Update on the mechanisms and roles of high-frequency oscillations in seizures and epileptic disorders

. 2017 Aug ; 58 (8) : 1330-1339. [epub] 20170706

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, přehledy, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid28681378

Grantová podpora
8109 CIHR - Canada
R01 NS095368 NINDS NIH HHS - United States
R01 NS094399 NINDS NIH HHS - United States
R01 NS084142 NINDS NIH HHS - United States
74609 CIHR - Canada

High-frequency oscillations (HFOs) are a type of brain activity that is recorded from brain regions capable of generating seizures. Because of the close association of HFOs with epileptogenic tissue and ictogenesis, understanding their cellular and network mechanisms could provide valuable information about the organization of epileptogenic networks and how seizures emerge from the abnormal activity of these networks. In this review, we summarize the most recent advances in the field of HFOs and provide a critical evaluation of new observations within the context of already established knowledge. Recent improvements in recording technology and the introduction of optogenetics into epilepsy research have intensified experimental work on HFOs. Using advanced computer models, new cellular substrates of epileptic HFOs were identified and the role of specific neuronal subtypes in HFO genesis was determined. Traditionally, the pathogenesis of HFOs was explored mainly in patients with temporal lobe epilepsy and in animal models mimicking this condition. HFOs have also been reported to occur in other epileptic disorders and models such as neocortical epilepsy, genetically determined epilepsies, and infantile spasms, which further support the significance of HFOs in the pathophysiology of epilepsy. It is increasingly recognized that HFOs are generated by multiple mechanisms at both the cellular and network levels. Future studies on HFOs combining novel high-resolution in vivo imaging techniques and precise control of neuronal behavior using optogenetics or chemogenetics will provide evidence about the causal role of HFOs in seizures and epileptogenesis. Detailed understanding of the pathophysiology of HFOs will propel better HFO classification and increase their information yield for clinical and diagnostic purposes.

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Jefferys JG, Menendez de la PL, Wendling F, et al. Mechanisms of physiological and epileptic HFO generation. Prog Neurobiol. 2012;98:250–264. PubMed PMC

Zijlmans M, Jiruska P, Zelmann R, et al. High-frequency oscillations as a new biomarker in epilepsy. Ann Neurol. 2012;71:169–178. PubMed PMC

Bragin A, Mody I, Wilson CL, et al. Local generation of fast ripples in epileptic brain. J Neurosci. 2002;22:2012–2021. PubMed PMC

Buzsaki G. Hippocampal Sharp Wave-Ripple: A Cognitive Biomarker for Episodic Memory and Planning. Hippocampus. 2015;25:1073–1188. PubMed PMC

Buzsaki G, Horvath Z, Urioste R, et al. High-frequency network oscillation in the hippocampus. Science. 1992;256:1025–1027. PubMed

Ylinen A, Bragin A, Nadasdy Z, et al. Sharp Wave-Associated High-Frequency Oscillation (200-Hz) in the Intact Hippocampus - Network and Intracellular Mechanisms. J Neurosci. 1995;15:30–46. PubMed PMC

Bragin A, Engel J, Jr, Wilson CL, et al. Hippocampal and entorhinal cortex high-frequency oscillations (100--500 Hz) in human epileptic brain and in kainic acid--treated rats with chronic seizures. Epilepsia. 1999;40:127–137. PubMed

Engel J, Jr, Bragin A, Staba R, et al. High-frequency oscillations: what is normal and what is not? Epilepsia. 2009;50:598–604. PubMed

Bragin A, Benassi SK, Kheiri F, et al. Further evidence that pathologic high-frequency oscillations are bursts of population spikes derived from recordings of identified cells in dentate gyrus. Epilepsia. 2011;52:45–52. PubMed PMC

D’Antuono M, de GP, Kano T, et al. Ripple activity in the dentate gyrus of dishinibited hippocampus-entorhinal cortex slices. J Neurosci Res. 2005;80:92–103. PubMed

Traub RD, Contreras D, Cunningham MO, et al. Single-column thalamocortical network model exhibiting gamma oscillations, sleep spindles, and epileptogenic bursts. J Neurophys. 2005;93:2194–2232. PubMed

Demont-Guignard S, Benquet P, Gerber U, et al. Distinct hyperexcitability mechanisms underlie fast ripples and epileptic spikes. Ann Neurol. 2012;71:342–352. PubMed

Foffani G, Uzcategui YG, Gal B, et al. Reduced spike-timing reliability correlates with the emergence of fast ripples in the rat epileptic hippocampus. Neuron. 2007;55:930–941. PubMed

