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缝隙连接蛋白 1 通道调节癫痫中的 ATP 释放。

Pannexin-1 Channel Regulates ATP Release in Epilepsy.

机构信息

Nantong University, Nantong, China.

Department of Neurology, Affiliated Hospital of Nantong University, Nantong, China.

出版信息

Neurochem Res. 2020 May;45(5):965-971. doi: 10.1007/s11064-020-02981-9. Epub 2020 Mar 13.

DOI:10.1007/s11064-020-02981-9
PMID:32170674
Abstract

With the deepening of research on epilepsy in recent decades, great progress has been made in the diagnosis and treatment of the disease. However, the clinical outcome remains unsatisfactory due to the confounding symptoms and complications, as well as complex intrinsic pathogenesis. A better understanding of the pathogenesis of epilepsy should be able to hinder the progress of the disease and improve the therapeutic effectiveness. Since the discovery of pannexin (Panx), unremitting efforts on the study of this gap junction protein family member have revealed its role in participating in the expression of various physiopathological processes. Among them, the activation or inhibition of Panx channel has been shown to regulate the release of adenosine triphosphate (ATP) and other signals, which is very important for the onset and control of nervous system diseases including epilepsy. In this article, we summarize the factors influencing the regulation of Panx channel opening, hoping to find a way to interfere with the activation or inhibition of Panx channel that regulates the signal transduction of ATP and other factors so as to control the progression of epilepsy and improve the quality of life of epileptic patients who fail to respond to the existing medical therapies and those at risk of surgical treatment.

摘要

近几十年来,随着对癫痫的研究不断深入,在癫痫的诊断和治疗方面取得了巨大进展。然而,由于症状和并发症复杂以及内在发病机制复杂,临床结果仍不尽如人意。更好地了解癫痫的发病机制应该能够阻止疾病的进展并提高治疗效果。自发现连接蛋白(Panx)以来,对这种间隙连接蛋白家族成员的不懈研究揭示了其参与各种生理病理过程表达的作用。其中,Panx 通道的激活或抑制已被证明可以调节三磷酸腺苷(ATP)和其他信号的释放,这对于包括癫痫在内的神经系统疾病的发作和控制非常重要。本文总结了影响 Panx 通道开放调节的因素,希望找到一种干预调节 ATP 和其他因素信号转导的 Panx 通道激活或抑制的方法,从而控制癫痫的进展,提高对现有医学治疗无反应和有手术治疗风险的癫痫患者的生活质量。

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Neuronal Panx1 drives peripheral sensitization in experimental plantar inflammatory pain.神经元 Panx1 驱动实验性足底炎性疼痛的外周敏化。

本文引用的文献

1
Pannexin 1 activation and inhibition is permeant-selective.缝隙连接蛋白 1 的激活和抑制是通透选择性的。
J Physiol. 2020 Jan;598(2):361-379. doi: 10.1113/JP278759. Epub 2020 Jan 6.
2
Selective inhibition of Panx1 channels decreases hemostasis and thrombosis in vivo.选择性抑制 Panx1 通道可减少体内止血和血栓形成。
Thromb Res. 2019 Nov;183:56-62. doi: 10.1016/j.thromres.2019.09.028. Epub 2019 Oct 18.
3
Pannexin-1 limits the production of proinflammatory cytokines during necroptosis.Pannexin-1 在细胞坏死性凋亡过程中限制促炎细胞因子的产生。
Mil Med Res. 2024 Apr 29;11(1):27. doi: 10.1186/s40779-024-00525-8.
4
Age-Dependent Activation of Pannexin1 Function Contributes to the Development of Epileptogenesis in Autosomal Dominant Sleep-related Hypermotor Epilepsy Model Rats.年龄依赖性的 Pannexin1 功能激活有助于常染色体显性遗传性睡眠相关运动性癫痫模型大鼠癫痫发生的发展。
Int J Mol Sci. 2024 Jan 28;25(3):1619. doi: 10.3390/ijms25031619.
5
Connexins Control Glial Inflammation in Various Neurological Diseases.连接蛋白在多种神经疾病中控制神经胶质炎症。
Int J Mol Sci. 2023 Nov 28;24(23):16879. doi: 10.3390/ijms242316879.
6
AR as a Prognostic Marker and a Potential Immunotherapy Target in Human Glioma.AR 作为人神经胶质瘤的预后标志物和潜在的免疫治疗靶点。
Int J Mol Sci. 2023 Apr 3;24(7):6688. doi: 10.3390/ijms24076688.
7
The P2X7 Receptor as a Mechanistic Biomarker for Epilepsy.P2X7 受体作为癫痫的机制生物标志物。
Int J Mol Sci. 2023 Mar 12;24(6):5410. doi: 10.3390/ijms24065410.
8
Contribution of large-pore channels to inflammation induced by microorganisms.大孔通道在微生物诱导的炎症中的作用。
Front Cell Dev Biol. 2023 Jan 9;10:1094362. doi: 10.3389/fcell.2022.1094362. eCollection 2022.
9
Pannexin-1 channel opening is critical for COVID-19 pathogenesis.泛连接蛋白-1通道开放对新冠病毒发病机制至关重要。
iScience. 2021 Dec 17;24(12):103478. doi: 10.1016/j.isci.2021.103478. Epub 2021 Nov 19.
10
Pannexin 1 channels and ATP release in epilepsy: two sides of the same coin : The contribution of pannexin-1, connexins, and CALHM ATP-release channels to purinergic signaling.缝隙连接蛋白 1 通道和癫痫中的 ATP 释放:同一枚硬币的两面:缝隙连接蛋白 1、连接蛋白和 CALHM ATP 释放通道对嘌呤能信号转导的贡献。
Purinergic Signal. 2021 Dec;17(4):533-548. doi: 10.1007/s11302-021-09818-2. Epub 2021 Sep 8.
EMBO Rep. 2019 Oct 4;20(10):e47840. doi: 10.15252/embr.201947840. Epub 2019 Aug 14.
4
Revealing epilepsy type using a computational analysis of interictal EEG.利用脑电信号的间期分析揭示癫痫类型
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Cannabinoids, hippocampal excitability and efficacy for the treatment of epilepsy.大麻素、海马兴奋性与癫痫治疗的疗效。
Pharmacol Ther. 2019 Oct;202:32-39. doi: 10.1016/j.pharmthera.2019.06.002. Epub 2019 Jun 7.
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An update for epilepsy research and antiepileptic drug development: Toward precise circuit therapy.癫痫研究和抗癫痫药物开发的新进展:迈向精确的电路治疗。
Pharmacol Ther. 2019 Sep;201:77-93. doi: 10.1016/j.pharmthera.2019.05.010. Epub 2019 May 23.
7
Elevation in plasma tRNA fragments precede seizures in human epilepsy.血浆 tRNA 片段升高先于人类癫痫发作。
J Clin Invest. 2019 Apr 30;129(7):2946-2951. doi: 10.1172/JCI126346.
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Extrinsic and intrinsic apoptosis activate pannexin-1 to drive NLRP3 inflammasome assembly.外在和内在凋亡途径激活连接蛋白-1 以驱动 NLRP3 炎性小体组装。
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The Role of Connexin and Pannexin Channels in Perinatal Brain Injury and Inflammation.连接蛋白和泛连接蛋白通道在围产期脑损伤与炎症中的作用
Front Physiol. 2019 Feb 27;10:141. doi: 10.3389/fphys.2019.00141. eCollection 2019.