An increase in persistent sodium current contributes to intrinsic neuronal bursting after status epilepticus

Journal of Neurophysiology

Volumn 105, Issue 1, 2011, Pages 117-129

  Chen, Shmuel ^a   Su, Hailing ^a   Yue, Cuiyong ^a   Remy, Stefan ^c   Royeck, Michel ^c   Sochivko, Dmitry ^c   Opitz, Thoralf ^c   Beck, Heinz ^c   Yaari, Yoel ^a,b  

^a HEBREW UNIVERSITY   (Israel)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^c UNIVERSITY HOSPITAL BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM ION; NICKEL; PILOCARPINE; SODIUM ION;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN ELECTROPHYSIOLOGY; CALCIUM CURRENT; CELL SURVIVAL; CONTROLLED STUDY; DENDRITE; EPILEPTIC STATE; MALE; NERVE CELL; NEURONAL BURSTING; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PYRAMIDAL NERVE CELL; RAT; SEIZURE THRESHOLD; SODIUM CURRENT; TEMPORAL LOBE EPILEPSY;

ANIMALS; CA1 REGION, HIPPOCAMPAL; CALCIUM CHANNEL BLOCKERS; CALCIUM CHANNELS, T-TYPE; MALE; MODELS, ANIMAL; NEURONS; PATCH-CLAMP TECHNIQUES; PILOCARPINE; RATS; RATS, INBRED STRAINS; RATS, WISTAR; SODIUM CHANNEL BLOCKERS; SODIUM CHANNELS; STATUS EPILEPTICUS; TETRODOTOXIN; TIME FACTORS;

EID: 78651429319     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.00184.2010     Document Type: Article

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