Russell Vivienne A, Sagvolden Terje, Johansen Espen Borgå
Center for Advanced Study, The Norwegian Academy of Science and Letters, Oslo, Norway.
Behav Brain Funct. 2005 Jul 15;1:9. doi: 10.1186/1744-9081-1-9.
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 alpha2-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.
虽然动物不能用于研究诸如语言等复杂的人类行为,但它们确实具有相似的基本功能。事实上,有动物模型的人类疾病比没有动物模型的疾病更容易理解。注意力缺陷多动障碍(ADHD)是一种异质性疾病。啮齿动物模型相对简单的神经系统使得能够识别出ADHD行为某些方面背后的神经生物学变化。几种ADHD动物模型表明多巴胺能系统功能受损。一些动物模型细胞外多巴胺浓度降低,突触后多巴胺D1受体(DRD1)上调,而另一些动物模型细胞外多巴胺浓度升高。在后一种情况下,提示多巴胺通路过度活跃。然而,在这些模型中,刺激诱发的多巴胺释放通常会减少,这与多巴胺传递受损一致。ADHD的行为特征可能是由于皮质-纹状体-丘脑-皮质回路中多巴胺对神经传递的调节受损所致。有大量证据表明,在某些模型中,去甲肾上腺素能系统受功能减退的α2-自受体控制不佳,导致去甲肾上腺素释放不适当增加。ADHD行为的某些方面可能是由于涉及前额叶皮质的神经回路中去甲肾上腺素能增加和多巴胺能调节减少之间的失衡所致。ADHD动物模型还表明,ADHD儿童的大脑神经回路可能发生改变。因此,研究该疾病的动物模型而非正常动物尤为重要。从动物模型获得的数据表明,精神兴奋剂可能不是通过作用于多巴胺转运体来使ADHD患者细胞外多巴胺浓度产生预期的升高。有证据表明,精神兴奋剂可能通过提高血清素水平来减少运动活动。除了为ADHD的神经生物学提供独特见解外,动物模型还被用于测试可用于缓解ADHD症状的新药。