{"id":1020,"date":"2018-05-08T14:54:35","date_gmt":"2018-05-08T12:54:35","guid":{"rendered":"http:\/\/semmelweis.hu\/psychophysiology\/?p=1020"},"modified":"2019-03-15T19:40:05","modified_gmt":"2019-03-15T18:40:05","slug":"long-range-alpha-and-beta-and-short-range-gamma-eeg-synchronization-distinguishes-phasic-and-tonic-rem-periods","status":"publish","type":"post","link":"https:\/\/semmelweis.hu\/psychophysiology\/2018\/05\/08\/long-range-alpha-and-beta-and-short-range-gamma-eeg-synchronization-distinguishes-phasic-and-tonic-rem-periods\/","title":{"rendered":"Long-range alpha and beta and short-range gamma EEG synchronization distinguishes phasic and tonic REM periods"},"content":{"rendered":"
SLEEP<\/em> 41: (3) (2018)<\/h5>\n
DOI: 10.1093\/sleep\/zsx210<\/a><\/h5>\n
P\u00e9ter Simor1,2<\/sup>, Ferenc Gombos3<\/sup>, Borb\u00e1la Blaskovich4<\/sup>, R\u00f3bert B\u00f3dizs5,6<\/sup><\/h5>\n
1<\/sup>Institute of Psychology, E\u00f6tv\u00f6s Lor\u00e1nd University, Hungary<\/h5>\n
2<\/sup>Ny\u00edr\u0151 Gyula Hospital, National Institute of Psychiatry and Addictions, Budapest, Hungary<\/h5>\n
3<\/sup>Department of General Psychology, P\u00e1zm\u00e1ny P\u00e9ter Catholic University, Budapest, Hungary<\/h5>\n
4<\/sup>Department of Cognitive Science, Budapest University of Technology and Economics, Budapest, Hungary<\/h5>\n
5<\/sup>Semmelweis University, Institute of Behavioural Sciences, Budapest, Hungary<\/h5>\n
6<\/sup>National Institute of Clinical Neuroscience, Budapest, Hungary<\/h5>\n
\u00a0<\/h5>\n
Abstract<\/strong><\/h5>\n
Rapid eye movement (REM) sleep is characterized by the alternation of two markedly different microstates, phasic and tonic REM. These periods differ in awakening and arousal thresholds, sensory processing, and spontaneous cortical oscillations. Previous studies indicate that although in phasic REM, cortical activity is independent of the external environment, attentional functions and sensory processing are partially maintained during tonic periods. Large-scale synchronization of oscillatory activity, especially in the \u03b1- and \u03b2-frequency ranges, can accurately distinguish different states of vigilance and cognitive processes of enhanced alertness and attention. Therefore, we examined long-range inter- and intrahemispheric as well as short-range electroencephalographic synchronization during phasic and tonic REM periods quantified by the weighted phase lag index. Based on the nocturnal polysomnographic data of 19 healthy adult participants, we showed that long-range inter- and intrahemispheric \u03b1 and \u03b2 synchrony was enhanced in tonic REM states in contrast to phasic ones, and resembled \u03b1 and \u03b2 synchronization of resting wakefulness. On the other hand, short-range synchronization within the \u03b3-frequency range was higher in phasic compared with tonic periods. Increased short-range synchrony might reflect local and inwardly driven sensorimotor activity during phasic REM periods, whereas enhanced long-range synchrony might index frontoparietal activity that reinstates environmental alertness after phasic REM periods.<\/h5>\n
Keywords<\/strong>: weighted phase lag index, frontoparietal, REM sleep, synchronization, EEG<\/h5>\n

 <\/p>\n

Statement of Significance<\/strong><\/p>\n

Rapid eye movement (REM) sleep is composed of the alternation of two microstates: phasic and tonic REM. Previous studies showed that cortical oscillations as measured by EEG spectral power densities show marked differences between phasic and tonic states. More specifically, \u03b1 and \u03b2 power is consistently higher during tonic, whereas \u03b3 activity is enhanced during phasic periods. We complemented these findings by analyzing synchronized activity within these frequency bands. We showed that \u03b1 and \u03b2 oscillations exhibit higher synchronization during tonic compared with phasic periods, especially between distant regions. On the other hand, phasic REM periods were characterized by relatively increased local (short-range) \u03b3 synchronization. Our findings contribute to the understanding of the complex and heterogeneous nature of REM sleep.<\/p>\n

 <\/p>\n

Introduction<\/strong><\/p>\n

Rapid eye movement (REM) sleep is a unique neural state that occupies 20%\u201325% of nighttime sleep in healthy human individuals [1]. REM sleep was termed as a paradoxical state [2], due to its combination of high cortical activity indexed by low voltage, mixed frequency electroencephalographic (EEG) oscillations, and low muscle tone [1]. In fact, intense sensorimotor and oneiric (dream) activity accompanied by inhibited motor output and reduced environmental processing [3\u20139] are essential features of REM sleep. Nevertheless, the nature of REM sleep seems to be even more complex, as it is composed of two markedly different brain states. The phasic<\/em> REM state is characterized by transient bursts of ocular movements, myoclonic twitches, and irregular vegetative activity that occur quasiperiodically [10] on the background of an apparently more quiescent, tonic<\/em> state [11\u201313]. Phasic REM sleep is accompanied by so-called ponto\u2013geniculo\u2013occipital (PGO) potentials originating spontaneously in the pontine reticular formation and transferred to the thalamocortical system and the hippocampal formation [14].<\/p>\n

