Biology subjects

Born, J.

Publications and source records attributed to Born, J..

24 records · Page 2Linked to original sources

bioRxiv2019

Susceptibility to auditory closed-loop stimulation of sleep slow oscillations changes with age

BackgroundCortical slow oscillations (SOs) and thalamo-cortical sleep spindles hallmark slow wave sleep and facilitate sleep-dependent memory consolidation. Experiments utilising auditory closed-loop stimulation to enhance these oscillations have shown great potential in young and older subjects. However, the magnitude of responses has yet to be compared between these age groups. ObjectiveWe examined the possibility of enhancing SOs and performance on different memory tasks in a healthy older population using auditory closed-loop stimulation and contrast effects to a young adult cohort. MethodsIn a within-subject design, subjects (n = 17, 55.7 {+/-} 1.0 years, 9 female) received auditory click stimulation in synchrony with SO up-states, which was compared to a no-stimulation sham condition. Overnight memory consolidation was assessed for declarative word-pairs and procedural finger-tapping skill. Post-sleep encoding capabilities were tested with a picture recognition task. Electrophysiological effects of stimulation were compared to those reported previously in a younger cohort (n = 11, 24.2 {+/-} 0.9 years, 8 female). ResultsOvernight retention and post-sleep encoding performance of the older cohort revealed no beneficial effect of stimulation, which contrasts with the enhancing effect the same stimulation protocol had in our younger cohort. Auditory stimulation prolonged endogenous SO trains and induced sleep spindles phase-locked to SO up-states in the older population. However, responses were markedly reduced compared to younger subjects. Additionally, the temporal dynamics of stimulation effects on SOs and spindles differed between age groups. ConclusionsOur findings suggest that the susceptibility to auditory stimulation during sleep drastically changes with age and reveal the difficulties of translating a functional protocol from younger to older populations. HighlightsO_LIAuditory closed-loop stimulation induced SOs and sleep spindles in older subjects C_LIO_LIStimulation effects were reduced and overall susceptibility diminished with age C_LIO_LISlow oscillation and sleep spindle dynamics deviated from those in younger subjects C_LIO_LIStimulation shows no evidence for memory effect in older subjects C_LI

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bioRxiv2019

The gap junction blocker mefloquine impairs sleep-dependent declarative memory consolidation in humans

During sleep, the time-compressed replay of engrams acquired during preceding wakefulness drives memory consolidation. We demonstrate in healthy humans that direct electrical coupling between neurons via gap junctions, i.e., electrical synapses, contributes to this beneficial effect of sleep. Twenty male participants learned a declarative word-pair task and a procedural finger sequence tapping task before receiving the antimalarial mefloquine that is known to block electrical synapses. Retrieval was tested after a retention interval of approximately 20.5 hours that included nocturnal sleep. As predicted, mefloquine given before sleep impaired the retention of declarative memory. In contrast, this effect was absent in control groups, which stayed awake or received mefloquine after sleep. Irrespective of sleep or administration time, mefloquine enhanced retention performance on the procedural memory control task. We conclude that sleep-dependent processes relying on electrical neuronal coupling enable hippocampus-dependent declarative memory consolidation, presumably via time-compressed hippocampal replay of memory traces within sharp-wave/ripple complexes. The recruitment of this understudied form of neuronal information transfer may be necessary to achieve fast-paced memory reprocessing during sleep. Considering that drugs targeting neurochemical synapses have recently fallen short of substantially advancing the treatment of memory impairments in Alzheimers disease, schizophrenia or during normal aging, unraveling the contribution of gap junctions to sleep-dependent declarative memory formation can be expected to open new therapeutic avenues. Significance statementSleep supports the strengthening and transformation of memory content via the active replay of previously encoded engrams. Surprisingly, blocking neurochemical synaptic transmission does not impair this function of sleep. Here we demonstrate that the direct electrical coupling between neurons via electrical synapses (gap junctions) is essential for the sleep-dependent formation of declarative memory, i.e., memory for episodes and facts. These findings are in line with the assumption that electrical synapses enable time-compressed neuronal firing patterns that emerge during sleep and drive declarative memory consolidation. Electrical synapses have so far not been linked to higher-order brain functions in humans; their contribution to sleep-dependent memory processing may provide a novel target for sleep-related clinical interventions.

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bioRxiv2019

Multimodal Study of the Effects of Varying Task Load Utilizing EEG, GSR and Eye-Tracking

