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. 2019 Aug 23;16:57. doi: 10.1186/s12986-019-0387-y

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© The Author(s). 2019

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 5 — a. Area of microtubule-associated protein 2 (MAP2) immunostaining in primary hippocampal neurons in culture b. Dendrite length c. Mean number of dendritic branches originating from soma d. Number of dendritic branching points. Neurons were challenged with BSA (control), 200 μm PA, 200 μM DHA or 200 μM PA plus 125 μM DHA for a period of 3 h followed by a further 3 h challenge either with the same or different treatment (* p < 0.05, *** p < 0.001). Data presented as mean ± SEM, n = 10 all groups. Bovine serum albumin (BSA), palmitic acid (PA) and docosahexaenoic acid (DHA)