Sprouting and synaptic reorganization in the subiculum and CA1 region of the hippocampus in acute and chronic models of partial-onset epilepsy
暂无分享,去创建一个
[1] Nobuaki Tamamaki,et al. Disposition of the slab‐like modules formed by axon branches originating from single CA1 pyramidal neurons in the rat hippocampus , 1990, The Journal of comparative neurology.
[2] A. Cole,et al. Neuronal stress and injury in C57/BL mice after systemic kainic acid administration , 1998, Brain Research.
[3] F. Dudek,et al. Spontaneous and stimulation-induced synchronized burst afterdischarges in the isolated CA1 of kainate-treated rats. , 1996, Journal of neurophysiology.
[4] D. Amaral,et al. Organization of CA1 projections to the subiculum: A PHA‐L analysis in the rat , 1991, Hippocampus.
[5] G. Danscher,et al. Zinc-containing neurons in hippocampus and related CNS structures. , 1990, Progress in brain research.
[6] Christophe Bernard,et al. Newly formed excitatory pathways provide a substrate for hyperexcitability in experimental temporal lobe epilepsy , 1999, The Journal of comparative neurology.
[7] B. Longo,et al. Supragranular mossy fiber sprouting is not necessary for spontaneous seizures in the intrahippocampal kainate model of epilepsy in the rat , 1998, Epilepsy Research.
[8] Y. Ben-Ari,et al. Hippocampal plasticity in the kindling model of epilepsy in rats , 1989, Neuroscience Letters.
[9] S. Laurberg,et al. Associational and commissural collaterals of neurons in the hippocampal formation (Hilus fasciae dentatae and subfield CA3) , 1981, Brain Research.
[10] G. Cascino,et al. Mossy fiber synaptic reorganization in the epileptic human temporal lobe , 1989, Annals of neurology.
[11] D. Riche,et al. Long-term effects of intrahippocampal kainic acid injection in rats: a method for inducing spontaneous recurrent seizures. , 1982, Electroencephalography and clinical neurophysiology.
[12] Morten Raastad,et al. The hippocampal lamella hypothesis revisited 1 1 Published on the World Wide Web on 12 October 2000. , 2000, Brain Research.
[13] T. Freund,et al. Total number and distribution of inhibitory and excitatory synapses on hippocampal CA1 pyramidal cells , 2001, Neuroscience.
[14] L. Slomianka. Neurons of origin of zinc-containing pathways and the distribution of zinc-containing boutons in the hippocampal region of the rat , 1992, Neuroscience.
[15] T. Hoogenraad. The neurobiology of zinc Part A: Physiochemistry, anatomy, and techniques (390 p.); Part B: Deficiency, toxicity, and pathology (345 p.). Edited by C.J. Frederickson, G.A. Howell, E.J. Kasarskis. Alan R. Liss Inc., New York, Figs and tables , 1985, Clinical Neurology and Neurosurgery.
[16] G. Golarai,et al. Mossy fiber synaptic reorganization induced by kindling: time course of development, progression, and permanence , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[17] R. S. Sloviter,et al. Commissurally projecting inhibitory interneurons of the rat hippocampal dentate gyrus: A colocalization study of neuronal markers and the retrograde tracer fluoro‐gold , 2001, The Journal of comparative neurology.
[18] W. Lanksch,et al. Alterations of Neuronal Connectivity in Area CA1 of Hippocampal Slices from Temporal Lobe Epilepsy Patients and from Pilocarpine‐Treated Epileptic Rats , 2000, Epilepsia.
[19] M. E. Corcoran,et al. Mossy fiber sprouting is dissociated from kindling of generalized seizures in the guinea‐pig , 2000, Neuroreport.
[20] J. Cavazos,et al. Synaptic reorganization in the hippocampus induced by abnormal functional activity. , 1988, Science.
[21] G. A. Howell,et al. A retrograde transport method for mapping zinc-containing fiber systems in the brain , 1990, Brain Research.
[22] P. Rutecki,et al. NMDA-dependent currents in granule cells of the dentate gyrus contribute to induction but not permanence of kindling. , 1999, Journal of neurophysiology.
[23] E. Cavalheiro. The pilocarpine model of epilepsy , 1995, The Italian Journal of Neurological Sciences.
[24] G. V. Goddard,et al. A permanent change in brain function resulting from daily electrical stimulation. , 1969, Experimental neurology.
[25] Jerome Engel,et al. Surgical treatment of the epilepsies , 1993 .
[26] José E Cavazos,et al. Ultrastructural features of sprouted mossy fiber synapses in kindled and kainic acid‐treated rats , 2003, The Journal of comparative neurology.
[27] William W. Lytton,et al. Computer models of hippocampal circuit changes of the kindling model of epilepsy , 1998, Artif. Intell. Medicine.
