Beneyto Monica, Lewis David A
Department of Psychiatry, University of Pittsburgh, W1656 Biomedical Science Tower, 3811 O'Hara Street, Pittsburgh, PA 15213, USA.
Int J Dev Neurosci. 2011 May;29(3):295-304. doi: 10.1016/j.ijdevneu.2010.08.003. Epub 2010 Aug 24.
The hypothesis that schizophrenia results from a developmental, as opposed to a degenerative, process affecting the connectivity and network plasticity of the cerebral cortex is supported by findings from morphological and molecular postmortem studies. Specifically, abnormalities in the expression of protein markers of GABA neurotransmission and the lamina- and circuit-specificity of these changes in the cortex in schizophrenia, in concert with knowledge of their developmental trajectories, offer crucial insight into the vulnerability of specific cortical networks to environmental insults during different periods of development. These findings reveal potential targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia, and provide guidance for future preventive strategies to preserve cortical neurotransmission in at-risk individuals.
精神分裂症源于影响大脑皮层连接性和网络可塑性的发育过程而非退行性过程这一假说,得到了形态学和分子尸检研究结果的支持。具体而言,精神分裂症患者大脑皮层中GABA神经传递蛋白标志物表达异常以及这些变化的层特异性和回路特异性,再结合其发育轨迹的知识,为特定皮层网络在不同发育阶段对环境损伤的易感性提供了关键见解。这些发现揭示了改善精神分裂症患者认知功能的治疗干预潜在靶点,并为保护高危个体皮层神经传递的未来预防策略提供了指导。