Weinberger D R
Arch Gen Psychiatry. 1987 Jul;44(7):660-9. doi: 10.1001/archpsyc.1987.01800190080012.
Recent research on schizophrenia has demonstrated that in this disorder the brain is not, strictly speaking, normal. The findings suggest that nonspecific histopathology exists in the limbic system, diencephalon, and prefrontal cortex, that the pathology occurs early in development, and that the causative process is inactive long before the diagnosis is made. If these findings are valid and not epiphenomena, then the pathogenesis of schizophrenia does not appear to fit either traditional metabolic, posttraumatic, or neurodegenerative models of adult mental illness. The data are more consistent with a neurodevelopmental model in which a fixed "lesion" from early in life interacts with normal brain maturational events that occur much later. Based on neuro-ontological principles and insights from animal research about normal brain development, it is proposed that the appearance of diagnostic symptoms is linked to the normal maturation of brain areas affected by the early developmental pathology, particularly the dorsolateral prefrontal cortex. The course of the illness and the importance of stress may be related to normal maturational aspects of dopaminergic neural systems, particularly those innervating prefrontal cortex. Some implications for future research and treatment are considered.
近期对精神分裂症的研究表明,严格来讲,在这种疾病中大脑并非正常。研究结果显示,边缘系统、间脑和前额叶皮质存在非特异性组织病理学变化,这种病变在发育早期就已出现,且致病过程在确诊前很久就已停止活动。如果这些发现是有效的而非附带现象,那么精神分裂症的发病机制似乎既不符合成人精神疾病的传统代谢、创伤后或神经退行性模型。这些数据更符合一种神经发育模型,即生命早期的固定“损伤”与很久之后发生的正常大脑成熟事件相互作用。基于神经本体论原则以及动物研究中关于正常大脑发育的见解,有人提出诊断症状的出现与受早期发育病理学影响的脑区(尤其是背外侧前额叶皮质)的正常成熟有关。疾病的进程以及压力的重要性可能与多巴胺能神经系统的正常成熟方面有关,尤其是那些支配前额叶皮质的部分。文中还考虑了对未来研究和治疗的一些启示。