Literature DB >> 8985701

Vulnerability and plasticity of the GABA system in the pilocarpine model of spontaneous recurrent seizures.

C R Houser1, M Esclapez.   

Abstract

Several similarities exist between the alterations observed in the chronic pilocarpine model of recurrent seizures in the rat and those found in human temporal lobe epilepsy. The present studies are focused on changes in the GABA system in this model. Following the initial pilocarpine-induced seizures, a substantial loss of glutamic acid decarboxylase (GAD) mRNA-containing neurons has been found in the hilus of the dentate gyrus (Obenaus et al., J. Neurosci., 13 (1993) 4470-4485), and, recently, a loss of GAD mRNA-labeled neurons has also been found in stratum oriens of CA1. Yet numerous other GABA neurons remain within the hippocampal formation, and there appear to be multiple compensatory changes in these neurons. Labeling for GAD65 mRNA and associated protein is substantially increased in the remaining GABA neurons at 2-4 months after the initial seizure episode. Such increased labeling suggests that the remaining GABA neurons are part of a functional circuit and may be responding to the need for increased activity. Alterations also occur in at least one subunit of the GABA-A receptor. Labeling for the alpha(5) subunit mRNA is substantially decreased in CA1 and CA2 of pilocarpine-treated rats during the chronic, seizure-prone period. These findings emphasize the complexity of changes in the GABA system and indicate a need for evaluating the functional consequences of each of the changes. The initial loss of specific groups of GABA neurons could be a critical first step in the gradual development of epileptiform activity. While many of the subsequent changes in the GABA system may be considered to be compensatory, significant deficits of GABAergic function could remain.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8985701     DOI: 10.1016/s0920-1211(96)00054-x

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  65 in total

Review 1.  Distinguishing between GABA(A) receptors responsible for tonic and phasic conductances.

Authors:  I Mody
Journal:  Neurochem Res       Date:  2001-09       Impact factor: 3.996

2.  Interneuron loss reduces dendritic inhibition and GABA release in hippocampus of aged rats.

Authors:  Emily M Stanley; Jim R Fadel; David D Mott
Journal:  Neurobiol Aging       Date:  2011-02-01       Impact factor: 4.673

3.  Axon sprouting and synaptic reorganization of GABAergic interneurons: a focused look at a general question.

Authors:  F Edward Dudek
Journal:  Epilepsy Curr       Date:  2010-09       Impact factor: 7.500

4.  Heterogeneity of the supramammillary-hippocampal pathways: evidence for a unique GABAergic neurotransmitter phenotype and regional differences.

Authors:  Rabia Soussi; Nianhui Zhang; Siroun Tahtakran; Carolyn R Houser; Monique Esclapez
Journal:  Eur J Neurosci       Date:  2010-08-16       Impact factor: 3.386

5.  Operative GABAergic inhibition in hippocampal CA1 pyramidal neurons in experimental epilepsy.

Authors:  M Esclapez; J C Hirsch; R Khazipov; Y Ben-Ari; C Bernard
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

6.  Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation.

Authors:  M Derchansky; S S Jahromi; M Mamani; D S Shin; A Sik; P L Carlen
Journal:  J Physiol       Date:  2007-11-08       Impact factor: 5.182

7.  Hilar mossy cell degeneration causes transient dentate granule cell hyperexcitability and impaired pattern separation.

Authors:  Seiichiro Jinde; Veronika Zsiros; Zhihong Jiang; Kazuhito Nakao; James Pickel; Kenji Kohno; Juan E Belforte; Kazu Nakazawa
Journal:  Neuron       Date:  2012-12-20       Impact factor: 17.173

8.  Structural plasticity of dentate granule cell mossy fibers during the development of limbic epilepsy.

Authors:  Steve C Danzer; Xiaoping He; Andreas W Loepke; James O McNamara
Journal:  Hippocampus       Date:  2010-01       Impact factor: 3.899

9.  Surviving hilar somatostatin interneurons enlarge, sprout axons, and form new synapses with granule cells in a mouse model of temporal lobe epilepsy.

Authors:  Wei Zhang; Ruth Yamawaki; Xiling Wen; Justin Uhl; Jessica Diaz; David A Prince; Paul S Buckmaster
Journal:  J Neurosci       Date:  2009-11-11       Impact factor: 6.167

Review 10.  Functional implications of seizure-induced neurogenesis.

Authors:  Helen E Scharfman
Journal:  Adv Exp Med Biol       Date:  2004       Impact factor: 2.622

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.