Phasic and tonic REM periods differ in awakening or arousal thresholds, and sensory processing, as the tonic episode shows generally lower thresholds [5, 15] and functional evoked responses to deviant tones, resembling evoked potentials during wakefulness [16]. In addition, acoustic stimuli presented during the tonic state elicited a residual blood oxygen level dependent response within the auditory cortex, whereas no such reactivity was evidenced during phasic periods [17]. The authors of this study speculate that phasic REM periods represent a functionally isolated brain state, in contrast to tonic periods, in which environmental processing is partially preserved [17]. Moreover, sensory stimulation seems to suppress phasic REM activity and facilitate the transition to the tonic state leading to arousals and microawakenings [18] that make the analyses of phasic REM sleep by functional magnetic resonance imaging (fMRI) quite challenging since sensory stimulation (noise and vibration) is always present in the MR environment [19].<\/p>\n

The analysis of spontaneous EEG oscillations is an efficient approach in order to compare phasic and tonic neural activities in an ecologically valid environment. A consistent finding of scalp EEG studies was a relative increase in \u03b1- (8\u201313 Hz) and \u03b2- (~14\u201330 Hz) frequency band power during tonic periods [20\u201322], which was also evidenced by intracranial sleep recordings [23, 24]. Oscillatory activity in the \u03b1- and \u03b2-frequency ranges measured during resting-state wakefulness reflects the activation of a widely distributed cingulo\u2013insular\u2013thalamic neural network [25] that underpins the maintenance of alertness, and facilitates accurate responses to incoming environmental stimuli [26\u201328].<\/p>\n

The other frequency specific activity that consistently distinguished phasic and tonic REM based on scalp and intracranial recordings was \u03b3 power (>30 Hz) that seemed to be relatively enhanced during phasic states [20, 21, 24, 29]. Increased \u03b3 power during phasic periods might reflect sensorimotor, emotional, and cognitive activity leading to intense dream experiences [29\u201331]. In fact, phenomenological observations showed that dream reports after phasic periods are more perceptual and hallucinatory-like than those collected after tonic episodes, which, in turn, are more thought-like [11, 32]. Based on these findings, we might assume that during phasic REM, the brain transitionally \u201cdecouples\u201d from the external environment and \u201csubmerges\u201d in inwardly generated sensory and motor activity, whereas during tonic states, vigilance, environmental awareness, and attentional processes reflecting a more wake-like state are partially reinstated [17, 21, 23].<\/p>\n

Large-scale synchronization of oscillatory activity is a crucial mechanism in the formation of functionally connected neuronal ensembles underlying a wide range of cognitive phenomena [33\u201335]. Accordingly, frequency-specific synchronous oscillations across distant electrode sites can characterize different states of vigilance [36, 37] or cognitive processes that vary in difficulty, attentional demands, or multimodal integration [38\u201340]. In spite of the advantages of such analyses, apart from one recent study in epileptic patients [41], phasic and tonic REM states were not systematically analyzed in terms of EEG synchronization.<\/p>\n

Our aim was to describe interareal (inter- and intrahemispheric) EEG synchronization during phasic and tonic periods based on the weighted phase lag index (WPLI) [42]. In light of the aforementioned data, we assumed that tonic REM sleep was a more wake-like state with enhanced alertness and reinstated attentional processes anticipating environmental stimuli. We were specifically interested in long-range \u03b1 synchronization that was shown to reflect increased arousal and alertness [25, 36] and to play a key role in cognitive processes that require enhanced attention [38, 39], multisensory integration [40, 43], or top-down control [34, 44]. Here, we show that long-range inter- and intrahemispheric \u03b1 or \u03b2 synchrony is enhanced in tonic periods in contrast to phasic ones. On the other hand, increased short-range \u03b3 synchrony differentiates phasic from tonic states.<\/p>\n

 <\/p>\n

Methods<\/strong><\/p>\n

Participants and procedure<\/strong><\/p>\n

\u00a0<\/strong>We analyzed nocturnal sleep EEG recordings that were collected in a previous study [21]. Our sample consisted of the polysomnographic data of 20 healthy individuals (10 males, Mage<\/sub> = 21.72 \u00b1 1.36 years). The recordings were collected the second night (after an adaptation night) in the sleep laboratory of the Semmelweis University. Participants were free from prior or current psychiatric, neurological, chronic somatic, or sleep disorders and showed no signs of anxiety or depressive symptoms according to standard psychometric measures. Participants were screened for depressive symptoms by the Hungarian version of the nine-itemed Beck depression inventory (BDI-9 [45]), for anxiety symptoms by the trait score of the adapted version of the Spielberger State-Trait Inventory (STAI-T [46]), and for sleep disorders by the Pittsburgh Sleep Quality Scale (PSQI [47]). Consumption of medicine (except oral contraceptives), alcohol, or drugs also belonged to exclusion criteria. Participants arrived at the laboratory between 20.00 and 21.00 hr and after the placement of electrodes were asked to go to bed at their habitual bedtimes. Before lights off, within a subsample (n<\/em> = 15) of our participants, resting state EEG with eyes closed was recorded, during which participants were instructed by the assistant to open their eyes for about 10\u201315 s in every 2 min. Lights off was scheduled between 22.00 and midnight, and participants were allowed to sleep until 8.30 in the morning unless they woke up earlier spontaneously. The data of one participant were excluded because technical artifacts in the electrooculogram (EOG) channel hindered the reliable selection of phasic periods. In addition, the resting state data of two participants were not included due to increased noise generated by muscle artifacts. Therefore, we could only include the data of 12 participants for the analyses of resting state wakeful data. The Ethical Committee of the Semmelweis University approved the study protocol and participants gave written informed consent to the procedure.<\/p>\n