[28] Christopher J. Frederickson,et al. Zinc-containing innervation of the subicular region in the rat , 1995, Neurochemistry International.
[29] Mark Stewart,et al. Propagation of synchronous epileptiform events from subiculum backward into area CA1 of rat brain slices , 2001, Brain Research.
[30] T. Bliss,et al. Lamellar organization of hippocampal excitatory pathways , 1971, Experimental Brain Research.
[31] G. A. Howell,et al. Zinc-containing neuronal innervation of the septal nuclei , 1993, Brain Research.
[32] F. Dudek,et al. Network properties of the dentate gyrus in epileptic rats with hilar neuron loss and granule cell axon reorganization. , 1997, Journal of neurophysiology.
[33] Thomas P. Sutula,et al. Progressive neuronal loss induced by kindling: a possible mechanism for mossy fiber synaptic reorganization and hippocampal sclerosis , 1990, Brain Research.
[34] S. Totterdell,et al. Morphology and distribution of electrophysiologically defined classes of pyramidal and nonpyramidal neurons in rat ventral subiculum in vitro , 1997, The Journal of comparative neurology.
[35] W. Lanksch,et al. Fluorescent tracer in pilocarpine‐treated rats shows widespread aberrant hippocampal neuronal connectivity , 2001, The European journal of neuroscience.
[36] N. Tamamaki,et al. Three-dimensional analysis of the whole axonal arbors originating from single CA2 pyramidal neurons in the rat hippocampus with the aid of a computer graphic technique , 1988, Brain Research.
[37] CR Houser,et al. Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[38] G. Golarai,et al. Activation of the dentate gyrus by pentylenetetrazol evoked seizures induces mossy fiber synaptic reorganization , 1992, Brain Research.
[39] P. Rutecki,et al. Spontaneous Seizures and Loss of Axo-Axonic and Axo-Somatic Inhibition Induced by Repeated Brief Seizures in Kindled Rats , 2003, The Journal of Neuroscience.
[40] A. Dahlström,et al. Localization of zinc-enriched neurons in the mouse peripheral sympathetic system , 2002, Brain Research.
[41] F. Dudek,et al. Short- and long-term changes in CA1 network excitability after kainate treatment in rats. , 2001, Journal of neurophysiology.
[42] F Edward Dudek,et al. Network interactions mediated by new excitatory connections between CA1 pyramidal cells in rats with kainate-induced epilepsy. , 2002, Journal of neurophysiology.
[43] G. Golarai,et al. Alteration of long-lasting structural and functional effects of kainic acid in the hippocampus by brief treatment with phenobarbital , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[44] N. Bannister,et al. Dendritic morphology of CA1 pyramidal neurones from the rat hippocampus: II. Spine distributions , 1995, The Journal of comparative neurology.
[45] J. H. Kim,et al. Hippocampal interneuron loss and plasticity in human temporal lobe epilepsy , 1989, Brain Research.
[46] L Menendez de la Prida,et al. Electrophysiological and morphological diversity of neurons from the rat subicular complex in vitro , 2003, Hippocampus.
[47] Y. Ben-Ari,et al. Hippocampal plasticity in childhood epilepsy , 1989, Neuroscience Letters.
[48] D. Amaral,et al. The three-dimensional organization of the hippocampal formation: A review of anatomical data , 1989, Neuroscience.
[49] F. Dudek,et al. Persistent hyperexcitability in isolated hippocampal CA1 of kainate-lesioned rats. , 1992, Journal of neurophysiology.
[50] A. Cole,et al. Early-life seizures in rats increase susceptibility to seizure-induced brain injury in adulthood , 1999, Neurology.
[51] W. J. Brown,et al. Temporal Lobe Volumetric Cell Densities in Temporal Lobe Epilepsy , 1984, Epilepsia.
[52] G. Golarai,et al. Assessing the functional significance of mossy fiber sprouting. , 1992, Epilepsy research. Supplement.
[53] G. Danscher,et al. Evidence from dithizone and selenium zinc histochemistry that perivascular mossy fiber boutons stain preferentially “in vivo” , 2004, Histochemistry.
[54] P. Andersen,et al. Organization of the hippocampal output , 1973, Experimental Brain Research.
[55] J. Cavazos,et al. Neuronal loss induced in limbic pathways by kindling: evidence for induction of hippocampal sclerosis by repeated brief seizures , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[56] D. Coulter,et al. Protracted postnatal development of inhibitory synaptic transmission in rat hippocampal area CA1 neurons. , 2000, Journal of neurophysiology.
[57] G. Danscher,et al. Retrograde tracing of zinc-enriched (ZEN) neuronal somata in rat spinal cord , 2001, Brain Research.
[58] S. Laurberg,et al. Commissural and intrinsic connections of the rat hippocampus , 1979, The Journal of comparative neurology.