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. 2017 Aug 23;7:9209. doi: 10.1038/s41598-017-08957-0

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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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The proposed working model of the neuroprotective effect of CE. Excessive extracellular glutamate overstimulates GluRs and induces excitotoxicity, which is blocked by CE via the PKC-GluA2 axis. CE further regulates the Akt-Bcl-2-Caspase signalling pathway to prevent cell death and promote cell survival, exerting a neuroprotective effect.