艾灸预处理可减轻癫痫状态发作的严重程度并抵消嘌呤能P2X7受体的促惊厥功能

IF 3 4区 医学 Q2 NEUROSCIENCES
Hong-Wei Zhang, Jia-Jia Li, Yulihan Tang, Mao-Lin Tian, Sheng Huang, Meng-Juan Sun
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引用次数: 0

摘要

艾灸是一种传统的中医治疗方法,包括使用点燃的中药材料对人体的特定穴位进行温灸。有证据表明,艾灸对包括癫痫在内的多种脑部疾病有益处,但艾灸预处理是否对癫痫发作有影响,其潜在机制是什么,仍有待确定。有证据表明,嘌呤能 ATP 门控 P2X7 受体(P2X7R)参与了艾灸的作用。此外,P2X7R 信号目前已被证实是导致癫痫发展的持久脑过度兴奋的基础。至于 P2X7R 信号是否参与了艾灸的癫痫发作抑制作用,迄今为止尚未进行过研究。在研究中,我们使用了 C57BL/6 雄性小鼠,这些小鼠在足三里(ST36)和大椎(GV14)穴位接受艾灸预处理,每天一次,持续 7、14 或 21 天。然后腹腔注射凯尼酸(KA,30 毫克/千克)诱发癫痫状态。根据拉辛量表分析了KA诱发癫痫状态期间的行为变化。通过皮质植入脑电图电极分析电图癫痫发作的变化。虽然艾灸预处理 7 天后未观察到对癫痫发作严重程度的影响,但在 ST36 和 GV14 处艾灸预处理 14 或 21 天后,KA 诱导的行为癫痫发作显著减少,减少率相似。皮层脑电图记录显示,艾灸预处理14天也能减少电图癫痫发作,证实了艾灸预处理的抗惊厥作用。为了确定艾灸是否会影响 P2X7R 信号的促惊厥作用,小鼠接受了 P2X7R 激动剂 BzATP 或 P2X7R 拮抗剂 A438079 的治疗。使用 P2X7R 激动剂 BzATP 会加重癫痫发作的严重程度,而使用 P2X7R 拮抗剂则会减轻癫痫发作的严重程度。我们还发现,艾灸预处理可抵消 BzATP 的作用,从而减轻癫痫发作。这些结果表明,在穴位 ST36 和 GV14 进行为期 14 天的艾灸预处理具有抗癫痫作用,这可能抵消了 P2X7R 的促惊厥功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Moxibustion pre-treatment attenuates seizure severity during status epilepticus and counteracts the proconvulsant function of the purinergic P2X7 receptor

Moxibustion pre-treatment attenuates seizure severity during status epilepticus and counteracts the proconvulsant function of the purinergic P2X7 receptor

Moxibustion, traditional Chinese medicine treatment, involves the warming of specific acupuncture points of the body using ignited herbal materials. Evidence suggests beneficial effects of moxibustion in several brain diseases including epilepsy, however, whether moxibustion pretreatment impacts on seizures and what are the underlying mechanisms remains to be established. Evidence has suggested the purinergic ATP-gated P2X7 receptor (P2X7R) to be involved in the actions of moxibustion. Moreover, P2X7R signalling is now well established to contribute to long-lasting brain hyperexcitability underlying epilepsy development. Whether P2X7R signalling is involved in the seizure-reducing actions of moxibustion has not been investigated to date. For our studies we used C57BL/6 male mice that received moxibustion pre-treatments at the acupoints Zusanli (ST36) and Dazhui (GV14) once daily for either 7, 14, or 21 days. This was followed by an intraperitoneal injection of kainic acid (KA, 30 mg/kg) to induce status epilepticus. Behavioral changes during KA-induced status epilepticus were analyzed according to the Racine scale. Changes in electrographic seizures were analyzed via cortical implanted electroencephalogram (EEG) electrodes. While no effect on seizure severity was observed following 7 days of moxibustion pre-treatment, moxibustion pre-treatment at both ST36 and GV14 for 14 or 21 days significantly reduced KA-induced behavior seizures at a similar rate. Cortical EEG recordings showed that 14 days of moxibustion pre-treatments also reduced electrographic seizures, confirming the anticonvulsant actions of moxibustion pre-treatment. To determine whether moxibustion impacts the pro-convulsant actions of P2X7R signaling, mice were treated with the P2X7R agonist BzATP or P2X7R antagonist A438079. While treatment with the P2X7R agonist BzATP exacerbated seizure severity, treatment with the P2X7R antagonist reduced seizure severity. We further found that moxibustion pre-treatment attenuated epileptic seizures by counteracting the effects of BzATP. These results suggest that moxibustion pre-treatment at the acupoints ST36 and GV14 for 14 days has anti-epileptic effects, which may counteract the proconvulsant functions of the P2X7R.

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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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