Table 2.
Type of epilepsy | Animal models* |
---|---|
Partial seizures | |
Acute seizures | Electrical stimulation, e.g. 6-Hz |
Chronic seizures | Electrical or chemical kindling Topical chemoconvulsants, which block inhibition, e.g. penicillin, bicuculline, picrotoxin, pentylentetrazol, strychnine Topical chemoconvulsants, which enhance excitation, e.g. carbachol, kainate Freeze lesion or partially isolated cortical slab Implanted metals, e.g. Al2O3, cobalt Experimental febrile seizures Post-traumatic epilepsy (PTE) induced by lateral fluid percussion brain injury Hippocampal sclerosis model, e.g. kainic acid, pilocarpine, post-status epilepticus models Focal dysplasia model, e.g. neonatal freeze, prenatal radiation, methylazoxymethanol |
Post-status epilepticus models with spontaneous recurrent seizures | Electrical status epilepticus induction, e.g. perforanth path, basolateral amygdala Chemical status epilepticus induction, e.g. pilocarpine, kainate |
Generalized seizures | |
Generalized tonic-clonic seizures | Electrical stimulation, e.g. maximal electroshock Chemoconvulsants, e.g. pilocarpine, kainate, penthylenetetrazol, bicuculline, picrotoxin, flurothyl Genetic models, e.g. genetically epilepsy-prone rats, Mongolian gerbil, DBA/2J mice, photosensitive baboons, knockout mice |
Absence seizure | Chemoconvulsants, e.g. low dose penthylenetetrazol, gamma-hydroxybutyrate Genetic models, e.g. genetic absence rats from Strasburg, Wistar Albino Glaxo/Rijswijk, tottering mice, stargazer mice, lethargic mice, slow-wave epilepsy mice, mocha mice, ducky mice |
*Common animals used are rats and mice