Biology subjects

Basso, J. C.

Publications and source records attributed to Basso, J. C..

5 recordsLinked to original sources

bioRxiv2026

Social attention and coordinated movement produce dissociable spectral and network changes during dyadic improvisational dance

Dance is increasingly delivered as an intervention for social and affective functioning, but a live dyadic encounter confounds several distinct ingredients - social attention, verbal engagement, coordinated movement, and in-the-moment generation - so its neural effects cannot be assigned to any one of them. We recorded dual-brain mobile EEG from adult human participants of both sexes (16 female, 2 male) and a dance instructor across six five-minute conditions that vary these ingredients independently: solitary rest, direct eye gaze, conversation, teacher-led and participant-led mirroring, and free improvisation, with concurrent head-mounted accelerometry. Referencing each condition to eye gaze - socially engaging but nearly motionless - rather than to solitary rest partitioned the response. The components proved dissociable. Nonverbal social attention alone reorganized the power spectrum, flattening the aperiodic exponent (g = -0.97) and desynchronizing alpha-band oscillations (g = -0.90), while leaving inter-regional connectivity unchanged (amplitude g = +0.15; phase g = +0.11). Verbal engagement added high-frequency amplitude coupling (g = +2.61) without further spectral change. Coordinated movement added a decrease in theta/alpha coupling involving the frontoparietal-control network (g = -0.59), the signature of an externally directed state, alongside a further spectral shift (g = -0.61). Movement-vigor covariates, corticokinematic coherence, and aperiodic-adjusted power indicated that the spectral effects were cortical rather than myogenic. Four weeks of improvisational dance training increased empathic responsiveness to others' distress relative to a movie control (g = 0.82). Coordinated social movement thus acts on the brain componentially, with mutual attention rather than motor load establishing the engaged state.

neuroscience↗

bioRxiv2026

Amplitude without phase: interpersonal movement coordination grades inter-brain coupling

Interpersonal movement coordination is a foundational feature of human sociality, scaffolding communication, affiliation, and joint action from infancy onward. Whether this behavioral coupling is accompanied by genuine coupling between brains, rather than one manufactured by shared sensory input or motion artifact, has proven difficult to establish. We recorded dual-brain EEG with synchronized head-mounted accelerometry from participant-partner dyads (16 dyads, 155 dyad-condition recordings) across six conditions grading interpersonal coordination from stillness to fully reciprocal joint movement, using improvisational dance to elicit sustained, naturalistic, gradable coordination. Windowed cross-correlation confirmed graded, partner-specific movement coordination, including a lead-lag signature that reversed with who led. Against a pseudo-dyad surrogate, inter-brain synchrony took one specific form: amplitude-envelope coupling in the high-beta and gamma bands, robust to a leakage-corrected measure, with no phase-based or slow-band coupling. Within dyads, movement synchrony predicted the strength of this amplitude coupling (standardized beta = 0.54 in gamma), an association that strengthened monotonically with frequency, held under a dyad fixed-effects estimator, and was undiminished when the amount of movement was entered into the model. Movement synchrony and inter-brain coupling also co-fluctuated within interactions, above surrogate. Two control analyses excluded the leading alternatives: the coupling was not sensorimotor rhythm-tracking, since corticokinematic coherence was present but non-localized and not movement-selective, and not a shared movement-frequency rhythm linking the brains. These results identify interpersonal movement coordination as an organizing variable for inter-brain coupling and specify that coupling as fast-band amplitude co-modulation, not phase synchrony. Brains couple when bodies coordinate, not when they merely move together.

neuroscience↗

bioRxiv2026

The Choreography of Coupled Brains: Coordinated Movement and Multi-Scale Neural Synchrony in Musical Theater for Individuals with Developmental Disabilities

Performing together, which demands moving, singing, and coordinating in real time, is among the most social things people do, yet whether such coordination synchronizes not only behavior but brain activity, within and between performers, has rarely been examined during genuine performance. In this pilot study, we used mobile electroencephalography, including dual-brain hyperscanning of co-performing partners, to resolve neural change over a 16-week musical-theater program in adolescents and adults with developmental disabilities, the majority autistic. We examined four levels: behavior, spectral power, within-brain (source-space) connectivity, and between-brain synchrony, framing all estimates as effect sizes. Anxiety decreased from pre- to post-intervention, consistently across participant and parent reports. During performance, high-beta and gamma power and within-brain amplitude connectivity rose broadly across the cortex, with maximal effects seen in parieto-occipital regions. Between-brain coupling was similarly carried by amplitude co-fluctuation rather than phase; however, it was graded by the degree of interpersonal movement coordination (strongest when partners mirrored one another) and scaled with movement vigor. Local and within-brain changes were thus broad and state-like, whereas coupling between brains was specific to interpersonal coordination. Coordinated movement may organize neural synchrony across scales, positioning musical theater as a tractable model for studying the social brain in motion.