 <\/p>\n

Recording and preprocessing<\/strong><\/p>\n

\u00a0<\/strong>Participants were fitted with gold-coated (Ag\/AgCl) scalp electrodes fixed with EC2 Grass Electrode Cream (Grass Technologies, Warwick, Rhode Island, USA). Nineteen scalp EEG derivations (Fp1, Fp2, F7, F3, Fz, F4, F8, T3, C3, Cz, C4, T4, T5, P3, Pz, P4, T6, O1, O2 referenced to the mathematically linked mastoids) as well as bipolar EOG and EMG electrodes were placed according to the standard 10\u201320 system [48]. Impedances were kept below 8 k\u03a9. Signals were collected, prefiltered (0.33\u20131500 Hz, 40 dB\/decade antialiasing hardware input filter), amplified, and digitized with 4096 Hz\/channel sampling rate (synchronous) with 12-bit resolution by using the 32-channel EEG\/polysystem (Brain-Quick BQ 132S; Micromed, Mogliano Veneto, Italy). A further 40 dB\/decade antialiasing digital filter was applied by digital signal processing, which low-pass filtered the data at 450 Hz. Finally, the digitized and filtered EEG was resampled to 1024 Hz. Sleep stages were previously scored manually according to standardized criteria of the American Academy of Sleep Medicine (AASM) [49] by an expert trained in sleep research.<\/p>\n

Sleep scoring and the inspection of eye movements (EMs) were carried out manually using a custom-made software tool for full night sleep EEG analysis (FerciosEEGPlus, Ferenc Gombos 2008\u20132017). After the scoring, we extracted the conventional parameters of sleep architecture (see Supplementary Material Table S1<\/em><\/strong>).<\/p>\n

REM sleep stages from the first four sleep cycles were considered for the selection of phasic and tonic segments. EMs were visually identified in 4 s time windows based on the presence of EOG deflections of an amplitude above 150 \u00b5V and shorter than 500 ms. Previous studies used less conservative amplitude criteria [50, 51]; however, EMs in bipolar EOG montages produce higher amplitudes; therefore, we restricted our analyses to relatively larger EMs. The velocity criterion was based on earlier studies indicating that EMs during REM do not exceed 2 Hz in terms of frequency [50, 51].<\/p>\n

A 4 s long segment was categorized as phasic if at least two consecutive EMs were detected in adjacent 2 s time windows. Segments were scored as tonic when no EMs occurred (EOG deflections below 25 \u00b5V) in adjacent 2 s time windows. In order to rule out possible intermediate periods and the contamination between the two states, phasic and tonic episodes separated from each other by less than two segments (8 s) were discarded. Segments containing technical and movement-related artifacts were visually inspected and excluded from further analyses. Given the larger amount of tonic compared with phasic periods, we randomly selected 100 phasic and 100 tonic segments (400 s) from each participant. In order to increase the stationarity of the data, we cut each 4 s long episode into three 2 s long overlapping (50%) segments. Awake resting state recordings were similarly split into 2 s long overlapping segments. The amount of awake segments was matched (by random selection) to the amount of analyzed REM periods (300 \u00d7 2 s). The continuous recordings were filtered by a discrete Fourier transform (DFT) filter removing (50 Hz) line noise and were band-pass filtered (Butterworth, zero phase forward and reverse digital filter between 0.5 and 46 Hz) before frequency analyses. The data were segmented into phasic and tonic trials.<\/p>\n

 <\/p>\n

Laplacian estimation<\/strong><\/p>\n

\u00a0<\/strong>Volume conduction, in general, as well as artifacts produced by microsaccades [52] or muscle activity [53], can largely influence the spatial topography of scalp EEG recordings yielding spurious synchronization even between distant electrode derivations. Therefore, prior to analyses of synchronization, we estimated the surface Laplacian of the EEG data [54\u201356]. The Laplacian estimation can be interpreted as a spatial filter that attenuates the influence of volume conduction, reference artifacts, and microsaccades and hence provides a more accurate localization of raw EEG signals [56, 57]. Although the WPLI is devoid of the effects of volume conduction originating from common source activity, Laplacian estimation proved to be useful and advisable in order to sharpen EEG topography prior to analyses of interareal synchronization, including the WPLI [39, 58]. We used a spherical spline interpolation (order of splines = 4, maximum degree of Legendre polynomials = 10, \u03bb = 10\u22125<\/sup>) and calculated the Laplacian, based on the second-order spatial derivatives. Previous work indicates that this procedure minimizes the unfavorable influence of REM-related microsaccades on fast frequency activity [59] and efficiently improves scalp topography even in the case of a small number (19 channels) of electrodes [60].<\/p>\n

 <\/p>\n

Frequency decomposition<\/strong><\/p>\n

\u00a0<\/strong>Spectral power analyses were performed between 4 and 46 Hz (from \u03b8 to \u03b3 range). We did not analyze slower frequency bins (i.e. within the \u03b4 range) due to the negligible contribution of \u03b4 oscillations to the differences between phasic and tonic states and due to the fact that slow frequency activity during phasic periods is largely contaminated by EMs rendering \u03b4 activity less reliable [20, 21, 51]. Two seconds long, artifact-free, Laplacian transformed phasic, tonic, and awake EEG data segments were tapered (with Hanning window for lower frequencies between 4 and 28 Hz, and by dpss multitaper method with \u00b12 Hz smoothing for higher frequencies between 29 and 46 Hz). The cross-power spectral densities were computed for each phasic, tonic, and awake trial, based on long-range interhemispheric and (frontoparietal) intrahemispheric channel combinations. Frontopolar and occipital channels were not included to provide a more homogeneous set of distances between pairs. As Figure 1 illustrates, interhemispheric channel pairs included F7-F8, F3-F4, T3-T4, C3-C4, T5-T6, and P3-P4. Intrahemispheric channel pairs included F7-T5, F3-P3, Fz-Pz, F4-P4, and F8-T6.<\/p>\n

