Cerebellar vermis proteome of chronic alcoholic individuals

被引:34
作者
Alexander-Kaufman, Kimberley
Harper, Clive
Wilce, Peter
Matsumoto, Izuru [1 ]
机构
[1] Univ Sydney, Fac Med, Discipline Pathol, Sydney, NSW 2006, Australia
[2] Univ Queensland, Dept Biochem & Mol Biol, St Lucia, Qld, Australia
关键词
alcohol-related disorders; proteomics; cerebellum; thiamine deficiency; hepatic encephalopathy;
D O I
10.1111/j.1530-0277.2007.00437.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Cerebellar changes are commonly associated with alcoholism and chronic alcohol consumption can produce profound impairments in motor functioning and various aspects of cognition. Although the mechanisms underlying alcohol-induced changes in the cerebellar vermis are poorly understood, observations in the alcoholic vermis are thought to be consequential to common alcohol-related factors, particularly thiamine deficiency. Methods: In the present study, we used a proteomics-based approach to compare protein expression profiles of the cerebellar vermis from human alcoholic individuals (both neurologically uncomplicated and alcoholic individuals complicated with liver cirrhosis) and healthy control brains. This article complements our recent studies performed on alcoholic prefrontal gray and white matter and splenium of the corpus callosum (CC). Results: Like the CC study, several liver cirrhosis-specific proteins were identified in the vermis, perhaps indicating the effects of liver dysfunction in this brain region. Among other protein expression changes observed are disturbances in the levels of thiamine-dependent enzymes. A derangement in energy metabolism perhaps related to thiamine deficiency seems to be important in both alcoholic groups, even where there are no clinical or pathological findings of Wernicke-Korsakoff syndrome. Conclusions: These results suggest that clinically and pathologically uncomplicated alcoholic cases may not in fact be "uncomplicated," as at the proteome level we seem to be isolating the confounding effects of nutritional deficiencies and liver dysfunction and perhaps their role in alcohol-related vermis damage. Together, these results indicate that the alcohol-related pathology of the vermis is more multifactorial than other brain regions examined previously (prefrontal region and CC splenium).
引用
收藏
页码:1286 / 1296
页数:11
相关论文
共 54 条
[31]  
MAJUMDAR SK, 1981, INT J VITAM NUTR RES, V51, P54
[32]  
Martin PR, 2003, ALCOHOL RES HEALTH, V27, P134
[33]   Vermal atrophy of alcoholics correlate with serum thiamine levels but not with dentate iron concentrations as estimated by MRI [J].
Maschke, M ;
Weber, J ;
Bonnet, U ;
Dimitrova, A ;
Bohrenkamper, J ;
Sturm, S ;
Müller, BW ;
Gastpar, M ;
Diener, HC ;
Forsting, M ;
Timmann, D .
JOURNAL OF NEUROLOGY, 2005, 252 (06) :704-711
[34]  
MILES MF, 1994, MOL PHARMACOL, V46, P873
[35]   Longitudinal brain metabolic characterization of chronic alcoholics with proton magnetic resonance spectroscopy [J].
Parks, MH ;
Dawant, BM ;
Riddle, WR ;
Hartmann, SL ;
Dietrich, MS ;
Nickel, MK ;
Price, RR ;
Martin, PR .
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH, 2002, 26 (09) :1368-1380
[36]   QUANTITATIVE-ANALYSIS OF ETHANOL EFFECTS ON PURKINJE-CELL DENDRITIC TREE [J].
PENTNEY, RJ .
BRAIN RESEARCH, 1982, 249 (02) :397-401
[37]  
PFEFFERBAUM R, 1993, ALCOHOL INDUCED BRAI, P71
[38]  
Phillips S C, 1990, Drug Alcohol Rev, V9, P53, DOI 10.1080/09595239000185071
[39]   A QUANTITATIVE HISTOLOGICAL STUDY OF THE CEREBELLAR VERMIS IN ALCOHOLIC PATIENTS [J].
PHILLIPS, SC ;
HARPER, CG ;
KRIL, J .
BRAIN, 1987, 110 :301-314
[40]   Comparison of false discovery rate methods in identifying genes with differential expression [J].
Qian, HR ;
Huang, SG .
GENOMICS, 2005, 86 (04) :495-503