Bielefeld Pascal, Sierra Amanda, Encinas Juan M, Maletic-Savatic Mirjana, Anderson Anne, Fitzsimons Carlos P
Neuroscience Program, Faculty of Sciences, Swammerdam Institute for Life Sciences, University of Amsterdam Amsterdam, Netherlands.
Achucarro Basque Center for NeuroscienceZamudio, Spain; Ikerbasque FoundationBilbao, Spain; University of the Basque Country (UPV/EHU)Leioa, Spain.
Front Neurosci. 2017 Mar 29;11:160. doi: 10.3389/fnins.2017.00160. eCollection 2017.
Lack of scientific reproducibility is a growing concern and weak experimental practices may contribute to irreproducibility. Here, we describe an optimized and versatile protocol for stereotaxic intrahippocampal administration of Kainic Acid (KA) in mice with a C57Bl6 background. In this protocol, KA administration is combined with recording of neuronal activity with wired and wireless setups. Following our protocol, KA administration results in a robust dose-dependent induction of low-level epileptiform activity or Status Epilepticus (SE) and induces previously characterized hallmarks of seizure-associated pathology. The procedure consists of three main steps: Craniotomy, stereotaxic administration of KA, and placement of recording electrodes in intrahippocampal, and subdural locations. This protocol offers extended possibilities compared to the systemic administration of KA, as it allows the researcher to accurately regulate the local dose of KA and resulting seizure activity, and permits the use and study of convulsive and non-convulsive KA doses, resulting in higher reproducibility and lower inter-individual variability and mortality rates. Caution should be taken when translating this procedure to different strains of mice as inter-strain sensitivity to KA has been described before. The procedure can be performed in ~1 h by a trained researcher, while intrahippocampal administration of KA without placing recording electrodes can be done in 25 min, and can be easily adapted to the titrated intrahippocampal administration of other drugs.
缺乏科学可重复性是一个日益受到关注的问题,薄弱的实验方法可能导致不可重复性。在此,我们描述了一种优化的通用方案,用于在C57Bl6背景的小鼠中进行立体定位海马内注射 kainic 酸(KA)。在该方案中,KA 注射与使用有线和无线装置记录神经元活动相结合。按照我们的方案,KA 注射会导致低水平癫痫样活动或癫痫持续状态(SE)的强烈剂量依赖性诱导,并诱导出先前已表征的癫痫相关病理学特征。该过程包括三个主要步骤:开颅、KA 的立体定位注射以及将记录电极放置在海马内和硬膜下位置。与全身注射 KA 相比,该方案提供了更多可能性,因为它允许研究人员精确调节 KA 的局部剂量和由此产生的癫痫活动,并允许使用和研究惊厥性和非惊厥性 KA 剂量,从而提高可重复性并降低个体间变异性和死亡率。在将此程序应用于不同品系的小鼠时应谨慎行事,因为之前已经描述了品系间对 KA 的敏感性。该程序由经过培训的研究人员在约1小时内即可完成,而不放置记录电极的海马内注射 KA 可在25分钟内完成,并且可以轻松适用于其他药物的滴定海马内注射。