\u00a0<\/strong><\/p>\n

\u00a0<\/strong>Figure 1.<\/strong><\/p>\n

\"\"<\/a><\/p>\n

Interhemispheric (blue) and intrahemispheric (orange) channel pairs for the calculation of long-range synchronization. Long-range connections refer to nonadjacent electrode pairs. Frontopolar and occipital electrodes were used for Laplacian estimation, but were excluded from the analyses of synchronization.<\/p>\n

\u00a0<\/strong><\/p>\n

\u00a0<\/strong>Synchronization: WPLI<\/strong><\/p>\n

\u00a0<\/strong>The phase lag index (PLI) was proposed by Stam and colleagues [61] in order to quantify phase synchronization based on the asymmetry of the distribution of phase-angle differences (usually represented as vectors in a circular plane) between two EEG signals. The PLI, such as the more widely used phase coherence, measures the consistency of phase relationships between two electric signals; however, it is less sensitive to the influence of volume conduction and common sources by discarding random and zero (or \u03c0) phase-angle differences [42, 61].<\/p>\n

The disadvantage of the PLI is that phase lags might turn into leads, and vice versa, yielding discontinuous measurements that can be problematic in the case of synchronization effects of small magnitude [42]. The modified version of the PLI, the WPLI, was introduced to attenuate this effect. This measure weights phase-angle differences by the magnitude of the imaginary component. Consequently, the procedure attenuates (deweights) the contribution of phase-angle difference vectors that are close to the real axis (close to zero or to \u03c0). Although the traditional measure of coherence appears to follow fluctuations in power, WPLI seems to be independent of spectral power [62]. The final estimate of the WPLI produces values between 0 and 1. Values closer to 1 indicate higher phase synchronization between signals [42]. The WPLI was computed for each channel pair and frequency between 4 and 46 Hz (1 Hz bin resolution). Filtering, segmentation, manual artifact rejection, Laplacian estimation, and frequency analyses (FFT and WPLI) were performed in Matlab (The Mathworks) using the Fieldtrip toolbox [63].<\/p>\n

 <\/p>\n

Statistical analyses<\/strong><\/p>\n

\u00a0<\/strong>Statistical testing was performed with R [64]. To reduce the number of statistical comparisons, we averaged the WPLI values of the corresponding channel pairs to obtain a mean value of interhemispheric and intrahemispheric synchronization, separately. WPLI values for the specific frequency bins were averaged into \u03b8 (4\u20137 Hz), \u03b1 (8\u201314 Hz), \u03b2 (15\u201330 Hz), and \u03b3 (31\u201346 Hz) ranges [65], but binwise values were retained for exploratory analyses. The assumption of normality was verified by the Shapiro\u2013Wilk test in each band and region (inter- and intrahemispheric). Repeated measures analyses of variance (ANOVA) with condition (phasic, tonic) and bands (\u03b8, \u03b1, \u03b2, \u03b3) as within-subject factors were performed for interhemispheric and intrahemispheric synchronization, separately. The Mauchly\u2019s test was used to verify the assumption of sphericity, and the Greenhouse\u2013Geiser correction on p<\/em>-values was applied if necessary. Additionally, paired sample t tests were performed to compare bandwise WPLI between phasic and tonic conditions. To address the issue of multiple comparisons, we applied the Benjamini\u2013Hochberg procedure to estimate false discovery rate [66], and we report corrected p<\/em>-values throughout the text. In order to examine whether phasic or tonic differences in \u03b1-band synchrony were specific for long-range synchronization, we performed two post hoc analyses. We calculated a grand average WPLI including all channel combinations (yielding 171 pairs of the 19 channels) and an average WPLI based only on short-range (adjacent) electrode combinations (yielding 26 channel pair combinations; e.g. Fp1-F7, F3-C3, C3-P3, F3-F7, T3-T5, T5-P3). The above statistical tests (ANOVAs and t tests) were performed similarly on these outcome measures. Binwise data of phasic or tonic REM and resting wakefulness were compared by bootstrap tests (permutation test). This approach is suitable to analyze sleep EEG data since it makes no assumptions of the distribution of the data [67\u201369]. Bootstrap tests in case of each frequency bin (from 4 to 46 Hz) and region (inter- and intrahemispheric WPLI) were based on 10000 random samples derived from the original pool of data (bootstrap distribution). Previous studies showed that such nonparametric tests are efficient in handling false alarm rate [70].<\/p>\n

 <\/p>\n

Results<\/strong><\/p>\n

\u00a0<\/strong>Long-range synchronization<\/strong><\/p>\n

\u00a0<\/strong>Inter- and intrahemispheric WPLI values of all frequency bands did not deviate from normal distribution as verified by Shapiro\u2013Wilk tests (all p<\/em> > 0.2). In case of interhemispheric synchronization, the main effect of condition showed a trend (F<\/em>1,18<\/sub> = 4.35, p<\/em> = 0.05, \u03b72<\/sup>= 0.19), and the effect of bands was not significant (F<\/em>3,54<\/sub> = 1.72, p<\/em> = 0.17), but a significant interaction between condition and bands emerged explaining 13% of the variance in WPLI values (F<\/em>3,54<\/sub> = 2.85, p<\/em> = 0.04, \u03b72<\/sup>= 0.13). As shown in Figure 2, post hoc comparisons between phasic and tonic conditions indicated that WPLI in the \u03b1 range was significantly higher in tonic in comparison to phasic periods (t<\/em>18<\/sub> = \u22122.8, p<\/em> < 0.05). Differences in other frequency bands were not significant (all p<\/em> > 0.05). Nevertheless, there was one outlier within the tonic \u03b2 band based on the interquartile range rule with a multiplier of 2.2 [71]; therefore, we repeated the above analyses excluding the outlier. The exclusion of the outlier did not change our results, except for the \u03b2 band, that showed a significant difference between phasic and tonic conditions (t<\/em>17<\/sub> = \u22122.72, p<\/em> = 0.04, d<\/em> = 0.64). Statistical parameters of paired comparisons (including the outlier) are summarized in Table 1.<\/p>\n

