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dc.contributor.authorAyyildiz, Mustafa
dc.contributor.authorCoskun, Sule
dc.contributor.authorYildirim, Mehmet
dc.contributor.authorAgar, Erdal
dc.date.accessioned2020-06-21T15:19:38Z
dc.date.available2020-06-21T15:19:38Z
dc.date.issued2007
dc.identifier.issn0013-9580
dc.identifier.issn1528-1167
dc.identifier.urihttps://doi.org/10.1111/j.1528-1167.2007.01080.x
dc.identifier.urihttps://hdl.handle.net/20.500.12712/19899
dc.descriptionAYYILDIZ, Mustafa/0000-0002-6594-3080; Yildirim, Mehmet/0000-0003-1798-5478; COSKUN CEVHER, SULE/0000-0001-6204-2845en_US
dc.descriptionWOS: 000248049200019en_US
dc.descriptionPubMed: 17433052en_US
dc.description.abstractPurpose: Epileptic seizure results from excessive discharge in a population of hyperexcitable neurons. A number of studies help to document the effects of active oxygen free radical scavengers such as alpha-tocopherol or ascorbic acid (vitamin C). In the present study, we examined the effects of ascorbic acid, at the six different doses, on penicillin-induced epileptiform activity. Methods: A single microinjection of penicillin (2.5 mu l, 500 units, intracortically) into the left sensorimotor cortex induced epileptiform activity within 2-5 min, progressing to full seizure activity lasting similar to 3-5 h. In the first set of experiments, 30 min after penicillin injection, six different doses of ascorbic acid (25, 50, 100, 200, 400, or 800 mg/kg) were administered intraperitoneally (IP). The other group of animals received the effective dose of ascorbic acid (100 mg/kg, IP) for 7 days. Ascorbic acid administration was stopped 24 h before penicillin treatment. Another group of rats received the effective dose of ascorbic acid (100 mg/kg, IP) 30 min before penicillin treatment. In the second set of experiments, the lipid peroxidation (NIDA) and reduced glutathione (GSH) levels of brain were measured in the control, control + ascorbic acid, penicillin, and penicillin + ascorbic acid groups. Results: Ascorbic acid, at the low dose (50, 100 mg/kg, 30 min after penicillin injection), decreased both the frequency and amplitude of penicillin-induced epileptiform activity in rats. Ascorbic acid, at intermediate doses (200, 400 mg/kg, 30 min after penicillin injection), decreased the frequency of epileptiform activity without changing the amplitude. Ascorbic acid, at the lowest dose (25 mg/kg) and highest dose (800 mg/kg) (30 min after penicillin injection), did not change either the frequency or amplitude of epileptiform activity. Ascorbic acid, at the low dose (100 mg/kg) was the most effective dose in changing the frequency and amplitude of penicillin-induced epileptiform activity. Pretreatment with ascorbic acid (100 mg/kg) 30 min before penicillin treatment caused a significant delay in the onset of penicillin-induced epileptiform activity. Pretreatment with ascorbic acid (100 mg/kg) for 7 days did not change the latency of epileptiform activity. The most effective dose of ascorbic acid (100 mg/kg) prevented both the decrease in GSH level and the increase in lipid peroxidation level (MDA) occurring after penicillin-induced epileptiform activity. Conclusions: These data indicate that ascorbic acid has neuroprotective activity against penicillin-induced epileptiform electrocorticogram activity.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.isversionof10.1111/j.1528-1167.2007.01080.xen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectepileptiform activityen_US
dc.subjectglutathioneen_US
dc.subjectlipid peroxidationen_US
dc.subjectpenicillinen_US
dc.subjectvitamin Cen_US
dc.titleThe effects of ascorbic acid on penicillin-induced epileptiform activity in ratsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume48en_US
dc.identifier.issue7en_US
dc.identifier.startpage1388en_US
dc.identifier.endpage1395en_US
dc.relation.journalEpilepsiaen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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