Department of Medicine, The University of Melbourne, Victoria, Australia; Department of Electrical and Electronic Engineering, The University of Melbourne, Victoria, Australia.
School of Biomedical Sciences, Monash University, Victoria, Australia.
Neuropharmacology. 2021 Jun 15;191:108572. doi: 10.1016/j.neuropharm.2021.108572. Epub 2021 Apr 24.
Local field potentials (LFPs) recorded intracranially display a range of location-specific oscillatory spectra which have been related to cognitive processes. Although the mechanisms producing LFPs are not completely understood, it is likely that voltage-gated ion channels which produce action potentials and patterned discharges play a significant role. It is also known that antipsychotic drugs (APDs) affect LFP spectra and a direct inhibitory effect on voltage-gated potassium channels has been reported. Additionally, voltage-gated potassium channels have been implicated in the pathophysiology of schizophrenia, a disorder for which APDs are primary therapies. In this study we sought to: i) better characterise the effects of two APDs on LFPs spectra and connectivity measures and ii) examine the effects of potassium channel modulators on LFPs and potential overlap of effects with APDs. Intracranial electrodes were implanted in hippocampus (HIP) and pre-frontal cortex (PFC) of C57BL/6J mice; power spectra, coherence and phase-amplitude cross-frequency coupling were measured. Drugs tested were APDs haloperidol and clozapine as well as voltage-gated potassium channel modulators (KVMs) 4-aminopyridine (4-AP), tetraethylammonium, retigabine and E-4031. Both APDs and KVMs significantly reduced gamma power except 4-AP, which conversely increased gamma power. Clozapine and retigabine additionally reduced gamma coherence between HIP and PFC, while 4-AP demonstrated the opposite effect. Phase-amplitude coupling between theta and gamma oscillations in HIP was significantly reduced by the administration of haloperidol and retigabine. These results provide previously undescribed effects of APDs on LFP properties and demonstrate novel modulation of LFP characteristics by KVMs that intriguingly overlap with the APD effects.
局部场电位 (LFPs) 经颅内记录显示出一系列与认知过程相关的特定位置振荡频谱。尽管产生 LFPs 的机制尚未完全理解,但产生动作电位和模式放电的电压门控离子通道很可能发挥重要作用。已知抗精神病药物 (APD) 会影响 LFPs 频谱,并且已经报道了对电压门控钾通道的直接抑制作用。此外,电压门控钾通道与精神分裂症的病理生理学有关,而 APD 是治疗该病的主要方法。在这项研究中,我们试图:i)更好地描述两种 APD 对 LFPs 频谱和连接性测量的影响,以及 ii)检查钾通道调节剂对 LFPs 的影响以及与 APD 重叠的潜在影响。颅内电极被植入 C57BL/6J 小鼠的海马体 (HIP) 和前额叶皮层 (PFC);测量了功率谱、相干性和相位-振幅交叉频率耦合。测试的药物是 APD 氟哌啶醇和氯氮平,以及电压门控钾通道调节剂 (KVM) 4-氨基吡啶 (4-AP)、四乙铵、瑞替加滨和 E-4031。除了 4-AP 相反地增加了伽马功率外,两种 APD 和 KVM 都显著降低了伽马功率。氯氮平和瑞替加滨还降低了 HIP 和 PFC 之间的伽马相干性,而 4-AP 则表现出相反的效果。海马体中 theta 和 gamma 振荡之间的相位-振幅耦合被氟哌啶醇和瑞替加滨的给药显著降低。这些结果提供了以前未描述的 APD 对 LFPs 特性的影响,并证明了 KVM 对 LFPs 特征的新颖调制,这些调制与 APD 效应令人好奇地重叠。