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Tahamtan, Mahshid, Shabani, Mohammad, Sheibani, Vahid. (1395). Possible Role of the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Memory Consolidation during Slow-Wave Sleep. سامانه مدیریت نشریات علمی, 2(3), 280-282. doi: 10.18869/nrip.jamsat.2.3.280
Mahshid Tahamtan; Mohammad Shabani; Vahid Sheibani. "Possible Role of the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Memory Consolidation during Slow-Wave Sleep". سامانه مدیریت نشریات علمی, 2, 3, 1395, 280-282. doi: 10.18869/nrip.jamsat.2.3.280
Tahamtan, Mahshid, Shabani, Mohammad, Sheibani, Vahid. (1395). 'Possible Role of the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Memory Consolidation during Slow-Wave Sleep', سامانه مدیریت نشریات علمی, 2(3), pp. 280-282. doi: 10.18869/nrip.jamsat.2.3.280
Tahamtan, Mahshid, Shabani, Mohammad, Sheibani, Vahid. Possible Role of the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Memory Consolidation during Slow-Wave Sleep. سامانه مدیریت نشریات علمی, 1395; 2(3): 280-282. doi: 10.18869/nrip.jamsat.2.3.280

Possible Role of the Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels in Memory Consolidation during Slow-Wave Sleep

Journal of Advanced Medical Sciences and Applied Technologies
مقاله 7، دوره 2، شماره 3، آذر 2016، صفحه 280-282    اصل مقاله (493.43 K)
نوع مقاله: Hypothesis
شناسه دیجیتال (DOI): 10.18869/nrip.jamsat.2.3.280
نویسندگان
Mahshid Tahamtan1؛ Mohammad Shabani2؛ Vahid Sheibani* 2
1Neuroscience research center, Neuropharmacology institute, Kerman University of Medical Sciences, Kerman, Iran
2Neuroscience Research Center, Neuropharmacology institute, Kerman University of Medical Sciences, Kerman, Iran
چکیده
Over more than a century of research has demonstrated that sleep is necessary for the retention of memory. The current review aim to discuss the functional brain network connectivity is important during slow-wave sleep (SWS) for memory consolidation. While several evidences indicated the importance of SWS for memory consolidation but information to understand the main mechanisms of it are not enough.  Although there is the likely involvement of various factors in this phenomenon, we hypothesize the key role of Ih current arising memory consolidation during SWS by generation of neuronal oscillations. Finding the possible mechanism involving in this process may provide lights to suggesting new treatments against memory impairments. 
کلیدواژه‌ها
Sleep؛ Memory consolidation؛ Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
مراجع
  1. Siapas AG, Wilson MA. Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep. Neuron. 1998;21(5):1123-8.
  2. Foote SL, Bloom FE, Aston-Jones G. Nucleus locus ceruleus: new evidence of anatomical and physiological specificity. Physiological reviews. 1983;63(3):844-914.
  3. Berridge CW, Waterhouse BD. The locus coeruleus–noradrenergic system: modulation of behavioral state and state-dependent cognitive processes. Brain Research Reviews. 2003;42(1):33-84.
  4. He C, Chen F, Li B, Hu Z. Neurophysiology of HCN channels: from cellular functions to multiple regulations. Progress in neurobiology. 2014;112:1-23.
  5. Kopp-Scheinpflug C, Tozer AJ, Robinson SW, Tempel BL, Hennig MH, Forsythe ID. The sound of silence: ionic mechanisms encoding sound termination. Neuron. 2011;71(5):911-25.
  6. Jahnsen H, Llinas R. Ionic basis for the electro‐responsiveness and oscillatory properties of guinea‐pig thalamic neurones in vitro. The Journal of physiology. 1984;349(1):227-47.
  7. Kocsis B, Li S. In vivo contribution of h‐channels in the septal pacemaker to theta rhythm generation. European Journal of Neuroscience. 2004;20(8):2149-58.
