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Aspesi, D.

Publications and source records attributed to Aspesi, D..

2 recordsLinked to original sources

Sex differences in the neural circuitry of aggression

The social behavior neural network (SBNN) is a circuit composed of reciprocally connected limbic structures that regulate a range of social behaviors, including aggression. Although both males and females of many species display aggressive behavior, studies of the neural circuitry underlying aggression have focused almost exclusively on males. In the present study, we investigated sex differences in neuronal activation of the neural circuitry controlling aggression in Syrian hamsters (Mesocricetus auratus). We employed c-Fos immunohistochemistry to quantify neuronal activation following aggressive encounters between same-sex male and female dyads. Animals were tested in their home cage either alone (n=7 per sex) or with a same-sex, non-aggressive intruder (n=7 per sex) for 10 minutes. Our data revealed substantial sex differences in the neuronal activation of the SBNN following aggression. In some regions, neuronal activity changed in opposite directions in males and females compared to controls (e.g., posterior lateral septum), while in others, there was a change in neuronal activation in only one sex (e.g., medial amygdala). These findings support the hypothesis that the neural circuitry regulating aggression exhibits marked sexual differentiation. HighlightsO_LIThe neural circuitry regulating aggression was differentially activated in males and females following aggressive encounters C_LIO_LISeveral brain regions exhibited opposite patterns of activation in males and females following aggression C_LIO_LIOnly the BNST had the same pattern of changes in neural activity in males and females following aggression C_LI

neuroscience↗

Comparative gene editing reduces dopamine receptor levels across rodent species

Translational challenges in neuroscience originate from species-specific differences that limit the generalizability of experimental findings. Comparative approaches can help distinguish conserved from species-specific mechanisms, but their application has been limited by the lack of molecular tools beyond traditional model organisms, complicating direct comparisons of conserved and divergent mechanisms of neural function. This gap is particularly evident for the dopaminergic system, a key regulator of motivated behaviors across species and the principal pharmacological target for current psychotherapies. Building on our recent development of comparative gene editing, we here present an adeno-associated virus-mediated CRISPR/Cas9 strategy to reduce in vivo dopamine receptors D1 and D2 levels across the rodent phylogeny. Using this approach, we achieved specific reduction of receptor levels in three rodent species (house mouse, prairie vole, and Syrian hamster), which we demonstrate with radioactive ligand binding assays. This toolkit expands the reach of comparative gene editing approaches, enabling functional investigation of the dopaminergic system across rodent species. Thereby, it supports comparative neuroscience by facilitating the identification of conserved versus species-specific neural mechanisms with enhanced translational potential.

neuroscience↗