Search bioRxiv⌕ Search

Biology subjects

Kumral, D.

Publications and source records attributed to Kumral, D..

14 recordsLinked to original sources

Learning sculpts microstructure in real time: evidence from dense temporal sampling of diffusion MRI

Learning induces rapid microstructural plasticity in the human brain, yet the precise temporal dynamics of these changes remain unclear. Using dense temporal sampling of diffusion-weighted MRI (DW-MRI) combined with task-based fMRI, we assessed microstructural changes throughout a declarative learning paradigm and subsequent rest. Seventy-four participants (36 females) learned image-location associations across four encoding-retrieval repetitions while undergoing interleaved functional and DW-MRI acquisitions. A matched control group (N=37, 21 females) underwent a similar imaging protocol without learning. Dense sampling of DW-MRI acquisitions (k=2146 across 22 time points in 127 min) revealed that learning-induced mean diffusivity (MD) decreases emerged shortly after learning onset and continued to develop during post-learning rest. The most robust and spatially consistent change was localized to the left middle occipital/temporal gyrus, a region also showing functional activation during encoding and retrieval. Linear mixed-effects modeling further confirmed a significant group-by-time interaction, with MD reductions in the left middle occipital/temporal gyrus emerging as early as {approx}7 min after learning onset, becoming robust by {approx}35-40 min, and persisting throughout the extended post-learning period, while controls showed no changes. Our findings demonstrate that learning-related microstructural plasticity unfolds continuously from encoding to offline consolidation, with learning-induced structural changes emerging in functionally engaged regions. Dense temporal sampling of DW-MRI offers a powerful approach to bridge functional activation and structural remodeling, providing evidence of when and where experience-dependent plasticity occurs during memory formation.

neuroscience↗

Rapid expansion and renormalization of parietal gray matter volume following associative learning

The human brain exhibits rapid structural plasticity following learning, yet its temporal dynamics and behavioral relevance remain elusive, particularly for declarative forms of learning. In this study, we tested whether T1-weighted MRI captures rapid structural reorganization following associative memory formation and whether such changes follow an expansion-renormalization trajectory. We combined three independent datasets (N = 198) to quantify gray matter volume (GMV) changes following an associative memory task using voxel-based morphometry across baseline, 2 h, and 12 h post-learning. We observed transient GMV increases in parietal, lateral occipital, and cerebellar regions at 2 h post-learning, which were no longer detectable relative to baseline by 12 h, consistent with rapid renormalization. Critically, GMV changes in left parietal cortex were associated with memory retention, such that greater maintenance of GMV was associated with better retention. In a separate, spatially distinct effect, sleep facilitated renormalization of GMV in the right parietal cortex, an effect that showed no association with memory retention. Our findings provide evidence that human gray matter undergoes hour-scale changes, reflecting dissociable memory- and sleep-related components.

neuroscience↗

Incorporation of complex narratives into dreaming

Reactivation of waking neuronal activity during sleep holds a functional role in memory consolidation. Reprocessing of daytime memory in dreams might aid later memory performance in a similar way. Numerous findings hint at a link between dreaming and sleep-dependent memory processing, however, studies investigating day-residue incorporation in dreaming led to mixed results so far. In this study, we used a naturalistic learning paradigm aimed at biasing dream content by manipulating pre-sleep experience. Participants listened to one of four different audiobooks while falling asleep and were awoken several times during the night to report their dreams. Afterwards, we tested how well they remembered the content of the audiobook. We then asked three blind raters to guess, based solely on anonymized dream reports, which audiobook someone had listened to before experiencing a dream. Our findings show that dreams across the whole night and from both NREM and REM awakenings contain specific information about the content of narratives studied before sleep. Moreover, participants with stronger incorporation of the audiobook in their dreams showed a tendency to recognize more audiobook content across the sleep period. Together, these findings suggest that salient day-time experiences resurface in dreams and that content selected for consolidation during sleep is more strongly incorporated.

neuroscience↗

Random auditory stimulation disturbs traveling slow waves and declarative memory

Sleep plays a crucial role in memory consolidation, and various methods have attempted to enhance this process by using auditory stimulation to modulate slow waves or trigger memory reactivation. However, the broader impact of auditory stimulation on sleep physiology and memory retention is not fully understood. Here, we apply random or sham auditory stimulation during an afternoon nap in a within-subject design to investigate its effects on declarative and procedural memory consolidation and electrical brain activity during sleep. Stimulation led to a specific reduction in slow-wave sleep, a decreased slow-wave count, and impaired declarative recall that correlated with the diminished sleep depth. Furthermore, we observed altered slow-wave traveling dynamics, with stimulation resulting in shorter traveling trajectories with less reach and reduced spatial spread, particularly impacting frontal regions. Disruptions in these features correlated with memory deficits. Our findings highlight the role of dynamic slow-wave properties in declarative memory consolidation and reveal some methodological limitations for using auditory cues during sleep, given their potential to disrupt complex processing patterns.

