利用微电极阵列评估方法研究Dravet综合征脑类器官的禁忌症药物反应

Organoids Pub Date : 2023-10-26 DOI:10.3390/organoids2040014
Remi Yokoi, Nami Nagafuku, Yuto Ishibashi, Naoki Matsuda, Ikuro Suzuki
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摘要

确保特定神经系统疾病患者的药物安全至关重要。例如,某些抗癫痫药物(aed)是Dravet综合征(DS)的禁忌症,其特征是Na+通道功能缺乏。构建能够检测退行性椎体变性患者神经细胞禁忌症药物反应和药物效应的体外评估方法,对药物安全性评估和治疗创新具有重要意义。本研究采用微电极阵列(MEA)测量和低频分析对人类ipsc衍生的DS类器官进行了AED反应研究。当暴露于禁忌药物卡马西平和苯妥英时,DS类器官的网络振荡数量增加,但振荡强度保持不变。此外,卡马西平似乎增强了振荡以外的活动,这与DS小鼠模型的发现部分一致。相反,用治疗药物丙戊酸钠治疗导致健康和DS类器官的活性下降相似。DS类器官的自发放电频率特征和aed反应性与体内观察到的典型脑电图模式部分相关。总之,本研究采用低频分析的MEA测量,揭示了DS类器官的禁忌症药物反应和疾病特异性功能特征,对DS患者安全性评估、精准医学和抗癫痫药物筛选有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contraindicated Drug Responses in Dravet Syndrome Brain Organoids Utilizing Micro Electrode Array Assessment Methods
Ensuring drug safety for patients with specific neurological disorders is of paramount importance. For instance, certain antiepileptic drugs (AEDs) are contraindicated in Dravet Syndrome (DS), which is characterized by a deficiency in Na+ channel function. Constructing in vitro assessment methods capable of detecting contraindicated drug responses and medication effects on neurons derived from DS patients is highly anticipated for drug safety assessment and therapeutic innovation. This study used micro electrode array (MEA) measurements with low-frequency analysis on human iPSC-derived DS organoids to investigate AED responses. When exposed to the contraindicated drugs carbamazepine and phenytoin, the number of network oscillations increased in DS organoids while maintaining oscillation intensity. Furthermore, carbamazepine administration appeared to enhance activities beyond oscillations which is partially consistent with findings in the DS mouse model. Conversely, treatment with the therapeutic drug sodium valproate resulted in a similar decrease in activity both in healthy and DS organoids. The frequency characteristics of spontaneous firings and AEDs responsiveness in DS organoids demonstrated partial correlation with typical electroencephalography patterns observed in vivo. In conclusion, this study, employing MEA measurements with low-frequency analysis, revealed contraindicated drug responses and disease-specific functional characteristics in DS organoids, effective for DS patient safety assessment, precision medicine, and antiepileptic drug screening.
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