Proteomic profiling of the rat hippocampus from the kindling models of electrical epilepsy and treatment with low-frequency deep brain stimulation: the important role of the cytoskeleton

[1]  K. Khajeh,et al.  Proteomic profiling of the rat hippocampus from the kindling and pilocarpine models of epilepsy: potential targets in calcium regulatory network , 2021, Scientific Reports.

[2]  J. Pilitsis,et al.  Potential indications for deep brain stimulation in neurological disorders: an evolving field , 2018, European journal of neurology.

[3]  Christian Eggeling,et al.  Cytoskeletal actin dynamics shape a ramifying actin network underpinning immunological synapse formation , 2017, Science Advances.

[4]  M. Mohammad-zadeh,et al.  The antiepileptogenic effect of low-frequency stimulation on perforant path kindling involves changes in regulators of G-protein signaling in rat , 2017, Journal of the Neurological Sciences.

[5]  A. Yadollahpour,et al.  Quantitative evaluation of antiepileptogenic effects of LFS either before or after kindling stimulation using spectral power analysis of extracellular EEG in rats , 2017, Brain Stimulation.

[6]  K. Khajeh,et al.  Hippocampal asymmetry: differences in the left and right hippocampus proteome in the rat model of temporal lobe epilepsy. , 2017, Journal of proteomics.

[7]  Y. Fathollahi,et al.  Effect of low frequency stimulation on impaired spontaneous alternation behavior of kindled rats in Y-maze test , 2016, Epilepsy Research.

[8]  J. Baizabal-Carvallo,et al.  Low-frequency deep brain stimulation for movement disorders. , 2016, Parkinsonism & related disorders.

[9]  C. González-Billault,et al.  The Presynaptic Microtubule Cytoskeleton in Physiological and Pathological Conditions: Lessons from Drosophila Fragile X Syndrome and Hereditary Spastic Paraplegias , 2016, Front. Mol. Neurosci..

[10]  Marco Y. Hein,et al.  The Perseus computational platform for comprehensive analysis of (prote)omics data , 2016, Nature Methods.

[11]  Yi Wang,et al.  Low-frequency stimulation in anterior nucleus of thalamus alleviates kainate-induced chronic epilepsy and modulates the hippocampal EEG rhythm , 2016, Experimental Neurology.

[12]  C. Heck,et al.  Neuromodulation in the Treatment of Epilepsy , 2015, Current Treatment Options in Neurology.

[13]  Jingyu Chang,et al.  Low-frequency stimulation of the pedunculopontine nucleus affects gait and the neurotransmitter level in the ventrolateral thalamic nucleus in 6-OHDA Parkinsonian rats , 2015, Neuroscience Letters.

[14]  Odilia Yim,et al.  Hierarchical Cluster Analysis: Comparison of Three Linkage Measures and Application to Psychological Data , 2015 .

[15]  R. Lamprecht The actin cytoskeleton in memory formation , 2014, Progress in Neurobiology.

[16]  D. Durand,et al.  Long‐lasting hyperpolarization underlies seizure reduction by low frequency deep brain electrical stimulation , 2013, The Journal of physiology.

[17]  Dominique M Durand,et al.  Low frequency stimulation of ventral hippocampal commissures reduces seizures in a rat model of chronic temporal lobe epilepsy , 2012, Epilepsia.

[18]  D. Durand,et al.  Low frequency stimulation decreases seizure activity in a mutation model of epilepsy , 2010, Epilepsia.

[19]  C. Hoogenraad,et al.  Actin in dendritic spines: connecting dynamics to function , 2010, The Journal of cell biology.

[20]  Kristl Vonck,et al.  Comparison of hippocampal Deep Brain Stimulation with high (130Hz) and low frequency (5Hz) on afterdischarges in kindled rats , 2010, Epilepsy Research.

[21]  Jack A. Tuszynski,et al.  Neural cytoskeleton capabilities for learning and memory , 2009, Journal of biological physics.

[22]  V. Sheibani,et al.  Serine/threonine protein phosphatases have no role in the inhibitory effects of low-frequency stimulation in perforant path kindling acquisition in rats , 2009, Neuroscience Letters.

[23]  A. Jahanshahi,et al.  The role of galanin receptors in anticonvulsant effects of low-frequency stimulation in perforant path–kindled rats , 2007, Neuroscience.

[24]  M. P. Howell,et al.  The immediate early gene early growth response gene 3 mediates adaptation to stress and novelty , 2007, Neuroscience.

[25]  C. Elger,et al.  Epileptic Seizures and Epilepsy: Definitions Proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE) , 2005, Epilepsia.

[26]  L. Rocha,et al.  Low frequency stimulation modifies receptor binding in rat brain , 2004, Epilepsy Research.

[27]  P. Shannon,et al.  Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks , 2003 .

[28]  M. Tyers,et al.  From genomics to proteomics , 2003, Nature.

[29]  P. Patsalos,et al.  The Importance of Drug Interactions in Epilepsy Therapy , 2002, Epilepsia.

[30]  E. Fuchs,et al.  Capillary changes in hippocampal CA1 and CA3 areas of the aging rhesus monkey , 2000, Acta Neuropathologica.

[31]  A. Matus,et al.  Actin-based plasticity in dendritic spines. , 2000, Science.

[32]  A. Podtelejnikov,et al.  Linking genome and proteome by mass spectrometry: large-scale identification of yeast proteins from two dimensional gels. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[33]  T. Sutula Experimental Models of Temporal Lobe Epilepsy: New Insights from the Study of Kindling and Synaptic Reorganization , 1990, Epilepsia.

[34]  K. Sobue,et al.  Control of the cytoskeleton by calmodulin and calmodulin-binding proteins , 1983 .

[35]  J. McNamara,et al.  The kindling model of epilepsy: A review , 1980, Progress in Neurobiology.

[36]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[37]  Victoria Barkley,et al.  Deep brain stimulation effects on learning, memory and glutamate and GABAA receptor subunit gene expression in kindled rats. , 2021, Acta neurobiologiae experimentalis.

[38]  H. Tao,et al.  Increased stathmin expression strengthens fear conditioning in epileptic rats. , 2015, Biomedical reports.

[39]  Howard Eichenbaum,et al.  Distinct roles for dorsal CA3 and CA1 in memory for sequential nonspatial events. , 2010, Learning & memory.

[40]  S. Hanash,et al.  Disease proteomics , 2003, Nature.

[41]  Liqun Luo,et al.  Actin cytoskeleton regulation in neuronal morphogenesis and structural plasticity. , 2002, Annual review of cell and developmental biology.