Mental Health Research Institute of Victoria, Parkville, Melbourne, Victoria 3052, Australia.
Schizophr Bull. 2010 Mar;36(2):246-70. doi: 10.1093/schbul/sbp132. Epub 2009 Nov 9.
In recent years, there have been huge advances in the use of genetically modified mice to study pathophysiological mechanisms involved in schizophrenia. This has allowed rapid progress in our understanding of the role of several proposed gene mechanisms in schizophrenia, and yet this research has also revealed how much still remains unresolved. Behavioral studies in genetically modified mice are reviewed with special emphasis on modeling psychotic-like behavior. I will particularly focus on observations on locomotor hyperactivity and disruptions of prepulse inhibition (PPI). Recommendations are included to address pharmacological and methodological aspects in future studies. Mouse models of dopaminergic and glutamatergic dysfunction are then discussed, reflecting the most important and widely studied neurotransmitter systems in schizophrenia. Subsequently, psychosis-like behavior in mice with modifications in the most widely studied schizophrenia susceptibility genes is reviewed. Taken together, the available studies reveal a wealth of available data which have already provided crucial new insight and mechanistic clues which could lead to new treatments or even prevention strategies for schizophrenia.
近年来,利用基因修饰小鼠研究精神分裂症相关的病理生理学机制已经取得了巨大进展。这使得我们对几种提出的精神分裂症基因机制的作用的理解迅速发展,但这项研究也揭示了仍有许多未解之谜。本文特别强调了基因修饰小鼠的行为研究,综述了类似精神病的行为模型。我将特别关注运动过度和前脉冲抑制(PPI)破坏的观察。本文还包括了对未来研究中药理学和方法学方面的建议。然后讨论了多巴胺能和谷氨酸能功能障碍的小鼠模型,反映了精神分裂症中最重要和广泛研究的神经递质系统。随后,综述了对最广泛研究的精神分裂症易感性基因进行修饰的小鼠的类似精神病的行为。总之,现有的研究提供了丰富的可用数据,这些数据已经提供了至关重要的新见解和机制线索,这可能为精神分裂症的治疗甚至预防策略提供新的方法。