Literature DB >> 26341658

Disruption of Endocytosis with the Dynamin Mutant shibirets1 Suppresses Seizures in Drosophila.

Jason R Kroll1, Karen G Wong2, Faria M Siddiqui2, Mark A Tanouye3.   

Abstract

One challenge in modern medicine is to control epilepsies that do not respond to currently available medications. Since seizures consist of coordinated and high-frequency neural activity, our goal was to disrupt neurotransmission with a synaptic transmission mutant and evaluate its ability to suppress seizures. We found that the mutant shibire, encoding dynamin, suppresses seizure-like activity in multiple seizure-sensitive Drosophila genotypes, one of which resembles human intractable epilepsy in several aspects. Because of the requirement of dynamin in endocytosis, increased temperature in the shi(ts1) mutant causes impairment of synaptic vesicle recycling and is associated with suppression of the seizure-like activity. Additionally, we identified the giant fiber neuron as critical in the seizure circuit and sufficient to suppress seizures. Overall, our results implicate mutant dynamin as an effective seizure suppressor, suggesting that targeting or limiting the availability of synaptic vesicles could be an effective and general method of controlling epilepsy disorders.
Copyright © 2015 by the Genetics Society of America.

Entities:  

Keywords:  Drosophila; behavior; dynamin; genetics; seizure

Mesh:

Substances:

Year:  2015        PMID: 26341658      PMCID: PMC4649637          DOI: 10.1534/genetics.115.177600

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  66 in total

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5.  A Systematic Review on Non-mammalian Models in Epilepsy Research.

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6.  FARS2 deficiency in Drosophila reveals the developmental delay and seizure manifested by aberrant mitochondrial tRNA metabolism.

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