neuroscience↗

bioRxiv2023

Granular retrosplenial cortex layer 2/3 generates high-frequency oscillations coupled with hippocampal theta and gamma in online states or sharp-wave ripples in offline states

Neuronal oscillations support information transfer by temporally aligning the activity of anatomically distributed writer and reader cell assemblies. High-frequency oscillations (HFOs) such as hippocampal CA1 sharp-wave ripples (SWRs; 100-250 Hz) are sufficiently fast to initiate synaptic plasticity between assemblies and are required for memory consolidation. HFOs are observed in parietal and midline cortices including granular retrosplenial cortex (gRSC). In offline brain states (e.g. quiet wakefulness) gRSC HFOs co-occur with CA1 SWRs, while in online states (e.g. ambulation) HFOs persist with the emergence of theta oscillations. The mechanisms of gRSC HFO oscillations, specifically whether the gRSC can intrinsically generate HFOs, and which layers support HFOs across states, remain unclear. We addressed these issues in behaving mice using optogenetic excitation in individual layers of the gRSC and high density silicon-probe recordings across gRSC layers and hippocampus CA1. Optogenetically induced HFOs (iHFOs) could be elicited by depolarizing excitatory neurons with 100 ms half-sine wave pulses in layer 2/3 (L2/3) or layer 5 (L5) though L5 iHFOs were of lower power than in L2/3. Critically, spontaneous HFOs were only observed in L2/3 and never in L5. Intra-laminar monosynaptic connectivity between excitatory and inhibitory neurons was similar across layers, suggesting other factors restrict HFOs to L2/3. To compare HFOs in online versus offline states we analyzed, separately, HFOs that did or did not co-occur with CA1 SWRs. Using current-source density analysis we found uniform synaptic inputs to L2/3 during all gRSC HFOs, suggesting layer-specific inputs may dictate the localization of HFOs to L2/3. HFOs occurring without SWRs were aligned with the descending phase of both gRSC and CA1 theta oscillations and were coherent with CA1 high frequency gamma oscillations (50-80 Hz). These results demonstrate that gRSC can internally generate HFOs without rhythmic inputs and that HFOs occur exclusively in L2/3, coupled to distinct hippocampal oscillations in online versus offline states.

neuroscience↗

bioRxiv2023

Hippocampal sharp wave-ripple dynamics in NREM sleep encode motivation for future physical activity

Physical activity is an integral part of every mammals daily life, and as a driver of Darwinian fitness, required coordinated evolution of the body and brain. The decision to engage in physical activity is driven either by survival needs or by motivation for the rewarding qualities of physical activity itself. Rodents exhibit innate and learned motivation for voluntary wheel running, and over time run longer and farther, reflecting increased incentive salience and motivation for this consummatory behavior. Dynamic coordination of neural and somatic physiology are necessary to ensure the ability to perform behaviors that are motivationally variable. Hippocampal sharp wave-ripples (SWRs) have evolved both cognitive and metabolic functions, which in modern mammals may facilitate body-brain coordination. To determine if SWRs encode aspects of exercise motivation we monitored hippocampal CA1 SWRs and running behaviors in adult mice, while manipulating the incentive salience of the running experience. During non-REM (NREM) sleep, the duration of SWRs before (but not after) running positively correlated with future running duration, and larger pyramidal cell assemblies were activated in longer SWRs, suggesting that the CA1 network encodes exercise motivation at the level of neuronal spiking dynamics. Inter-Ripple-intervals (IRI) before but not after running were negatively correlated with running duration, reflecting more SWR bursting, which increases with learning. In contrast, SWR rates before and after running were positively correlated with running duration, potentially reflecting a tuning of metabolic demand for that days anticipated and actual energy expenditure rather than motivation. These results suggest a novel role for CA1 in exercise behaviors and specifically that cell assembly activity during SWRs encodes motivation for anticipated physical activity. SIGNIFICANCE STATEMENTDarwinian fitness is increased by body-brain coordination through internally generated motivation, though neural substrates are poorly understood. Specific hippocampal rhythms (i.e., CA1 SWRs), which have a well-established role in reward learning, action planning and memory consolidation, have also been shown to modulate systemic [glucose]. Using a mouse model of voluntary physical activity that requires body-brain coordination, we monitored SWR dynamics when animals were highly motivated and anticipated rewarding exercise (i.e., when body-brain coordination is of heightened importance). We found that during non-REM sleep before exercise, SWR dynamics (which reflect cognitive and metabolic functions) were correlated with future time spent exercising. This suggests that SWRs support cognitive and metabolic facets that motivate behavior by coordinating the body and brain.

neuroscience↗