Homeostatic synaptic plasticity can explain post-traumatic epileptogenesis in chronically isolated neocortex

Cerebral Cortex

Volumn 15, Issue 6, 2005, Pages 834-845

  Houweling, Arthur R ^a,b,e   Bazhenov, Maxim ^a   Timofeev, Igor ^d   Steriade, Mircea ^d   Sejnowski, Terrence J ^a,c  

^a SALK INSTITUTE FOR BIOLOGICAL STUDIES   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF CALIFORNIA SAN DIEGO   (United States)

^d UNIVERSITÉ LAVAL   (Canada)

^e ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Brain trauma; Computational model; Deafferentation; Epilepsy; Injury; Slow oscillation

Indexed keywords

ACTION POTENTIAL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CAT; COMPUTER MODEL; CONTROLLED STUDY; DEAFFERENTATION; DEPOLARIZATION; DOWN REGULATION; EPILEPTIC DISCHARGE; EPILEPTOGENESIS; HOMEOSTASIS; NEOCORTEX; NERVE CELL PLASTICITY; NERVE CONDUCTION; NERVE EXCITABILITY; NONHUMAN; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; SYNAPTIC TRANSMISSION; TRAUMATIC EPILEPSY; UPREGULATION;

ACTION POTENTIALS; ACUTE DISEASE; ANIMALS; BRAIN INJURIES; CATS; CHRONIC DISEASE; DENERVATION; ELECTRODES, IMPLANTED; EPILEPSY; HOMEOSTASIS; MODELS, NEUROLOGICAL; NEOCORTEX; NEURONAL PLASTICITY; PERIODICITY;

EID: 18844410288     PISSN: 10473211     EISSN: None     Source Type: Journal    
DOI: 10.1093/cercor/bhh184     Document Type: Article

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