Bachus S E, Kleinman J E
Clinical Brain Disorders Branch, NIMH Neuroscience Center at St. Elizabeths, Washington, D.C. 20032, USA.
J Clin Psychiatry. 1996;57 Suppl 11:72-83.
Neuropharmacologic discoveries have driven much of the research on neural substances of schizophrenia since the advent of neuroleptic drugs, which appear to share blockade of dopamine receptors. as their common denominator. Yet, despite concerted efforts to identify the source of putative dopaminergic hyperactivity in the brain in schizophrenia, definitive evidence for the "dopamine hypothesis of schizophrenia" remains elusive. More recently, a "neural systems" approach, focussing on the limbic system, has yielded substantial convergent evidence, from both in vivo imaging and postmortem morphological, biochemical, and molecular biological methods, implicating limbic cortex in the neuropathology underlying schizophrenia. Moreover, these limbic cortical regions modulate dopaminergic function in the striatum and nucleus accumbens, via glutamatergic projections. Increasingly, focus is shifting to a role for glutamatergic dysfunction in schizophrenia, opening the possibility that drugs that act upon glutamate function, either directly or indirectly via co-modulators of glutamate transmission, could potentially be developed as adjunctive or primary novel pharmacotherapeutic strategies.
自从抗精神病药物问世以来,神经药理学的发现推动了对精神分裂症神经物质的大量研究,这些药物似乎都具有多巴胺受体阻断作用,这是它们的共同特征。然而,尽管人们齐心协力寻找精神分裂症患者大脑中假定的多巴胺能活动亢进的来源,但“精神分裂症多巴胺假说”的确凿证据仍然难以捉摸。最近,一种“神经系统”方法,聚焦于边缘系统,已经从活体成像以及死后形态学、生物化学和分子生物学方法中获得了大量趋同证据,表明边缘皮层与精神分裂症潜在的神经病理学有关。此外,这些边缘皮层区域通过谷氨酸能投射调节纹状体和伏隔核中的多巴胺能功能。越来越多的研究焦点转向谷氨酸能功能障碍在精神分裂症中的作用,这使得直接作用于谷氨酸功能或通过谷氨酸传递的共调节剂间接作用于谷氨酸功能的药物有可能被开发为辅助或主要新型药物治疗策略。