Sleep Medicine Reviews
Volume 6, Issue 2 , Pages 139-149 , May 2002

The functional significance of K-complexes

References 

  1. Loomis AL, Harvey N, Hobart GA III. Distribution of disturbance patterns in the human electroencephalogram, with special reference to sleep. J Neurophysiol. 1938;1:413–430
  2. IFSECN . A glossary of terms most commonly used by clinical electroencephalographers. Electroencephalogr Clin Neurophysiol. 1974;37:538–548
  3. Roth M, Shaw J, Green J. The form, voltage distribution and physiological significance of the K-complex. Electroencephalogr Clin Neurophysiol. 1956;8:385–402
  4. Bremer G, Smith JR, Karacan I. Automatic detection of the K-complex in sleep electroencephalograms. IEEE Trans Biomed Eng. 1970;17:314–323
  5. Rosa AC, Kemp B, Paiva T, Lopes da Silva FH, Kamphuisen HAC. A model-based detector of vertex waves and K complexes in sleep electroencephalogram. Electroencephalogr Clin Neurophysiol. 1991;78:71–79
  6. Bankman IN, Sigillito VG, Wise RA, Smith PL. Feature-based detection of the K-complex wave in the human electroencephalogram using neural networks. IEEE Trans Biomed Eng. 1992;39:1305–1310
  7. Jobert M, Poiseau E, Jähnig P, Schulz H, Kubicki S. Pattern recognition by matched filtering: an analysis of sleep spindle and K-complex density under the influence of Lormetazepam and Zopiclone. Pharmacoencephalography. 1992;26:100–107
  8. Jansen BH, Desai PR. K-complex detection using multilayer perceptrons and recurrent networks. Int J Biomed Comput. 1994;37:249–257
  9. Amzica F, Steriade M. The K-complex: its slow (<1-Hz) rhythmicity and relation to delta waves. Neurology. 1997;49:952–959
  10. Amzica F, Steriade M. Cellular substrates and laminar profile of sleep K-complex. Neuroscience. 1998;82:671–686
  11. Steriade M, Nuñez A, Amzica F. A novel slow (<1 Hz) oscillation of neocortical neurons in vivo: depolarizing and hyperpolarizing components. J Neurosci. 1993;13:3252–3265
  12. Steriade M, Amzica F, Contreras D. Synchronization of fast (30–40 Hz) spontaneous cortical rhythms during brain activation. J Neurosci. 1996;16:392–417
  13. Achermann P, Borbély AA. Low-frequency (<1 Hz) oscillations in the human sleep EEG. Neuroscience. 1997;81:213–222
  14. Simon NR, Manshanden I, Lopes da Silva FH. A MEG study of sleep. Brain Res. 2000;860:64–76
  15. Amzica F, Steriade M. Short- and long-range neuronal synchronization of the slow (<1 Hz) cortical oscillation. J Neurophysiol. 1995;75:20–38
  16. Contreras D, Steriade M. Cellular basis of EEG slow rhythms: a study of dynamic corticothalamic relationships. J Neurosci. 1995;15:604–622
  17. Massimini M, Amzica F. Extracellular calcium fluctuations and intracellular potentials in the cortex during the slow sleep oscillation. J Neurophysiol. 2001;85:1346–1350
  18. Contreras D, Timofeev I, Steriade M. Mechanisms of long-lasting hyperpolarizations underlying slow sleep oscillations in cat corticothalamic networks. J Physiol (Lond). 1996;494:251–264
  19. Niedermeyer E. Sleep and EEG. In: Niedermeyer E, Lopes da Silva FH (eds) Electroencephalography. Basic Principles, Clinical Applications, and Related Fields. Baltimore, MD: Williams & Wilkins. 1999;174–188
  20. Steriade M, Oakson G, Ropert N. Firing rates and patterns of midbrain reticular neurons during steady and transitional states of the sleep–waking cycle. Exp Brain Res. 1982;46:37–51
  21. Steriade M, Datta S, Oakson G, Curró Dossi R. Neuronal activities in brain-stem cholinergic nuclei related to tonic activation processes in thalamocortical systems. J Neurosci. 1990;10:2541–2559
  22. Hirsch JC, Fourment A, Marc ME. Sleep-related variations of membrane potential in the lateral geniculate body relay neurons of the cat. Brain Res. 1983;259:308–312
  23. Steriade M, Contreras D, Curró Dossi R, Nuñez A. The slow (<1 Hz) oscillation in reticular thalamic and thalamocortical neurons: scenario of sleep rhythm generation in interacting thalamic and neocortical networks. J Neurosci. 1993;13:3284–3299
  24. Steriade M, Nuñez A, Amzica F. Intracellular analysis of relations between the slow (<1 Hz) neocortical oscillation and other sleep rhythms of the electroencephalogram. J Neurosci. 1993;13:3266–3283
  25. Sanchez-Vives MV, McCormick DA. Cellular and network mechanisms of rhythmic recurrent activity in neocortex. Nat Neurosci. 2000;3:1027–1034
  26. Timofeev I, Steriade M. Low-frequency rhythms in the thalamus of intact-cortex and decorticated cats. J Neurophysiol. 1996;76:4152–4168
