Schizophrenia and Neuropharmacology Research Group, VA Connecticut Healthcare System, West Haven, CT, USA.
Abraham Ribicoff Research Facilities, Connecticut Mental Health Center, New Haven, CT, USA.
Mol Psychiatry. 2017 Nov;22(11):1633-1640. doi: 10.1038/mp.2017.6. Epub 2017 Feb 28.
There is a need to develop treatments for cognitive impairment associated with schizophrenia (CIAS). The significant role played by N-methyl-d-aspartate receptors (NMDARs) in both the pathophysiology of schizophrenia and in neuronal plasticity suggests that facilitation of NMDAR function might ameliorate CIAS. One strategy to correct NMDAR hypofunction is to stimulate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs) as AMPAR and NMDAR functioning are coupled and interdependent. In rats and nonhuman primates (NHP), AMPAR potentiators reduce spatial working memory deficits caused by the nonselective NMDAR antagonist ketamine. The current study assessed whether the AMPAR potentiator PF-04958242 would attenuate ketamine-induced deficits in verbal learning and memory in humans. Healthy male subjects (n=29) participated in two randomized treatment periods of daily placebo or PF-04958242 for 5 days separated by a washout period. On day 5 of each treatment period, subjects underwent a ketamine infusion for 75 min during which the effects of PF-04958242/placebo were assessed on ketamine-induced: (1) impairments in verbal learning and recall measured by the Hopkins Verbal Learning Test; (2) impairments in working memory on a CogState battery; and (3) psychotomimetic effects measured by the Positive and Negative Syndrome Scale and Clinician-Administered Dissociative Symptoms Scale. PF-04958242 significantly reduced ketamine-induced impairments in immediate recall and the 2-Back and spatial working memory tasks (CogState Battery), without significantly attenuating ketamine-induced psychotomimetic effects. There were no pharmacokinetic interactions between PF-04958242 and ketamine. Furthermore, PF-04958242 was well tolerated. 'High-impact' AMPAR potentiators like PF-04958242 may have a role in the treatment of the cognitive symptoms, but not the positive or negative symptoms, associated with schizophrenia. The excellent concordance between the preclinical (rat, NHP) and human studies with PF-04958242, and in silico modeling of AMPAR-NMDAR interactions in the hippocampus, highlights the translational value of this study.
需要开发治疗与精神分裂症相关的认知障碍(CIAS)的方法。N-甲基-D-天冬氨酸受体(NMDAR)在精神分裂症的病理生理学和神经元可塑性中都起着重要作用,这表明促进 NMDAR 功能可能改善 CIAS。纠正 NMDAR 功能低下的一种策略是刺激α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPAR),因为 AMPAR 和 NMDAR 的功能是耦合和相互依赖的。在大鼠和非人灵长类动物(NHP)中,AMPAR 增强剂可减少非选择性 NMDAR 拮抗剂氯胺酮引起的空间工作记忆缺陷。本研究评估了 AMPAR 增强剂 PF-04958242 是否会减轻人类氯胺酮引起的言语学习和记忆缺陷。健康男性受试者(n=29)参加了为期 5 天的每日安慰剂或 PF-04958242 两种随机治疗期,每个治疗期之间有一个洗脱期。在每个治疗期的第 5 天,受试者接受氯胺酮输注 75 分钟,在此期间评估 PF-04958242/安慰剂对氯胺酮引起的以下影响:(1)霍普金斯言语学习测试测量的言语学习和回忆受损;(2)CogState 电池上的工作记忆受损;(3)阳性和阴性综合征量表和临床医生管理的分离症状量表测量的精神病样效应。PF-04958242 显著降低了氯胺酮引起的即时回忆和 2-Back 和空间工作记忆任务(CogState 电池)的损害,而没有显著减轻氯胺酮引起的精神病样效应。PF-04958242 与氯胺酮之间没有药代动力学相互作用。此外,PF-04958242 具有良好的耐受性。像 PF-04958242 这样的“高影响”AMPAR 增强剂可能在治疗与精神分裂症相关的认知症状方面发挥作用,但不能治疗阳性或阴性症状。PF-04958242 在临床前(大鼠、NHP)和人类研究中的极好一致性,以及在海马中 AMPAR-NMDAR 相互作用的计算机建模,突出了这项研究的转化价值。