Animal models of attention-deficit hyperactivity disorder

被引:191
作者
Russell, Vivienne A. [1 ,2 ]
Sagvolden, Terje [1 ,3 ]
Johansen, Espen Borga [1 ,3 ]
机构
[1] Norwegian Acad Sci & Letters, Ctr Adv Study, Oslo, Norway
[2] Univ Cape Town, Dept Human Biol, ZA-7700 Rondebosch, South Africa
[3] Univ Oslo, Inst Basic Med Sci, Dept Physiol, N-0316 Oslo, Norway
基金
英国医学研究理事会;
关键词
D O I
10.1186/1744-9081-1-9
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
Although animals cannot be used to study complex human behaviour such as language, they do have similar basic functions. In fact, human disorders that have animal models are better understood than disorders that do not. ADHD is a heterogeneous disorder. The relatively simple nervous systems of rodent models have enabled identification of neurobiological changes that underlie certain aspects of ADHD behaviour. Several animal models of ADHD suggest that the dopaminergic system is functionally impaired. Some animal models have decreased extracellular dopamine concentrations and upregulated postsynaptic dopamine D1 receptors (DRD1) while others have increased extracellular dopamine concentrations. In the latter case, dopamine pathways are suggested to be hyperactive. However, stimulus-evoked release of dopamine is often decreased in these models, which is consistent with impaired dopamine transmission. It is possible that the behavioural characteristics of ADHD result from impaired dopamine modulation of neurotransmission in cortico-striato-thalamo-cortical circuits. There is considerable evidence to suggest that the noradrenergic system is poorly controlled by hypofunctional alpha(2)-autoreceptors in some models, giving rise to inappropriately increased release of norepinephrine. Aspects of ADHD behaviour may result from an imbalance between increased noradrenergic and decreased dopaminergic regulation of neural circuits that involve the prefrontal cortex. Animal models of ADHD also suggest that neural circuits may be altered in the brains of children with ADHD. It is therefore of particular importance to study animal models of the disorder and not normal animals. Evidence obtained from animal models suggests that psychostimulants may not be acting on the dopamine transporter to produce the expected increase in extracellular dopamine concentration in ADHD. There is evidence to suggest that psychostimulants may decrease motor activity by increasing serotonin levels. In addition to providing unique insights into the neurobiology of ADHD, animal models are also being used to test new drugs that can be used to alleviate the symptoms of ADHD.
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页数:17
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共 191 条
[81]  
Homer CJ, 2000, PEDIATRICS, V105, P1158
[82]   DIMINISHED BRAIN SYNAPTIC PLASMA-MEMBRANE CA2+-ATPASE ACTIVITY IN SPONTANEOUSLY HYPERTENSIVE RATS - ASSOCIATION WITH REDUCED ANESTHETIC REQUIREMENTS [J].
HORN, JL ;
JANICKI, PK ;
FRANKS, JJ .
LIFE SCIENCES, 1995, 56 (22) :PL427-PL432
[83]   Glutamate receptor-dependent modulation of dopamine efflux in the nucleus accumbens by basolateral, but not central, nucleus of the amygdala in rats [J].
Howland, JG ;
Taepavarapruk, P ;
Phillips, AG .
JOURNAL OF NEUROSCIENCE, 2002, 22 (03) :1137-1145
[84]   Changes in open field behavior, spatial memory, and hippocampal parvalbumin immunoreactivity following enrichment in rats exposed to neonatal anoxia [J].
Iuvone, L ;
Geloso, MC ;
DellAnna, E .
EXPERIMENTAL NEUROLOGY, 1996, 139 (01) :25-33
[85]   Attention-deficit/hyperactivity disorder (ADHD) behaviour explained by dysfunctioning reinforcement and extinction processes [J].
Johansen, EB ;
Aase, H ;
Meyer, A ;
Sagvolden, T .
BEHAVIOURAL BRAIN RESEARCH, 2002, 130 (1-2) :37-45
[86]   Norepinephrine regulates locomotor hyperactivity in the mouse mutant coloboma [J].
Jones, MD ;
Hess, EJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2003, 75 (01) :209-216
[87]   Expression of catecholaminergic mRNAs in the hyperactive mouse mutant coloboma [J].
Jones, MD ;
Williams, ME ;
Hess, EJ .
MOLECULAR BRAIN RESEARCH, 2001, 96 (1-2) :114-121
[88]   Abnormal presynaptic catecholamine regulation in a hyperactive SNAP-25-deficient mouse mutant [J].
Jones, MD ;
Williams, ME ;
Hess, EJ .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2001, 68 (04) :669-676
[89]   Profound neuronal plasticity in response to inactivation of the dopamine transporter [J].
Jones, SR ;
Gainetdinov, RR ;
Jaber, M ;
Giros, B ;
Wightman, RM ;
Caron, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :4029-4034
[90]   Loss of autoreceptor functions in mice lacking the dopamine transporter [J].
Jones, SR ;
Gainetdinov, RR ;
Hu, XT ;
Cooper, DC ;
Wightman, RM ;
White, FJ ;
Caron, MG .
NATURE NEUROSCIENCE, 1999, 2 (07) :649-655