neuroscience↗

Daytime experiences shape neural activity and dream content in the sleeping brain

Dreams incorporate recent experiences, and memory-related brain activity is reactivated during sleep, suggesting that dreaming, memory consolidation and reactivation are tightly linked. We devised a paradigm to investigate whether memory reprocessing during sleep contributes to dreaming. Participants listened to different audiobooks before falling asleep, introducing dissimilar experiences to be processed at night. We show that audiobook content was reprocessed at the neural level using multivariate pattern analyses. Brain activity during rapid eye movement sleep, particularly in the beta range, carried information about the audiobook. While the amount of neural reinstatement did not correlate with memory retention, global beta power during REM sleep was associated with better memory performance. Moreover, blind raters could determine which audiobook participants had studied based on dream reports. Participants who dreamt of the audiobook also showed stronger neural reinstatement. Reprocessing of pre-sleep experiences during sleep may thus shape our brain activity, our dreams, and our memories.

neuroscience↗

Spindle-dependent memory consolidation in healthy adults: A meta-analysis

Accumulating evidence suggests a central role for sleep spindles in the consolidation of new memories. However, no metaanalysis of the association between sleep spindles and memory performance has been conducted so far. Here, we report meta-analytical evidence for spindle-memory associations and investigate how multiple factors, including memory type, spindle type, spindle characteristics, and EEG topography affect this relationship. The literature search yielded 53 studies reporting 1427 effect sizes, resulting in a small to moderate effect for the average association. We further found that spindle-memory associations were significantly stronger for procedural memory than for declarative memory. Neither spindle types nor EEG scalp topography had an impact on the strength of the spindle-memory relation, but we observed a distinct functional role of global and fast sleep spindles, especially for procedural memory. We also found a moderation effect of spindle characteristics, with power showing the largest effect sizes. Collectively, our findings suggest that sleep spindles are involved in learning, thereby representing a general physiological mechanism for memory consolidation. HighlightsO_LISpindle measures showed a small to medium-sized association with memory performance. C_LIO_LIThis relationship was stronger for procedural memory than declarative memory. C_LIO_LINo moderation effects of spindle type and EEG scalp topography have been observed. C_LIO_LISpindle power emerged as the strongest predictors. C_LIO_LINaps showed similar spindle-related consolidation mechanisms to whole-night sleep. C_LI

neuroscience↗

Rapid volumetric brain changes after acute psychosocial stress

Stress is an important trigger for brain plasticity: Acute stress can rapidly affect brain activity and functional connectivity, and chronic or pathological stress has been associated with structural brain changes. Measures of structural magnetic resonance imaging (MRI) can be modified by short-term motor learning or visual stimulation, suggesting that they also capture rapid brain changes. Here, we investigated volumetric brain changes (together with changes in T1 relaxation rate and cerebral blood flow) after acute stress in humans as well as their relation to psychophysiological stress measures. Sixty-seven healthy men (25.8{+/-}2.7 years) completed a standardized psychosocial laboratory stressor (Trier Social Stress Test) or a control version while blood, saliva, heart rate, and psychometrics were sampled. Structural MRI (T1 mapping / MP2RAGE sequence) at 3T was acquired 45 min before and 90 min after intervention onset. Grey matter volume (GMV) changes were analysed using voxel-based morphometry. Associations with endocrine, autonomic, and subjective stress measures were tested with linear models. We found significant group-by-time interactions in several brain clusters including anterior/mid-cingulate cortices and bilateral insula: GMV was increased in the stress group relative to the control group, in which several clusters showed a GMV decrease. We found a significant group-by-time interaction for cerebral blood flow, and a main effect of time for T1 values (longitudinal relaxation time). In addition, GMV changes were significantly associated with state anxiety and heart rate variability changes. Such rapid GMV changes assessed with VBM may be induced by local tissue adaptations to changes in energy demand following neural activity. Our findings suggest that endogenous brain changes are counteracted by acute psychosocial stress, which emphasizes the importance of considering homeodynamic processes and generally highlights the influence of stress on the brain. HighlightsO_LIWe investigated rapid brain changes using MRI in a stress and a control group C_LIO_LIVBM-derived GMV showed a significant group-by-time interaction in several clusters C_LIO_LIMain pattern: GMV in the stress group increased relative to the control group, in which GMV decreased C_LIO_LIGMV changes across groups were associated with state anxiety and heart rate variability C_LIO_LINeither cerebral blood flow, nor T1 values fully account for the VBM results C_LI

neuroscience↗

Alterations in rhythmic and non-rhythmic resting-state EEG activity and their link to cognition in older age

