全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Age-Dependent Increase of Absence Seizures and Intrinsic Frequency Dynamics of Sleep Spindles in Rats

DOI: 10.1155/2014/370764

Full-Text   Cite this paper   Add to My Lib

Abstract:

The risk of neurological diseases increases with age. In WAG/Rij rat model of absence epilepsy, the incidence of epileptic spike-wave discharges is known to be elevated with age. Considering close relationship between epileptic spike-wave discharges and physiologic sleep spindles, it was assumed that age-dependent increase of epileptic activity may affect time-frequency characteristics of sleep spindles. In order to examine this hypothesis, electroencephalograms (EEG) were recorded in WAG/Rij rats successively at the ages 5, 7, and 9 months. Spike-wave discharges and sleep spindles were detected in frontal EEG channel. Sleep spindles were identified automatically using wavelet-based algorithm. Instantaneous (localized in time) frequency of sleep spindles was determined using continuous wavelet transform of EEG signal, and intraspindle frequency dynamics were further examined. It was found that in 5-months-old rats epileptic activity has not fully developed (preclinical stage) and sleep spindles demonstrated an increase of instantaneous frequency from beginning to the end. At the age of 7 and 9 months, when animals developed matured and longer epileptic discharges (symptomatic stage), their sleep spindles did not display changes of intrinsic frequency. The present data suggest that age-dependent increase of epileptic activity in WAG/Rij rats affects intrinsic dynamics of sleep spindle frequency. 1. Introduction Sleep spindles are well-known EEG phenomena that reflect spontaneous rhythmic activity of thalamocortical neuronal network during non-REM sleep [1–3]. In vivo experiments demonstrated a close relationship between sleep spindles and epileptic spike-wave discharges (SWD) [4–6]. SWD are electroencephalographic (EEG) manifestation of absence epilepsy, and they are triggered by the cortex, opposite to sleep spindles, which are known to originate from the thalamus (reviewed in [7]). In comparison to sleep spindles, SWD are underlain by more intensive excitation and/or synchronization processes in thalamocortical network [7–9]. Previously we demonstrated that sleep spindles and SWD showed different time-frequency characteristics, as measured in the cortex and thalamus [10]. Intraspindle frequency is an important parameter characterizing intrinsic properties of thalamocortical network activity [11, 12] with respect to generation of autonomous oscillations. In healthy human subjects, the frequency of sleep spindles is known to vary from 10 to 16?Hz (e.g., [2, 12, 13]), and in animals (rats and cats) from 7 to 14?Hz [1, 14]. Recently we compared

