Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.10.28.762252

Dog and Human Brains Represent Human Emotional Bodies with Asymmetric Encoding of Happiness and Anger

Abstract

Dogs live in an environment rich in human emotional signals, yet most of what we know about their visual emotion perception comes from faces. Our study shifts this focus to the body, a central channel of emotional communication in dogs and a source of social information when they observe human emotional expressions. Here, we investigated how the brains of dogs and humans represent emotions conveyed by human bodies. Using fMRI, we examined 24 awake companion dogs and 40 humans viewing videos of bodily happiness, anger, and neutral actions, alongside phase-scrambled controls. Both dogs and humans showed occipito-temporal sensitivity to human bodies, with emotional modulation in the right caudal suprasylvian gyrus in dogs and the right extrastriate body area in humans. Multivariate response patterns also differentiated bodily happiness from anger in both dogs and humans. Emotion-specific RSA further showed a similar representational asymmetry: happiness showed consistent category-specific neural patterns, whereas anger showed no comparable category effect but could still be differentiated from happiness and neutral actions. Despite this shared representational asymmetry, the anatomical distribution differed, with happiness represented across more distributed regions in dogs, whereas anger differentiation involved a broader cortical network in humans. No corresponding effects were found for phase-scrambled controls. Together, these findings provide the first direct neural evidence of how the dog brain represents affective information conveyed by human bodies, while leaving open whether emotions expressed by conspecific bodies evoke similar neural representations. More broadly, our results suggest similar representational relationships between bodily emotions in dogs and humans, despite differences in the anatomical distribution of these effects, while highlighting the role of human bodily expressions in dogs' social cognition, and advancing our understanding of the neural basis of emotional communication across species.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Cuaya, L. V., Hernandez-Perez, R., Boch, M., Rumpf, J., Reyes-Aguilar, A., Huber, L., Lamm, C.. 2026-11-03. Dog and Human Brains Represent Human Emotional Bodies with Asymmetric Encoding of Happiness and Anger. https://doi.org/10.64898/2026.10.28.762252

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

KEEP EXPLORING

Related preprints

Epidermal Langerhans Cells Act as Neuroimmune Regulators of Pain and Itch

Neuroimmune interactions in the skin coordinate immune defense and somatosensory perception, yet how immune cells shape sensory signaling remains poorly defined. Here, we show that Langerhans cells (LCs), epidermal antigen-presenting cells, function as local immune-derived amplifiers of cutaneous sensory signaling. Anatomical and transcriptomic analyses reveal preferential LC association with non-peptidergic sensory neurons. LC activation increases neuronal and behavioral responses to thermal, mechanical, and pruritic stimuli without directly exciting sensory neurons, whereas LC inhibition or ablation selectively reduces pruritogen-evoked itch. We identified semaphorin 7A as a candidate LC-expressed mediator. Semaphorin 7A sensitized cultured sensory neurons to chloroquine and histamine, and neutralizing semaphorin 7A abolished the increase in chloroquine-evoked scratching produced by LC activation. Its receptor PlexinC1 was expressed by most MrgprA3 pruriceptors and blocking PlexinC1 reduced semaphorin 7A-evoked neuronal responses. Together, these findings identify epidermal LCs as local immune-derived amplifiers that regulate the responsiveness of cutaneous sensory circuits and identify semaphorin 7A as a mediator of LC-induced itch potentiation.

neuroscience↗

Feasible closed-loop stimulation for neural latent dynamics control

Modern neuroscience benefits from powerful computational and experimental methods for studying neural populations, including latent dynamics models that predict behavior with few dimensions. But despite their explanatory utility, latent factors are seldom targeted explicitly with experimental perturbations, leaving causal relationships to behavior and inferred dynamical landscapes untested. A promising solution is closed-loop, multi-channel optogenetic control, which, when paired with model predictions, could steer neural trajectories in real time--a feat impossible for traditional, hand-designed stimulation. However, because closed-loop latent control has not been demonstrated in vivo, the hardware and software requirements remain unclear--particularly the necessary stimulation dimensionality and how limited resources such as implant volume and bandwidth should be allocated between stimulation and recording capabilities. Preliminary experiments would thus help guide ongoing technological development. As large-scale exploration of these design spaces in vivo is prohibitively expensive, we conducted a high-throughput simulation survey using biophysically grounded spiking neural networks. We found that low-dimensional actuation is sufficient: in the reference configuration, ~20% of the stimulation channels achieved ~85% of peak control performance, far fewer than the number of neurons. Furthermore, allocating channels roughly equally between stimulation and recording optimized behavioral control, whereas pairing many electrodes with a single light source--the prevailing practice in experimental labs--performed poorly. Even without heavily optimizing modeling or control, we obtained >60% tracking error reduction and >90% evoked behavior accuracy on average for optimal channel counts. These results held across extensive parameter variations, suggesting that closed-loop latent control is feasible with accessible channel counts and establishing design principles for future tool development and in vivo experiments.

neuroscience↗

Identification of Kinome Biomarkers and Therapeutic Rescue in cGMP-Linked Retinal Degeneration

Inherited retinal degenerations, such as Retinitis Pigmentosa (RP) and Leber's congenital amaurosis (LCA), are major causes of progressive and irreversible vision loss. The large number of genes associated with these disorders makes their clinical and molecular characterization difficult, while systemic biomarkers for disease progression or treatment response remain limited. These challenges were addressed by targeting cGMP-associated mechanisms shared by RP and LCA and integrating systemic biomarker profiling with retinal outcomes. Kinase activity analysis (kinome analysis) in peripheral blood mononuclear cells distinguished healthy and diseased states and captured therapy-associated signatures in rd10 mice treated with LP-CN03, a liposomal formulation of the cGMP analog CN03. This first systemic analysis in a therapeutically responsive animal model highlights kinome analysis as a potential translational readout. Given shared cGMP signaling in RP and AIPL1-associated LCA, LP-CN03's therapeutic potential was further evaluated in a new CRISPR-Cas9-generated Aipl1-/- mouse model. Treatment with LP-CN03 preserved retinal structure and function, as shown by electroretinography, longitudinal optical coherence tomography, fundus imaging, optomotor testing, and photoreceptor-specific gene expression. Together, these findings provide independent in vivo evidence for the neuroprotective effect of LP-CN03 in both cGMP-related RP and LCA, also highlighting the translational value of kinome profiling.

neuroscience↗