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  • Audiogenic seizures  (1)
  • Nuclear Reaction  (1)
  • rat  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 441 (1985), S. 261-270 
    ISSN: 0375-9474
    Keywords: Nuclear Reaction
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1463
    Keywords: Audiogenic seizures ; kindling ; EEG
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A strain of Wistar rats was inbred for susceptibility to audiogenic seizures characterized by one or two wild running fits followed by tonic dorsiflexion with open mouth and then a catatonic state. During the tonic phase, the cortical EEG was flat for 1 to 2 sec, then changed to a slow, regular lowamplitude discharge, 9 to 12c/s, for 25 to 60 sec. In these rats exposed to 40 daily 90-sec auditory stimuli, behavior and EEG changed. The wild running became disorganized by myoclonic jerks of the limbs and body. In some animals, the tonic extension disappeared and a myoclonic seizure developed progressively, with facial and forelimb clonus, and rearing and falling. In others, the tonic phase was followed by a generalized clonic phase. The EEG during the myoclonic and tonic-clonic seizures showed high-amplitude rhythmic spikes, polyspikes and spike-waves, 1 to 10 c/s, for 40 to 120 sec, often outlasting the sound stimulus. The effects of ethosuximide, carbamazepine and phenytoin were the same on primary and modified audiogenic seizures. The progressive behavioral and EEG modifications of audiogenic seizures following repeated auditory stimuli suggest that kindling had developed, the seizures being propagated from the brain stem to forebrain structures.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 16 (1995), S. 113-118 
    ISSN: 1590-3478
    Keywords: absence epilepsy ; model ; rat ; genetic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Il 100% degli animali appartenenti al ceppo GAERS (Genetic Absence Epilepsy Rats from Strasbourg) presenta crisi generalizzate non convulsive ricorrenti caratterizzate da scariche di punta-onda (PO) accompagnate da arresto comportamentale, immobilità e talora movimenti rapidi delle vibrisse. Le scariche spontanee di PO (7–11 Hz) iniziano e cessano bruscamente su una attività di fondo EEG normale alla frequenza media di 1.5 per minuto. I farmaci efficaci nella epilessia con assenze tipo piccolo male dell'uomo sopprimono le PO in modo dose-dipendente, mentre i farmaci specifici per le crisi convulsive o parziali sono inefficaci. Registrazioni con elettrodi profondi ed esperimenti di lesione dimostrano che le PO nei GAERS dipendono da strutture corticali e talamiche con una possibile origine del ritmo nella porzione laterale del talamo; i recettori GABAA sembrano giocare un ruolo critico. Le PO sono geneticamente determinate con una ereditarietà autosomica dominante. La variabile espressività delle PO nei nati da incroci tra GAERS e controlli può essere dovuta all'esistenza di geni multipli.
    Notes: Abstract In Genetic Absence Epilepsy Rats from Strasbourg (GAERS), 100% of the animals present recurrent generalized non-convulsive seizures characterized by bilateral and synchronous spike-and-wave discharges (SWD) accompanied with behavioural arrest, staring and sometimes twitching of the vibrissae. Spontaneous SWD (7–11 cps) start and end abruptly on a normal background EEG at a mean frequency of 1.5 per min. Drugs effective against absence seizures in humans suppress the SWD dose-dependently, whereas drugs specific for convulsive or focal seizures are ineffective. Depth EEG recordings and lesion experiments show that SWD in GAERS depend on cortical and thalamic structures with a possible rhythmic triggering by the lateral thalamus; GABAA and GABAB receptors seem to play a critical role. SWD are genetically determined with an autosomal dominant inheritance. The variable expression of SWD in offsprings from GAERS and control reciprocal crosses may be due to the existence of multiple genes.
    Type of Medium: Electronic Resource
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