Department of Neurology Massachusetts General Hospital Boston Massachusetts; Harvard Medical School Boston Massachusetts.
Ann Clin Transl Neurol. 2015 Oct 27;2(12):1055-70. doi: 10.1002/acn3.259. eCollection 2015 Dec.
Although benzodiazepines and other GABAA receptors allosteric modulators are used to treat neonatal seizures, their efficacy may derive from actions on subcortical structures. Side effects of benzodiazepines in nonseizing human neonates include myoclonus, seizures, and abnormal movements. Excitatory actions of GABA may underlie both side effects and reduced anticonvulsant activity of benzodiazepines. Neocortical organotypic slice cultures were used to study: (1) spontaneous cortical epileptiform activity during early development; (2) developmental changes in [Cl(-)]i and (3) whether diazepam's anticonvulsant effect correlated with neuronal [Cl(-)]i.
Epileptiform activity in neocortical organotypic slice cultures was measured by field potential recordings. Cl(-) changes during development were assessed by multiphoton imaging of neurons transgenically expressing a Cl-sensitive fluorophore. Clinically relevant concentrations of diazepam were used to test the anticonvulsant effectiveness at ages corresponding to premature neonates through early infancy.
(1) Neocortical organotypic slices at days in vitro 5 (DIV5) exhibited spontaneous epileptiform activity. (2) Epileptiform event duration decreased with age. (3) There was a progressive decrease in [Cl(-)]i over the same age range. (4) Diazepam was ineffective in decreasing epileptiform activity at DIV5-6, but progressively more effective at older ages through DIV15. (5) At DIV5-6, diazepam worsened epileptiform activity in 50% of the slices.
The neocortical organotypic slice is a useful model to study spontaneous epileptiform activity. Decreasing [Cl(-)]i during development correlates with decreasing duration of spontaneous epileptiform activity and increasing anticonvulsant efficacy of diazepam. We provide a potential explanation for the reports of seizures and myoclonus induction by benzodiazepines in newborn human neonates and the limited electrographic efficacy of benzodiazepines for the treatment of neonatal seizures.
尽管苯二氮䓬类药物和其他 GABA A 受体变构调节剂被用于治疗新生儿癫痫发作,但它们的疗效可能源于对皮质下结构的作用。在非惊厥的人类新生儿中,苯二氮䓬类药物的副作用包括肌阵挛、癫痫发作和异常运动。GABA 的兴奋作用可能是这些副作用和苯二氮䓬类药物抗惊厥活性降低的基础。使用皮质器官型切片培养物来研究:(1)早期发育过程中的皮质癫痫样活动;(2)[Cl(-)]i 的发育变化;(3)地西泮的抗惊厥作用是否与神经元[Cl(-)]i 相关。
通过场电位记录测量皮质器官型切片培养物中的癫痫样活动。通过转染表达 Cl-敏感荧光染料的神经元的多光子成像评估发育过程中的 Cl-变化。使用临床相关浓度的地西泮测试对应于早产儿到婴儿早期的年龄的抗惊厥效果。
(1)在体外培养 5 天(DIV5)的皮质器官型切片中显示出自发性癫痫样活动。(2)癫痫样事件持续时间随年龄而减少。(3)在相同的年龄范围内,[Cl(-)]i 逐渐降低。(4)地西泮在 DIV5-6 时不能减少癫痫样活动,但在较老的年龄阶段通过 DIV15 时效果逐渐增强。(5)在 DIV5-6 时,地西泮在 50%的切片中加重了癫痫样活动。
皮质器官型切片是研究自发性癫痫样活动的有用模型。发育过程中[Cl(-)]i 的减少与自发性癫痫样活动持续时间的减少以及地西泮抗惊厥作用的增强相关。我们为苯二氮䓬类药物在新生人类新生儿中引起癫痫发作和肌阵挛以及苯二氮䓬类药物对新生儿癫痫发作的电疗效果有限提供了潜在的解释。