Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 5 | Molecular Autism

Fig. 5

From: Sociability deficits after prenatal exposure to valproic acid are rescued by early social enrichment

Fig. 5

VPA-VPA mice show increased c-Fos immunoreactivity and dopaminergic turnover in the piriform cortex. af Density of c-Fos-positive nuclei was measured in the whole Pir (a). Schemes in b show the posterior limit of the aPir and the anterior limit of the pPir, where the posterior part of the anterior commissure (acp, dark gray) is visible. Data is also presented discriminating between the anterior part of the Pir (c, aPir) and the posterior part of the Pir (e, pPir). n = 5–7 mice/group. Representative images of the aPir (d) and pPir (f) for the four experimental groups are shown. c-Fos-positive nuclei (black, arrows show examples) in Nissl stained slices. Bars, 200 μm. gl Monoamine levels in the Pir were measured by HPLC-ED. g DA, h DOPAC, i DA turnover (DOPAC/DA), j 5-HT, k 5-HIAA, and l 5-HT turnover (5-HIAA/5-HT). n = 4–5 mice/group. Two-way ANOVA followed by Tukey’s post hoc tests, *p < 0.05, **p < 0.01. Graphs indicate means + s.e.m. Detailed statistical information is available in Additional file 1: Table S3

Back to article page