Gamma Oscillations and Potassium Channel Modulation in Schizophrenia: Targeting GABAergic Dysfunction.

IF 1.6 4区 医学 Q3 CLINICAL NEUROLOGY Clinical EEG and Neuroscience Pub Date : 2024-03-01 Epub Date: 2023-01-02 DOI:10.1177/15500594221148643
Stephen J Kaar, Judith F Nottage, Ilinca Angelescu, Tiago Reis Marques, Oliver D Howes
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Abstract

Impairments in gamma-aminobutyric acid (GABAergic) interneuron function lead to gamma power abnormalities and are thought to underlie symptoms in people with schizophrenia. Voltage-gated potassium 3.1 (Kv3.1) and 3.2 (Kv3.2) channels on GABAergic interneurons are critical to the generation of gamma oscillations suggesting that targeting Kv3.1/3.2 could augment GABAergic function and modulate gamma oscillation generation. Here, we studied the effect of a novel potassium Kv3.1/3.2 channel modulator, AUT00206, on resting state frontal gamma power in people with schizophrenia. We found a significant positive correlation between frontal resting gamma (35-45 Hz) power (n = 22, r = 0.613, P < .002) and positive and negative syndrome scale (PANSS) positive symptom severity. We also found a significant reduction in frontal gamma power (t13 = 3.635, P = .003) from baseline in patients who received AUT00206. This provides initial evidence that the Kv3.1/3.2 potassium channel modulator, AUT00206, may address gamma oscillation abnormalities in schizophrenia.

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精神分裂症中的伽马振荡和钾通道调节:针对 GABA 能功能障碍。
γ-氨基丁酸(GABA)能中间神经元功能受损会导致γ功率异常,被认为是精神分裂症患者症状的根源。GABA能中间神经元上的电压门控钾3.1(Kv3.1)和3.2(Kv3.2)通道对伽马振荡的产生至关重要,这表明靶向Kv3.1/3.2可增强GABA能功能并调节伽马振荡的产生。在这里,我们研究了新型 Kv3.1/3.2 钾通道调节剂 AUT00206 对精神分裂症患者静息状态额叶伽玛功率的影响。我们发现,在接受 AUT00206 治疗的患者中,额叶静息伽马(35-45 Hz)功率(n = 22,r = 0.613,P t13 = 3.635,P = .003)与基线之间存在明显的正相关。这初步证明了 Kv3.1/3.2 钾通道调节剂 AUT00206 可以解决精神分裂症患者伽马振荡异常的问题。
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来源期刊
Clinical EEG and Neuroscience
Clinical EEG and Neuroscience 医学-临床神经学
CiteScore
5.20
自引率
5.00%
发文量
66
审稿时长
>12 weeks
期刊介绍: Clinical EEG and Neuroscience conveys clinically relevant research and development in electroencephalography and neuroscience. Original articles on any aspect of clinical neurophysiology or related work in allied fields are invited for publication.
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