研究论文

基于 1H NMR谱的给药赭石大鼠血清代谢组学研究

  • 魏莹1 ,
  • 2 ,
  • 章文军1 ,
  • 薛蓉2 ,
  • 李晓晶2* ,
  • 裴奉奎2
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  • 1. 河北工业大学 化工学院,天津 300130
    2. 中国科学院 长春应用化学研究所,吉林 长春 130022
魏莹(1989-),女,河北唐山人,硕士研究生,应用化学专业. *通讯联系人:李晓晶,电话: 0431-85262219,E-mail: xjli@ciac.ac.cn.

收稿日期: 2014-12-04

  修回日期: 2015-10-23

  网络出版日期: 2015-12-05

基金资助

国家自然科学基金资助项目(20975097, 21305134)

A 1H NMR-Based Metabonomic Study on the Serum of Haematitum-Treated Rats

  • WEI Ying1 ,
  • 2 ,
  • ZHANG Wen-jun1 ,
  • XUE Rong2 ,
  • LI Xiao-jing2* ,
  • PEI Feng-kui2
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  • 1. Department of Chemistry, Hebei University of Technology, Tianjin 300130, China;
    2. Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
*Corresponding author: LI Xiao-jing, Tel: +86-431-85262219, E-mail: xjli@ciac.ac.cn.

Received date: 2014-12-04

  Revised date: 2015-10-23

  Online published: 2015-12-05

Supported by

国家自然科学基金资助项目(20975097, 21305134)

摘要

基于1H NMR 的代谢组学方法对灌胃给药赭石的成年 Wistar 大鼠血清进行分析,运用主成分分析模式识别方法对所得数据进行处理,并对给药大鼠血清进行生化指标检测.研究结果表明,大鼠体内β-羟异丁酸、乙酸、丙酮、胆碱、甘油磷脂酰胆碱、葡萄糖、乳酸、低密度脂蛋白、极低密度脂蛋白和脂质等内源性代谢物浓度发生明显变化,可作为赭石的特征代谢物. 2 g/kg 5 g/kg 体重剂量赭石使大鼠机体产生大量活性氧化物(ROS)造成过氧化损伤,导致能量代谢和糖代谢紊乱,糖酵解反应增强,并且对肝功能造成了影响.

本文引用格式

魏莹1 , 2 , 章文军1 , 薛蓉2 , 李晓晶2* , 裴奉奎2 . 基于 1H NMR谱的给药赭石大鼠血清代谢组学研究
[J]. 波谱学杂志, 2015
, 32(4) : 628 -636 . DOI: 10.11938/cjmr20150408

Abstract

Wistar rats were intragastrically administered with different doses (0, 2, 5 g/kg body weight) of haematitum. 1H NMR-based metabonomic techniques were used to analyze the metabolic profiles of the serum samples collected from the treated rats. Significant treatment-related changes were observed for the levels of β-hydroxybutyate, acetate, acetone, choline, glycerophosphorylcholine, glucose, lactate, low density lipoprotein, very low density lipoprotein and lipids. Such biochemical changes indicated that haematitum treatment at the dose of 2 or 5 g/kg body weight gave rise to reactive oxygen species (ROS) and caused peroxidation damage. It is concluded that haematitum treatment affects glucose, lipid and energy metabolism in rats.

参考文献

[1] Chinese Pharmacopoeia Commission(国家药典委员会). Chinese Pharmacopoeia(中国药典)[M]. Beijing(北京): China Medical Science Press(中国医药科技出版社), 2012.

[2] Liu Shu-hua(刘淑花), Bi Jun-ying(毕俊英). The investigation of trace element and pharmacological action of ocher or calcined ocher (生或煅赭石微量元素含量及药理作用比较)[J]. Stud Trace Elem Health(微量元素与健康研究), 2003, 20(1): 6―7.

[3] Zheng Jian-han(郑建涵), Wu Zhen-hua(吴振华). Discussoin of best ways of processnig ruddle(中药代赭石最佳炮制方法探讨)[J]. CATCM(中医药学刊), 2006, 24(8): 1 559―1 560.

[4] Liu Dan(刘丹), Li Jun-song(李俊松), Li Wei-dong(李伟东), et al. Studies on changes of content of eleven elements in crude and calcined ochre(赭石炮制前后 11 种元素的含量变化研究)[J]. CATCM(中华中医药学刊), 2008, 26(12): 2 577―2 578.

[5] Li Hong-liang(李红亮). The study of Fu-xuan-dai-zhe-tang in treatment of post-stroke hiccup(旋覆代赭汤治疗中风后呃逆浅析)[J]. World Chinese Med(世界中医药), 2013, 8(1): 65―66.

