Drugs, sweat, and fears: a comparison of the effects of diazepam and methylphenidate on fear conditioning

被引:17
作者
Brignell, Catherine M. [1 ]
Curran, H. Valerie
机构
[1] Univ Southampton, Sch Psychol, Southampton SO17 1BJ, Hants, England
[2] UCL, Subdept Clin Hlth Psychol, Clin Psychopharmacol Unit, London WC1H 6BT, England
关键词
diazepam; methylphenidate; fear conditioning; human; emotional memory; skin conductance;
D O I
10.1007/s00213-006-0363-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Classical conditioning of a fear response involves the formation of an association between a stimulus and an emotional response and can be seen as a basic form of emotional memory. While both benzodiazepines and stimulant drugs may influence the formation of episodic memories for emotional events, their effects on fear conditioning are less clear. This study compared the effects of diazepam with methylphenidate on fear conditioning. In a single-session between groups design with three conditions [placebo, diazepam (10 mg), and methylphenidate (40 mg)], classical conditioning of a skin conductance response to a visual stimulus previously paired with a 100-db white noise was tested in 45 healthy volunteers. Diazepam blocked fear conditioning, despite responses to the unconditioned aversive stimulus and neutral control stimulus being unimpaired. Conditioning remained intact after methylphenidate. Conditioned responses were not extinguished completely by the end of the experiment, and it was not possible to draw conclusions about the effects of the drugs on extinction. Although diazepam has well-documented amnesic effects, it has not been found to affect implicit forms of memory like perceptual and conceptual priming. As the present study found impaired fear conditioning after diazepam, it adds weight to recent findings that emotional memories are disproportionately impaired by the benzodiazepines.
引用
收藏
页码:504 / 516
页数:13
相关论文
共 69 条
[21]   INTACT DELAY-EYEBLINK CLASSICAL-CONDITIONING IN AMNESIA [J].
GABRIELI, JDE ;
CARRILLO, MC ;
CERMAK, LS ;
MCGLINCHEYBERROTH, R ;
GLUCK, MA ;
DISTERHOFT, JF .
BEHAVIORAL NEUROSCIENCE, 1995, 109 (05) :819-827
[22]   SKIM CONDUCTANCE RESPONSES IN PATIENTS SEDATED WITH MIDAZOLAM OR PROPOFOL [J].
GEDDES, SM ;
GRAY, WM ;
ASBURY, AJ .
BRITISH JOURNAL OF ANAESTHESIA, 1994, 73 (03) :345-349
[23]   SKIN-CONDUCTANCE RESPONSES TO AUDITORY-STIMULI AND ANTICIPATORY RESPONSES BEFORE VENIPUNCTURE IN PATIENTS PREMEDICATED WITH DIAZEPAM OR MORPHINE [J].
GEDDES, SM ;
GRAY, WM ;
MILLAR, K ;
ASBURY, AJ .
BRITISH JOURNAL OF ANAESTHESIA, 1993, 71 (04) :512-516
[24]  
Gray JA, 1997, SCIENCE, V278, P1548
[25]   Emotional arousal does not affect delay eyeblink conditioning [J].
Grillon, C ;
Hill, J .
COGNITIVE BRAIN RESEARCH, 2003, 17 (02) :400-405
[26]   Comments on the use of the startle reflex in psychopharmacological challenges: impact of baseline startle on measurement of fear-potentiated startle [J].
Grillon, C ;
Baas, JMP .
PSYCHOPHARMACOLOGY, 2002, 164 (02) :236-238
[27]   Contextual fear conditioning and baseline startle responses in the rat fear-potentiated startle test:: a comparison of benzodiazepine/γ-aminobutyric acid-A receptor agonists [J].
Guscott, MR ;
Cook, GP ;
Bristow, LJ .
BEHAVIOURAL PHARMACOLOGY, 2000, 11 (06) :495-504
[28]   Impaired fear conditioning in Alzheimer's disease [J].
Hamann, S ;
Monarch, ES ;
Goldstein, FC .
NEUROPSYCHOLOGIA, 2002, 40 (08) :1187-1195
[29]  
Hardman J., 2001, GOODMAN GILMANS PHAR
[30]   Contextual control over the expression of fear in rats conditioned under a benzodiazepine [J].
Harris, JA ;
Westbrook, RF .
PSYCHOPHARMACOLOGY, 2001, 156 (01) :92-97