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Abstract
Epilepsy is among the most common neurological diseases, affecting more than 50 million people worldwide. Unfortunately, one-third of people with epilepsy fail to respond to any current treatment and present a decreased quality of life. Nevertheless, different studies suggest that epilepsies acquired from an initial insult as status epilepticus (SE) followed by epileptogenesis can be prevented. Therefore, it is necessary to establish animal models of epileptogenesis induced by SE. Thus, here we proposed an animal model of epileptogenesis triggered by SE that occurred during the neurodevelopment of zebrafish (Danio rerio). Zebrafish larvae at the 7th day post-fertilization (dpf) were randomly assigned to two experimental groups. One group was exposed to embryo medium. The other group was exposed to pentylenetetrazol (15 mM PTZ) to induce SE. At the 8th dpf, each larva was subjected to the open tank test (OTT) to analyze locomotion and behavioral parameters. After the OTT, each initial group was divided into two groups: animals maintained in embryo medium and animals exposed to PTZ (3 mM), and the susceptibility to PTZ-induced seizure-like behavior was analyzed. Data showed that animals submitted to SE on the 7th dpf showed altered locomotion and behavior 24 hours later. Interestingly, zebrafish larvae submitted to SE on the 7th dpf showed decreased latency to reach seizure-like behavioral stages when exposed to a low concentration of PTZ on the 8th dpf. Concluding, our results show that SE during neurodevelopment increases the susceptibility of zebrafish larvae to present PTZ-induced seizure-like behavior. Our study contributes to the establishment of a model of epileptogenesis in developing zebrafish. Finally, the next step is to improve this model by characterizing molecular, biochemical and physiological markers.
Competing Interest Statement
The authors have declared no competing interest.
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