In this study, a novel series of 4-(2-(alkylthio)benzo[]oxazol-5-yl)-2,4-dihydro-3-1,2,4-triazol-3-ones (-) was designed and synthesized. The anticonvulsant activities of these compounds were evaluated by using the maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole (scPTZ) seizure models in mice. The neurotoxicity of these compounds was evaluated using the rotarod neurotoxicity test. The majority of compounds showed anti-MES activities at 100 or 300 mg/kg. Compound was considered to be the most promising, based on its potency against MES- and PTZ-induced seizures with ED values of 23.7 and 18.9 mg/kg, respectively. The TD value of was 284.0 mg/kg, which resulted in a higher protective index (PI = TD/ED) value than that of carbamazepine and valproate. In an ELISA test, compound significantly increased the γ-aminobutyric acid (GABA) content in mouse brain. In addition, pretreatment with thiosemicarbazide (an inhibitor of the GABA synthesizing enzyme) significantly decreased the activity of in the MES model, which suggests that the mechanism through which compound elicits its anticonvulsive action is at least in part through increasing the GABA level in the brain.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017283PMC
http://dx.doi.org/10.3390/molecules23040756DOI Listing

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