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. 2017 Sep 22;7:12191. doi: 10.1038/s41598-017-12368-6

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Treatment with a combination of NBQX and ifenprodil during the latent period of the intrahippocampal kainate mouse model retards the development of spontaneous clinical seizures. Data are combined from experiments 2 and 3 (see Fig. 1) and are shown for 4 periods (2, 3, 4, 6 weeks) after kainate. In each graph, the number of clinical seizures in individual mice is shown; the group median is indicated by the horizontal line. Analysis of data by two-way ANOVA indicated a significant difference between vehicle and drug treated groups (P < 0.05); post hoc analysis by Dunn’s multiple comparisons test indicated that drug treatment significantly reduced seizure frequency at 2 weeks after kainate (P = 0.0418).