Effects of ethanol on locomotor and anxiety-like behaviors and the acquisition of ethanol intake in Lewis and spontaneously hypertensive rats

被引:28
作者
Da Silva, GE
Vendruscolo, LF
Takahashi, RN
机构
[1] Univ Fed Santa Catarina, Ctr Ciencias Biol, Dept Farmacol, BR-88015420 Florianopolis, SC, Brazil
[2] Univ Reg Blumenau, Dept Ciencias Farmaceut, BR-89030000 Blumenau, SC, Brazil
关键词
Lewis; SHR; anxiety; locomotor activity; elevated plus-maze; open-field; ethanol self-administration;
D O I
10.1016/j.lfs.2005.01.013
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The purpose of the present study was to investigate whether Lewis (LEW) and spontaneously hypertensive rats (SHR), characterized in numerous behavioral tests as strains with high-anxiety and low-anxiety, respectively, could differ in their sensitivity to the effects of ethanol in the elevated plus maze (EPM) and the open field (OF), two classical models of anxiety/emotionality, as well as in the acquisition of ethanol drinking behavior. It was also of interest to examine the relationship between sweet and bitter fluids preference and ethanol intake. SHR and LEW rats were given saline or ethanol injections (0.6 or 1.2 g/kg, ip.) and tested in the EPM and OF. Subsequently the same animals were given continuous free choice between water and ethanol solution (2-8%). Additional groups of animals were exposed to a free-choice regimen between saccharin (0.002-0.09%) or quinine (0.0001-0.0015%) and water. The low dose of ethanol (0.6 g/kg) induced anxiolytic-like effects and intensive locomotor activation mainly in SHR rats tested in the OF arena. Overall, LEW counterparts were unaffected in OF test. In oral self-administration paradigm, SHR rats consumed significantly more ethanol than LEW rats. Concerning other solutions, SHR rats consumed large amounts of saccharin compared with LEW rats. These data indicate that the SHR preference for ethanol intake may be positively related to their differential sensitivity to the anxiolytic/ stimulant effects of ethanol and to the sensitivity of this strain for saccharin reinforcement. In addition, these findings provide evidence that the SHR strain may represent a useful genetic and pharmacological toot to investigate ethanol drinking traits. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:693 / 706
页数:14
相关论文
共 46 条
[1]   Alcohol stimulates motor activity in selectively bred Sardinian alcohol-preferring (sP), but not in Sardinian alcohol-nonpreferring (sNP), rats [J].
Agabio, R ;
Carai, MAM ;
Lobina, C ;
Pani, M ;
Reali, R ;
Vacca, G ;
Gessa, GL ;
Colombo, G .
ALCOHOL, 2001, 23 (02) :123-126
[2]   Psychobiology of novelty seeking and drug seeking behavior [J].
Bardo, MT ;
Donohew, RL ;
Harrington, NG .
BEHAVIOURAL BRAIN RESEARCH, 1996, 77 (1-2) :23-43
[3]   ALCOHOL AND ANXIETY - ETHOPHARMACOLOGICAL APPROACHES [J].
BLANCHARD, RJ ;
MAGEE, L ;
VENIEGAS, R ;
BLANCHARD, C .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1993, 17 (02) :171-182
[4]   Shared genes influence sensitivity to the effects of ethanol on locomotor and anxiety-like behaviors, and the stress axis [J].
Boehm, SL ;
Reed, CL ;
McKinnon, CS ;
Phillips, TJ .
PSYCHOPHARMACOLOGY, 2002, 161 (01) :54-63
[5]   Does the increase in locomotion induced by ethanol indicate its stimulant or anxiolytic properties? [J].
Boerngen-Lacerda, R ;
Souza-Formigoni, MLO .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2000, 67 (02) :225-232
[6]   A 4-year longitudinal study on risk factors for alcoholism [J].
Cheng, ATA ;
Gau, SF ;
Chen, THH ;
Chang, JC ;
Chang, YT .
ARCHIVES OF GENERAL PSYCHIATRY, 2004, 61 (02) :184-191
[7]   NEUROGENETIC ADAPTIVE-MECHANISMS IN ALCOHOLISM [J].
CLONINGER, CR .
SCIENCE, 1987, 236 (4800) :410-416
[8]   EFFECTS OF ETHANOL AND RO-15-4513 IN AN ELECTROPHYSIOLOGICAL MODEL OF ANXIOLYTIC ACTION [J].
COOP, CF ;
MCNAUGHTON, N ;
WARNOCK, K ;
LAVERTY, R .
NEUROSCIENCE, 1990, 35 (03) :669-674
[9]   Locomotor stimulant effects of intraventricular injections of low doses of ethanol in rats: acute and repeated administration [J].
Correa, M ;
Arizzi, MN ;
Betz, A ;
Mingote, S ;
Salamone, JD .
PSYCHOPHARMACOLOGY, 2003, 170 (04) :368-375
[10]   Comparison of voluntary ethanol intake by two pairs of rat lines used as genetic models of anxiety [J].
Da Silva, GE ;
Ramos, A ;
Takahashi, RN .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2004, 37 (10) :1511-1517