Ibarz JM, Foffani G, Cid E, et al. Emergent dynamics of fast ripples in the epileptic hippocampus. J Neurosci. 2010;30:16249–16261. PubMed PMC

Gliske SV, Stacey WC, Lim E, et al. Emergence of Narrowband High Frequency Oscillations from Asynchronous, Uncoupled Neural Firing. Int J Neural Systems. 2017:27. PubMed PMC

Draguhn A, Traub RD, Schmitz D, et al. Electrical coupling underlies high-frequency oscillations in the hippocampus in vitro. Nature. 1998;394:189–192. PubMed

Jefferys JG. Nonsynaptic modulation of neuronal activity in the brain: electric currents and extracellular ions. Physiol Rev. 1995;75:689–723. PubMed

Jiruska P, de Curtis M, Jefferys JG, et al. Synchronization and desynchronization in epilepsy: controversies and hypotheses. J Physiol. 2013;591:787–797. PubMed PMC

Bikson M, Fox JE, Jefferys JG. Neuronal aggregate formation underlies spatiotemporal dynamics of nonsynaptic seizure initiation. J Neurophys. 2003;89:2330–2333. PubMed

Jiruska P, Csicsvari J, Powell AD, et al. High-frequency network activity, global increase in neuronal activity, and synchrony expansion precede epileptic seizures in vitro. J Neurosci. 2010;30:5690–5701. PubMed PMC

Staba RJ, Frighetto L, Behnke EJ, et al. Increased fast ripple to ripple ratios correlate with reduced hippocampal volumes and neuron loss in temporal lobe epilepsy patients. Epilepsia. 2007;48:2130–2138. PubMed

Wendling F, Benquet P, Bartolomei F, et al. Computational models of epileptiform activity. J Neurosci Met. 2016;260:233–251. PubMed

Roopun AK, Simonotto JD, Pierce ML, et al. A nonsynaptic mechanism underlying interictal discharges in human epileptic neocortex. PNAS. 2010;107:338–343. PubMed PMC

Stacey WC, Lazarewicz MT, Litt B. Synaptic Noise and Physiological Coupling Generate High-Frequency Oscillations in a Hippocampal Computational Model. J Neurophys. 2009;102:2342–2357. PubMed PMC

Stacey WC, Krieger A, Litt B. Network recruitment to coherent oscillations in a hippocampal computer model. J Neurophys. 2011;105:1464–1481. PubMed PMC

Fink CG, Gliske S, Catoni N, et al. Network Mechanisms Generating Abnormal and Normal Hippocampal High-Frequency Oscillations: A Computational Analysis. eNeuro. 2015:2. PubMed PMC

Alvarado-Rojas C, Huberfeld G, Baulac M, et al. Different Mechanisms of Ripple-like Oscillations in the Human Epileptic Subiculum. Ann Neurol. 2015;77:281–290. PubMed PMC

Valero M, Cid E, Averkin RG, et al. Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples. Nat Neurosci. 2015;18:1281. PubMed PMC

Aivar P, Valero M, Bellistri E, et al. Extracellular Calcium Controls the Expression of Two Different Forms of Ripple-Like Hippocampal Oscillations. J Neurosci. 2014;34:2989–3004. PubMed PMC

Weiss SA, Lemesiou A, Connors R, et al. Seizure localization using ictal phase-locked high gamma A retrospective surgical outcome study. Neurology. 2015;84:2320–2328. PubMed PMC

Kucewicz MT, Cimbalnik J, Matsumoto JY, et al. High frequency oscillations are associated with cognitive processing in human recognition memory. Brain. 2014;137:2231–2244. PubMed PMC

Jacobs J, LeVan P, Chatillon CE, et al. High frequency oscillations in intracranial EEGs mark epileptogenicity rather than lesion type. Brain. 2009;132:1022–1037. PubMed PMC

Klausberger T, Somogyi P. Neuronal diversity and temporal dynamics: the unity of hippocampal circuit operations. Science. 2008;321:53–57. PubMed PMC

Fries P, Nikolic D, Singer W. The gamma cycle. Trends Neurosci. 2007;30:309–316. PubMed

Karlocai MR, Kohus Z, Kali S, et al. Physiological sharp wave-ripples and interictal events in vitro: what’s the difference? Brain. 2014;137:463–485. PubMed

Morris G, Jiruska P, Jefferys JG, et al. A New Approach of Modified Submerged Patch Clamp Recording Reveals Interneuronal Dynamics during Epileptiform Oscillations. Front Neurosci. 2016;10:519. PubMed PMC