ObjectiveThe effect of task load on performance is investigated by simultaneously collecting multi-modal physiological data and participant response data. Periodic response to a questionnaire is also obtained. The goal is to determine combinations of modalities that best serve as predictors of task performance.\n\nApproachA group of participants performed a computer-based visual search task mimicking postal code sorting. A five-digit number had to be assigned to one of six different non-overlapping numeric ranges. Trials were presented in blocks of progressively increasing task difficulty. The participants responses were collected simultaneously with 32 channels of electroencephalography (EEG) data, eye-tracking data, and Galvanic Skin Response (GSR) data. The NASA Task-Load-Index self-reporting instrument was administered at discrete time points in the experiment.\n\nMain resultsLow beta frequency EEG waves (12.5-18 Hz) were more prominent as cognitive task load increased, with most activity in frontal and parietal regions. These were accompanied by more frequent eye blinks and increased pupillary dilation. Blink duration correlated strongly with task performance. Phasic components of the GSR signal were related to cognitive workload, whereas tonic components indicated a more general state of arousal. Subjective data (NASA TLX) as reported by the participants showed an increase in frustration and mental workload. Based on one-way ANOVA, EEG and GSR provided the most reliable correlation to perceived workload level and were the most informative measures (taken together) for performance prediction.\n\nSignificanceNumerous modalities come into play during task-related activity. Many of these modalities can provide information on task performance when appropriately grouped. This study suggests that while EEG is a good predictor of task performance, additional modalities such as GSR increase the likelihood of more accurate predictions. Further, in controlled laboratory conditions, the most informative or minimum number of modalities can be isolated for monitoring in real work environments.

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bioRxiv2019

Consolidation of reward memory during sleep does not require dopaminergic activation

Sleep enhances memories, especially, if they are related to future rewards. Although dopamine has been shown to be a key determinant during reward learning, the role of dopaminergic neurotransmission for amplifying reward-related memories during sleep remains unclear. In the present study, we scrutinize the idea that dopamine is needed for the preferential consolidation of rewarded information. We blocked dopaminergic neurotransmission, thereby aiming to wipe out preferential sleep-dependent consolidation of high over low rewarded memories during sleep. Following a double-blind, balanced, crossover design 20 young healthy men received the dopamine d2-like receptor blocker Sulpiride (800 mg) or placebo, after learning a Motivated Learning Task. The task required participants to memorize 80 highly and 80 lowly rewarded pictures. Half of them were presented for a short (750 ms) and a long duration (1500 ms), respectively, which enabled to dissociate effects of reward on sleep-associated consolidation from those of mere encoding depth. Retrieval was tested after a retention interval of 20 h that included 8 h of nocturnal sleep. As expected, at retrieval, highly rewarded memories were remembered better than lowly rewarded memories, under placebo. However, there was no evidence for an effect of blocking dopaminergic neurotransmission with Sulpiride during sleep on this differential retention of rewarded information. This result indicates that dopaminergic activation is not required for the preferential consolidation of reward-associated memory. Rather it appears that dopaminergic activation only tags such memories at encoding for intensified reprocessing during sleep.

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bioRxiv2018

Variable training but not sleep improves consolidation of motor adaptation

How motor memory consolidates still remains elusive. Motor tasks consolidation were shown to depend on periods of sleep, whereas pure non-hippocampal dependent tasks, like motor adaptation, might not. Some research suggests that the mode of training might affect the sleep dependency of motor adaptation tasks. Here we investigated whether sleep differentially impacts memory consolidation dependent on the variability during training. Healthy men were trained with their dominant, right hand on a force field adaptation task and re-tested after an 11-h consolidation period either involving overnight sleep (Sleep) or daytime wakefulness (Wake). Retesting also included a transfer to the non-dominant hand. Half of the subjects in each group adapted to different force field magnitudes with low inter-trial variability (Sleep-Blocked; Wake-Blocked), the other half with high variability (Sleep-Random; Wake-Random). EEG was recorded during task execution and overnight polysomnography. Motor adaptation was comparable between Wake and Sleep groups, although performance changes over sleep correlated with sleep spindles nesting in slow wave upstates. Higher training variability improved retest, including transfer learning, and these improvements correlated with higher alpha power in contralateral parietal areas. Enhanced consolidation after training might foster the ability to correct ongoing movements by responsive feedback rather than their pre-execution prediction.

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bioRxiv2017

Overnight memory consolidation facilitates rather than interferes with new learning of similar materials - a study probing NMDA-receptors

Whereas sleep-dependent consolidation and its neurochemical underpinnings have been strongly researched, less is known about how consolidation during sleep affects subsequent learning. Since sleep enhances memory, it can be expected to pro-actively interfere with learning after sleep, in particular of similar materials. This pro-active interference should be enhanced by substances that benefit consolidation during sleep, such as D-cycloserine. We tested this hypothesis in two groups (Sleep, Wake) of young healthy participants receiving on one occasion D-cycloserine (175 mg) and on another occasion placebo, according to a double-blind balanced cross-over design. Treatment was administered after participants had learned a set of word-pairs (A-B list) and before nocturnal retention periods of sleep vs. wakefulness. After D-cycloserine blood plasma levels had dropped to negligible amounts, i.e., the next day in the evening, participants learned, in three sequential runs, new sets of word-pairs. One list - to enhance interference - consisted of the same cue words as the original set paired with a new target word (A-C list) and the other of completely new cue words (D-E set). Unexpectedly, during post-retention learning the A-C interference list was generally better learned than the completely new D-E list, which suggests that consolidation of previously encoded similar material enhances memory integration rather than pro-active interference. Consistent with this view, new learning of word-pairs was better after sleep than wakefulness. Similarly, D-cycloserine generally enhanced learning of new word-pairs, compared to placebo. This effect being independent of sleep or wakefulness, leads us to speculate that D-cycloserine, in addition to enhancing sleep-dependent consolidation, might mediate a time-dependent process of active forgetting.

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