GC-MS-based plasma metabolomic investigations of morphine dependent rats at different states of euphoria, tolerance and naloxone-precipitated withdrawal

被引:12
作者
Liu, Ruoxu [1 ,2 ,4 ]
Cheng, Jianhua [3 ]
Yang, Jingwen [1 ,2 ]
Ding, Xinghua [1 ,2 ]
Yang, Shuguang [1 ,2 ]
Dong, Fangting [3 ]
Guo, Ning [4 ,5 ]
Liu, Shaojun [1 ,2 ]
机构
[1] Inst Basic Med Sci, State Key Lab Prote, Beijing 100850, Peoples R China
[2] Inst Basic Med Sci, Dept Neurobiol, Beijing 100850, Peoples R China
[3] Natl Ctr Biomed Anal, Beijing 100850, Peoples R China
[4] Inst Basic Med Sci, Dept Cell Immunol, Beijing 100850, Peoples R China
[5] Inst Basic Med Sci, Dept Mol Immunol, Beijing 100850, Peoples R China
关键词
GC-MS; Metabolomics; Morphine dependence; Plasma; Rats; MU-OPIOID RECEPTOR; FULMINANT HEPATIC-FAILURE; GASTROINTESTINAL-TRACT; FUNCTIONAL EXPRESSION; MICE; CLONING; KAPPA; MODEL; LOCALIZATION; CHOLESTEROL;
D O I
10.1007/s11011-014-9638-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Long-term or excessive application of morphine leads to tolerance and addiction, which hindered its conventional applications as a drug. Although tremendous progress has been made on the mechanisms of morphine, crucial evidence elaborating the neurobiological basis of tolerance and dependence is still lacking. To further explore the physiological adaptions during morphine's application, a systematic screening of small molecules in blood has been carried out. The plasma of morphine dependent rats was collected at different time points with or without naloxone treatment, and was analyzed by gas chromatography-mass spectrometry (GC-MS). Partial least squares discriminate analysis (PLS-DA) and the Student's t Tests with the false discovery rate (FDR) correction were conducted on the normalized data for the distinction of groups and the identification of the most contributed metabolites. Clear separation is observed between different treatments, and 29 out of 41 metabolites changes significantly compared with the corresponding controls. The concentration of threonine, glycine, serine, beta-d-glucose and oxalic acid are consistently changed in all morphine treated groups compared with controls. Through this experiment we find characteristic metabolites in different dependent states and discuss the possible compensation effects. The interpretation of these metabolites would throw light on the biological effects of morphine and reveal the possibilities to become marker of morphine addiction.
引用
收藏
页码:767 / 776
页数:10
相关论文
共 42 条
[1]   A20 protects mice from D-galactosamine/lipopolysaccharide acute toxic lethal hepatitis [J].
Arvelo, MB ;
Cooper, JT ;
Longo, C ;
Daniel, S ;
Grey, ST ;
Mahiou, J ;
Czismadia, E ;
Abu-Jawdeh, G ;
Ferran, C .
HEPATOLOGY, 2002, 35 (03) :535-543
[2]   Cellular localization and distribution of the cloned mu and kappa opioid receptors in rat gastrointestinal tract [J].
Bagnol, D ;
Mansour, A ;
Akil, H ;
Watson, SJ .
NEUROSCIENCE, 1997, 81 (02) :579-591
[3]   Opioids: cellular mechanisms of tolerance and physical dependence [J].
Bailey, CP ;
Connor, M .
CURRENT OPINION IN PHARMACOLOGY, 2005, 5 (01) :60-68
[4]   Metabolomics and its potential in drug development [J].
Beyoglu, Diren ;
Idle, Jeffrey R. .
BIOCHEMICAL PHARMACOLOGY, 2013, 85 (01) :12-20
[5]  
Bh HAR, 2013, TOMES R INFORM SYSTE, V158
[6]   IMMUNOSUPPRESSIVE EFFECTS OF CHRONIC MORPHINE TREATMENT IN MICE [J].
BRYANT, HU ;
BERNTON, EW ;
HOLADAY, JW .
LIFE SCIENCES, 1987, 41 (14) :1731-1738
[7]   Association between low plasma levels of cholesterol and relapse in cocaine addicts [J].
Buydens-Branchey, L ;
Branchey, M .
PSYCHOSOMATIC MEDICINE, 2003, 65 (01) :86-91
[8]  
CHEN Y, 1993, MOL PHARMACOL, V44, P8
[9]   75 years of opioid research: the exciting but vain quest for the Holy Grail [J].
Corbett, AD ;
Henderson, G ;
McKnight, AT ;
Paterson, SJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 147 :S153-S162
[10]   CLONING OF A DELTA OPIOID RECEPTOR BY FUNCTIONAL EXPRESSION [J].
EVANS, CJ ;
KEITH, DE ;
MORRISON, H ;
MAGENDZO, K ;
EDWARDS, RH .
SCIENCE, 1992, 258 (5090) :1952-1955