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. 2016 Oct 20;11(10):e0165071. doi: 10.1371/journal.pone.0165071

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© 2016 Gómez-Galán et al

This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Fig 3 — A-C. Representative western blots with their corresponding molecular weights (kDa) (A) and densitometry analysis for the different tested proteins: AMPA-R subunits: GluA1-2 (B), the astrocytic marker GFAP (C) and glial glutamate transporters: GLAST and GLT-1 (D) presented as percentage (%) of GH (control group) after normalization to β-actin or vinculin (loading control). Bar-graph data represent means ± s.e.m. (N = 6–8 animals per group). GH: group-housed, SI: social-isolated, SI +R: social-isolated with access to a running wheel. ***, * vs. GH; # vs. SI+R; one-way ANOVA followed by Bonferroni’s multiple comparisons test. GH:group-housed, SI: social-isolated, SI +R: social-isolated with access to a running wheel.