Chronic low-dose cocaine treatment during adolescence facilitates aggression in hamsters

被引:42
作者
Harrison, RJ
Connor, DF
Nowak, C
Melloni, RH
机构
[1] Northeastern Univ, Dept Psychol, Behav Neurosci Program, Boston, MA 02115 USA
[2] Univ Massachusetts, Med Ctr, Dept Psychiat, Worcester, MA 01655 USA
关键词
aggression; behavior; cocaine; adolescence; drug abuse;
D O I
10.1016/S0031-9384(00)00220-1
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Cocaine abuse Juring adolescence represents a significant health risk because of the potential fur both acute and long-term negative physical and psychological sequclae, including increased aggressive behavior. This study examined the effects of chronic adolescent cocaine exposure on aggression in an animal model. It was hypothesized that chronic cocaine exposure during adolescence predisposes animals to heightened levels of aggressive behavior. To test this hypothesis, adolescent male golden hamsters (Mesocricetus auratus) were administered cocaine hydrochloride during their entire adolescent development (Postnatal Days 27-54) and then tested for offensive aggression using the resident-intruder model. Animals treated with low-dose cocaine during adolescence showed significantly elevated measures of offensive aggression (i.e., increased number of bites, attacks, and decreased latencies to bite), whereas measures of social communication, sexual motivation and motor activity remained constant. Cocaine-treated animals did not differ in body weight gain from controls, suggesting no dramatic physiological effects of adolescent cocaine exposure on body growth at the doses tested. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:555 / 562
页数:8
相关论文
共 68 条
[1]   BRAIN MECHANISMS FOR OFFENSE, DEFENSE, AND SUBMISSION [J].
ADAMS, DB .
BEHAVIORAL AND BRAIN SCIENCES, 1979, 2 (02) :201-213
[2]   Involvement of the 5-HT1A subtype receptor in the neonatal organization of agonistic behaviour in the rat [J].
Albonetti, E ;
Gonzalez, MI ;
Siddiqui, A ;
Wilson, CA ;
Farabollini, F .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1996, 54 (01) :189-193
[3]  
[Anonymous], 1994, COCAINE
[4]   REPEATED COCAINE ADMINISTRATION REDUCES 5-HT1A-MEDIATED PROLACTIN SECRETION IN RATS [J].
BAUMANN, MH ;
ROTHMAN, RB .
NEUROSCIENCE LETTERS, 1995, 193 (01) :9-12
[5]   EVIDENCE FOR ALTERATIONS IN PRESYNAPTIC SEROTONERGIC FUNCTION DURING WITHDRAWAL FROM CHRONIC COCAINE IN RATS [J].
BAUMANN, MH ;
BECKETTS, KM ;
ROTHMAN, RB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 282 (1-3) :87-93
[6]   BIOSYNTHESIS OF DOPAMINE AND SEROTONIN IN THE RAT-BRAIN AFTER REPEATED COCAINE INJECTIONS - A MICRODISSECTION MAPPING STUDY [J].
BAUMANN, MH ;
RALEY, TJ ;
PARTILLA, JS ;
ROTHMAN, RB .
SYNAPSE, 1993, 14 (01) :40-50
[7]  
BLANCHARD DC, 1988, ANNU REV PSYCHOL, V39, P43, DOI 10.1146/annurev.psych.39.1.43
[8]   Cocaine potentiates defensive behaviors related to fear and anxiety [J].
Blanchard, DC ;
Blanchard, RJ .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1999, 23 (07) :981-991
[9]   THE UNDERREPORTING OF COCAINE-RELATED TRAUMA - DRUG-ABUSE WARNING NETWORK REPORTS VS HOSPITAL TOXICOLOGY TESTS [J].
BROOKOFF, D ;
CAMPBELL, EA ;
SHAW, LM .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1993, 83 (03) :369-371
[10]  
BROWN GL, 1982, AM J PSYCHIAT, V139, P741