[6] Nicholson J K, Lindon J C, 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(11): 1 181―1 189.

[7] Duarte I F, Diaz S O, Gil A M. NMR metabolomics of human blood and urine in disease research[J]. J Pharmaceut Biomed, 2014, 93(S1): 17―26.

[8] Liu S, Wang W, Zhou X Y, et al. Dose responsive effects of cisplatin in L02 cells using NMR-based metabolomics[J]. Environ Toxicol Phar, 2014, 37(1): 150―157.

[9] Li M H, Wang J S, Lu Z G, et al. NMR-based metabolomics approach to study the toxicity of lambda-cyhalothrin to goldfish (Carassius auratus)[J]. Aquat Toxicol, 2014, 146: 82―92.

[10] Anni L, Riikka J, Jari S, et al. Postprandial response on fatty meal is affected by sea buckthorn (Hippophaë rhamnoides) supplementation: NMR metabolomics study[J]. Food Res Int, 2014, 58: 23―34.

[11] Ernst M, Silva D B, Silva R R, et al. Mass spectrometry in plant metabolomics strategies: from analytical platforms to data acquisition and processing[J]. Nat prod Rep, 2014, 31 (6): 784―806.

[12] Feng J H, Zhao J, Tang H R, et al. NMR-based metabonomic analyses of the effects of ultrasmall superparamagnetic particles of iron oxide (USPIO) on macrophage metabolism[J]. J Nanopart Res, 2011, 13(5): 2 049―2 062.

[13] Qiu Yu-jie(邱玉洁), Xia Sheng-an (夏圣安), Liu Mai-li(刘买利), et al. Pattern recognition methods in biomedical magnetic resonance(生物医学核磁共振中的模式识别方法)[J]. Chinese J Magn Reson(波谱学杂志), 2005, 22(1): 99―111.

[14] Zhang Pan-pan(张盼盼), Zhang Wen-jun(章文军), Li Xiao-jing(李晓晶), et al. Studies on the serum of arsenic trionxide treated rats by 1H NMR based metabonomics(基于 1H NMR 的代谢组学方法对大鼠砒霜给药后血清的研究)[J]. Chinese J Anal Chem (分析化学), 2013, 41(9): 1 434―1 438.

[15] Wei L, Liao P Q, Li X J, et al. Metabolic profiling studies on the toxicological effects of realgar in rats by 1H NMR spectroscopy[J]. Toxicol Appl Pharm, 2009, 234(3): 314―325.

[16] Dong Ji-yang(董继扬), Xu Le(徐乐), Xu Jing-jing(许晶晶), et al. Adaptive binning method for NMR spectroscopic metabonmics data preprocessing(核磁共振代谢组学数据处理中的自适应分段积分方法)[J]. Chem J of Chinese U(高等学校化学学报), 2009, 30(6): 1 101―1 108.

[17] Zheng X F, Tian J S, Liu P, et al. Analysis of the restorative effect of Bu-zhong-yi-qi-tang in the spleen-qi deficiency rat model using 1H NMR-based metabonomics[J]. J Ethnopharmacol, 2014, 151(2): 912―920.

[18] Eaton J W, Qian M. Molecular bases of cellular iron toxicity[J]. Free Radical Bio Med, 2002, 32(9): 833―840.

[19] Hershko C, Link G, Ioav C. Pathophysiology of iron over load[J]. Ann NY Acad Sci, 1998, 850(1): 191―201.

[20] Bacon B R, Tavill A S, Brittenham G M, et al. Hepatic lipid peroxidation in vivo in rats with chronic iron overload[J]. J Clin Invest, 1983, 71(3): 429―439.

[21] Warburg O, Wind F, Negelein E. The metabolism of tumors in the body[J]. J Gen Physiol, 1927, 8(6): 519―530.

[22] McGarry J D, Foster D W. Regulation of hepatic fatty acid oxidation and ketone body production[J]. Annu Rev Biochem, 1980, 49: 395―420.

[23] Knowles S E, Jarrett I G, Filsell O H, et al. Production and utilization of acetate in mammals[J]. Biochem J, 1974, 142(2): 401―411.


[24] Zeisel S H. Dietary choline: biochemistry, physiology, and pharmacology[J]. Annu Rev Nutr, 1981, 1(1): 95―121.

[25] Griffin J L, Mann C J, Scott J, et al. Choline containing metabolites during cell transfection: an insight into magnetic resonance spectroscopy detectable changes[J]. FEBS Lett, 2001, 509(2): 263―266.

[26] Peters T J, Selden C, Seymour C A. Lysosomal disruption in the pathogenesis of hepatic damage in primary and secondary haemochromatosis[J]. Ciba Found Symp, 1976, 51: 317―329.


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