Jiruska P, Finnerty GT, Powell AD, et al. Epileptic high-frequency network activity in a model of non-lesional temporal lobe epilepsy. Brain. 2010;133:1380–1390. PubMed PMC

Ferecsko AS, Jiruska P, Foss L, et al. Structural and functional substrates of tetanus toxin in an animal model of temporal lobe epilepsy. Brain Struct Funct. 2015;220:1013–1029. PubMed PMC

Bragin A, Azizyan A, Almajano J, et al. Analysis of chronic seizure onsets after intrahippocampal kainic acid injection in freely moving rats. Epilepsia. 2005;46:1592–1598. PubMed

Weiss SA, Alvarado-Rojas C, Bragin A, et al. Ictal onset patterns of local field potentials, high frequency oscillations, and unit activity in human mesial temporal lobe epilepsy. Epilepsia. 2016;57:111–121. PubMed PMC

Levesque M, Salami P, Gotman J, et al. Two seizure-onset types reveal specific patterns of high-frequency oscillations in a model of temporal lobe epilepsy. J Neurosci. 2012;32:13264–13272. PubMed PMC

Shiri Z, Manseau F, Levesque M, et al. Activation of Specific Neuronal Networks Leads to Different Seizure Onset Types. Ann Neurol. 2016;79:354–365. PubMed PMC

Perucca P, Dubeau F, Gotman J. Intracranial electroencephalographic seizure-onset patterns: effect of underlying pathology. Brain. 2014;137:183–196. PubMed

Spencer SS, Guimaraes P, Katz A, et al. Morphological Patterns of Seizures Recorded Intracranially. Epilepsia. 1992;33:537–545. PubMed

Gnatkovsky V, Librizzi L, Trombin F, et al. Fast Activity at Seizure Onset Is Mediated by Inhibitory Circuits in the Entorhinal Cortex In Vitro. Ann Neurol. 2008;64:674–686. PubMed

Shiri Z, Manseau F, Levesque M, et al. Interneuron Activity Leads to Initiation of Low-Voltage Fast-Onset Seizures. Ann Neurol. 2015;77:541–546. PubMed PMC

Yekhlef L, Breschi GL, Lagostena L, et al. Selective activation of parvalbumin- or somatostatin-expressing interneurons triggers epileptic seizurelike activity in mouse medial entorhinal cortex. J Neurophys. 2015;113:1616–1630. PubMed

Uva L, Breschi GL, Gnatkovsky V, et al. Synchronous Inhibitory Potentials Precede Seizure-Like Events in Acute Models of Focal Limbic Seizures. J Neurosci. 2015;35:3048–3055. PubMed PMC

Lopantsev V, Avoli M. Participation of GABA(A)-mediated inhibition in ictallike discharges in the rat entorhinal cortex. J Neurophys. 1998;79:352–360. PubMed

Memarian N, Madsen SK, Macey PM, et al. Ictal Depth EEG and MRI Structural Evidence for Two Different Epileptogenic Networks in Mesial Temporal Lobe Epilepsy. Plos One. 2015:10. PubMed PMC

Ogren JA, Bragin A, Wilson CL, et al. Three-dimensional hippocampal atrophy maps distinguish two common temporal lobe seizure-onset patterns. Epilepsia. 2009;50:1361–1370. PubMed PMC

Kohling R, D’Antuono M, Benini R, et al. Hypersynchronous ictal onset in the perirhinal cortex results from dynamic weakening in inhibition. Neurobiol Dis. 2016;87:1–10. PubMed PMC

Bragin A, Wilson CL, Engel J., Jr Chronic epileptogenesis requires development of a network of pathologically interconnected neuron clusters: a hypothesis. Epilepsia. 2000;41(Suppl 6):S144–S152. PubMed

Trevelyan AJ, Baldeweg T, van Drongelen W, et al. The source of afterdischarge activity in neocortical tonic-clonic epilepsy. J Neurosci. 2007;27:13513–13519. PubMed PMC

Trevelyan AJ, Sussillo D, Watson BO, et al. Modular propagation of epileptiform activity: evidence for an inhibitory veto in neocortex. J Neurosci. 2006;26:12447–12455. PubMed PMC

Schevon CA, Weiss SA, McKhann G, Jr, et al. Evidence of an inhibitory restraint of seizure activity in humans. Nat Commun. 2012;3:1060. PubMed PMC

Truccolo W, Donoghue JA, Hochberg LR, et al. Single-neuron dynamics in human focal epilepsy. Nat Neurosci. 2011;14:635–641. PubMed PMC