  27. Davis H, Davis PA, Loomis AL, Harvey N, Hobart G. Electrical reactions of the human brain to auditory stimulation during sleep. J Neurophysiol. 1939;6:500–514
  28. Amzica F, Steriade M. Disconnection of intracortical synaptic linkages disrupts synchronization of a slow oscillation. J Neurosci. 1995;15:4658–4677
  29. Steriade M, McCarley RW. Brainstem Control of Wakefulness and Sleep. New York: Plenum. 1990;
  30. Morison RS, Bassett DL. Electrical activity of the thalamus and basal ganglia in decorticated cats. J Neurophysiol. 1945;8:309–314
  31. Steriade M, Deschênes M, Domich L, Mulle C. Abolition of spindle oscillations in thalamic neurons disconnected from nucleus reticularis thalami. J Neurophysiol. 1985;54:1473–1497
  32. Steriade M, Domich L, Oakson G, Deschênes M. The deafferented reticularis thalami nucleus generates spindle rhythmicity. J Neurophysiol. 1987;57:260–273
  33. Contreras D, Destexhe A, Sejnowski TJ, Steriade M. Control of spatiotemporal coherence of a thalamic oscillation by corticothalamic feedback. Science. 1996;274:771–774
  34. McCormick DA, Pape HC. Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillations in thalamic relay neurones. J Physiol (Lond). 1990;431:291–318
  35. Leresche N, Lightowler S, Soltesz I, Jassik-Gerschenfeld D, Crunelli V. Low-frequency oscillatory activities intrinsic to rat and cat thalamocortical cells. J Physiol (Lond). 1991;441:155–174
  36. Steriade M, Curró Dossi R, Nuñez A. Network modulation of a slow intrinsic oscillation of cat thalamocortical neurons implicated in sleep delta waves: cortically-induced synchronization and brainstem cholinergic suppression. J Neurosci. 1991;11:3200–3217
  37. Jones EG. The Thalamus. New York: Plenum. 1985;
  38. Amzica F, Steriade M. Electrophysiological correlates of sleep delta waves. Electroencephalogr Clin Neurophysiol. 1998;107:69–83
  39. Villablanca J, Salinas-Zeballos ME. Sleep-wakefulness, EEG and behavioral studies of chronic cats without the thalamus: the «athalamic» cat. Arch Ital e Biol. 1972;110:383–411
  40. Jahnsen H, Llinás RR. Electrophysiological properties of guinea-pig thalamic neurons: an in vitro study. J Physiol (Lond). 1984;349:205–226
  41. Steriade M, Llinás R. The functional states of the thalamus and the associated neuronal interplay. Physiol Rev. 1988;68:649–742
  42. Niiyama Y, Satoh N, Kutsuzawa O, Hishikawa Y. Electrophysiological evidence suggesting that sensory stimuli of unknown origin induce spontaneous K-complexes. Electroencephalogr Clin Neurophysiol. 1996;98:394–400
  43. Halasz P. Hierarchy of micro-arousals and the microstructure of sleep. Neurophysiol Clin. 1998;28:461–475
  44. Steriade M, Amzica F, Nuñez A. Cholinergic and noradrenergic modulation of the slow (0.3 Hz) oscillation in neocortical cells. J Neurophysiol. 1993;70:1384–1400
  45. Steriade M, Amzica F, Contreras D. Synchronization of fast (30–40 Hz) spontaneous cortical rhythms during brain activation. J Neurosci. 1996;16:392–417
  46. Moruzzi G, Magoun HW. Brain stem reticular formation and activation of the EEG. Electroencephalogr Clin Neurophysiol. 1949;1:445–473
  47. Sato S, Dreifuss FE, Penry JK. The effect of sleep on spike-wave discharges in absence seizures. Neurology. 1973;23:1335–1345
  48. Steriade M, Amzica F. Dynamic coupling among neocortical neurons during evoked and spontaneous spike-wave seizure activity. J Neurophysiol. 1994;72:2051–2069
  49. Steriade M, Contreras D. Relations between cortical and thalamic cellular events during transition from sleep patterns to paroxysmal activity. J Neurosci. 1995;15:623–642
  50. Steriade M, Amzica F, Neckelmann D, Timofeev I. Spike-wave complexes and fast components of cortically generated seizures. II. Extra- and intracellular patterns. J Neurophysiol. 1998;80:1456–1479
  51. Matsumoto H, Ajmone-Marsan C. Cortical cellular phenomena in experimental epilepsy: ictal manifestations. Exp Neurol. 1964;9:305–326
  52. Ayala GF, Dichter M, Gumnit RJ, Matsumoto H, Spencer WA. Genesis of epileptic interictal spikes. New knowledge of cortical feedback systems suggests a neurophysiological explanation of brief paroxysms. Brain Res. 1973;52:1–17
  53. Johnston D, Brown TH. Giant synaptic potential hypothesis for epileptiform activity. Science. 1981;21:294–297

PII: S1087-0792(01)90181-9

doi: 10.1053/smrv.2001.0181

Sleep Medicine Reviews
Volume 6, Issue 2 , Pages 139-149 , May 2002