McCullumsmith Robert E, Hammond John H, Shan Dan, Meador-Woodruff James H
Department of Psychiatry, University of Cincinnati, Cincinnati, OH, USA.
Neuropsychopharmacology. 2014 Jan;39(1):65-87. doi: 10.1038/npp.2013.239. Epub 2013 Oct 4.
We propose that postmortem tissue is an underutilized substrate that may be used to translate genetic and/or preclinical studies, particularly for neuropsychiatric illnesses with complex etiologies. Postmortem brain tissues from subjects with schizophrenia have been extensively studied, and thus serve as a useful vehicle for illustrating the challenges associated with this biological substrate. Schizophrenia is likely caused by a combination of genetic risk and environmental factors that combine to create a disease phenotype that is typically not apparent until late adolescence. The complexity of this illness creates challenges for hypothesis testing aimed at understanding the pathophysiology of the illness, as postmortem brain tissues collected from individuals with schizophrenia reflect neuroplastic changes from a lifetime of severe mental illness, as well as treatment with antipsychotic medications. While there are significant challenges with studying postmortem brain, such as the postmortem interval, it confers a translational element that is difficult to recapitulate in animal models. On the other hand, data derived from animal models typically provide specific mechanistic and behavioral measures that cannot be generated using human subjects. Convergence of these two approaches has led to important insights for understanding molecular deficits and their causes in this illness. In this review, we discuss the problem of schizophrenia, review the common challenges related to postmortem studies, discuss the application of biochemical approaches to this substrate, and present examples of postmortem schizophrenia studies that illustrate the role of the postmortem approach for generating important new leads for understanding the pathophysiology of severe mental illness.
我们认为,尸检组织是一种未得到充分利用的样本,可用于转化遗传和/或临床前研究,特别是对于病因复杂的神经精神疾病。来自精神分裂症患者的尸检脑组织已得到广泛研究,因此可作为一个有用的载体,用以说明与这种生物样本相关的挑战。精神分裂症可能是由遗传风险和环境因素共同作用导致的,这些因素共同形成一种疾病表型,通常直到青春期后期才会显现。这种疾病的复杂性给旨在理解其病理生理学的假设检验带来了挑战,因为从精神分裂症患者身上采集的尸检脑组织反映了终生严重精神疾病以及抗精神病药物治疗所导致的神经可塑性变化。虽然研究尸检脑组织存在重大挑战,如死后间隔时间,但它具有一种在动物模型中难以重现的转化要素。另一方面,从动物模型获得的数据通常提供了无法通过人类受试者产生的特定机制和行为测量结果。这两种方法的结合为理解该疾病中的分子缺陷及其原因带来了重要见解。在本综述中,我们讨论精神分裂症问题,回顾与尸检研究相关的常见挑战,讨论生化方法在这种样本上的应用,并展示尸检精神分裂症研究的实例,这些实例说明了尸检方法在为理解严重精神疾病的病理生理学产生重要新线索方面的作用。