Sleep loss diminishes hippocampal reactivation and replay.

Memories benefit from sleep1, and the reactivation and replay of waking experiences during hippocampal sharp-wave ripples (SWRs) are considered to be crucial for this process2. However, little is known about how these patterns are impacted by sleep loss. Here we recorded CA1 neuronal activity over 12 h in rats across maze exploration, sleep and sleep deprivation, followed by recovery sleep. We found that SWRs showed sustained or higher rates during sleep deprivation but with lower power and higher frequency ripples. Pyramidal cells exhibited sustained firing during sleep deprivation and reduced firing during sleep, yet their firing rates were comparable during SWRs regardless of sleep state. Despite the robust firing and abundance of SWRs during sleep deprivation, we found that the reactivation and replay of neuronal firing patterns was diminished during these periods and, in some cases, completely abolished compared to ad libitum sleep. Reactivation partially rebounded after recovery sleep but failed to reach the levels found in natural sleep. These results delineate the adverse consequences of sleep loss on hippocampal function at the network level and reveal a dissociation between the many SWRs elicited during sleep deprivation and the few reactivations and replays that occur during these events.

Zebrafish optomotor response to second-order motion illustrates that age-related changes in motion detection depend on the activated motion system.

Various aspects of visual functioning, including motion perception, change with age. Yet, there is a lack of comprehensive understanding of age-related alterations at different stages of motion processing and in each motion system. To understand the effects of aging on second-order motion processing, we investigated optomotor responses (OMR) in younger and older wild-type (AB-strain) and acetylcholinesterase (achesb55/+) mutant zebrafish. The mutant fish with decreased levels of acetylcholinesterase have been shown to have delayed age-related cognitive decline. Compared to previous results on first-order motion, we found distinct changes in OMR to second-order motion. The polarity of OMR was dependent on age, such that second-order stimulation led to mainly negative OMR in the younger group while older zebrafish had positive responses. Hence, these findings revealed an overall aging effect on the detection of second-order motion. Moreover, neither the genotype of zebrafish nor the spatial frequency of motion significantly changed the response magnitude. Our findings support the view that age-related changes in motion detection depend on the activated motion system.

Sleep loss diminishes hippocampal reactivation and replay.

Memories benefit from sleep, and sleep loss immediately following learning has a negative impact on subsequent memory storage. Several prominent hypotheses ascribe a central role to hippocampal sharp-wave ripples (SWRs), and the concurrent reactivation and replay of neuronal patterns from waking experience, in the offline memory consolidation process that occurs during sleep. However, little is known about how SWRs, reactivation, and replay are affected when animals are subjected to sleep deprivation. We performed long duration (~12 h), high-density silicon probe recordings from rat hippocampal CA1 neurons, in animals that were either sleeping or sleep deprived following exposure to a novel maze environment. We found that SWRs showed a sustained rate of activity during sleep deprivation, similar to or higher than in natural sleep, but with decreased amplitudes for the sharp-waves combined with higher frequencies for the ripples. Furthermore, while hippocampal pyramidal cells showed a log-normal distribution of firing rates during sleep, these distributions were negatively skewed with a higher mean firing rate in both pyramidal cells and interneurons during sleep deprivation. During SWRs, however, firing rates were remarkably similar between both groups. Despite the abundant quantity of SWRs and the robust firing activity during these events in both groups, we found that reactivation of neurons was either completely abolished or significantly diminished during sleep deprivation compared to sleep. Interestingly, reactivation partially rebounded upon recovery sleep, but failed to reach the levels characteristic of natural sleep. Similarly, the number of replays were significantly lower during sleep deprivation and recovery sleep compared to natural sleep. These results provide a network-level account for the negative impact of sleep loss on hippocampal function and demonstrate that sleep loss impacts memory storage by causing a dissociation between the amount of SWRs and the replays and reactivations that take place during these events.

Audiovisual interactions in speeded discrimination of a visual event.

The integration of information from different senses is central to our perception of the external world. Audiovisual interactions have been particularly well studied in this context and various illusions have been developed to demonstrate strong influences of these interactions on the final percept. Using audiovisual paradigms, previous studies have shown that even task-irrelevant information provided by a secondary modality can change the detection and discrimination of a primary target. These modulations have been found to be significantly dependent on the relative timing between auditory and visual stimuli. Although these interactions in time have been commonly reported, we have still limited understanding of the relationship between the modulations of event-related potentials (ERPs) and final behavioral performance. Here, we aimed to shed light on this important issue by using a speeded discrimination paradigm combined with electroencephalogram (EEG). During the experimental sessions, the timing between an auditory click and a visual flash was varied over a wide range of stimulus onset asynchronies and observers were engaged in speeded discrimination of flash location. Behavioral reaction times were significantly changed by click timing. Furthermore, the modulations of evoked activities over medial parietal/parieto-occipital electrodes were associated with this effect. These modulations were within the 126-176 ms time range and more importantly, they were also correlated with the changes in reaction times. These results provide an important functional link between audiovisual interactions at early stages of sensory processing and reaction times. Together with previous research, they further suggest that early crossmodal interactions play a critical role in perceptual performance.

