Department of Psychology, Division of Molecular Neuroscience, Psychiatric University Clinics, Transfaculty Research Platform, Department Biozentrum, Life Sciences Training Facility, and Department of Psychology, Division of Cognitive Neuroscience, University of Basel, 4055 Basel, Switzerland.
Proc Natl Acad Sci U S A. 2013 Nov 12;110(46):E4369-74. doi: 10.1073/pnas.1314478110. Epub 2013 Oct 21.
In the last decade there has been an exponential increase in knowledge about the genetic basis of complex human traits, including neuropsychiatric disorders. It is not clear, however, to what extent this knowledge can be used as a starting point for drug identification, one of the central hopes of the human genome project. The aim of the present study was to identify memory-modulating compounds through the use of human genetic information. We performed a multinational collaborative study, which included assessment of aversive memory--a trait central to posttraumatic stress disorder--and a gene-set analysis in healthy individuals. We identified 20 potential drug target genes in two genomewide-corrected gene sets: the neuroactive ligand-receptor interaction and the long-term depression gene set. In a subsequent double-blind, placebo-controlled study in healthy volunteers, we aimed at providing a proof of concept for the genome-guided identification of memory modulating compounds. Pharmacological intervention at the neuroactive ligand-receptor interaction gene set led to significant reduction of aversive memory. The findings demonstrate that genome information, along with appropriate data mining methodology, can be used as a starting point for the identification of memory-modulating compounds.
在过去的十年中,人们对复杂人类特征(包括神经精神障碍)的遗传基础的了解呈指数级增长。然而,尚不清楚这些知识在多大程度上可以作为药物识别的起点,这是人类基因组计划的核心希望之一。本研究的目的是通过使用人类遗传信息来识别具有记忆调节作用的化合物。我们进行了一项多国合作研究,包括对创伤后应激障碍核心特征的厌恶记忆评估,以及对健康个体的基因集分析。我们在两个全基因组校正的基因集中确定了 20 个潜在的药物靶基因:神经活性配体-受体相互作用和长时程抑郁基因集。在随后的一项健康志愿者的双盲、安慰剂对照研究中,我们旨在为基于基因组的记忆调节化合物的鉴定提供概念验证。在神经活性配体-受体相互作用基因集中进行药物干预可显著降低厌恶记忆。这些发现表明,基因组信息以及适当的数据挖掘方法可以作为识别具有记忆调节作用的化合物的起点。