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Behavioral/Systems/Cognitive

Sleep-Dependent θ Oscillations in the Human Hippocampus and Neocortex

Jose L. Cantero, Mercedes Atienza, Robert Stickgold, Michael J. Kahana, Joseph R. Madsen and Bernat Kocsis
Journal of Neuroscience 26 November 2003, 23 (34) 10897-10903; DOI: https://doi.org/10.1523/JNEUROSCI.23-34-10897.2003
Jose L. Cantero
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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Mercedes Atienza
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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Robert Stickgold
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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Michael J. Kahana
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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Joseph R. Madsen
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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Bernat Kocsis
1Laboratory of Neurophysiology, Department of Psychiatry, Massachusetts Mental Health Center, Harvard Medical School, Boston, Massachusetts 02115, 2Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts 02454, and 3Department of Neurosurgery, Children's Hospital, and Department of Surgery, Harvard Medical School, Boston, Massachusetts 02115
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    Figure 1.

    A, High-speed computed tomography view of the bilateral localization of multicontact depth electrodes in one of the participants. Aligned white dots correspond with the positions of the electrodes. B, Locations of recordings sites across all nine participants. These topographic maps show electrode locations on four views of a standard brain. Top left, Right lateral view. Top right, Left lateral view. Bottom left, Inferior view. Bottom right, Mid-axial-hippocampal view. Different shapes denote locations in different participants. Color-filled shapes indicate electrodes showed state-dependent θ oscillations. Note that some similar depth electrodes (bottom right, blue) showed θ oscillations during both REM and arousals from sleep.

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    Figure 2.

    Human θ oscillations generated in the hippocampal formation during awakenings from natural sleep and during REM sleep in bursts. A, Examples of unfiltered EEG traces containing hippocampal θ oscillations associated with awakenings and REM bursts in one patient. Talairach coordinates (L-R, A-P, I-S) (in mm): (24.0, -26.9, -7.2). Identical findings were observed in the remaining two patients (Talairach coordinates: 24.0, -32.3, 1.1; and 24.0, -32.1, -0.8). The same electrodes exhibited maximal θ power during awakenings and REM θ. B, Spectra obtained from the EEG segments shown in A (thin lines) and from averaging all θ segments (thick lines) in the same hippocampal electrode for that patient. Mean frequencies are shown for averaged segments.

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    Figure 3.

    Comparison of θ-burst activity in REM sleep and SWS. A, Representative pattern of θ power within the human hippocampus across 30 min of REM and SWS in a patient with hippocampal-depth electrodes as determined by the discrete-Fourier transform algorithms. The horizontal dashed line indicates the spectral power threshold used to quantify the number of θ bursts in each brain state. The threshold was computed using the averaged peak of θ power per minute during the entire period of each cerebral state. Talairach coordinates (L-R, A-P, I-S) (in mm): (24.0, -32.1, -0.8). B, Enlarged view of 1 min (indicated by the short, thick, black line under both plots in A) of θ power across time during REM and SWS, emphasizing the presence of short θ bursts selectively during REM sleep. C, Histogram of REM-θ burst durations computed for the same patient and recording site. Results similar to those shown in A-C were obtained in the other two patients with hippocampal recordings as well.

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    Figure 4.

    Human θ oscillations in different regions of the neocortex during quiet wakefulness. A, Approximate location of the electrodes that showed the maximum amplitude of θ activity in five of eight patients with neocortical recordings (each symbol denotes a different patient). Talairach coordinates (L-R, A-P, I-S) (in mm): •, 14.8, 13.3, 41.2; ♦, -20.2, 47.7, 8.9; ▴, -29.0, 0.4, -27.4; ✚, -60.5, -26.9, -11.4; and ★, -44.1, -44.8, -15.7). B, Unfiltered EEG recordings from locations indicated in A. Note that each EEG trace belongs to a different patient and is highly representative of the pattern of electrophysiological activity observed during quiet wakefulness in each individual patient. For each patient, most of the electrodes placed within the same cortical region showed the same pattern of θ oscillations during quiet wakefulness. C, Spectral power density computed for a representative electrode in each neocortical region involved in θ generation during quiet wakefulness. Thick lines, Averaged spectra for all θ epochs; thin lines, spectra for single epochs shown in B. Peak frequencies are for averaged spectra.

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    Figure 5.

