bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.05.25.727611

Sex differences in neural activity across amygdalo-striatal network during social behaviour

Abstract

BackgroundSocial behaviour is essential for the survival of most mammalian species and is shaped by sex-dependent genetic and endocrine factors. However, how sex influences brain-wide neural dynamics during social interactions remains poorly understood. MethodsHere, we investigated sex differences in neural activity across a distributed amygdalo-striatal network in freely behaving mice. Using chronically implanted electrode arrays, we simultaneously recorded extracellular activity from multiple amygdalo-striatal regions while mice performed four social discrimination tasks. Neural signals were analysed alongside video-based behavioural tracking and head acceleration measurements. ResultsWe identified significant sex differences in neural activity that emerged even before social interaction, suggesting distinct anticipatory network states. During social interaction, sex differences were distributed across brain regions and electrophysiological features, but were most consistently expressed in the basolateral amygdala (BLA). Notably, BLA activity exhibited pronounced sex-specific, context- and time-dependent dynamics, particularly during the initial phase of social interaction. These neural differences were associated with variations in behavioural responses and movement dynamics. ConclusionsTogether, our findings reveal that sex shapes both baseline and interaction-driven neural activity across the social brain network, and highlight the BLA as a key node underlying sex-specific dynamics of social behaviour. Plain English summarySocial behaviour is essential for survival and differs between males and females in many species, including humans and mice. These differences are influenced by biological factors such as genes and hormones, but how they are reflected in brain activity during social interactions is still not fully understood. In this study, we examined how brain activity differs between male and female mice during social behaviour. We recorded neural activity simultaneously from several brain regions involved in social and emotional processing while mice performed four different social interaction tasks. These tasks tested preferences for social versus non-social stimuli, opposite-sex animals, isolated animals, and stressed animals. At the same time, we monitored behaviour and head movements using video tracking and motion sensors. We found that males and females showed distinct patterns of brain activity even before social interaction began, suggesting that the brain may enter different "anticipatory" states depending on sex. During social interaction, sex differences in neural activity varied depending on the social context and the stage of the interaction. The strongest and most consistent differences were observed in the basolateral amygdala, a brain region known to regulate emotional and social behaviour. Interestingly, these neural differences were linked to differences in movement dynamics and social responses, particularly during the first moments of interaction. Our findings suggest that sex shapes both baseline brain activity and the way the brain responds during social encounters. This work improves our understanding of the neural basis of sex differences in social behaviour and may help inform future research on psychiatric conditions that affect social functioning differently in males and females. HighllightsO_LISimultaneous multi-site recordings revealed sex-dependent neural dynamics across an amygdalo-striatal social brain network during social behaviour. C_LIO_LIMale and female mice exhibited distinct electrophysiological signatures even before social interaction, suggesting sex-specific anticipatory neural states. C_LIO_LIHigh-frequency local field potential oscillations showed the strongest and most consistent sex differences across behavioural contexts and brain regions. C_LIO_LIThe basolateral amygdala (BLA) emerged as a key region displaying context- and time-dependent sex differences during early social interaction. C_LIO_LISex-specific BLA activity correlated with movement dynamics during investigation of isolated conspecifics, linking neural network activity to behavioural responses. C_LI Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=139 SRC="FIGDIR/small/727611v1_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@82f8a7org.highwire.dtl.DTLVardef@92d085org.highwire.dtl.DTLVardef@b7dc78org.highwire.dtl.DTLVardef@eb4dba_HPS_FORMAT_FIGEXP M_FIG C_FIG

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Phalip, A., Netser, S., Wagner, S.. 2026-05-28. Sex differences in neural activity across amygdalo-striatal network during social behaviour. https://doi.org/10.64898/2026.05.25.727611

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Different hippocampal subfield volumes predict source memory performance and general cognitive ability in an adult lifespan sample