Table 1.<\/strong><\/em><\/p>\n

Paired sample t tests (n = 19) contrasting bandwise long-range interhemispheric and long-range intrahemispheric WPLI in phasic and tonic REM sleep<\/em><\/p>\n

Table1<\/a><\/p>\n

\u2020<\/sup>Long-range interhemispheric WPLI within the \u03b2 range was significantly higher in tonic vs. phasic REM after the exclusion of one outlier (see Long-range synchronization).<\/em><\/p>\n


\nFigure 2.<\/em><\/strong><\/p>\n

\"\"<\/a><\/p>\n

Long-range interhemispheric and intrahemispheric WPLI in phasic and tonic REM periods in different frequency bands. Dots show individual data points, the vertical line within the boxes shows the medians, boxes represent the first and third quartiles, and whiskers indicate the interquartile range of 1.5. *Statistical parameters after the exclusion of the outlier.<\/em><\/p>\n

 <\/p>\n

Regarding intrahemispheric synchronization, the main effect of condition was significant explaining a large portion of the variance in the outcome measure (F<\/em>1,18<\/sub> = 19.8, p<\/em> < 0.001, \u03b72<\/sup>= 0.52). The effect of bands was not significant (F<\/em>3,54<\/sub> = 1.48, p<\/em> = 0.23), but the interaction between condition and bands yielded a significant effect (F<\/em>3,54<\/sub> = 5.35, p<\/em> = 0.003, \u03b72<\/sup>= 0.23). Post hoc comparisons showed that WPLI in the \u03b1- (t<\/em>18<\/sub> = \u22124.76, p<\/em> = 0.0006) and \u03b2- (t<\/em>18<\/sub> = \u22124.01, p<\/em> = 0.002) frequency bands were significantly different across phasic and tonic periods, both showing higher values in tonic in comparison to phasic REM sleep (see Figure 2 and Table 1). The exclusion of outliers (n<\/em> = 2) did not modify the results of the statistical tests.<\/p>\n

 <\/p>\n

WPLI in REM states compared with wakefulness<\/strong><\/p>\n

\u00a0<\/strong>In order to explore peak frequencies and frequency specific increases in long-range synchronization, we visualized WPLI in phasic and tonic REM states from 4 to 46 Hz. As shown in Figure 3, interhemispheric synchronization was relatively higher in tonic conditions, especially in frequencies pertaining to the high \u03b1 and \u03b2 ranges (12\u201316 and 28\u201331 Hz). In case of intrahemispheric synchronization, tonic REM showed relative increases in several frequency bins (5\u20136, 9\u201310, 13\u201316, and 25\u201331 Hz), except in those that belong to the \u03b3 range.<\/p>\n

Figure 3.<\/strong><\/em><\/p>\n

\"\"<\/a><\/p>\n

Inter- and intrahemispheric WPLI in phasic and tonic REM sleep between 4 and 46 Hz (1 Hz resolution). The line graph depicts the mean values of 19 participants in each frequency bin. Vertical lines indicate standard errors. Black horizontal lines correspond to bins that are significantly different (p < 0.05) between phasic and tonic conditions.<\/em><\/p>\n

To compare inter- and intrahemispheric synchronization during wakefulness with that of phasic and tonic REM states, we visualized binwise WPLI in these three vigilance states, based on the data of our subsample (n<\/em> = 12) in which wakeful resting state recordings were also available. Due to the large amount of muscle-related and technical artifacts that affected specifically high-frequency activity in recordings collected during the awake state, in this case, binwise WPLI was visualized only until 27 Hz (Figure 4). Wakefulness was characterized by increased inter- and intrahemispheric synchronization within the \u03b1 range, peaking around 10 Hz. Although WPLI in the \u03b1-frequency range was markedly increased in resting wakefulness, compared with REM sleep periods, tonic REM, particularly in case of intrahemispheric synchronization, exhibited an intermediate state between wakefulness and phasic REM sleep in this regard. Furthermore, long-range synchronization within the \u03b2 range exhibited overlapping values between wakefulness and tonic REM sleep, exceeding the values found in phasic REM (see Figure 4).<\/p>\n

Figure 4.<\/strong><\/em><\/p>\n

\"\"<\/a><\/p>\n

Inter- and intrahemispheric WPLI in phasic REM, tonic REM, and resting wakefulness, between 4 and 27 Hz (1 Hz resolution). The linegraph (smoothed for visualization) depicts the mean values of 12 participants in each frequency bin. Vertical lines indicate standard errors. Blue horizontal lines correspond to statistically significant differences between tonic REM and wakefulness. Red horizontal lines correspond to statistically significant differences between phasic REM and wakefulness.<\/em><\/p>\n

