Stimulants: use and abuse in the treatment of attention deficit hyperactivity disorder

被引:81
作者
Fone, KCF [1 ]
Nutt, DJ
机构
[1] Univ Nottingham, Queens Med Ctr, Inst Neurosci, Sch Biomed Sci, Nottingham NG7 2UH, England
[2] Univ Bristol, Psychopharmacol Res Unit, Bristol BS8 1TD, Avon, England
关键词
D O I
10.1016/j.coph.2004.10.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Attention deficit hyperactivity disorder (ADHD) is the most prevalent childhood developmental disorder and is also of unclear neurobiological aetiology. However, recent advances in molecular genetics and brain imaging implicate dopaminergic hypofunction in the frontal lobes and basal ganglia in ADHD. Psychostimulants (e.g. methylphenidate and amphetamine, which are potent inhibitors of the dopamine transporter) are the first choice medication for ADHD and have a good acute efficacy and safety profile when used for this disorder. Whether long-term psychostimulant administration to adolescents alters neural development and behaviour or increases the risk of substance abuse is less certain. The precise molecular mechanism of action of psychostimulants is beginning to be established. Furthermore, preclinical studies have begun to use lower clinically relevant doses and oral administration of psychostimulants to determine their long-term effect on development, behaviour and neurochemistry, which is an important public health issue associated with chronic medication of adolescents with ADHD.
引用
收藏
页码:87 / 93
页数:7
相关论文
共 54 条
[21]   The dopamine transporter and neuroimaging in attention deficit hyperactivity disorder [J].
Krause, KH ;
Dresel, SH ;
Krause, J ;
la Fougere, C ;
Ackenheil, M .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2003, 27 (07) :605-613
[22]  
Kuczenski R, 2002, J NEUROSCI, V22, P7264
[23]  
Kuczenski R, 2001, J PHARMACOL EXP THER, V296, P876
[24]   International consensus statement on attention-deficit/hyperactivity disorder (ADHD) and disruptive behaviour disorders (DBDs): Clinical implications and treatment practice suggestions [J].
Kutcher, S ;
Aman, M ;
Brooks, SJ ;
Buitelaar, J ;
van Daalen, E ;
Fegert, J ;
Findling, RL ;
Fisman, S ;
Greenhill, LL ;
Huss, M ;
Kusumakar, V ;
Pine, D ;
Taylor, E ;
Tyano, S .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2004, 14 (01) :11-28
[25]   Expression of dopamine transporter and vesicular monoamine transporter 2 mRNAs in rat midbrain after repeated amphetamine administration [J].
Lu, WX ;
Wolf, ME .
MOLECULAR BRAIN RESEARCH, 1997, 49 (1-2) :137-148
[26]   The dopamine transporter: relevance to attention deficit hyperactivity disorder (ADHD) [J].
Madras, BK ;
Miller, GM ;
Fischman, AJ .
BEHAVIOURAL BRAIN RESEARCH, 2002, 130 (1-2) :57-63
[27]   Effects of repeated methylphenidate treatment in the young rat: Sensitization of both locomotor activity and stereotyped sniffing [J].
McDougall, SA ;
Collins, RL ;
Karper, PE ;
Watson, JB ;
Crawford, CA .
EXPERIMENTAL AND CLINICAL PSYCHOPHARMACOLOGY, 1999, 7 (03) :208-218
[28]   Subchronic methylphenidate administration has no effect on locomotion, emotional behavior, or water maze learning in prepubertal mice [J].
McFayden, MP ;
Brown, RE ;
Carrey, N .
DEVELOPMENTAL PSYCHOBIOLOGY, 2002, 41 (02) :123-132
[29]   MODAFINIL BINDS TO THE DOPAMINE UPTAKE CARRIER SITE WITH LOW-AFFINITY [J].
MIGNOT, E ;
NISHINO, S ;
GUILLEMINAULT, C ;
DEMENT, WC .
SLEEP, 1994, 17 (05) :436-437
[30]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159