Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2020 Apr 30;45(11):1931–1941. doi: 10.1038/s41386-020-0686-z

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2020

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/.

PMC Copyright notice

Fig. 2 — Representative photomicrographs (scale bar = 500 μm, a) showing c-Fos immunostaining within the ventral pallidum (VP), nucleus accumbens (Acb), caudate putamen (CPu), paraventricular nucleus (PVN), amygdala (AMY), pedunculopontine nucleus (PP), substantia nigra (SN), and ventral tegmental area (VTA) in brain slices collected from both NR + S (non restricted + stressed) and R + S (restricted + stressed) rats treated with either vehicle (veh) or OEA (10 mg kg⁻¹, i.p.) and sacrificed 120 min after treatment. Semiquantitative densitometric analysis of c-Fos expression within the VP (b), Acb (c), CPu (d), PVN (e), AMY (f), PP (g), SN (h), and VTA (i) of NR + S and R + S rats treated with either veh or OEA (10 mg kg⁻¹, i.p.) and sacrificed 120 min after treatment. Data are expressed as mean ± SEM. *P < 0.05; ***P < 0.001 vs veh in the same diet regimen group; °P < 0.05; °°P < 0.01; °°°P < 0.001 vs NR + S in the same treatment group (Tukey’s post hoc test, N = 3).