While many structural and biochemical changes in the brain have been previously associated with aging, the findings concerning electrophysiological signatures, reflecting functional properties of neuronal networks, remain rather controversial. To try resolve this issue, we took advantage of a large population study (N=1703) and comprehensively investigated the association of multiple EEG biomarkers (power of alpha and theta oscillations, individual alpha peak frequency (IAF), the slope of 1/f power spectral decay), aging, and aging and cognitive performance. Cognitive performance was captured with three factors representing processing speed, episodic memory, and interference resolution. Our results show that not only did IAF decline with age but it was also associated with interference resolution over multiple cortical areas. To a weaker extent, 1/f slope of the PSD showed age-related reductions, mostly in frontal brain regions. Finally, alpha power was negatively associated with the speed of processing in the right frontal lobe, despite the absence of age-related alterations. Our results thus demonstrate that multiple electrophysiological features, as well as their interplay, should be considered when investigating the association between age, neuronal activity, and cognitive performance.

neuroscience↗

Relationship between Regional White Matter Hyperintensities and Alpha Oscillations in Older Adults

Aging is associated with increased white matter hyperintensities (WMHs) and with the alterations of alpha oscillations (7-13 Hz). However, a crucial question remains, whether changes in alpha oscillations relate to aging per se or whether this relationship is mediated by age-related neuropathology like WMHs. Using a large cohort of cognitively healthy older adults (N=907, 60-80 years), we assessed relative alpha power, alpha peak frequency, and long-range temporal correlations (LRTC) from resting-state EEG. We further associated these parameters with voxel-wise WMHs from 3T MRI. We found that a higher prevalence of WMHs in the superior and posterior corona radiata as well as in the thalamic radiation was related to elevated alpha power, with the strongest association in the bilateral occipital cortex. In contrast, we observed no significant relation of the WMHs probability with alpha peak frequency and LRTC. Finally, higher age was associated with elevated alpha power via total WMH volume. Although an increase in alpha oscillations due to WMH can have a compensatory nature, we rather suggest that an elevated alpha power is a consequence of WMH affecting a spatial organization of alpha sources.

neuroscience↗

Hemispheric asymmetries in resting-state EEG and fMRI are related to approach and avoidance behaviour, but not to eating behaviour or BMI

Much of our behaviour is driven by two motivational dimensions - approach and avoidance. These have been related to frontal hemispheric asymmetries in clinical and resting-state EEG studies: approach was linked to higher activity of the left relative to the right hemisphere, while avoidance was related to the opposite pattern. Increased approach behaviour, specifically towards unhealthy foods, is also observed in obesity and has been linked to asymmetry in the framework of the right-brain hypothesis of obesity. Here, we aimed to replicate previous EEG findings of hemispheric asymmetries for self-reported approach/avoidance behaviour and to relate them to eating behaviour. Further, we assessed whether resting fMRI hemispheric asymmetries can be detected and whether they are related to approach/avoidance, eating behaviour, and BMI. We analysed 3 samples: Sample 1 (n=117) containing EEG and fMRI data from lean participants, and Samples 2 (n=89) and 3 (n=152) containing fMRI data from lean, overweight, and obese participants. While in Sample 1 approach in women was related to EEG and fMRI hemispheric asymmetries, in Samples 2 and 3 this effect was not significant. Here, hemispheric asymmetries were neither related to BMI nor eating behaviour. Our study partly replicates previous EEG findings regarding hemispheric asymmetries and indicates that this relationship could also be captured using fMRI. Our findings suggest that eating behaviour and obesity are likely to be mediated by mechanisms not directly relating to frontal asymmetries in neuronal activation quantified with EEG and fMRI.

neuroscience↗

BOLD and EEG Signal Variability at Rest Differently Relate to Aging in the Human Brain

Variability of neural activity is regarded as a crucial feature of healthy brain function, and several neuroimaging approaches have been employed to assess it noninvasively. Studies on the variability of both evoked brain response and spontaneous brain signals have shown remarkable changes with aging but it is unclear if the different measures of brain signal variability - identified with either hemodynamic or electrophysiological methods - reflect the same underlying physiology. In this study, we aimed to explore age differences of spontaneous brain signal variability with two different imaging modalities (EEG, fMRI) in healthy younger (25{+/-}3 years, N=135) and older (67{+/-}4 years, N=54) adults. Consistent with the previous studies, we found lower blood oxygenation level dependent (BOLD) variability in the older subjects as well as less signal variability in the amplitude of low-frequency oscillations (1-12 Hz), measured in source space. These age-related reductions were mostly observed in the areas that overlap with the default mode network. Moreover, age-related increases of variability in the amplitude of beta-band frequency EEG oscillations (15-25 Hz) were seen predominantly in temporal brain regions. There were significant sex differences in EEG signal variability in various brain regions while no significant sex differences were observed in BOLD signal variability. Bivariate and multivariate correlation analyses revealed no significant associations between EEG- and fMRI-based variability measures. In summary, we show that both BOLD and EEG signal variability reflect aging-related processes but are likely to be dominated by different physiological origins, which relate differentially to age and sex.