  8. Timo-Iaria C, Negrào N, Schmidek WR, Hoshino K, de Menezes CEL, Da Rocha TL. Phases and states of sleep in the rat. Physiology & Behavior. 1970;5(9):1057-62.
  9. Hobson JA. REM sleep and dreaming: towards a theory of protoconsciousness. Nature Reviews Neuroscience. 2009;10(11):803-13.
  10. Hanlon EC, Faraguna U, Vyazovskiy VV, Tononi G, Cirelli C. Effects of skilled training on sleep slow wave activity and cortical gene expression in the rat. Sleep. 2009;32(6):719-29.
  11. Landsness EC, Crupi D, Hulse BK, Peterson MJ, Huber R, Ansari H, et al. Sleep-dependent improvement in visuomotor learning: a causal role for slow waves. Sleep. 2009;32(10):1273-84.
  12. Meerlo P, de Bruin EA, Strijkstra AM, Daan S. A social conflict increases EEG slow-wave activity during subsequent sleep. Physiology & behavior. 2001;73(3):331-5.
  13. Marshall L, Born J. The contribution of sleep to hippocampus-dependent memory consolidation. Trends in cognitive sciences. 2007;11(10):442-50.
  14. Csicsvari J, Hirase H, Czurko A, Mamiya A, Buzsaki G. Oscillatory coupling of hippocampal pyramidal cells and interneurons in the behaving rat. The Journal of neuroscience. 1999;19(1):274-87.
  15. BuzsÁk G. Memory consolidation during sleep: a neurophysiological perspective. Journal of sleep research. 1998;7(S1):17-23.
  16. Kali S, Dayan P. Off-line replay maintains declarative memories in a model of hippocampal-neocortical interactions. Nature neuroscience. 2004;7(3):286-94.
  17. Sara SJ. Locus Coeruleus in time with the making of memories. Current opinion in neurobiology. 2015;35:87-94.
  18. Eschenko O, Sara SJ. Learning-dependent, transient increase of activity in noradrenergic neurons of locus coeruleus during slow wave sleep in the rat: Brain stem–cortex interplay for memory consolidation? Cerebral Cortex. 2008;18(11):2596-603.
  19. Bernabeu R, Bevilaqua L, Ardenghi P, Bromberg E, Schmitz P, Bianchin M, et al. Involvement of hippocampal cAMP/cAMP-dependent protein kinase signaling pathways in a late memory consolidation phase of aversively motivated learning in rats. Proceedings of the National Academy of Sciences. 1997;94(13):7041-6.
  20. Kety S. The possible role of the adrenergic systems of the cortex in learning. Research publications-Association for Research in Nervous and Mental Disease. 1972;50:376.
  21. Cirelli C, Tononi G. Locus ceruleus control of state-dependent gene expression. The Journal of neuroscience. 2004;24(23):5410-9.
  22. Ludwig A, Budde T, Stieber J, Moosmang S, Wahl C, Holthoff K, et al. Absence epilepsy and sinus dysrhythmia in mice lacking the pacemaker channel HCN2. The EMBO journal. 2003;22(2):216-24.
  23. McCormick DA, Bal T. Sleep and arousal: thalamocortical mechanisms. Annual review of neuroscience. 1997;20(1):185-215.
  24. Mellor J, Nicoll RA, Schmitz D. Mediation of hippocampal mossy fiber long-term potentiation by presynaptic Ih channels. Science. 2002;295(5552):143-7.
  25. Fan Y, Fricker D, Brager DH, Chen X, Lu H-C, Chitwood RA, et al. Activity-dependent decrease of excitability in rat hippocampal neurons through increases in Ih. Nature neuroscience. 2005;8(11):1542-51.
  26. Pouille F, Scanziani M. Enforcement of temporal fidelity in pyramidal cells by somatic feed-forward inhibition. Science. 2001;293(5532):1159-63.
  27. Nolan MF, Malleret G, Lee KH, Gibbs E, Dudman JT, Santoro B, et al. The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells. Cell. 2003;115(5):551-64.
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