Harrison Paul J
Department of Psychiatry, Neurosciences Building, Warneford Hospital, University of Oxford, Oxford, OX3 7JX, UK.
Psychopharmacology (Berl). 2004 Jun;174(1):151-62. doi: 10.1007/s00213-003-1761-y. Epub 2004 Mar 6.
This paper puts the case for the hippocampus as being central to the neuropathology and pathophysiology of schizophrenia. The evidence comes from a range of approaches, both in vivo (neuropsychology, structural and functional imaging) and post mortem (histology, morphometry, gene expression, and neurochemistry). Neuropathologically, the main positive findings concern neuronal morphology, organisation, and presynaptic and dendritic parameters. The results are together suggestive of an altered synaptic circuitry or "wiring" within the hippocampus and its extrinsic connections, especially with the prefrontal cortex. These changes plausibly represent the anatomical component of the aberrant functional connectivity that underlies schizophrenia. Glutamatergic pathways are prominently but not exclusively affected. Changes appear somewhat greater in the left hippocampus than the right, and CA1 is relatively uninvolved compared to other subfields. Hippocampal pathology in schizophrenia may be due to genetic factors, aberrant neurodevelopment, and/or abnormal neural plasticity; it is not due to any recognised neurodegenerative process. Hippocampal involvement is likely to be associated with the neuropsychological impairments of schizophrenia rather than with its psychotic symptoms.
本文阐述了海马体在精神分裂症神经病理学和病理生理学中处于核心地位的观点。证据来源于一系列研究方法,包括活体研究(神经心理学、结构和功能成像)以及尸检研究(组织学、形态测量学、基因表达和神经化学)。在神经病理学方面,主要的阳性发现涉及神经元形态、组织以及突触前和树突参数。这些结果共同表明海马体内及其外在连接,尤其是与前额叶皮质的连接,存在突触回路或“布线”改变。这些变化可能代表了精神分裂症潜在的异常功能连接的解剖学组成部分。谷氨酸能通路受到显著但并非唯一的影响。左侧海马体的变化似乎比右侧更大,与其他亚区相比,CA1相对未受影响。精神分裂症中的海马体病理可能归因于遗传因素、异常神经发育和/或异常神经可塑性;而非任何公认的神经退行性过程。海马体受累可能与精神分裂症的神经心理学损害有关,而非其精神病性症状。