 <\/p>\n

Grand average and short-range WPLI<\/strong><\/p>\n

\u00a0<\/strong>To verify whether the above differences between phasic and tonic conditions in \u03b1 or \u03b2 synchronization were specific to long-range synchrony, we first computed a grand average of bandwise synchronization by averaging WPLI values of all channel combinations. The repeated measures ANOVA for this outcome measure yielded a significant main effect of band (F<\/em>3,54<\/sub> = 11.64, p<\/em> < 0.0001, \u03b72<\/sup>= 0.41) and a significant interaction between condition and band (F<\/em>3,54<\/sub> = 13.34, p<\/em> < 0.0001, \u03b72<\/sup>= 0.46), whereas the main effect of condition (F<\/em>1,18<\/sub> = 2.35, p<\/em> = 0.14) was not significant. Paired comparisons revealed significantly higher WPLI in phasic REM in case of the \u03b3 (t<\/em>18<\/sub> = 5.45, p<\/em> < 0.001, Cohens\u2019 d = 1.25) band, whereas increased synchronization was found in the \u03b2 range (t<\/em>18<\/sub> = \u22122.63, p<\/em> < 0.05, Cohens\u2019 d = 0.61) during the tonic state. Differences in the \u03b1 band were not significant (t<\/em>18<\/sub> = \u22121.58, p<\/em> > 0.1, Cohens\u2019 d = 0.36).<\/p>\n

As the grand average of WPLI including all channel pair combinations intermingles long- and short-range synchronization, we extracted bandwise short-range synchronization averaging WPLI values of only adjacent electrode pairs (e.g. F3-C3, C3-P3, F4-F8, P3-T5). In case of short-range WPLI, the main effect of condition (F<\/em>1,18<\/sub> = 18.71, p<\/em> < 0.001, \u03b72<\/sup>= 0.51), band (F<\/em>3,54<\/sub> = 12.16, p<\/em> < 0.0001, \u03b72<\/sup>= 0.4), and their interaction (F<\/em>3,54<\/sub> = 13.76, p<\/em> < 0.0001, \u03b72<\/sup>= 0.45) were significant. Paired t tests indicated relatively increased WPLI values in the phasic condition compared with the tonic state within the \u03b3 (t<\/em>18<\/sub> = 6.74, p<\/em> < 0.00001, Cohens\u2019 d = 1.54) band. In contrast to long-range synchrony, WPLI within the \u03b1- and \u03b2-frequency ranges did not differentiate phasic and tonic conditions (Figure 5<\/em><\/strong> and Supplementray Table S2<\/em><\/strong>).<\/p>\n

Figure 5.<\/strong><\/em><\/p>\n

\"\"<\/a><\/p>\n

Average WPLI of adjacent (short-range) electrode combinations in phasic and tonic REM periods in different frequency bands. Dots show individual data points, the vertical line within the boxes shows the medians, boxes represent the first and third quartiles, whiskers indicate the interquartile range of 1.5.<\/em><\/p>\n

 <\/p>\n

Topographical aspects<\/strong><\/p>\n

\u00a0<\/strong>In order to examine (on an exploratory level) the topographical aspects of EEG synchronization, we contrasted phasic and tonic WPLI values of each interhemispheric and intrahemispheric electrode pair. WPLI within the \u03b1 band showed consistently higher values in tonic REM in all electrode combinations, peaking at posterior interhemispheric pairs (P3-P4). WPLI within the \u03b2 band showed \u201ctonic peaks\u201d at left frontoparietal (F3-P3), right frontotemporal (F8-T6), and central interhemispheric derivations (C3-C4). Although the averages of inter- and intrahemispheric long-range synchronization in \u03b8 and \u03b3 ranges were not significant (see Long-range synchronization), frontoparietal \u03b8 and \u03b3 synchronization (in two electrode pairs: F4-P4, Fz-Pz) showed clear peaks in phasic REM. Long-range synchronization in different frequency bands and electrode pairs is visualized in Supplementary Figure S1.<\/em><\/strong><\/p>\n

Additionally, we analyzed average WPLI values in anterior, central, and posterior regions, by computing the mean WPLI score of all possible electrode combinations of these regions. In case of the anterior region, the main effects of condition (F<\/em>1,18<\/sub> = 7.20, p<\/em> = 0.02, \u03b72<\/sup>= 0.23) and band (F<\/em>3,54<\/sub> = 12.18, p<\/em> < 0.0001, \u03b72<\/sup>= 0.29) were significant, as well as the interaction between condition and band (F<\/em>3,54<\/sub> = 24.96, p<\/em> < 0.0001, \u03b72<\/sup>= 0.6). Post hoc comparisons showed increased \u03b3 synchronization (t<\/em>18<\/sub> = 5.3, p<\/em> < 0.0005, Cohens\u2019 d = 1.23) in phasic, and a trend of higher \u03b1 synchronization (t<\/em>18<\/sub> = \u22122.48, p<\/em> = 0.08, Cohens\u2019 d = 0.54) in tonic REM. In central channel pairs, only the effect of band (F<\/em>3,54<\/sub> = 17.38, p<\/em> < 0.0001, \u03b72<\/sup>= 0.48) was significant, but condition (F<\/em>1,18<\/sub> = 0.08, p<\/em> = 0.78) and condition \u00d7 band (F<\/em>1,18<\/sub> = 1.63, p<\/em> = 019) were not significant factors of the model. Accordingly, no significant differences between phasic and tonic states emerged in any frequency band (Supplementary Table S3<\/em><\/strong>). Similarly, in case of posterior channel pairs, only the main effect of band was significant (F<\/em>3,54<\/sub> = 19.38, p<\/em> < 0.0001, \u03b72<\/sup>= 0.5248), whereas no significant effect of condition (F<\/em>1,18<\/sub> = 0.05, p<\/em> = 0.82) or of condition \u00d7 band (F<\/em>1,18<\/sub> = 2.35, p<\/em> = 0.08) emerged. The only band differentiating phasic and tonic conditions was \u03b3 showing a trend (t<\/em>18<\/sub> = 2.62, p<\/em> = 0.08, Cohens\u2019 d = 0.6) of higher synchronization in phasic REM (Supplementary Table S3<\/em><\/strong>).<\/p>\n

