Comparative Analysis of Anticonvulsant Activity of Trans and Cis 5,5′-Diphenylhydantoin Schiff Bases
creativework.keywords | 5,5′-diphenylhydantoin Schiff bases, KA SE, MES, mice, trans–cis | |
creativework.publisher | Multidisciplinary Digital Publishing Institute (MDPI) | en |
dc.contributor.author | Tchekalarova J. | |
dc.contributor.author | Todorov P. | |
dc.contributor.author | Stoyanova T. | |
dc.contributor.author | Atanasova M. | |
dc.date.accessioned | 2024-07-10T14:27:06Z | |
dc.date.accessioned | 2024-07-10T14:51:05Z | |
dc.date.available | 2024-07-10T14:27:06Z | |
dc.date.available | 2024-07-10T14:51:05Z | |
dc.date.issued | 2023-11-01 | |
dc.description.abstract | Recently, the four 5,5′-diphenylhydantoin Schiff bases, possessing different aromatic species (SB1-Ph, SB2-Ph, SB3-Ph and SB4-Ph) were synthesized, characterized, and evaluated for anticonvulsant activity in combination with phenytoin. In the present study, the SB1-Ph and SB4-Ph compounds were selected, based on their anticonvulsant potency, and compared with their cis isomers, prepared after a one-hour exposure to the UV source, for their anticonvulsant potency in the maximal electroshock (MES) test and the kainate (KA)-induced status epilepticus (SE) test in mice. In the MES test, the cis SB1-Ph compound exhibited superior to phenytoin and trans isomer activity in the three tested doses, while the cis SB4-Ph compound entirely suppressed the electroshock-induced seizure spread at the highest dose of 40 mg/kg. Pretreatment with the cis SB1-Ph compound and the cis SB4-Ph at the doses of 40 mg/kg, respectively, for seven days, significantly attenuated the severity of KA SE compared to the matched control group pretreated with a vehicle, while phenytoin was ineffective in this test. The cis SB4-Ph but not the cis SB1-Ph demonstrated an antioxidant effect against the KA-induced SE in the hippocampus. Our results suggest that trans–cis conversion of 5,5′-diphenylhydantoin Schiff bases has potential against seizure spread in the MES test and mitigated the KA-induced SE. The antioxidant potency of cis SB4-Ph might be associated with its efficacy in mitigating the SE. | |
dc.identifier.doi | 10.3390/ijms242216071 | |
dc.identifier.issn | 1422-0067 | |
dc.identifier.issn | 1661-6596 | |
dc.identifier.scopus | SCOPUS_ID:85177744730 | en |
dc.identifier.uri | https://rlib.uctm.edu/handle/123456789/884 | |
dc.language.iso | en | |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85177744730&origin=inward | |
dc.title | Comparative Analysis of Anticonvulsant Activity of Trans and Cis 5,5′-Diphenylhydantoin Schiff Bases | |
dc.type | Article | |
oaire.citation.issue | 22 | |
oaire.citation.volume | 24 |