neuroscience↗

The age-dependent relationship between resting heart rate variability and functional brain connectivity

Resting heart rate variability (HRV), an index of parasympathetic cardioregulation and an individual trait marker related to mental and physical health, decreases with age. Previous studies have associated resting HRV with structural and functional properties of the brain - mainly in cortical midline and limbic structures. We hypothesized that HRV may alter its relationship with brain structure and function across the adult lifespan. In 388 healthy subjects of three age groups (140 younger: 26.0{+/-}4.2 years, 119 middle-aged: 46.3{+/-}6.2 years, 129 older: 66.9{+/-}4.7 years), gray matter structure (voxel-based morphometry) and resting-state functional connectivity (eigenvector centrality mapping and exploratory seed-based functional connectivity) were related to resting HRV, measured as the root mean square of successive differences (RMSSD). Confirming previous findings, resting HRV decreased with age. For HRV-related gray matter volume, there were no statistically significant differences between the age groups, nor similarities across all age groups. In whole-brain functional connectivity analyses, we found an age-dependent association between resting HRV and eigenvector centrality in the bilateral ventromedial prefrontal cortex (vmPFC), driven by the younger adults. Across all age groups, HRV was positively correlated with network centrality in bilateral posterior cingulate cortex. Seed-based functional connectivity analysis using the vmPFC cluster revealed an HRV-related cortico-cerebellar network in younger but not in middle-aged or older adults. Our results indicate that the decrease of HRV with age is accompanied by changes in functional connectivity along the cortical midline. This extends our knowledge of brain-body interactions and their changes over the lifespan.

neuroscience↗

Association of Peripheral Blood Pressure with Grey Matter Volume in 19- to 40-Year-Old Adults

ObjectiveTo test whether elevated blood pressure (BP) relates to grey matter volume (GMV) changes in young adults who had not previously been diagnosed as hypertensive (systolic BP (SBP)/diastolic BP (DBP)[&ge;]140/90 mmHg).\n\nMethodsWe associated BP with GMV from structural 3 Tesla T1-weighted MRI of 423 healthy adults between 19-40 years (mean age=27.7{+/-}5.3 years, 177 women, SBP/DBP=123.2/73.4{+/-}12.2/8.5 mmHg). Data originated from four previously unpublished cross-sectional studies conducted in Leipzig, Germany. We performed voxel-based morphometry on each study separately and combined results in image-based meta-analyses (IBMA) to assess cumulative effects across studies. Resting BP was assigned to one of four categories: (1) SBP<120 and DBP<80 mmHg, (2) SBP 120-129 or DBP 80-84 mmHg, (3) SBP 130-139 or DBP 85-89 mmHg, (4) SBP[&ge;]140 or DBP[&ge;]90 mmHg.\n\nResultsIBMA yielded: (a) lower regional GMV was correlated with higher peripheral BP; (b) lower GMV with higher BP when comparing individuals in sub-hypertensive categories 3 and 2, respectively, to those in category 1; (c) lower BP-related GMV was found in regions including hippocampus, amygdala, thalamus, frontal and parietal structures (e.g. precuneus).\n\nConclusionsBP[&ge;]120/80 mmHg was associated with lower GMV in regions that have previously been related to GM decline in older individuals with manifest hypertension. Our study shows that BP-associated GM alterations emerge continuously across the range of BP and earlier in adulthood than previously assumed. This suggests that treating hypertension or maintaining lower BP in early adulthood might be essential for preventing the pathophysiological cascade of asymptomatic cerebrovascular disease to symptomatic end-organ damage, such as stroke or dementia.

neuroscience↗

A functional connectome phenotyping dataset including cognitive state and personality measures

The dataset enables exploration of higher-order cognitive faculties, self-generated mental experience, and personality features in relation to the intrinsic functional architecture of the brain. We provide multimodal magnetic resonance imaging (MRI) data and a broad set of state and trait phenotypic assessments: mind-wandering, personality traits, and cognitive abilities. Specifically, 194 healthy participants (between 20 and 75 years of age) filled out 31 questionnaires, performed 7 tasks, and reported 4 probes of in-scanner mind-wandering. The scanning session included four 15.5-min resting-state functional MRI runs using a multiband EPI sequence and a high-resolution structural scan using a 3D MP2RAGE sequence. This dataset constitutes one part of the MPI-Leipzig Mind-Brain-Body database.

neuroscience↗