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dc.contributor.authorErdogan, Mumin Alper
dc.contributor.authorYusuf, Dimas
dc.contributor.authorErdogan, Arife
dc.contributor.authorErbas, Oytun
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T15:55:28Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T15:55:28Z
dc.date.issued2019
dc.identifier.issn0920-1211
dc.identifier.issn1872-6844
dc.identifier.urihttps://dx.doi.org/10.1016/j.eplepsyres.2018.12.011
dc.identifier.urihttp://hdl.handle.net/11446/2037
dc.descriptionWOS: 000461404200005en_US
dc.descriptionPubMed ID: 30610970en_US
dc.description.abstractBackground: Millions of individuals worldwide suffer from epilepsy, and up to 25% of patients have seizures that are resistant to currently available antiepileptic drugs. Hence, there continues to be a need for more seizure medications that are effective yet tolerable. Levodropropizine (LVDP) is an established antitussive drug that, based on preclinical data, may also have antiepileptic activity. Methods: We treated rats with either intraperitoneal (IP) LVDP at two different doses or placebo in randomized fashion and then exposed them to IP pentylenetetrazol (PTZ), a potent seizure-inducing compound. We measured the rats' subsequent seizure activity with electroencephalography (EEG), Racine's convulsion scale (RCS) and time to first myoclonic jerk (TFMJ) to determine whether LVDP has antiepileptic properties in our murine model for epilepsy. Results: When compared to placebo, LVDP at both doses significantly suppressed seizure activity. Mean EEG spike wave percentage score decreased from 76.8% (placebo) to 13.1% (lower dose) and 7.6% (higher dose, both p < 0.0001). RCS decreased from a mean of 5.8 (placebo) to 1.83 (lower dose) and 1.16 (higher dose, both p < 0.05). TFMJ had increased from a mean of 65.1 s (placebo), to 247.3 s (lower dose) and 295.5 s (higher dose, both p < 0.0001). Conclusions: Levodropropizine, a common antitussive drug, suppresses seizure activity in rats with PTZ-induced status epilepticus. Given the ongoing need to find effective therapies for refractory epilepsy, the possibility of using levodropropizine as an antiepilepticshould be further explored.en_US
dc.language.isoengen_US
dc.publisherELSEVIER SCIENCE BVen_US
dc.identifier.doi10.1016/j.eplepsyres.2018.12.011en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSeizureen_US
dc.subjectEpilepsyen_US
dc.subjectLevodropropizineen_US
dc.subjectPentylenetetrazolen_US
dc.subjectRaten_US
dc.titleLevodropropizine suppresses seizure activity in rats with pentylenetetrazol-induced epilepsyen_US
dc.typearticleen_US
dc.relation.journalEPILEPSY RESEARCHen_US
dc.departmentDBÜen_US
dc.identifier.volume150en_US
dc.identifier.startpage32en_US
dc.identifier.endpage37en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Erdogan, Mumin Alper] Izmir Katip Celebi Univ, Fac Med, Dept Physiol, Izmir, Turkey -- [Yusuf, Dimas] Univ British Columbia, Fac Med, Vancouver, BC, Canada -- [Erdogan, Arife] Izmir Bozyaka Training & Res Hosp, Dept Emergency Med, Izmir, Turkey -- [Erbas, Oytun] Bilim Univ, Fac Med, Dept Physiol, Istanbul, Turkey -- [Yusuf, Dimas] Jefferson Cary Canc Ctr, 163 Van Buren Rd, Caribou, ME 04736 USAen_US


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