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An in Silico, Biomarker-Based Method for the Evaluation of Virtual Neuropsychiatric Drug Effects

机译:一种基于计算机模拟,基于生物标记的虚拟神经精神药物疗效评估方法

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摘要

The recent explosion in neuroscience research has markedly increased our understanding of the neurobiological correlates of many psychiatric illnesses, but this has unfortunately not translated into more effective pharmacologic treatments for these conditions. At the same time, researchers have increasingly sought out biological markers, or biomarkers, as a way to categorize psychiatric illness, as these are felt to be closer to underlying genetic and neurobiological vulnerabilities. While biomarker-based drug discovery approaches have tended to employ in vivo (e.g., rodent) or in vitro test systems, relatively little attention has been paid to the potential of computational, or in silico, methodologies. Here we describe such a methodology, using as an example a biophysically detailed computational model of hippocampus that is made to generate putative schizophrenia biomarkers by the inclusion of a number of neuropathological changes that have been associated with the illness (NMDA system deficit, decreased neural connectivity, hyperdopaminergia). We use the specific inability to attune to gamma band (40 Hz) auditory stimulus as our illness biomarker. We expose this system to a large number of virtual medications, defined by systematic variation of model parameters corresponding to five cellular-level effects. The potential efficacy of virtual medications is determined by a wellness metric (WM) that we have developed. We identify a number of virtual agents that consist of combinations of mechanisms, which are not simply reversals of the causative lesions. The manner in which this methodology could be extended to other neuropsychiatric conditions, such as Alzheimer’s disease, autism, and fragile X syndrome, is discussed.
机译:神经科学研究的最新发展显着增加了我们对许多精神疾病的神经生物学相关性的理解,但是不幸的是,这并未转化为针对这些疾病的更有效的药物治疗方法。同时,研究人员越来越多地寻找生物标记物作为一种对精神疾病进行分类的方法,因为人们认为这些标记物更接近潜在的遗传和神经生物学脆弱性。尽管基于生物标志物的药物发现方法倾向于在体内(例如啮齿动物)或体外测试系统中使用,但是相对较少地关注计算方法或计算机方法学的潜力。在这里,我们描述了这样一种方法,以海马的生物物理详细计算模型为例,该模型通过包含与疾病相关的许多神经病理学改变(NMDA系统缺陷,神经连通性降低)而产生推定的精神分裂症生物标志物,多巴胺痛)。我们使用特定的无能调节到伽马带(40 Hz)的听觉刺激作为我们的疾病生物标记。我们将这个系统暴露于大量的虚拟药物,这些药物由对应于五个细胞水平效应的模型参数的系统变化定义。虚拟药物的潜在功效取决于我们开发的健康指标(WM)。我们确定了由机制组合组成的许多虚拟代理,这些组合不仅是病因病变的逆转。讨论了将该方法扩展到其他神经精神疾病(例如阿尔茨海默氏病,自闭症和脆弱X综合征)的方式。

著录项

  • 来源
    《Neural computation》 |2017年第4期|1021-1052|共32页
  • 作者

    Peter J. Siekmeier;

  • 作者单位

    Harvard Medical School, Boston, MA 02115, and Laboratory for Computational Neuroscience, McLean Hospital, Belmont, MA 02478, U.S.A. psiekmeier@mclean.harvard.edu;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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