Highlights d Presenting odors to one nostril in sleep achieves local TMR in one brain hemisphere d Local TMR selectively improves hemisphere-related memories for specific words d Local TMR differentially modulates slow-wave and spindle power across hemispheres

Memory consolidation can be promoted via Targeted Memory Reactivation (TMR)that re-presents training cues or context during sleep. Whether TMR acts locally or globally on cortical sleep oscillations remains unknown. Here we exploit the unique functional neuroanatomy of olfaction with its ipsilateral stimulus processing to perform local TMR in one brain hemisphere. Participants learned associations between words and locations in left or right visual fields with contextual odor throughout. During post-learning naps, odors were presented to one nostril throughout NREM sleep. We found improved memory for specific words processed in the cued hemisphere (ipsilateral to stimulated nostril). Unilateral odor cues locally modulated slow wave activity (SWA) such that regional SWA increase in the cued hemisphere negatively correlated with select memories for cued words.Moreover, local TMR improved slow wave-spindle coupling specifically in the cued hemisphere. Thus, TMR in human sleep transcends global action by selectively promoting specific memories associated with local sleep oscillations.

Sniffing a molecule emitted from baby heads makes men less aggressive yet women more aggressive.

Adolescence is often filled with positive and negative emotional experiences that may change how individuals remember and respond to stimuli in their environment. In adults, aversive events can both enhance memory for associated stimuli as well as generalize to enhance memory for unreinforced but conceptually related stimuli. The present study tested whether learned aversive associations similarly lead to better memory and generalization across a category of stimuli in adolescents. Participants completed an olfactory Pavlovian category conditioning task in which trial-unique exemplars from one of two categories were partially reinforced with an aversive odor. Participants then returned 24 h later to complete a recognition memory test. We found better corrected recognition memory for the reinforced versus the unreinforced category of stimuli in both adults and adolescents. Further analysis revealed that enhanced recognition memory was driven specifically by better memory for the reinforced exemplars. Autonomic arousal during learning was also related to subsequent memory. These findings build on previous work in adolescent and adult humans and rodents showing comparable acquisition of aversive Pavlovian conditioned responses across age groups and demonstrate that memory for stimuli with an acquired aversive association is enhanced in both adults and adolescents.

Terrestrial mammals use pheromones to effectively trigger or block conspecific aggression. Here we tested whether hexadecanal (HEX), a human body-volatile implicated as a mammalian-wide social odor, impacts human aggression. Using validated behavioral paradigms, we observed a remarkable dissociation: sniffing HEX blocked aggression in men, but triggered aggression in women. Next, using functional brain imaging, we uncovered a pattern of brain activity mirroring behaviour: In both men and women, HEX increased activity in the left angular gyrus, an area implicated in perception of social cues. Hex then modulated functional connectivity between the angular gyrus and a brain network implicated in social appraisal (temporal pole) and aggressive execution (amygdala and orbitofrontal cortex) in a sex-dependent manner consistent with behaviour: increasing connectivity in men, but decreasing connectivity in women. These findings implicate HEX as a human pheromone, whose sex-specific brain processing is at the mechanistic heart of human aggressive behavior.