Weiss SA, Banks GP, McKhann GM, Jr, et al. Ictal high frequency oscillations distinguish two types of seizure territories in humans. Brain. 2013;136:3796–3808. PubMed PMC

Eissa TL, Tryba AK, Marcuccilli CJ, et al. Multiscale Aspects of Generation of High-Gamma Activity during Seizures in Human Neocortex. eNeuro. 2016:3. PubMed PMC

Kanazawa K, Matsumoto R, Imamura H, et al. Intracranially recorded ictal direct current shifts may precede high frequency oscillations in human epilepsy. Clin Neurophys. 2015;126:47–59. PubMed

Bragin A, Wilson CL, Almajano J, et al. High-frequency oscillations after status epilepticus: epileptogenesis and seizure genesis. Epilepsia. 2004;45:1017–1023. PubMed

Salami P, Levesque M, Benini R, et al. Dynamics of interictal spikes and high-frequency oscillations during epileptogenesis in temporal lobe epilepsy. Neurobiol Dis. 2014;67:97–106. PubMed PMC

Zijlmans M, Jacobs J, Zelmann R, et al. High-frequency oscillations mirror disease activity in patients with epilepsy. Neurology. 2009;72:979–986. PubMed PMC

Levesque M, Behr C, Avoli M. The anti-ictogenic effects of levetiracetam are mirrored by interictal spiking and high-frequency oscillation changes in a model of temporal lobe epilepsy. Seizure. 2015;25:18–25. PubMed PMC

Behr C, Levesque M, Ragsdale D, et al. Lacosamide modulates interictal spiking and high-frequency oscillations in a model of mesial temporal lobe epilepsy. Epilepsy Res. 2015;115:8–16. PubMed PMC

Bragin A, Engel J, Jr, Wilson CL, et al. Electrophysiologic analysis of a chronic seizure model after unilateral hippocampal KA injection. Epilepsia. 1999;40:1210–1221. PubMed

Bragin A, Engel J, Jr, Staba RJ. High-frequency oscillations in epileptic brain. Curr Opin Neurol. 2010;23:151–156. PubMed PMC

Jones RT, Barth AM, Ormiston LD, et al. Evolution of temporal and spectral dynamics of pathologic high-frequency oscillations (pHFOs) during epileptogenesis. Epilepsia. 2015;56:1879–1889. PubMed PMC

Levesque M, Bortel A, Gotman J, et al. High-frequency (80–500 Hz) oscillations and epileptogenesis in temporal lobe epilepsy. Neurobiology of Disease. 2011;42:231–241. PubMed PMC

O’Connor WT, Smyth A, Gilchrist MD. Animal models of traumatic brain injury: A critical evaluation. Pharmac Ther. 2011;130:106–113. PubMed

Pitkanen A, Immonen RJ, Grohn OHJ, et al. From traumatic brain injury to posttraumatic epilepsy: What animal models tell us about the process and treatment options. Epilepsia. 2009;50:21–29. PubMed

D’Ambrosio R, Fairbanks JP, Fender JS, et al. Post-traumatic epilepsy following fluid percussion injury in the rat. Brain. 2004;127:304–314. PubMed PMC

Kharatishvili I, Nissinen JP, McIntosh TK, et al. A model of posttraumatic epilepsy induced by lateral fluid-percussion brain injury in rats. Neuroscience. 2006;140:685–697. PubMed

Bragin A, Li L, Almajano J, et al. Pathologic electrographic changes after experimental traumatic brain injury. Epilepsia. 2016;57:735–745. PubMed PMC

Jefferys JGR, Jiruska P. The Tetanus Toxin Model of Temporal Lobe Epilepsy. Encyclopedia of Basic Epilepsy Research. 2009;1–3:804–807.

Wykes RC, Heeroma JH, Mantoan L, et al. Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy. Sci Transl Med. 2012;4:161ra152. PubMed PMC

Frost JD, Lee CL, Hrachovy RA, et al. High frequency EEG activity associated with ictal events in an animal model of infantile spasms. Epilepsia. 2011;52:53–62. PubMed PMC

Frost JD, Lee CL, Le JT, et al. Interictal high frequency oscillations in an animal model of infantile spasms. Neurobiol Dis. 2012;46:377–388. PubMed PMC

Kobayashi K, Akiyama T, Oka M, et al. A storm of fast (40–150Hz) oscillations during hypsarrhythmia in West syndrome. Ann Neurol. 2015;77:58–67. PubMed

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