    Evidence of different θ generator sources within the human hippocampal formation and neocortex. A, Averaged partial coherence results between pairs of electrodes for each wake-sleep state after removing common influences from other sources. Electrode pairs were located within the hippocampal formation (hipp-hipp; coordinates: 24.0, -26.9, -7.2; and 24.0, -36.2, 3.1), the basal surface of the temporal lobe (ctx-ctx; coordinates: -29.0, 0.4, -27.4; and -43.8, -38.3, -14.6), or had one electrode in each structure (hipp-ctx; coordinates: 24.0, -26.9, -7.2; and -29.0, 0.4, -27.4). B, Comparison of averaged θ power (4-7 Hz) within hippocampus and neocortex for each wake-sleep state. Data are from the same subject as in A. C, Same as A, but for a different patient. Corticocortical coupling in this patient was determined using a pair of electrodes located in the frontal lobe. Talairach coordinates (in mm): hipp-hipp, 24.0, -32.1, -0.8, and 24.0, -15.7, -12.1; ctx-ctx, 14.8, 13.3, 41.2, and 25.0, 21.9, 31.2; hipp-ctx, 24.0, -32.1, -0.8, and 14.8, 13.3, 41.2. D, Same as B, but for the patient shown in C. Results for both partial coherence and spectral analysis were essentially unchanged when other combinations of electrodes were used in each patient.

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    Figure 6.

    Absence of phase relationship between θ cycle and γ amplitude in human hippocampus. Averaged peak of γ amplitude (bottom, thick line) showed an inconsistent relationship with the θ cycle (top) as revealed by the high variability observed in γ peak (±SD values represented by thin lines). θ cycle (top) was obtained after averaging all θ cycles contained in REM-θ bursts recorded in three patients with hippocampal implants.

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    Table 1.

    Summary of demographic and clinical information for each patient

    Patient Gender Age (years) Seizure type MRI findings Implant type Medication Surgical procedure
    1 M 15 Left temporal lobe focus None Subdural plus depth Antibiotics, anticonvulsives, analgesics Left lateral temporal lobe and left mesial temporal lobe resections
    2 M 14 Right frontal and temporal lobe focus Chiari-I malformation Subdural Analgesics, anticonvulsives Anterior right temporal and right frontal resecctions
    3 M 19 Left temporal lobe focus Right choroidal cyst, cerebellar tonsils below foramen magnum Subdural Analgesics, anticonvulsives Left inferior temporal lobe resection
    4 M 15 Left mesial temporal lobe focus None Depth Analgesics, anticonvulsives, antibiotics Small resections of left lateral temporal lobe, hippocampus, and amygdala
    5 M 19 Left occipital focus Left temporoparietal lesions Subdural plus depth Analgesics, anticonvulsives Left occipital resection and multiple subpial transectiopns through parieto-occipital regions
    6 M 10 Right parietotemporal focus None Subdural Analgesics, anticonvulsives Left temporal lobectomy and left mesial hippocampectomy
    7 M 19 Left parieto-occipital focus Dysplasia in the left posterior frontal lobe Subdural Analgesics, anticonvulsives Left parieto-occipital resection
    8 M 11 Left frontal focus None Subdural Analgesics, anticonvulsives Left frontotemporal and anterior frontal resections
    9 M 11 Left temporal lobe focus None Subdural Analgesics, anticonvulsives Left anterior temporal resection
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The Journal of Neuroscience: 23 (34)
Journal of Neuroscience
Vol. 23, Issue 34
26 Nov 2003
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Sleep-Dependent θ Oscillations in the Human Hippocampus and Neocortex
Jose L. Cantero, Mercedes Atienza, Robert Stickgold, Michael J. Kahana, Joseph R. Madsen, Bernat Kocsis
Journal of Neuroscience 26 November 2003, 23 (34) 10897-10903; DOI: 10.1523/JNEUROSCI.23-34-10897.2003

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Sleep-Dependent θ Oscillations in the Human Hippocampus and Neocortex
Jose L. Cantero, Mercedes Atienza, Robert Stickgold, Michael J. Kahana, Joseph R. Madsen, Bernat Kocsis
Journal of Neuroscience 26 November 2003, 23 (34) 10897-10903; DOI: 10.1523/JNEUROSCI.23-34-10897.2003
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Keywords

  • θ oscillations
  • hippocampus
  • cerebral cortex
  • sleep
  • intracranial recordings
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