Stress affects theta activity in limbic networks and impairs novelty-induced ex...

• Author(s): Jacinto, Luís ; Reis, Joana ; Dias, Nuno S. ; Cerqueira, João J. ; Correia, José Higino ; Sousa, Nuno
• Date: 2013
• Persistent ID: http://hdl.handle.net/11110/532
• Origin: CiencIPCA
• Subject(s): Amygdala; Local Field Potentials; Anxiety; pre-frontal cortex; stress; ventral hippocampus
• Document Type: Article
• Language: English

Description

Exposure to a novel environment triggers the response of several brain areas that regulate emotional behaviors. Here, we studied theta oscillations within the hippocampus (HPC)-amygdala (AMY)-medial prefrontal cortex (mPFC) network in exploration of a novel environment and subsequent familiarization through repeated exposures to that same environment; in addition, we assessed how concomitant stress exposure could disrupt this activity and impair both behavioral processes. Local field potentials were simultaneously recorded from dorsal and ventral hippocampus (dHPC and vHPC respectively), basolateral amygdala (BLA) and mPFC in freely behaving rats while they were exposed to a novel environment, then repeatedly re-exposed over the course of 3 weeks to that same environment and, finally, on re-exposure to a novel unfamiliar environment. A longitudinal analysis of theta activity within this circuit revealed a reduction of vHPC and BLA theta power and vHPC-BLA theta coherence through familiarization which was correlated with a return to normal exploratory behavior in control rats. In contrast, a persistent over-activation of the same brain regions was observed in stressed rats that displayed impairments in novel exploration and familiarization processes. Importantly, we show that stress also affected intra-hippocampal synchrony and heightened the coherence between vHPC and BLA. In summary, we demonstrate that modulatory theta activity in the aforementioned circuit, namely in the vHPC and BLA, is correlated with the expression of anxiety in novelty-induced exploration and familiarization in both normal and pathological conditions. Luis R. Jacinto was supported by the Portuguese Foundation for Science and Technology (FCT) under grant SFRH/BD/40459/2007. This work was supported by FCT and FEDER funds through Programa Operacional Factores de Competitividade (COMPETE) with project references FCOMP- 01-0124-FEDER-021145 (FCT/PTDC/SAU-ENB/118383/2010) and FCOMP-01-0124-FEDER-022674; ADI Project “DoIT— Desenvolvimento e Operacionalização da Investigação de Translação” (“MyHealth-PPS4”; project n◦ 13853); and a BIAL Foundation Grant (138/2008 to João J. Cerqueira).