Department of Zoology, University of Otago, Dunedin, New Zealand.
Brain Health Research Centre, University of Otago, Dunedin, New Zealand.
J Neurochem. 2024 Dec;168(12):4014-4024. doi: 10.1111/jnc.15836. Epub 2023 May 17.
Epilepsy, a clinical diagnosis characterised by paroxysmal episodes known as seizures, affects 1% of people worldwide. Safe and patient-specific treatment is vital and can be achieved by the development of rapid pre-clinical models of for identified epilepsy genes. Epilepsy can result from either brain injury or gene mutations, and can also be induced chemically. Xenopus laevis tadpoles could be a useful model for confirmation of variants of unknown significance found in epilepsy patients, and for drug re-purposing screens that could eventually lead to benefits for patients. Here, we characterise and quantify seizure-related behaviours in X. laevis tadpoles arrayed in 24-well plates. To provoke acute seizure behaviours, tadpoles were chemically induced with either pentylenetetrazole (PTZ) or 4-aminopyridine (4-AP). To test the capacity to adapt this method for drug testing, we also exposed induced tadpoles to the anti-seizure drug valproate (VPA). Four induced seizure-like behaviours were described and manually quantified, and two of these (darting, circling) could be accurately detected automatically, using the video analysis software TopScan. Additionally, we recorded swimming trajectories and mean swimming velocity. Automatic detection showed that either PTZ or 4-AP induced darting behaviour and increased mean swimming velocity compared to untreated controls. Both parameters were significantly reduced in the presence of VPA. In particular, darting behaviour was a shown to be a sensitive measure of epileptic seizure activity. While we could not automatically detect the full range of seizure behaviours, this method shows promise for future studies since X. laevis is a well-characterised and genetically tractable model organism.
癫痫是一种以阵发性癫痫发作为特征的临床诊断,影响全球 1%的人口。安全且针对患者个体的治疗至关重要,而这可以通过开发针对已确定的癫痫基因的快速临床前模型来实现。癫痫可能由脑损伤或基因突变引起,也可能由化学诱导引起。非洲爪蟾(Xenopus laevis)蝌蚪可能是确认癫痫患者未知意义变异体的有用模型,也是药物再利用筛选的有用模型,最终可能使患者受益。在这里,我们在 24 孔板中排列的非洲爪蟾蝌蚪中对与癫痫发作相关的行为进行了特征描述和定量分析。为了诱发急性癫痫行为,我们用戊四氮(PTZ)或 4-氨基吡啶(4-AP)化学诱导蝌蚪。为了测试这种方法用于药物测试的能力,我们还将诱导的蝌蚪暴露于抗癫痫药物丙戊酸钠(VPA)中。描述并手动定量了四种诱导的癫痫样行为,其中两种(猛冲、盘旋)可以使用视频分析软件 TopScan 自动准确地检测到。此外,我们还记录了游泳轨迹和平均游泳速度。自动检测表明,与未处理的对照组相比,PTZ 或 4-AP 诱导了猛冲行为并增加了平均游泳速度。VPA 的存在使这两个参数都显著降低。特别是,猛冲行为是癫痫发作活动的敏感测量指标。虽然我们不能自动检测到所有类型的癫痫发作行为,但这种方法具有广阔的未来研究前景,因为非洲爪蟾是一种特征明确且遗传上易于操作的模式生物。