Conn Kyna-Anne, Burne Thomas H J, Kesby James P
Queensland Brain Institute, The University of Queensland, St Lucia, QLD, Australia.
Queensland Centre for Mental Health Research, Wacol, QLD, Australia.
Front Neurosci. 2020 Jun 3;14:542. doi: 10.3389/fnins.2020.00542. eCollection 2020.
Schizophrenia is characterized by positive, negative and cognitive symptoms. All current antipsychotic treatments feature dopamine-receptor antagonism that is relatively effective at addressing the psychotic (positive) symptoms of schizophrenia. However, there is no clear evidence that these medications improve the negative or cognitive symptoms, which are the greatest predictors of functional outcomes. One of the most robust pathophysiological observations in patients with schizophrenia is increased subcortical dopamine neurotransmission, primarily in the associative striatum. This brain area has an important role in a range of cognitive processes. Dopamine is also known to play a major part in regulating a number of cognitive functions impaired in schizophrenia but much of this research has been focused on cortical dopamine. Emerging research highlights the strong influence subcortical dopamine has on a range of cognitive domains, including attention, reward learning, goal-directed action and decision-making. Nonetheless, the precise role of the associative striatum in the cognitive impairments observed in schizophrenia remains poorly understood, presenting an opportunity to revisit its contribution to schizophrenia. Without a better understanding of the mechanisms underlying cognitive dysfunction, treatment development remains at a standstill. For this reason, improved preclinical animal models are needed if we are to understand the complex relationship between subcortical dopamine and cognition. A range of new techniques are facillitating the discrete manipulation of dopaminergic neurotransmission and measurements of cognitive performance, which can be investigated using a variety of sensitive translatable tasks. This has the potential to aid the successful incorporation of recent clinical research to address the lack of treatment strategies for cognitive symptoms in schizophrenia. This review will give an overview on the current state of research focused on subcortical dopamine and cognition in the context of schizophrenia research. We also discuss future strategies and approaches aimed at improving the translational outcomes for the treatment of cognitive deficits in schizophrenia.
精神分裂症的特征包括阳性、阴性和认知症状。目前所有的抗精神病药物治疗均以多巴胺受体拮抗作用为特点,这在治疗精神分裂症的精神病性(阳性)症状方面相对有效。然而,尚无明确证据表明这些药物能改善阴性或认知症状,而这些症状是功能预后的最强预测因素。精神分裂症患者最有力的病理生理学观察结果之一是皮质下多巴胺神经传递增加,主要发生在联合纹状体。这个脑区在一系列认知过程中发挥着重要作用。多巴胺在调节精神分裂症中受损的多种认知功能方面也起着主要作用,但大部分此类研究都集中在皮质多巴胺上。新出现的研究突出了皮质下多巴胺对一系列认知领域的强大影响,包括注意力、奖赏学习、目标导向行为和决策。尽管如此,联合纹状体在精神分裂症中观察到的认知障碍中的确切作用仍知之甚少,这为重新审视其对精神分裂症的影响提供了契机。如果我们不更好地理解认知功能障碍背后的机制,治疗进展将停滞不前。因此,如果我们要理解皮质下多巴胺与认知之间的复杂关系,就需要改进临床前动物模型。一系列新技术有助于对多巴胺能神经传递进行离散操作和认知表现测量,这可以通过各种敏感的可转化任务进行研究。这有可能有助于成功整合近期的临床研究,以解决精神分裂症认知症状治疗策略的不足。本综述将概述精神分裂症研究背景下关于皮质下多巴胺与认知的研究现状。我们还将讨论旨在改善精神分裂症认知缺陷治疗转化结果的未来策略和方法。