 <\/p>\n

Discussion<\/strong><\/p>\n

\u00a0<\/strong>In this study, we examined frequency-specific cortical synchronization in phasic and tonic REM sleep. Our analyses indicate that inter- and intrahemispheric \u03b1 and \u03b2 synchrony as quantified by the WPLI is enhanced in tonic REM states in contrast to phasic ones. In case of short-range synchronization, however, WPLI in the \u03b3-frequency range is higher in phasic compared with tonic periods.<\/p>\n

Our findings complement and extend earlier studies that emphasized the differences between these two microstates in terms of alertness [5], environmental processing [16], neuronal network activity [17] and mental experiences [11]. Phasic and tonic REM sleep shows marked differences in EEG spectral power: \u03b1 and \u03b2 oscillations are increased during the tonic state, whereas \u03b3 power is relatively enhanced during the phasic state [20\u201323]. Beyond local EEG power, phase synchronization between distant electrode sites reflects functional coupling and integration between cortical regions [33, 34, 72]. Accordingly, frequency-specific phase synchronization between distant cortical regions clearly distinguished different states of vigilance, including non-REM (NREM) sleep, REM sleep, and wakefulness [67, 73, 74].<\/p>\n

Here, we extended this line of inquiry to examine cortical synchronization between phasic and tonic REM sleep, and focused on long-range \u03b1 synchronization as it has been linked to the frontoparietal network supporting alertness, attention, and top-down control [34, 38, 44, 75]. In line with our expectations, we found increased inter- and intrahemispheric long-range \u03b1 synchronization during tonic in contrast to phasic REM sleep. Additionally, relatively increased synchronization was evidenced within the tonic state in faster frequencies comprising the \u03b2 range. Our analyses indicated that these differences were specific to long-range synchrony, as short-range synchronization in the \u03b1 and \u03b2 ranges was not significantly different across phasic and tonic conditions.<\/p>\n

Long-range inter- and intrahemispheric \u03b1 synchronization is a prominent feature of a variety of cognitive processes that characterize the awake state [44]; therefore, it is tempting to speculate that increased long-range \u03b1 synchronization found in the tonic state supports the assumption that tonic REM sleep resembles wakefulness. In fact, long-range WPLI values showed a prominent peak within the \u03b1 range during resting wakefulness, and intrahemispheric \u03b1 synchrony in tonic REM exhibited intermediate values between phasic REM and wakefulness. Our data corroborate the findings of two previous studies showing increased synchrony in the \u03b1 range during (eyes closed) wakefulness compared with REM sleep (although these studies applied phase coherence [59] and global field synchronization [67], as measures of synchronization). Although phasic REM periods are characterized by reduced long-range \u03b1 synchrony, our findings suggest that inter- and intrahemispheric \u03b1 synchronization is partially reinstated during tonic REM states. Long-range \u03b1 synchronization during tonic states might restore sensory awareness and responsiveness [34] after phasic periods in which the brain temporarily decouples from the external environment [17]. It is important to note that enhanced long-range synchronization in the tonic state was also found in the \u03b2 band. Although increased \u03b1 synchronization in tonic REM seemed to be a consistent pattern of all examined electrode pairs, higher \u03b2 band synchrony was evident among frontocentral interhemispheric, as well as frontoparietal, and frontotemporal intrahemispheric electrode pairs. This finding coheres with other studies indicating that frontoparietal network activity is not constrained to \u03b1 oscillations, but extends to the \u03b2 range [25, 40, 76, 77].<\/p>\n

Reduced inter- and intrahemispheric synchronization between distant cortical ensembles during phasic REM sleep might be related to attenuated environmental processing as reflected by increased awakening threshold and attenuated cortical reactivity in response to external stimulation [5, 16, 17]. On the other hand, enduring external stimulation seems to suppress phasic REM sleep and triggers tonic REM, presumably due to the reengagement of frontoparietal attentional networks [17, 18]. Reduced long-range synchrony during phasic REM is also in line with clinical data indicating that phasic REM periods have a suppressing effect on interictal epileptiform discharges [41, 78], as epileptic activity seems to be facilitated by wide-spread neuronal synchronization [79].<\/p>\n

Although long-range \u03b1 or \u03b2 synchrony decreased, \u03b3 synchronization between the adjacent electrode sites was relatively enhanced during phasic REM periods. Oscillations in the \u03b3 range were consistently reported in phasic REM sleep [21, 30, 80]. Our findings complement these data and suggest that these oscillations may arise from local instead of wide-spread cortical regions. Although we can only speculate about the underlying mechanism of such oscillations, we might assume that these are driven by cholinergic and glutamatergic activity linked to PGO waves. First of all, cholinergic and glutamatergic projections have a crucial role in the generation of phasic REM sleep [81\u201384]. Moreover, a large amount of data indicate that ascending cholinergic and glutamatergic activity facilitates \u03b3 oscillations in the neocortex during wakefulness and REM sleep [85\u201389]. Increased \u03b3 synchronization during phasic periods was prominent between anterior electrode pairs. Nevertheless, given the lack of similar findings, further studies should corroborate whether phasic \u03b3 synchronization is specifically enhanced in frontal regions.<\/p>\n

Increased short-range \u03b3 synchrony might reflect intense limbic and sensorimotor activity during phasic REM sleep leading to highly emotional and perceptually vivid dream experiences [11, 32, 90]. On the other hand, synchronization of cortical ensembles within the \u03b3 bands might be related to mechanisms facilitating neural plasticity and memory-consolidation [91] that might also influence mental activity during sleep. Nevertheless, information-processing and mental activity during phasic REM sleep in relation to frequency-specific synchronization is far from being understood and needs to be addressed in future studies.<\/p>\n

