We provide a variety of internationally recognized epilepsy animal model construction services, covering three categories: chemical induction, physical stimulation, and genetic engineering, to facilitate basic research and drug development.
Model Name |
Induction method |
Applicable animals |
Type of attack |
Application Areas |
Model Features |
PTZ Model |
Intraperitoneal/subcutaneous injection of PTZ |
Rats and mice |
Acute/chronic myoclonus, spasticity |
Drug screening, attack mechanism research |
Easy to operate, suitable for initial screening of anti-epileptic drugs; can simulate absence seizures |
GHB/GBL Model |
Systemic injection of gamma-hydroxybutyrate or its precursors |
Rat |
Absence seizures (SWDs EEG) |
Mechanism of absence epilepsy and evaluation of drug efficacy |
Highly specific absence model; requires EEG monitoring |
KA Model |
Intraventricular or systemic injection of KA |
Rats and mice |
Focal→generalized seizures |
The pathogenesis of temporal lobe epilepsy and the development of more effective targeted therapeutic drugs |
The operation is simple and permanent; the latency period and EEG characteristics are highly similar to those of human temporal lobe epilepsy. |
Model Name |
Induction method |
Applicable animals |
Type of attack |
Application Areas |
Model Features |
Electric ignition model |
Repetitive electrical stimulation of the hippocampus/amygdala |
Rat |
Focal→generalized seizures |
Drug-resistant epilepsy and neuroplasticity research |
Simulate the progression of epilepsy; requires surgical implantation of electrodes, which takes a long time |
6Hz corneal stimulation model |
6Hz current stimulation of the cornea |
Rat |
Psychomotor epilepsy |
Drug resistance screening |
Non-invasive, high success rate; simulates complex partial seizures |
MES Model |
Maximum electric shock stimulation |
Mice, rat |
Generalized tonic-clonic seizure |
Gold standard screening for anticonvulsant drugs |
Rapid and standardized; biased towards ion channel drug testing |
Gene Targets |
Mutation type |
Applicable animals |
Phenotypic characteristics |
Application Areas |
Model advantages |
SCN1A knockout |
Gene knockout |
Mice |
Dravet syndrome, spontaneous seizures |
Genetic epilepsy mechanisms and gene therapy |
Highly simulates human Dravet syndrome; suitable for studying sodium channel-related pathologies |
CHRNA4 knock-in |
Point mutation knock-in |
Mice |
Nocturnal frontal lobe epilepsy |
Neural receptor targeted drug development |
Accurate simulation of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) |
KCNQ2 mutations |
Conditional dominant negative |
Transgenic mice |
Benign familial neonatal epilepsy |
Study on the relationship between potassium channel function and epilepsy |
Simulate BFNC, suitable for neonatal epilepsy mechanism and drug screening |
LGI1 knockout |
Gene knockout |
Mice |
Idiopathic temporal lobe epilepsy |
Autoimmune epilepsy research |
Simulates genetic epilepsy with auditory features; can be used to explore immunomodulatory treatment |
Accurate Modeling :Provides a full-cycle model from acute onset to chronic spontaneous epilepsy, supporting customized induction plans.
Data support :Supporting electroencephalogram (EEG/Video-EEG), behavioral analysis and histopathology testing services.
Compliance assurance : Comply with AAALAC international animal welfare standards and provide ethical approval assistance services.
Research Advisory Team :Recommend the best model solution based on your experimental goals (such as drug targets, pathological stages, species requirements).
Technical Support : Full-process service from model building to data analysis to help you complete your research efficiently!
Note : For specific model parameters, cycles and quotations, please consult our dedicated customer service.
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