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鉴别苯环利定和 MK-801 的运动和感觉运动效应:精神分裂症样模型中含 GluN2C 的 NMDA 受体的参与。

Discrimination of motor and sensorimotor effects of phencyclidine and MK-801: Involvement of GluN2C-containing NMDA receptors in psychosis-like models.

机构信息

Institut d'Investigacions Biomèdiques de Barcelona (IIBB-CSIC), Barcelona, Spain; Institut d'Investigacions Biomèdiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain; Centro de Investigación Biomédica en Red de Salud Mental (CIBERSAM), ISCIII, Madrid, Spain; Universitat de Barcelona, Barcelona, Spain.

Instituto de Investigaciones Biológicas Clemente Estable, Montevideo, Uruguay.

出版信息

Neuropharmacology. 2022 Aug 1;213:109079. doi: 10.1016/j.neuropharm.2022.109079. Epub 2022 May 11.

Abstract

Non-competitive NMDA receptor (NMDA-R) antagonists like ketamine, phencyclidine (PCP) and MK-801 are routinely used as pharmacological models of schizophrenia. However, the NMDA-R subtypes, neuronal types (e.g., GABA vs. glutamatergic neurons) and brain regions involved in psychotomimetic actions are not fully understood. PCP activates thalamo-cortical circuits after NMDA-R blockade in reticular thalamic GABAergic neurons. GluN2C subunits are densely expressed in thalamus and cerebellum. Therefore, we examined their involvement in the behavioral and functional effects elicited by PCP and MK-801 using GluN2C knockout (GluN2CKO) and wild-type mice, under the working hypothesis that psychotomimetic effects should be attenuated in mutant mice. PCP and MK-801 induced a disorganized and meandered hyperlocomotion in both genotypes. Interestingly, stereotyped behaviors like circling/rotation, rearings and ataxia signs were dramatically reduced in GluN2CKO mice, indicating a better motor coordination in absence of GluN2C subunits. In contrast, other motor or sensorimotor (pre-pulse inhibition of the startle response) aspects of the behavioral syndrome remained unaltered by GluN2C deletion. PCP and MK-801 evoked a general pattern of c-fos activation in mouse brain (including thalamo-cortical networks) but not in the cerebellum, where they markedly reduced c-fos expression, with significant genotype differences paralleling those in motor coordination. Finally, resting-state fMRI showed an enhanced cortico-thalamic-cerebellar connectivity in GluN2CKO mice, less affected by MK-801 than controls. Hence, the GluN2C subunit allows the dissection of the behavioral alterations induced by PCP and MK-801, showing that some motor effects (in particular, motor incoordination), but not deficits in sensorimotor gating, likely depend on GluN2C-containing NMDA-R blockade in cerebellar circuits.

摘要

非竞争性 NMDA 受体 (NMDA-R) 拮抗剂,如氯胺酮、苯环利定 (PCP) 和 MK-801,通常被用作精神分裂症的药理学模型。然而,NMDA-R 亚型、神经元类型(例如 GABA 与谷氨酸能神经元)以及涉及致幻作用的脑区尚未完全了解。PCP 在网状丘脑 GABA 能神经元中 NMDA-R 阻断后激活丘脑皮质回路。GluN2C 亚基在丘脑和小脑中有高密度表达。因此,我们使用 GluN2C 敲除 (GluN2CKO) 和野生型小鼠,检验了它们在 PCP 和 MK-801 诱发的行为和功能效应中的作用,假设致幻作用在突变小鼠中应该减弱。PCP 和 MK-801 在两种基因型中均诱导出紊乱和蜿蜒的过度活跃。有趣的是,刻板行为,如转圈/旋转、后肢抬起和共济失调迹象,在 GluN2CKO 小鼠中显著减少,表明在缺乏 GluN2C 亚基的情况下运动协调更好。相比之下,其他运动或感觉运动(惊跳反应的预脉冲抑制)方面的行为综合征在 GluN2C 缺失时没有改变。PCP 和 MK-801 在小鼠大脑中引起了 c-fos 激活的一般模式(包括丘脑皮质网络),但在小脑中没有引起,它们显著降低了 c-fos 的表达,基因型差异显著,与运动协调相似。最后,静息态 fMRI 显示 GluN2CKO 小鼠的皮质-丘脑-小脑连接增强,对 MK-801的影响小于对照小鼠。因此,GluN2C 亚基允许对 PCP 和 MK-801 诱导的行为改变进行剖析,表明一些运动效应(特别是运动不协调),而不是感觉运动门控缺陷,可能依赖于小脑回路中含有 GluN2C 的 NMDA-R 阻断。

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