AUTHOR=Utsumi Yuichi , Taketoshi Makiko , Miwa Michiko , Tominaga Yoko , Tominaga Takashi TITLE=Assessing seizure liability in vitro with voltage-sensitive dye imaging in mouse hippocampal slices JOURNAL=Frontiers in Cellular Neuroscience VOLUME=Volume 17 - 2023 YEAR=2023 URL=https://www.frontiersin.org/journals/cellular-neuroscience/articles/10.3389/fncel.2023.1217368 DOI=10.3389/fncel.2023.1217368 ISSN=1662-5102 ABSTRACT=Non-clinical toxicology is a major cause of drug candidate attrition during development. In particular, drug-induced seizures are the most common finding in central nervous system (CNS) toxicity. Current safety pharmacology tests for assessing CNS functions are often inadequate in detecting seizure-inducing compounds early in drug development, leading to significant delays. This paper presents an in vitro seizure liability assay using voltage-sensitive dye (VSD) imaging techniques in hippocampal brain slices, offering a powerful alternative to traditional electrophysiological methods. Hippocampal slices were isolated from mice, and VSD optical responses evoked by stimulating the Schaffer collateral pathway were recorded and analyzed in the stratum radiatum (SR) and stratum pyramidale (SP). VSDs allow for the comprehensive visualization of neuronal action potentials and postsynaptic potentials on a millisecond timescale. By employing this approach, we investigated the in vitro drug-induced seizure liability of representative proconvulsant compounds. Picrotoxin (PiTX; 1-100 µM), gabazine (GZ; 0.1-10 µM), and 4aminopyridine (4AP; 10-100 µM) exhibited seizure-like responses in the hippocampus, but pilocarpine hydrochloride (Pilo; 10-100 µM) did not. Our findings demonstrate the potential of VSDbased assays in identifying seizurogenic compounds during early drug discovery, thereby reducing delays in drug development and providing insights into the mechanisms underlying seizure induction and the associated risks of pro-convulsant compounds.Non-clinical toxicity is a leading cause of drug candidate attrition during drug development (Waring et al., 2015). To address this issue, regulatory agencies, such as the International Council for Harmonisation (ICH), have developed guidelines for safety pharmacology testing that require the evaluation of cardiovascular, respiratory, and central nervous system (CNS) functions prior to human administration. Specifically, the ICH guideline S7A mandates safety pharmacology tests including those that evaluate CNS function. The Irwin test (Irwin, 1968) and functional observational battery (Moser et al., 1995) have been frequently used in preclinical safety studies to detect the potential