期刊文献+

基于气相色谱的铅中毒大鼠尿液代谢指纹图谱研究

A Gas Chromatography-based Metabonomics Approach to Study Urine Metabolite Fingerprint of SD Rats Treated by Lead Acetate
在线阅读 下载PDF
导出
摘要 代谢组学是近年来新发展起来的一门学科,其在毒理学领域的应用越来越受到关注。本文通过对色谱条件的优化建立了一种基于气相色谱的代谢组学技术,检测铅染毒大鼠内源性代谢物谱变化,并运用主成分分析的模式识别方法对这一变化过程进行分析。发现正常组、低剂量染毒组、中剂量染毒组以及高剂量染毒组大鼠处于不同的空间位置,说明随着染毒剂量的不同,各组大鼠的尿液代谢指纹图谱发生了明显的变化。进一步分析发现,各组大鼠的气相色谱图谱在保留时间为3.5 min和5.5 min时的差异对上述总体差异的贡献最大。表明不同剂量的铅染毒能导致大鼠的尿液代谢指纹图谱发生明显的改变,这种改变能用结合模式识别的气相色谱技术检测出来;气相色谱技术可作为核磁共振技术等其它平台的补充工具用于代谢组学研究. Metabonomics is a newly has attracted more and more attention. developing subject, and its application in toxicology In this study, the chromatographic of Gas chromatog- raphy was optimized to detect the. urine metabonomics change of lead exposed rats and this process was analyed by principal component analysis (PCA). It was found that the normal group, low doses of lead poisoning group, middle doses of lead poisoning group and highdose of lead poisoning group were distributed in different position in the space of three-di- mensional scatter plot chart and these four groups can be clearly distinguished, which illus- trated that with the change of poisoning doses, there was notable difference in the rats urine metabolic fingerprint. Further analysis found that variance of peak area at retention time of 3.5 and 5.5 have the greatest contribution to the overall difference. That is to say different doses of lead exposure can cause obvious change this change in rat urine metabolic fingerprinting, and can be detected by the method of gas chromatography based metabonomics combined with pattern recognition;and gas chromatography can be used as complementary tool for other metabonomics studying platform such as nuclear magnetic resonance.
出处 《南华大学学报(自然科学版)》 2012年第4期69-74,80,共7页 Journal of University of South China:Science and Technology
基金 湖南省教育厅科技基金资助项目(10C1173) 湖南省卫生厅科技基金资助项目(B2010-043)
关键词 气相色谱 铅中毒 代谢组学 主成分分析法 GC lead poisoning metabonomics principal component analysis
  • 相关文献

参考文献10

二级参考文献328

  • 1赵剑宇,颜贤忠,彭双清.关木通肾毒性的代谢组学研究[J].中草药,2006,37(5):725-730. 被引量:48
  • 2刘丽丽,马增春,王宇光,秦红霖,谭洪玲,肖成荣,高月.四物汤对环磷酰胺致血虚证小鼠骨髓蛋白质组的影响[J].中国中药杂志,2006,31(14):1172-1175. 被引量:25
  • 3谢跃生,潘桂湘,高秀梅,刘昌孝.高效液相色谱技术在代谢组学研究中的应用[J].分析化学,2006,34(11):1644-1648. 被引量:25
  • 4Nicholson JK, Lindon JC, Holmes E.“Metabonomics”:understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data [J].Xenobiotica, 1999,29 : 1181 - 1189.
  • 5Lindon JC, Nicholson JK, Holmes E, et al.Contemporary issues in toxicology the role of metabonomics in toxicology and its evaluation by the COMET project [J]. Toxicol Appl Pharmacol, 2003,187 : 137 - 146.
  • 6Liu CX, Li C, Lin DH, et al. Significance of metabonomics in drug discovery and development [J].Asian J Drug Metab Pharmacokinet, 2004,4:87 -96.
  • 7Liu CX. Application of metabonomics in drug discovery and development [M] // He FC. Post-gene-time: Drug Diascovery. Beijing: Military Medical Science Press,2004:17 -20.
  • 8Nicholson JK, Connelly J, Lindon JC, et al.Metabonomics: a platform for studying drug toxicity and gene function [J]. Nat Rev Drug Discov, 2002,1 : 153 -161.
  • 9Pumb RS, Stumpf CL, Gorenstein MV, et al.Metabonomics: the use of electrospry mass spectrometry coupled to revesed-phase liquid chromatography show a potential for the screening of rat urine in drug development [J]. Rapid Commun Mass Spectrum, 2002,16 : 1991 - 1996.
  • 10Plumb RS, Stumpf CL, Granger JH, et al. Use of liquid chromatography/time-of-flight mass spectrometry and multivariate statistical analysis shows promise for the detection of drug metabolites in biological fluids [J].Rapid Commun Mass Spectrom, 2003,17:2632 - 2638.

共引文献273

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部