Alcohol drinking produces brain region-selective changes in expression of inducible transcription factors

被引:123
作者
Bachtell, RK [1 ]
Wang, YM [1 ]
Freeman, P [1 ]
Risinger, FO [1 ]
Ryabinin, AE [1 ]
机构
[1] Oregon Hlth Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA
关键词
ethanol; c-Fos; FosB; Zif268; Edinger-Westphal;
D O I
10.1016/S0006-8993(99)02019-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mapping the effects of alcohol consumption on neural activity could provide valuable information on mechanisms of alcohol's effects on behavior. The present study sought to identify effects of alcohol consumption on expression of inducible transcription factors (ITFs) in mouse brain. C57BL/6J mice were trained to consume 10% ethanol/10% sucrose solution during a 30-min limited access period. Control animals were given access to 10% sucrose solution or water. Following the final day of the procedure, animals were sacrificed and immunohistochemical analyses were performed for three ITFs (c-Fos, FosB, and Zif268). Alcohol-consuming animals had increased ITF expression in several brain areas. Specifically, c-Fos was significantly induced in the nucleus accumbens core (AcbC), the medial posteroventral portion of the central nucleus of the amygdala (CeMPV), and the Edinger-Westphal nucleus (EW), Expression of c-Fos was significantly lower in the dentate gyrus of alcohol-consuming animals vs. sucrose-consuming animals. However, it was not significantly different from the water controls. Induction of c-Fos in AcbC, CeMPV and EW was significantly related to blood alcohol concentrations (BAC). Furthermore, FosB expression in the CeMPV and the EW was also significantly higher in the alcohol-consuming animals vs. water controls. FosB expression in the EW was significantly related to BAG. The significance of these results is two-fold. First, our experiments demonstrate that ITF mapping is an effective strategy in identifying alcohol-induced changes following voluntary consumption. Second, they suggest a relationship between ITF expression in AcbC, CeMPV and EW and the level of alcohol intoxication. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 165
页数:9
相关论文
共 54 条
[1]  
Bradshaw C.M., 1989, NEUROPHARMACOLOGICAL, P320
[2]   INDUCTION OF THE C-FOS PROTOONCOGENE IN RAT AMYGDALA DURING UNCONDITIONED AND CONDITIONED FEAR [J].
CAMPEAU, S ;
HAYWARD, MD ;
HOPE, BT ;
ROSEN, JB ;
NESTLER, EJ ;
DAVIS, M .
BRAIN RESEARCH, 1991, 565 (02) :349-352
[3]  
CECATELLI S, 1989, P NATL ACAD SCI USA, V86, P9569
[4]   ACTIVATION AND DESENSITIZATION OF FOS IMMUNOREACTIVITY IN THE RAT-BRAIN FOLLOWING ETHANOL ADMINISTRATION [J].
CHANG, SL ;
PATEL, NA ;
ROMERO, AA .
BRAIN RESEARCH, 1995, 679 (01) :89-98
[5]   Ethanol-induced expression of c-Fos differentiates the FAST and SLOW selected lines of mice [J].
Demarest, K ;
Hitzemann, B ;
Phillips, T ;
Hitzemann, R .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1999, 23 (01) :87-95
[6]  
Demarest K, 1998, ALCOHOL CLIN EXP RES, V22, P1531
[8]   Addiction and imaging of the living human brain [J].
Gatley, SJ ;
Volkow, ND .
DRUG AND ALCOHOL DEPENDENCE, 1998, 51 (1-2) :97-108
[9]   Topographic organization of Fos-like immunoreactivity in the rostral nucleus of the solitary tract evoked by gustatory stimulation with sucrose and quinine [J].
Harrer, MI ;
Travers, SP .
BRAIN RESEARCH, 1996, 711 (1-2) :125-137
[10]  
Hitzemann B, 1997, ALCOHOL CLIN EXP RES, V21, P1497