bioRxiv Science⌕ Search

Biology subjects

Morais-Silva, G.

Publications and source records attributed to Morais-Silva, G..

2 recordsLinked to original sources

Left-to-right dorsomedial prefrontal cortex interhemispheric projections mediate psychosocial stress vulnerability

Functional asymmetries in the medial prefrontal cortex (mPFC) are significant attributes of this brain area, implicated in its role in emotional processing and executive function. Evidence suggests that, under normal conditions, there is a tonic inhibition of the right (R) mPFC by the left (L) mPFC, and a dysregulation of this hemispheric functional lateralization is implicated in detrimental chronic stress effects. Considering the wide interhemispheric connection and the inhibitory tone from the LmPFC to the RmPFC, we hypothesize that alterations in the activity of the direct projections between the mPFC hemispheres during stressful situations are related to stress vulnerability. To address this question, we used a chemogenetic approach to modulate the activity of L-to-R dorsomedial prefrontal cortex (dmPFC) monosynaptic projections during psychosocial stress (PSS) exposure in mice. We found that activating LdmPFC projections during a repeated PSS protocol prevents stress-induced apathy-like behavior in females and males and social avoidance in male mice. On the other hand, inhibiting such projections during a single session of PSS increases vulnerability to stress effects in male mice, increasing social avoidance and anxiety-like behaviors. Both glutamatergic and GABAergic cells compose the projecting interhemispheric neurons in the dmPFC. However, the LdmPFC showed a higher density of glutamatergic projections to the RdmPFC than the opposite. In conclusion, our results revealed an involvement of the monosynaptic projections from the LdmPFC to RdmPFC in the vulnerability to the behavioral alterations induced by PSS in female and male mice.

neuroscience↗

Activation of Npas1-neurons in the Ventral Pallidum Mediates Stress Susceptibility

AbstractAltered activity of the ventral pallidum (VP) underlies disrupted motivation in stress and drug exposure. The VP is a very heterogeneous structure comprised of many neuron types with distinct physiological properties and projections. Neuronal PAS 1-positive (Npas1+) VP neurons are thought to send projections to brain regions critical for motivational behavior. While Npas1+ neurons have been characterized in the globus pallidus external, there is limited information on these neurons in the VP. To address this limitation, we evaluated the projection targets of the VP Npas1+ neurons and performed RNA-seq on ribosome-associated mRNA from VP Npas1+ neurons to determine their molecular identity. Finally, we used a chemogenetic approach to manipulate VP Npas1+ neurons during social defeat stress (SDS) and behavioral tasks related to anxiety and motivation in Npas1-Cre mice. We employed a similar approach in females using the chronic witness defeat stress (CWDS). We identified VP Npas1+ projections to the nucleus accumbens, ventral tegmental area, medial and lateral habenula, lateral hypothalamus, thalamus, medial and lateral septum, and periaqueductal gray area. VP Npas1+ neurons displayed distinct transcriptomes representing distinct biological processes. Chemogenetic activation of VP Npas1+ neurons increased susceptibility to a subthreshold (S)SDS and anxiety-like behavior in the elevated plus maze and open field while the inhibition of VP Npas1+ neurons enhanced resilience to chronic (C)SDS and CWDS. Thus, the activity of VP Npas1+ neurons modulates susceptibility to social stressors and anxiety-like behavior. Our studies provide new information into VP Npas1+ neuron circuitry, molecular identity, and their role in stress response.

neuroscience↗