Representing multiple agents and their mutual relations is a prerequisite to understand social events such as interactions. Using functional magnetic resonance imaging on human adults, we show that visual areas dedicated to body form and body motion perception contribute to processing social events, by holding the representation of multiple moving bodies and encoding the spatial relations between them. In particular, seeing animations of human bodies facing and moving toward (vs. away from) each other increased neural activity in the body-selective cortex [extrastriate body area (EBA)] and posterior superior temporal sulcus (pSTS) for biological motion perception. In those areas, representation of body postures and movements, as well as of the overall scene, was more accurate for facing body (vs. nonfacing body) stimuli. Effective connectivity analysis with dynamic causal modeling revealed increased coupling between EBA and pSTS during perception of facing body stimuli. The perceptual enhancement of multiple-body scenes featuring cues of interaction (i.e., face-to-face positioning, spatial proximity, and approaching signals) was supported by the participants’ better performance in a recognition task with facing body versus nonfacing body stimuli. Thus, visuospatial cues of interaction in multiple-person scenarios affect the perceptual representation of body and body motion and, by promoting functional integration, streamline the process from body perception to action representation.

Luminance contrast is a fundamental visual cue. Using a dedicated neuroimaging framework, we sought to characterize typical Blood Oxygen Level Dependent (BOLD) responses in two subcortical regions, the superior colliculus (SC) and the lateral geniculate nucleus (LGN), and V1, the primary visual cortex area, and how they change over the lifespan. For imaging subcortical activity related to luminance contrast modulation, specific measurements were introduced to rule out possible signal contamination by cardiovascular activity and vascular alterations with age that could hamper the BOLD signal interpretation. Clearly, BOLD responses increased in these three regions with luminance contrast, with a statistically significant diminution in LGN and V1 for older compared to younger participants, while basal perfusion remained unchanged. Additionally, perceptual responses, as assessed with psychophysical experiments, were highly correlated to BOLD measures in the three studied regions. Taken together, fMRI and psychophysics results indicate an alteration of luminance contrast processing with normal aging. Based on this knowledge we can better recognize when age-related brain changes vary from these expectations especially during neurodegenerative diseases progression where the functioning of subcortical structures is altered. The proposed fMRI-physchophysics methodology allows performing such investigation.