Modest positive associations between episodic memory performance and whole hippocampal and hippocampal subfield volumes have been reported in numerous prior studies. A smaller number of studies have reported associations between hippocampal volume and performance on tests of non-mnemonic cognition. The present study examined whether these associations were evident in a lifespan sample of cognitively healthy adults. Of particular interest was whether any identified associations were sensitive to age, and whether associations between subfield volumes and mnemonic and non-mnemonic performance were subfield dependent. We acquired high-resolution T1- and T2-weighted structural images from 163 adults (18-87 years of age). Participants also undertook a comprehensive neuropsychological test battery and an in-scanner test of source memory. Principal components analysis was employed to reduce the neuropsychological test scores to 5 cognitive components. Two components reflected memory performance while the other three reflected different aspects of non-mnemonic cognition. Hippocampal subfields (Cornu Ammonis (CA)1, CA2-3, dentate gyrus (DG) and subiculum) were segmented and measured with the Automated Segmentation of Hippocampus Subfields (ASHS) package. Source memory performance was selectively associated across participants with CA2-3 volume. By contrast, both mnemonic and non-mnemonic component scores derived from the test battery were associated exclusively with the volume of the DG. All associations were age-invariant. The findings indicate that different cognitive domains can be dissociated by virtue of their associations with different hippocampal subfields. Of importance, these associations appear to be life-long and hence are unlikely to reflect individual differences in age-related decline in structural integrity.

neuroscience↗

Cell type specific astrocytic feedback regulates excitation inhibition balance and cortical network dynamics

Astrocytes actively regulate synaptic transmission and neuronal excitability, yet their role in orchestrating macroscopic cortical network regimes and slow-wave oscillations remains an active area of reasearch. This study investigates how bidirectional neuron astrocyte interactions shape emergent population dynamics using a computational network model of excitatory and inhibitory neurons coupled to an astrocyte. The results identify astrocytic feedback topology, rather than astrocytic coupling strength alone, as a key determinant of emergent cortical network dynamics. By systematically dissecting pathway-specific connectivity, it has been shown that the neuronal population driving astrocytic activation and the neuronal population receiving gliotransmission jointly determine whether the network occupies asynchronous irregular (AI), synchronous irregular (SI), synchronous regular(SR), asynchronous regular(AR) or quiescent regimes.Directing gliotransmission selectively onto excitatory neurons consistently promotes population synchrony regardless of the population influencing astrocytic dynamics, whereas selective modulation of inhibitory interneurons induces network quiescence via strong suppression. Under dual-target gliotransmission, network synchrony is dictated by the population driving astrocytic dynamics: excitatory-only drive promotes synchrony, while combined or inhibitory-specific drive preserves asynchronous states. Furthermore, the model reveals that astrocytic signaling kinetics provide an additional temporal control mechanism that regulates the frequency and persistence of self sustained up states.

neuroscience↗

VCP inhibition prevents cone photoreceptor degeneration in the cpfl1 mouse model of achromatopsia

Achromatopsia (ACHM) is a rare autosomal recessive retinal disorder characterized by absent cone photoreceptor function from early life, leading to severe visual impairment. Mutations in genes involved in the cone phototransduction cascade frequently result in elevated cyclic guanosine monophosphate (cGMP) levels and activation of stress pathways, including endoplasmic reticulum (ER) stress and the unfolded protein response. Targeting common downstream mechanisms rather than individual mutations may provide a broadly applicable therapeutic strategy. Here, we investigated whether pharmacological inhibition of valosin-containing protein (VCP), a key regulator of ER and protein homeostasis, can prevent cone degeneration in the spontaneous cone photoreceptor function loss 1 (cpfl1) mouse model of ACHM. Organotypic culture of retinal explants from cpfl1 mice were treated with the selective VCP inhibitor ML240. Cone survival, cell death, opsin expression and localization were assessed by TUNEL assay, immunohistochemistry, and quantitative image analysis. ML240 treatment significantly increased cone density and improved cone opsin expression and trafficking to the outer segments (OSs) in cpfl1 explants compared to controls. Importantly, rhodopsin trafficking in rod photoreceptors was unaffected, indicating that VCP inhibition did not impair normal rod phototransduction. These findings demonstrate that VCP inhibition by ML240 effectively preserves cone photoreceptors and improves cone-specific functional markers in the cpfl1 model. Targeting VCP may represent a mutation-independent therapeutic strategy for preventing cone death in ACHM.

neuroscience↗