References

[1]  M. Steriade, Neuronal Substrates of Sleep and Epilepsy, Cambridge University Press, Cambridge, Mass, USA, 2003.
[2]  L. de Gennaro and M. Ferrara, “Sleep spindles: an overview,” Sleep Medicine Reviews, vol. 7, no. 5, pp. 423–440, 2003.
[3]  A. Destexhe and T. J. Sejnowski, Thalamocortical Assemblies, Oxford University Press, Oxford, UK, 2001.
[4]  P. Gloor, “Generalized epilepsy with bilateral synchronous spike and wave discharge. New findings concerning its physiological mechanisms,” Electroencephalography and Clinical Neurophysiology, no. 34, pp. S245–S249, 1978.
[5]  E. L. J. M. van Luijtelaar, “Spike-wave discharges and sleep spindles in rats,” Acta Neurobiologiae Experimentalis, vol. 57, no. 2, pp. 113–121, 1997.
[6]  G. K. Kostopoulos, “Spike-and-wave discharges of absence seizures as a transformation of sleep spindles: the continuing development of a hypothesis,” Clinical Neurophysiology, vol. 111, supplement 2, pp. S27–S38, 2000.
[7]  N. Leresche, R. C. Lambert, A. C. Errington, and V. Crunelli, “From sleep spindles of natural sleep to spike and wave discharges of typical absence seizures: is the hypothesis still valid?” Pflugers Archiv European Journal of Physiology, vol. 463, no. 1, pp. 201–212, 2012.
[8]  E. Sitnikova, “Thalamo-cortical mechanisms of sleep spindles and spike-wave discharges in rat model of absence epilepsy (a review),” Epilepsy Research, vol. 89, no. 1, pp. 17–26, 2010.
[9]  A. Lüttjohann and G. van Luijtelaar, “The dynamics of cortico-thalamo-cortical interactions at the transition from pre-ictal to ictal LFPs in absence epilepsy,” Neurobiology of Disease, vol. 47, no. 1, pp. 49–60, 2012.
[10]  E. Sitnikova, A. E. Hramov, A. A. Koronovsky, and G. van Luijtelaar, “Sleep spindles and spike-wave discharges in EEG: their generic features, similarities and distinctions disclosed with Fourier transform and continuous wavelet analysis,” Journal of Neuroscience Methods, vol. 180, no. 2, pp. 304–316, 2009.
[11]  T. Andrillon, Y. Nir, R. J. Staba et al., “Sleep spindles in humans: insights from intracranial EEG and unit recordings,” Journal of Neuroscience, vol. 31, no. 49, pp. 17821–17834, 2011.
[12]  Y. Urakami, A. A. Ioannides, and G. K. Kostopoulos, “Sleep spindles—as a biomarker of brain function and plasticity,” in Advances in Clinical Neurophysiology, I . M. Ajeena, Ed., chapter 4, 2012.
[13]  C. Iber, S. Ancoli-Israel, A. Chesson, and S. F. Quan, The AASM Manual for the Scoring of Sleep and Associated Events: Rules, Terminology, and Technical Specification, American Academy of Sleep Medicine, Westchester, Ill, USA, 1st edition, 2007.
[14]  G. Gandolfo, L. Glin, and C. Gottesmann, “Study of sleep spindles in the rat: a new improvement,” Acta Neurobiologiae Experimentalis, vol. 45, no. 5-6, pp. 151–162, 1985.
[15]  E. Sitnikova, A. E. Hramov, V. V. Grubov, and A. A. Koronovsky, “Time-frequency characteristics and dynamics of sleep spindles in WAG/Rij rats with absence epilepsy,” Brain Research, vol. 1543, pp. 290–299, 2014.
[16]  E. I. Sitnikova, V. V. Grubov, A. E. Khramov, and A. A. Koronovskiǐ, “[Age-related changes in time-frequency structure of sleep spindles in EEG in rats with genetic predisposition to absence epilepsy (Wag/Rij)],” Zhurnal Vyssheǐ Nervnoǐ Deiatelnosti Imeni I P Pavlova, vol. 62, no. 6, pp. 733–744, 2012.
[17]  A. M. L. Coenen and E. L. J. M. van Luijtelaar, “Genetic animal models for absence epilepsy: a review of the WAG/Rij strain of rats,” Behavior Genetics, vol. 33, no. 6, pp. 635–655, 2003.
[18]  A. M. L. Coenen and E. L. J. M. van Luijtelaar, “The WAG/Rij rat model for absence epilepsy: age and sex factors,” Epilepsy Research, vol. 1, no. 5, pp. 297–301, 1987.
[19]  G. van Luijtelaar and A. Bikbaev, “Midfrequency cortico-thalamic oscillations and the sleep cycle: genetic, time of day and age effects,” Epilepsy Research, vol. 73, no. 3, pp. 259–265, 2007.
[20]  A. Ovchinnikov, A. Lüttjohann, A. Hramov, and G. van Luijtelaar, “An algorithm for real-time detection of spike-wave discharges in rodents,” Journal of Neuroscience Methods, vol. 194, no. 1, pp. 172–178, 2010.
[21]  E. I. Sitnikova, T. N. Egorova, and V. V. Raevskiǐ, “Reduction of the number of neurons in substantia nigra (Pars compacta) positively correlates with a reduction of seizure activity in WAG/Rij rats,” Zhurnal Vyssheǐ Nervnoǐ Deiatelnosti Imeni I P Pavlova, vol. 62, no. 5, pp. 619–628, 2012 (Russian).
[22]  N. ?ar?ak, R. G. Aker, O. ?zdemir, T. Demiralp, and F. Y. Onat, “The relationship between age-related development of spike-and-wave discharges and the resistance to amygdaloid kindling in rats with genetic absence epilepsy,” Neurobiology of Disease, vol. 32, no. 3, pp. 355–363, 2008.
[23]  M. Steriade, “The corticothalamic system in sleep,” Frontiers in Bioscience, vol. 8, pp. d878–d899, 2003.
[24]  S. V. Sch?nwald, D. Z. Carvalho, G. Dellagustin, E. L. de Santa-Helena, and G. J. L. Gerhardt, “Quantifying chirp in sleep spindles,” Journal of Neuroscience Methods, vol. 197, no. 1, pp. 158–164, 2011.
[25]  D. Z. Carvalho, G. J. Gerhardt, G. Dellagustin et al., “Loss of sleep spindle frequency deceleration in Obstructive Sleep Apnea,” Clinical Neurophysiology, vol. 125, pp. 306–312, 2014.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133