Long-term potentiation enhancing effect of epileptic insult in the CA1 area is dependent on prior-application of primed-burst stimulation

[1]  J. Behr,et al.  A novel method using ambient glutamate for the electrophysiological quantification of extrasynaptic NMDA receptor function in acute brain slices , 2019, The Journal of physiology.

[2]  S. Traynelis,et al.  Functional and pharmacological properties of triheteromeric GluN1/2B/2D NMDA receptors , 2019, The Journal of physiology.

[3]  A. Zaitsev,et al.  Changes in Functional Properties of Rat Hippocampal Neurons Following Pentylenetetrazole-induced Status Epilepticus , 2019, Neuroscience.

[4]  A. Zaitsev,et al.  Transient Switching of NMDA-Dependent Long-Term Synaptic Potentiation in CA3-CA1 Hippocampal Synapses to mGluR1-Dependent Potentiation After Pentylenetetrazole-Induced Acute Seizures in Young Rats , 2019, Cellular and Molecular Neurobiology.

[5]  R. Morris,et al.  Silent Learning , 2018, Current Biology.

[6]  S. Sylantyev,et al.  Spontaneously opening GABAA receptors play a significant role in neuronal signal filtering and integration , 2018, Cell Death & Disease.

[7]  C. Papatheodoropoulos,et al.  β-adrenergic receptors reduce the threshold for induction and stabilization of LTP and enhance its magnitude via multiple mechanisms in the ventral but not the dorsal hippocampus , 2018, Neurobiology of Learning and Memory.

[8]  P. Paoletti,et al.  Triheteromeric NMDA receptors: from structure to synaptic physiology. , 2018, Current opinion in physiology.

[9]  M. Topf,et al.  Disease-associated missense mutations in GluN2B subunit alter NMDA receptor ligand binding and ion channel properties , 2018, Nature Communications.

[10]  V. Kotak,et al.  GABAergic inhibition gates excitatory LTP in perirhinal cortex , 2017, Hippocampus.

[11]  A. Zaitsev,et al.  Status epilepticus impairs synaptic plasticity in rat hippocampus and is followed by changes in expression of NMDA receptors , 2017, Biochemistry (Moscow).

[12]  C. Papatheodoropoulos,et al.  Theta burst stimulation‐induced LTP: Differences and similarities between the dorsal and ventral CA1 hippocampal synapses , 2016, Hippocampus.

[13]  N. Naghdi,et al.  Chronic sodium salicylate administration enhances population spike long-term potentiation following a combination of theta frequency primed-burst stimulation and the transient application of pentylenetetrazol in rat CA1 hippocampal neurons. , 2015, European journal of pharmacology.

[14]  K. Newell,et al.  GluN2B protein deficits in the left, but not the right, hippocampus in schizophrenia , 2014, BMC Psychiatry.

[15]  Rüdiger Köhling,et al.  Enhanced NMDA receptor-dependent LTP in the epileptic CA1 area via upregulation of NR2B , 2013, Neurobiology of Disease.

[16]  J. Frey,et al.  Continuous blockade of GABA-ergic inhibition induces novel forms of long-lasting plastic changes in apical dendrites of the hippocampal cornu ammonis 1 (CA1) in vitro , 2010, Neuroscience.

[17]  Benjamin D. Philpot,et al.  Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity , 2008, Neuropharmacology.

[18]  W. Abraham.  Metaplasticity: tuning synapses and networks for plasticity , 2008, Nature Reviews Neuroscience.

[19]  Stephen F Traynelis,et al.  Subunit‐specific gating controls rat NR1/NR2A and NR1/NR2B NMDA channel kinetics and synaptic signalling profiles , 2005, The Journal of physiology.

[20]  G. Collingridge,et al.  Differential Roles of NR2A and NR2B-Containing NMDA Receptors in Cortical Long-Term Potentiation and Long-Term Depression , 2004, The Journal of Neuroscience.

[21]  M. Sheng,et al.  Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity , 2004, Science.

[22]  O. Paulsen,et al.  Maturation of Long-Term Potentiation Induction Rules in Rodent Hippocampus: Role of GABAergic Inhibition , 2003, The Journal of Neuroscience.

[23]  Y. Fathollahi,et al.  Reversal of pentylenetetrazol‐induced potentiation phenomenon by theta pulse stimulation in the CA1 region of rat hippocampal slices , 2003, Synapse.

[24]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[25]  Y. Fathollahi,et al.  Primed-burst potentiation occludes the potentiation phenomenon and enhances the epileptiform activity induced by transient pentylenetetrazol in the CA1 region of rat hippocampal slices , 2000, Brain Research.

[26]  S. Hrabetova,et al.  Distinct NMDA Receptor Subpopulations Contribute to Long-Term Potentiation and Long- Term Depression Induction , 2000, The Journal of Neuroscience.

[27]  M. Bear,et al.  Bidirectional, experience-dependent regulation of N-methyl-D-aspartate receptor subunit composition in the rat visual cortex during postnatal development. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[28]  E. B. Roberts,et al.  Enhanced NR2A subunit expression and decreased NMDA receptor decay time at the onset of ocular dominance plasticity in the ferret. , 1999, Journal of neurophysiology.

[29]  M. Bear,et al.  Metaplasticity: the plasticity of synaptic plasticity , 1996, Trends in Neurosciences.

[30]  Kurths,et al.  Phase synchronization of chaotic oscillators. , 1996, Physical review letters.

[31]  J. L. Stringer.  Pentylenetetrazol causes polysynaptic responses to appear in the dentate gyrus , 1995, Neuroscience.

[32]  T. Bird.  Major Patterns of Human Inheritance: Relevance to the Epilepsies , 1994, Epilepsia.

[33]  N. Matsokis,et al.  Pentylenetetrazol‐Induced Seizures Decrease γ‐Aminobutyric Acid‐Mediated Recurrent Inhibition and Enhance Adenosine‐Mediated Depression , 1994, Epilepsia.

[34]  Eric R. Kandel,et al.  Tissue-plasminogen activator is induced as an immediate–early gene during seizure, kindling and long-term potentiation , 1993, Nature.

[35]  T. Bliss,et al.  A synaptic model of memory: long-term potentiation in the hippocampus , 1993, Nature.

[36]  W. Abraham,et al.  Priming of associative long-term depression in the dentate gyrus by θ frequency synaptic activity , 1992, Neuron.

[37]  R. Malenka,et al.  The influence of prior synaptic activity on the induction of long-term potentiation. , 1992, Science.

[38]  G. Collingridge,et al.  GABAB autoreceptors regulate the induction of LTP , 1991, Nature.

[39]  Y. Ben-Ari,et al.  Novel form of long-term potentiation produced by a K+channel blocker in the hippocampus , 1991, Nature.

[40]  U. Heinemann,et al.  Effects of pentetrazol on neuronal activity and on extracellular calcium concentration in rat hippocampal slices , 1990, Epilepsy Research.

[41]  G. Collingridge,et al.  Low-frequency activation of the NMDA receptor system can prevent the induction of LTP , 1989, Neuroscience Letters.

[42]  T. Dunwiddie,et al.  Characteristics of hippocampal primed burst potentiation in vitro and in the awake rat , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[43]  H. Wigström,et al.  Facilitation of hippocampal long-lasting potentiation by GABA antagonists. , 1985, Acta physiologica Scandinavica.

[44]  T. Bliss,et al.  Long‐lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path , 1973, The Journal of physiology.

[45]  E. Speckmann,et al.  Actions of pentylenetetrazol (PTZ) on CA3 neurons in hippocampal slices of guinea pigs , 2004, Experimental Brain Research.