Conditioned increases in anxiogenic-like behavior following exposure to contextual stimuli associated with cocaine are mediated by corticotropin releasing factor

被引:65
作者
DeVries, AC [1 ]
Pert, A [1 ]
机构
[1] NIMH, Biol Psychiat Branch, Bethesda, MD 20892 USA
关键词
anxiety; elevated plus-maze; classical conditioning; drug abuse; CRF antagonist;
D O I
10.1007/s002130050627
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although cocaine is a powerful reinforcer, it has been reported to produce anxiety in humans and anxiogenic-like behavior in animals. The goal of this study was three-fold: (1) to determine the doses of cocaine that induce anxiogenic-like behavior in the elevated plus-maze in rats, (2) to determine if cocaine-associated contextual cues are capable of eliciting anxiogenic-like behavior in the absence of the drug, and (3) to identify possible mechanisms through which cocaine-associated cues affect behavior in the elevated plus-maze. Measurement of the amount of time that the animals spend exploring the open arms of the maze provides a sensitive index of anxiogenic-like behavior in rats. In experiment 1, rats were injected with 10 mg/kg, 20 mg/kg, or 30 mg/kg cocaine HCl or saline for 6 days. On day 6, the rats were tested in the elevated plus-maze 25 min after injection with cocaine or saline. The animals chronically treated with the three doses of cocaine exhibited a dose-dependent increase in anxiogenic-like behavior in the elevated plus-maze, compared to the saline-treated group. In experiment 2, cocaine-induced (30 mg/kg) conditioning was achieved using a simple contextual design. On the final day of the experiment (day 6), after 5 days of conditioning, the rats were exposed for 25 min to the cocaine-associated contextual cues, then placed in the elevated plus-maze. Animals that had been exposed to cocaine-associated contextual cues prior to being placed in the elevated plus-maze exhibited a significant increase.in anxiogenic-like behavior compared to the control groups. However, pretreatment of the rats with the CRF antagonist, proportional to-helical CRF9-41, (1 mu g, ICV), on the test day, prior to exposure to cocaine-associated contextual cues, attenuated the subsequent anxiogenic-like behavioral response in the elevated plus-maze (experiment 3). The results suggest that contextual cues associated with repeated treatment with 30 mg/kg cocaine are capable of eliciting anxiogenic-like behavior in the absence of the drug and that CRF mediates the expression of anxiogenic-like behaviors in the elevated plus-maze following exposure to cocaine-associated cues. The conditioned anxiogenic action elicited by cocaine-associated cues may have relevance for understanding the complex addictive nature of this drug and some of the clinical phenomena related to its use.
引用
收藏
页码:333 / 340
页数:8
相关论文
共 50 条
  • [21] JOHANSON CE, 1989, PHARMACOL REV, V41, P3
  • [22] FACILITATION OF COCAINE KINDLING BY GLUCOCORTICOIDS IN RATS
    KLING, MA
    SMITH, MA
    GLOWA, JR
    PLUZNIK, D
    DEMAS, J
    DEBELLIS, MD
    GOLD, PW
    SCHULKIN, J
    [J]. BRAIN RESEARCH, 1993, 629 (01) : 163 - 166
  • [23] POSTCOCAINE DEPRESSION AND SENSITIZATION OF BRAIN-STIMULATION REWARD - ANALYSIS OF REINFORCEMENT AND PERFORMANCE EFFECTS
    KOKKINIDIS, L
    MCCARTER, BD
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 36 (03) : 463 - 471
  • [24] CELLULAR AND MOLECULAR MECHANISMS OF DRUG-DEPENDENCE
    KOOB, GF
    BLOOM, FE
    [J]. SCIENCE, 1988, 242 (4879) : 715 - 723
  • [25] LISTER RG, 1987, PSYCHOPHARMACOLOGY, V92, P180
  • [26] LOUIE AK, 1989, AM J PSYCHIAT, V146, P40
  • [27] MARKOU A, 1991, NEUROPSYCHOPHARMACOL, V4, P17
  • [28] COCAINE INDUCED SECRETION OF ACTH, BETA-ENDORPHIN, AND CORTICOSTERONE
    MOLDOW, RL
    FISCHMAN, AJ
    [J]. PEPTIDES, 1987, 8 (05) : 819 - 822
  • [29] VALIDATION OF OPEN - CLOSED ARM ENTRIES IN AN ELEVATED PLUS-MAZE AS A MEASURE OF ANXIETY IN THE RAT
    PELLOW, S
    CHOPIN, P
    FILE, SE
    BRILEY, M
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1985, 14 (03) : 149 - 167
  • [30] PERT A, 1990, NIDA RES MG, V97, P208