The optomotor response of aging zebrafish reveals a complex relationship between visual motion characteristics and cholinergic system.

Understanding the principles underlying age-related changes in motion perception is paramount for improving the quality of life and health of older adults. However, the mechanisms underlying age-related alterations in this aspect of vision, which is essential for survival in a dynamic world, still remain unclear. Using optomotor responses to drifting gratings, we investigated age-related changes in motion detection of adult zebrafish (wild-type/AB-strain and achesb55/+ mutants with decreased levels of acetylcholinesterase). Our results pointed out negative optomotor responses that significantly depend on the spatial frequency and contrast level of stimulation, providing supporting evidence for the visual motion-driven aspect of this behavior mainly exhibited by adult zebrafish. Although there were no significant main effects of age and genotype, we found a significant three-way interaction between contrast level, age, and genotype. In the contrast domain, the changes in optomotor responses and thus in the detection of motion direction were age- and genotype-specific. Accordingly, these behavioral findings suggest a strong but complicated relationship between visual motion characteristics and the cholinergic system during neural aging.

Short- and long-term forms of neural adaptation: An ERP investigation of dynamic motion aftereffects.

Adaptation is essential to interact with a dynamic and changing environment, and can be observed on different timescales. Previous studies on a motion paradigm called dynamic motion aftereffect (dMAE) showed that neural adaptation can establish even in very short timescales. However, the neural mechanisms underlying such rapid form of neural plasticity is still debated. In the present study, short- and long-term forms of neural plasticity were investigated using dynamic motion aftereffect combined with EEG (Electroencephalogram). Participants were adapted to directional drifting gratings for either short (640 msec) or long (6.4 sec) durations. Both adaptation durations led to motion aftereffects on the perceived direction of a dynamic and directionally ambiguous test pattern, but the long adaptation produced stronger dMAE. In line with behavioral results, we found robust changes in the event-related potentials elicited by the dynamic test pattern within 64-112 msec time range. These changes were mainly clustered over occipital and parieto-occipital scalp sites. Within this time range, the aftereffects induced by long adaptation were stronger than those by short adaptation. Moreover, the aftereffects by each adaptation duration were in the opposite direction. Overall, these EEG findings suggest that dMAEs reflect changes in cortical areas mediating low- and mid-level visual motion processing. They further provide evidence that short- and long-term forms of motion adaptation lead to distinct changes in neural activity, and hence support the view that adaptation is an active time-dependent process which involves different neural mechanisms.

Cortical processes underlying the effects of static sound timing on perceived visual speed.

It is well known that the timing of brief static sounds can alter different aspects of visual motion perception. For instance, previous studies have shown that time intervals demarcated by brief sounds can modulate perceived visual speed such that apparent motions with short auditory time intervals are typically perceived as faster than those with long time intervals. Yet, little is known about the principles and cortical processes underlying such effects of auditory timing. Using a speed judgment paradigm combined with EEG recording, we aimed to identify when and where in the cortex auditory timing takes place for motion processing. Our results indicated significant effects of auditory timing over the medial parieto-occipital and parietal, right centro-parietal, and frontal scalp sites. In addition, these effects were not restricted to a single ERP component and we observed both significant changes in early and late components. Therefore, our findings here suggest that auditory timing may take place at both early and late stages of motion processing and its influences on motion perception may be the outcome of the dynamic interplay between different cortical regions. Together with accumulating evidence, these findings also support the notion that audiovisual integration is a multistage process and it may be achieved through more diversified processes than previously thought.

The involvement of centralized and distributed processes in sub-second time interval adaptation: an ERP investigation of apparent motion.

Accumulating evidence suggests that the timing of brief stationary sounds affects visual motion perception. Recent studies have shown that auditory time interval can alter apparent motion perception not only through concurrent stimulation but also through brief adaptation. The adaptation after-effects for auditory time intervals was found to be similar to those for visual time intervals, suggesting the involvement of a central timing mechanism. To understand the nature of cortical processes underlying such after-effects, we adapted observers to different time intervals using either brief sounds or visual flashes and examined the evoked activity to the subsequently presented visual apparent motion. Both auditory and visual time interval adaptation led to significant changes in the ERPs elicited by the apparent motion. However, the changes induced by each modality were in the opposite direction. Also, they mainly occurred in different time windows and clustered over distinct scalp sites. The effects of auditory time interval adaptation were centred over parietal and parieto-central electrodes while the visual adaptation effects were mostly over occipital and parieto-occipital regions. Moreover, the changes were much more salient when sounds were used during the adaptation phase. Taken together, our findings within the context of visual motion point to auditory dominance in the temporal domain and highlight the distinct nature of the sensory processes involved in auditory and visual time interval adaptation.