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痛风性关节炎大鼠模型尿液的代谢组学研究 被引量:7

Metabonomic Study of the Urine of Rat Acute Gouty Arthritis Model
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摘要 目的通过代谢组学研究,了解痛风性关节炎大鼠模型尿液中代谢组的变化规律。方法基于代谢组学方法,以LC/MS为数据采集平台,并结合主成分分析方法等化学计量学手段,研究空白大鼠、痛风性关节炎大鼠尿液中代谢物组时量的轨迹变化。结果造模后大鼠的代谢状态相对其造模前及空白对照组大鼠出现了偏离,随着时间的推移又逐渐回复到造模前的初始代谢状态,以此代谢组学方法所得的大鼠代谢轨迹变化很好地反映了大鼠痛风性关节炎的发生、发展、恢复的病程状况。结论模型的整体代谢状态通过代谢组学方法可以得到很好的体现,因而代谢组学技术为痛风性关节炎模型提供了良好的研究手段。 Objective To analysis the metabonome characteristics of the urine of MSU crystal-induced acute gouty arthritis rats by the method of metabolomics.Methods Based on the method of metabolomics, which applies LC/MS as data acquisition platform,incorporating with the means of stoechiometry such as principal component analysis,we analyzed the metabonome difference between the urine of acute gouty arthritis rats and that of normal rats.Results Compare with control group,the metabolism status of acute gouty arthritis model group deviated.After that,with the time lapsed,it retrieved gradually to the incipient metabolism status.The variation of metabolism locus of rats measured by the methods of metabolomics properly reflects the genesis,development,and recuperation course of acute gouty arthritis.Conclusion The whole metabolism status of rat model is able to be presented finely with the method of metabolomics.The metabolomics study could offer a satisfactory research approach to acute gouty arthritis.
出处 《四川大学学报(医学版)》 CAS CSCD 北大核心 2010年第4期660-663,共4页 Journal of Sichuan University(Medical Sciences)
基金 四川省科学和技术平台项目(项目编号:08PT-06)支持
关键词 痛风性关节炎 大鼠 尿液 代谢组学 Gouty arthritis Rat Urine Metabonomics(or metabolomics)
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  • 1林春驿,魏德庆,马春全,包丽颖,孙力.鸡混合型痛风的诊治报告[J].当代畜牧,1993,22(3):23-23. 被引量:2
  • 2黄玉荣,魏广力,龙红,肖淑华,王淑芳,刘昌孝.钩藤多动合剂的药效作用及用代谢物组学方法研究其生化机制[J].中草药,2005,36(3):398-402. 被引量:57
  • 3董纯武,顾耀志,吴祖立,姚龙涛,王秀贤,徐永根,蔡玉书.鸡痛风病研究报告[J].中国兽医杂志,1989,15(2):24-27. 被引量:7
  • 4刘文革,李凤莲,孙凤发.高钙饲料引起鸡痛风的诊治[J].养禽与禽病防治,1996(10):29-29. 被引量:5
  • 5Yagnik DR, Hillyer P, Marshall D, et al. Noninflammatory phagocytosis of monosodium urate monohydrate crystals by mouse macrophages.Implications for the control of joint inflammation in gout. Arthritis Rheum, 2000,43 (8): 1779-1789.
  • 6Dan T, Yoneya T,Onoma M,et al. Hyperuricemic and uricosuric actions of AA-193 in a hyperuricemic rat model. Metabolism, 1994,43(1): 123-128.
  • 7Wu X, Wakamiya M, Vaishnav S,et al. Hyperuricemia and urate oxidase-deficient mice. Proc Natl Acad Sci,1994,91(2):742-746.
  • 8Coderre TJ,Wall PD. Ankle joint arthritis in rats: An alternative animal modle of arthritis to that produce by Freud's adjuvant. Pain,1987,28: 379-393.
  • 9Wyngaarden JB, Kelley WN. Gout and hyperuricemia. Philadelphia:Grune&Stration, 1978.39-49.
  • 10Phelps T J,Palumbo A V,Beliaev A S.Metabolomics and microarrays for improved understanding of phenotypic characteristics controlled by both genomics and environmental constraints[J].Curr Opin Biotechnol,2002,13:20-4.

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