Chronic prenatal ethanol exposure increases disinhibition and perseverative responding in the adult guinea pig

被引:10
作者
Olmstead, Mary C. [1 ,2 ,3 ]
Martin, Amanda [1 ]
Brien, James F. [2 ,3 ]
Reynolds, James N. [2 ,3 ]
机构
[1] Queens Univ, Dept Psychol, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Pharmacol & Toxicol, Kingston, ON K7L 3N6, Canada
[3] Queens Univ, Ctr Neurosci Studies, Kingston, ON K7L 3N6, Canada
来源
BEHAVIOURAL PHARMACOLOGY | 2009年 / 20卷 / 5-6期
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
foetal alcohol spectrum disorder; Go/No-Go; guinea pig; impulsivity; inhibition; operant responding; perseveration; PREFRONTAL CORTEX; FETAL ALCOHOL; CHILDREN; ACETALDEHYDE; HIPPOCAMPUS; RECEPTORS; BEHAVIOR; DEFICITS; RATS;
D O I
10.1097/FBP.0b013e3283305e27
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Cognitive and behavioural deficits, including increased impulsivity and perseveration, are associated with chronic prenatal ethanol exposure (CPEE) in humans. We tested whether these same deficits occur in the guinea pig after CPEE treatment. Pregnant guinea pigs received oral administration of ethanol (4g/kg maternal body weight/day), or isocaloric-sucrose/pair-feeding throughout gestation. Young adult offspring were trained in lever-pressing paradigms to work for a sucrose-pellet food reward. CPEE increased No-Go, but not Go, responses in the Go/No-Go paradigm, indicative of a disinhibition deficit in these animals. Perseverative responses in the Cued Alternation task were also increased in CPEE offspring. These data show that CPEE induces behavioural deficits in the guinea pig that are remarkably similar to the executive function deficits that follow prenatal ethanol exposure in humans. Behavioural Pharmacology 20:554-557 (C) 2009 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:554 / 557
页数:4
相关论文
共 24 条
[1]   How do physicians define "light", "moderate", and "heavy" drinking? [J].
Abel, EL ;
Kruger, ML ;
Friedl, J .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1998, 22 (05) :979-984
[2]   MRI findings in children with school problems who had been exposed prenatally to alcohol [J].
Autti-Rämo, I ;
Autti, T ;
Korkman, M ;
Kettunen, S ;
Salonen, O ;
Valanne, L .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2002, 44 (02) :98-106
[3]   Dissociable contribution of 5-HT1A and 5-HT2A receptors in the medial prefrontal cortex to different aspects of executive control such as impulsivity and compulsive perseveration in rats [J].
Carli, M ;
Baviera, M ;
Invernizzi, RW ;
Balducci, C .
NEUROPSYCHOPHARMACOLOGY, 2006, 31 (04) :757-767
[4]   DOSE-DEPENDENT EFFECTS OF PRENATAL ETHANOL EXPOSURE IN THE GUINEA-PIG [J].
CATLIN, MC ;
ABDOLLAH, S ;
BRIEN, JF .
ALCOHOL, 1993, 10 (02) :109-115
[5]   PHARMACOKINETICS OF ETHANOL AND ITS METABOLITE, ACETALDEHYDE, AND FETOLETHALITY IN THE 3RD-TRIMESTER PREGNANT GUINEA-PIG FOR ORAL-ADMINISTRATION OF ACUTE, MULTIPLE-DOSE ETHANOL [J].
CLARKE, DW ;
STEENAART, NAE ;
SLACK, CJ ;
BRIEN, JF .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1986, 64 (08) :1060-1067
[6]   Dissociation in prefrontal cortex of affective and attentional shifts [J].
Dias, R ;
Robbins, TW ;
Roberts, AC .
NATURE, 1996, 380 (6569) :69-72
[7]  
Elvidge H., 1972, J Instit Animal Technicians, V23, P111
[8]   A COMPARISON OF THE EFFECTS OF DORSAL OR MEDIAN RAPHE INJECTIONS OF 8-OH-DPAT IN 3 OPERANT TASKS MEASURING RESPONSE-INHIBITION [J].
FLETCHER, PJ .
BEHAVIOURAL BRAIN RESEARCH, 1993, 54 (02) :187-197
[9]   Chronic prenatal ethanol exposure impairs conditioned responding and enhances GABA release in the hippocampus of the adult guinea pig [J].
Hayward, ML ;
Martin, AE ;
Brien, JF ;
Dringenberg, HC ;
Olmstead, MC ;
Reynolds, JN .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 308 (02) :644-650
[10]   Memory-related acetylcholine efflux from rat prefrontal cortex and hippocampus: a microdialysis study [J].
Hironaka, N ;
Tanaka, K ;
Izaki, Y ;
Hori, K ;
Nomura, M .
BRAIN RESEARCH, 2001, 901 (1-2) :143-150