Interestingly, in case of long-range synchrony, the main effect of frequency band was not significant, indicating the lack of a frequency gradient in synchronization when REM microstates were treated as a whole. This finding is apparently at odds with a previous study indicating clear peaks in synchronization during REM as measured by global field synchrony [67], but resembles the finding of another study showing no evident peaks in coherence during REM sleep after Laplacian transformation [59]. Given the paucity of previous studies in this regard, as well as the differences in the applied methodologies, it is not easy to explain the lack of differences between frequency bands. Nevertheless, it seems plausible that frequency-specific peaks in long-range synchronization do not overlap in phasic and tonic conditions (as it was apparent in the binwise analysis (Figure 3), and hence, the main effects of frequency bands were masked due to these differences. In sharp contrast to long-range synchronization, a pronounced main effect of frequency band did emerge in case of short-range synchrony. We might assume that local cortical activity (and hence, frequency-specific variations in amplitude) might contribute to increased synchronization between electrode sites that are close to each other. Moreover, we should note that measures of synchronization between adjacent electrodes are less immune to the effects of field spread even when these are mitigated by Laplacian transformation and by discarding zero phase lags [92]. This might explain why our measures of short-range synchronization resemble more the frequency gradient of spectral power measures [21].<\/p>\n

We showed that frequency-specific coherent activity among local and distant neural ensembles differentiates phasic from tonic REM periods and provides further evidence on the heterogeneity of REM sleep. We applied a measure of synchronization that is independent of the fluctuations of spectral power [62] and showed that beyond the differences in spectral power [20\u201322], different frequencies show different topographical patterns of synchronization during tonic and phasic REM periods.<\/p>\n

Among the limitations of our work, we should note that our analyses are based on a relatively low number of electrode combinations. Therefore, our findings, especially the topographical aspects, should be corroborated by future studies that apply high density EEG or intracerebral recordings allowing for a more precise analyses of long- and short-range synchronization. Furthermore, we should emphasize that the assumption of partially reinstated alertness during tonic REM periods is still speculative and needs to be examined in further experiments that involve direct measurements of attentional processes during tonic and phasic REM periods. Accordingly, the functional significance of the alternation between phasic and tonic microstates within REM sleep remains unanswered. Interestingly, in contrast to REM sleep, the heterogeneity of NREM sleep regarding sleep stability and arousability is relatively well established [93]. These studies suggest that the dynamic structure of NREM sleep reflects two opposing, but at the same time complementary processes: an \u201coffline\u201d mode promoting the stability of sleep as well as internal memory processing and an \u201conline\u201d mode facilitating environmental alertness [93, 94]. The interchange of two microstates within REM sleep might reflect a similar process, alternating between phasic REM periods featured by intrinsic neuronal activity and reduced sensory processing [17], and tonic states characterized by reinstated environmental alertness.<\/p>\n

 <\/p>\n

Funding
\n\u00a0<\/strong>The project was supported by the \u00daNKP-17-4 New National Excellence Program of the Ministry of Human Capacities. P.S. was supported by the Hungarian Scientific Research Fund (NKFI PD 115432) of the National Research, Development and Innovation Office.<\/p>\n

 <\/p>\n

Notes<\/strong><\/p>\n

Conflicts of interest statement<\/em>. None declared.<\/p>\n

Work Performed: Department of Affective Psychology, E\u00f6tv\u00f6s Lor\u00e1nd University and Semmelweis University, Institute of Behavioural Sciences, Budapest, Hungary<\/p>\n

 <\/p>\n

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       <\/p>\n

      \u00a9 Sleep Research Society 2017. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com<\/a><\/p>\n

       <\/p>\n

      Supplementary figure<\/p>\n

      <\/strong>Figure S1. <\/strong>Long-range synchronization in different frequency bands and electrode pairs. The y-axis shows the ratio of the medians of phasic and tonic WPLI scores in the specific electrode pairs. Points below the horizontal dashed line indicate higher values in tonic, whereas points above the line indicate higher WPLI scores in the phasic state<\/em>
      \n<\/strong><\/p>\n

      \u00a0 \"\"<\/a><\/p>\n

      Supplementary material<\/a>
      \n(Table S1, Table S2, Table S3<\/em><\/strong>)<\/p>\n

       <\/p>\n","protected":false},"excerpt":{"rendered":"

      SLEEP 41: (3) (2018) DOI: 10.1093\/sleep\/zsx210<\/a> P\u00e9ter Simor1,2, Ferenc Gombos3, Borb\u00e1la Blaskovich4, R\u00f3bert B\u00f3dizs5,6 1Institute of Psychology, E\u00f6tv\u00f6s Lor\u00e1nd University, Hungary 2Ny\u00edr\u0151 Gyula Hospital, National Institute of Psychiatry and Addictions, Budapest, Hungary 3Department of General Psychology, P\u00e1zm\u00e1ny P\u00e9ter Catholic University, Budapest, Hungary 4Department of Cognitive Science, Budapest University of Technology and Economics, Budapest, Hungary 5Semmelweis University, …<\/p>\n","protected":false},"author":101277,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[6],"tags":[45,136,127,137,135],"class_list":["post-1020","post","type-post","status-publish","format-standard","hentry","category-articles-in-professional-journals","tag-eeg","tag-frontoparietal","tag-rem-sleep","tag-synchronization","tag-weighted-phase-lag-index"],"acf":[],"_links":{"self":[{"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/posts\/1020","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/users\/101277"}],"replies":[{"embeddable":true,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/comments?post=1020"}],"version-history":[{"count":10,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/posts\/1020\/revisions"}],"predecessor-version":[{"id":1581,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/posts\/1020\/revisions\/1581"}],"wp:attachment":[{"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/media?parent=1020"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/categories?post=1020"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/semmelweis.hu\/psychophysiology\/wp-json\/wp\/v2\/tags?post=1020"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}