Alterations of serum brain-derived neurotrophic factor levels in early alcohol withdrawal

被引:60
作者
Huang, Ming-Chyi [1 ,2 ,3 ]
Chen, Chun-Hsin [3 ,4 ]
Chen, Chia-Hui [5 ]
Liu, Shing-Cheng [2 ,3 ]
Ho, Chia-Jen [2 ]
Shen, Winston W. [3 ,4 ]
Leu, Sy-Jye [1 ]
机构
[1] Taipei Med Univ, Inst Cell & Mol Biol, Taipei, Taiwan
[2] Taipei City Hosp, Taipei City Psychiat Ctr, Dept Psychiat, Taipei, Taiwan
[3] Taipei Med Univ, Sch Med, Dept Psychiat, Taipei, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Dept Psychiat, Taipei, Taiwan
[5] Natl Hlth Res Inst, Div Mental Hlth & Subst Abuse Res, Taipei, Taiwan
来源
ALCOHOL AND ALCOHOLISM | 2008年 / 43卷 / 03期
关键词
D O I
10.1093/alcalc/agm172
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
Aims: Alcohol withdrawal-enhanced neurotoxicity contributes to the addictive process. Brain-derived neurotrophic factor (BDNF) plays an important role in neuronal plasticity and learning. In this study, we explored the changes of serum BDNF levels in alcoholic patients at baseline and after one-week alcohol withdrawal. Methods: Twenty-five alcoholic patients were admitted for alcohol detoxification treatment, and 22 healthy control subjects were also enrolled. We collected blood samples of the patient group on the first and seventh day of alcohol withdrawal, and measured serum BDNF level with sandwich enzyme-linked immunosorbent assay. The severity of withdrawal symptoms was evaluated by the Clinical Institute Withdrawal Assessment-Alcohol, Revised every eight hours. Results: Serum BDNF levels did not differ significantly between alcoholic patients and control subjects. But BDNF levels were found to be significantly increased one week after alcohol withdrawal (from 13.9 +/- 3.8 ng/ml to 15.4 +/- 3.8 ng/ml, P = 0.03). A significant positive correlation was found between baseline BDNF level and baseline withdrawal severity (r = 0.45, P = 0.03). Conclusions: The present study suggests that elevated serum BDNF levels were found in early alcohol withdrawal, implying that BDNF may involve in neuroadaptation during the period.
引用
收藏
页码:241 / 245
页数:5
相关论文
共 42 条
[1]   Changes in human plasma nerve growth factor level after chronic alcohol consumption and withdrawal [J].
Aloe, L ;
Tuveri, MA ;
Guerra, G ;
Pinna, L ;
Tirassa, P ;
Micera, A ;
Alleva, E .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1996, 20 (03) :462-465
[2]  
BISON S, 2003, ALCOHOLISM CLIN EXPT, V27
[3]   In vivo up-regulation of brain-derived neurotrophic factor in specific brain areas by chronic exposure to Δ9-tetrahydrocannabinol [J].
Butovsky, E ;
Juknat, A ;
Goncharov, I ;
Elbaz, J ;
Eilam, R ;
Zangen, A ;
Vogel, Z .
JOURNAL OF NEUROCHEMISTRY, 2005, 93 (04) :802-811
[4]   Alcohol-induced neurodegeneration: When, where and why? [J].
Crews, FT ;
Collins, MA ;
Dlugos, C ;
Littleton, J ;
Wilkins, L ;
Neafsey, EJ ;
Pentney, R ;
Snell, LD ;
Tabakoff, B ;
Zou, J ;
Noronha, A .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2004, 28 (02) :350-364
[5]   Increased plasma fibrinolysis and tissue-type plasminogen activator/tissue-type plasminogen activator inhibitor ratios after ethanol withdrawal in chronic alcoholics [J].
Delahousse, B ;
Maillot, F ;
Gabriel, I ;
Schellenberg, F ;
Lamisse, F ;
Gruel, Y .
BLOOD COAGULATION & FIBRINOLYSIS, 2001, 12 (01) :59-66
[6]  
Grimm JW, 2003, J NEUROSCI, V23, P742
[7]   BDNF controls dopamine D3 receptor expression and triggers behavioural sensitization [J].
Guillin, O ;
Diaz, J ;
Carroll, P ;
Griffon, N ;
Schwartz, JC ;
Sokoloff, P .
NATURE, 2001, 411 (6833) :86-89
[8]   Reduced Behavioral effects of cocaine in heterozygous brain-derived neurotrophic factor (BDNF) knockout mice [J].
Hall, FS ;
Drgonova, J ;
Goeb, M ;
Uhl, GR .
NEUROPSYCHOPHARMACOLOGY, 2003, 28 (08) :1485-1490
[9]   Rapid and selective induction of BDNF expression in the hippocampus during contextual learning [J].
Hall, J ;
Thomas, KL ;
Everitt, BJ .
NATURE NEUROSCIENCE, 2000, 3 (06) :533-535
[10]   Chronic antidepressant medication attenuates dexamethasone-induced neuronal death and sublethal neuronal damage in the hippocampus and striatum [J].
Haynes, LE ;
Barber, D ;
Mitchell, IJ .
BRAIN RESEARCH, 2004, 1026 (02) :157-167