Reduced ethanol-induced conditioned taste aversion and conditioned place preference in GIRK2 null mutant mice

被引:51
作者
Hill, KG
Alva, H
Blednov, YA
Cunningham, CL
机构
[1] Oregon Hlth & Sci Univ, Dept Behav Neurosci L407, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Portland Alcohol Res Ctr, Portland, OR 97201 USA
[4] Univ Texas, Waggoner Ctr Alcohol & Addict Res, Austin, TX 78712 USA
[5] Univ Texas, Neurobiol Sect, Austin, TX 78712 USA
关键词
GIRK2; channel; ethanol; conditioned taste aversion; conditioned place preference; locomotor activity; learning and memory; knockout mice;
D O I
10.1007/s00213-003-1472-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rationale. Previous studies have shown that GIRK2 channel function is enhanced by ethanol and that GIRK2 null mutant mice are less sensitive to some of ethanol's effects, including anxiolysis, habituated locomotor stimulation, and acute handling-induced convulsions than wild types. Under some conditions, GIRK2 knockout mice consume more ethanol than wild types, but it is unclear whether they do so because they are more sensitive to ethanol's rewarding effects or less sensitive to its aversive effects. <LF>Objective. To further assess the role of GIRK2 in ethanol action, GIRK2 null mutant and wild type mice were tested in conditioning models that measure the motivational effects of ethanol. Method. In a conditioned taste aversion (CTA) procedure, knockout and wild type mice were given ethanol (0.0, 2.0, 2.5, or 3.5 g/kg, IP) following 1-h access to saccharin every 48 h over a 10 day period. In a conditioned place preference (CPP) procedure, knockout and wild type mice were given ethanol (2.0 or 3.0 g/kg, IP) paired with one stimulus (grid or hole floor) and saline paired with the other. After four 5-min trials with each stimulus, a 60-min choice test was done. Results. The results demonstrated a genotypic difference in both paradigms. In CTA, there was no difference between genotypes at 0.0 or 3.5 g/kg ethanol, but at the 2.0 and 2.5 g/kg doses, wild types developed a stronger aversion to saccharin than knockouts. In CPP, wild types developed place preference, but knockouts did not. Conclusions. These studies show that GIRK2 deletion reduced ethanol's impact in tasks that are commonly used to index the drug's rewarding and aversive effects. These findings could reflect either a learning/memory deficit or decreased sensitivity to ethanol's motivational effects in null mutant mice. The latter interpretation is more consistent with previous data showing that knockout mice consume higher doses of ethanol than wild type mice.
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收藏
页码:108 / 114
页数:7
相关论文
共 39 条
[1]   Hyperactivity and dopamine D1 receptor activation in mice lacking girk2 channels [J].
Blednov, YA ;
Stoffel, M ;
Cooper, R ;
Wallace, D ;
Mane, N ;
Harris, RA .
PSYCHOPHARMACOLOGY, 2002, 159 (04) :370-378
[2]  
Blednov YA, 2001, J PHARMACOL EXP THER, V298, P521
[3]   GIRK2 deficient mice - Evidence for hyperactivity and reduced anxiety [J].
Blednov, YA ;
Stoffel, M ;
Chang, SR ;
Harris, RA .
PHYSIOLOGY & BEHAVIOR, 2001, 74 (1-2) :109-117
[4]   Enhancement of ethanol reward by dopamine D3 receptor blockade [J].
Boyce, JM ;
Risinger, FO .
BRAIN RESEARCH, 2000, 880 (1-2) :202-206
[5]   Dopamine D3 receptor antagonist effects on the motivational effects of ethanol [J].
Boyce, JM ;
Risinger, FO .
ALCOHOL, 2002, 28 (01) :47-55
[6]   Genetic differences in naloxone enhancement of ethanol-induced conditioned taste aversion [J].
Broadbent, J ;
Linder, HV ;
Cunningham, CL .
PSYCHOPHARMACOLOGY, 1996, 126 (02) :147-155
[7]   Ethanol-induced conditioned taste aversion in 15 inbred mouse strains [J].
Broadbent, J ;
Muccino, KJ ;
Cunningham, CL .
BEHAVIORAL NEUROSCIENCE, 2002, 116 (01) :138-148
[8]  
Carr HA., 1989, NEUROPHARMACOLOGICAL, P264
[9]  
Cunningham C.L., 1993, METHODS BEHAV PHARM, P349, DOI DOI 10.1016/B978-0-444-81444-9.50019-5
[10]   Naloxone Facilitates Extinction but Does Not Affect Acquisition or Expression of Ethanol-Induced Conditioned Place Preference [J].
Cunningham, Christopher L. ;
Dickinson, Shelly D. ;
Okorn, Dobrina M. .
EXPERIMENTAL AND CLINICAL PSYCHOPHARMACOLOGY, 1995, 3 (04) :330-343