Lesion-induced axonal sprouting and hyperexcitability in the hippocampus in vitro : Implications for the genesis of posttraumatic epilepsy
The delayed development of recurring seizures is a common consequence of traumatic head injury; the cause of such epilepsy is unknown. We demonstrate here that transection of the mature axons of CA3 pyramidal cells in hippocampal slice cultures leads to the formation by CA3 pyramidal cells of new ax...
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Veröffentlicht in: | Nature medicine 1997-09, Vol.3 (9), p.990-996 |
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creator | Mckinney, R. Anne Debanne, Dominique Gähwiler, Beat H Thompson, Scott M |
description | The delayed development of recurring seizures is a common consequence of traumatic head injury; the cause of such epilepsy is unknown. We demonstrate here that transection of the mature axons of CA3 pyramidal cells in hippocampal slice cultures leads to the formation by CA3 pyramidal cells of new axon collaterals that are immunoreactive with the growth-associated protein GAP-43. Individual CA3 cell axons had an elevated number of presynaptic boutons 14 days after the lesion, and dual intracellular recordings revealed an increased probability that any two CA3 pyramidal cells were connected by an excitatory synapse. Lesioned cultures were hyperexcitable and synaptic responses often displayed unusual prolonged polysynaptic components. We thus demonstrate that recurrent axon collaterals are newly sprouted by pyramidal cells as a consequence of axonal injury and suggest that this underlies the development of posttraumatic epilepsy. |
doi_str_mv | 10.1038/nm0997-990 |
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Anne</creatorcontrib><creatorcontrib>Debanne, Dominique</creatorcontrib><creatorcontrib>Gähwiler, Beat H</creatorcontrib><creatorcontrib>Thompson, Scott M</creatorcontrib><title>Lesion-induced axonal sprouting and hyperexcitability in the hippocampus in vitro : Implications for the genesis of posttraumatic epilepsy</title><title>Nature medicine</title><addtitle>Nat Med</addtitle><description>The delayed development of recurring seizures is a common consequence of traumatic head injury; the cause of such epilepsy is unknown. We demonstrate here that transection of the mature axons of CA3 pyramidal cells in hippocampal slice cultures leads to the formation by CA3 pyramidal cells of new axon collaterals that are immunoreactive with the growth-associated protein GAP-43. 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We thus demonstrate that recurrent axon collaterals are newly sprouted by pyramidal cells as a consequence of axonal injury and suggest that this underlies the development of posttraumatic epilepsy.</description><subject>Animals</subject><subject>Axons - pathology</subject><subject>Axons - physiology</subject><subject>Culture Techniques</subject><subject>Disease Models, Animal</subject><subject>Epilepsy, Post-Traumatic - etiology</subject><subject>Epilepsy, Post-Traumatic - pathology</subject><subject>Epilepsy, Post-Traumatic - physiopathology</subject><subject>GAP-43 Protein</subject><subject>Hippocampus - injuries</subject><subject>Hippocampus - pathology</subject><subject>Hippocampus - physiopathology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Pyramidal Cells - pathology</subject><subject>Pyramidal Cells - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Time Factors</subject><issn>1078-8956</issn><issn>1546-170X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1LHTEUhoO0-NVu3Bey6qIwNZlMvtyJVCtc6KaCuyE3c8abMpPEJCPev9BfbfRe7LKrE8778B7Cg9AZJd8pYercz0Rr2WhNDtAx5Z1oqCT3H-qbSNUozcUROsn5DyGEEa4P0aFulZItP0Z_V5Bd8I3zw2JhwOY5eDPhHFNYivMP2PgBb7YREjxbV8zaTa5ssfO4bABvXIzBmjku-XX15EoK-ALfznFy1pRanPEY0hv7AL6eyjiMOIZcSjLLXBGLIboJYt5-Qh9HM2X4vJ-n6O76x--rn83q183t1eWqsR3pSmNbWBswHeOccSkEHUHolikuR9J2bD0SK7W0wFoYiJZCW6KAUTUAGygdLTtFX3e99Y-PC-TSzy5bmCbjISy5l7oVXCnyX5CKTrT1bgW_7UCbQs4Jxj4mN5u07SnpXw31O0N9NVThL_vWZT3D8I7uldQc73JvypLgPf8nmb0AJ3yZ8A</recordid><startdate>199709</startdate><enddate>199709</enddate><creator>Mckinney, R. 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subjects | Animals Axons - pathology Axons - physiology Culture Techniques Disease Models, Animal Epilepsy, Post-Traumatic - etiology Epilepsy, Post-Traumatic - pathology Epilepsy, Post-Traumatic - physiopathology GAP-43 Protein Hippocampus - injuries Hippocampus - pathology Hippocampus - physiopathology Humans Immunohistochemistry Membrane Glycoproteins - metabolism Nerve Tissue Proteins - metabolism Pyramidal Cells - pathology Pyramidal Cells - physiology Rats Rats, Wistar Time Factors |
title | Lesion-induced axonal sprouting and hyperexcitability in the hippocampus in vitro : Implications for the genesis of posttraumatic epilepsy |
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