WB qualitatively reflecting the changes in lung and liver. It will be important to determine whether these changes are due to alterations in the intrinsic capacity for GSH synthesis and/or availability of amino acid precursors of GSH.

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