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  • Journal of Experimental and Clinical Medicine
  • Volume:39 Issue:3
  • Investigation of the Effects of Pinacidil and Glibenclamide Administration on HCN1, KCNT1, Kir 6.1, ...

Investigation of the Effects of Pinacidil and Glibenclamide Administration on HCN1, KCNT1, Kir 6.1, SUR1 Gene Expressions in Hippocampus and Cortex Regions in Epileptic Rats

Authors : Ümit KILIÇ, Hayriye SOYTÜRK
Pages : 868-873
View : 43 | Download : 8
Publication Date : 2022-08-30
Article Type : Research Paper
Abstract :The purpose of this study was to look into the effects of pinacidil and glibenclamide on HCN1, KCNT1, Kir 6.1, and SUR1 gene expression in epileptic rats hippocampus and cortex. Male Wistar-Albino rats were used in this study. The drugs pinacidil and glibenclamide were utilized. Control, Epilepsy, Epilepsy-O, and Epilepsy-B were the five groups formed. The epileptic focus was created by intracortical administration of penicillin at a dose of 500 IU/2 μl. Hippocampus and Cortex are removed from all animals and Kir 6.1, SUR1, HCN1, and KCNT1 gene expression levels were determined by qPCR. The SPSS 21 program was used for statistics. HCN1 gene expression level is equal in the hippocampus and cortex insert ignore into journalissuearticles values(p<0.05);. KCNT1, SUR1, and KIR6.1 are more expressed in the hippocampus than in the cortex insert ignore into journalissuearticles values(p<0.05);. In epilepsy groups, HCN1 gene expression level was found to be higher than KCNT1, SUR1, and KIR6.1 gene expression levels insert ignore into journalissuearticles values(p<0.05);. KIR6.1, SUR1, gene expression levels decreased with the application of pinacidil and glibenclamide insert ignore into journalissuearticles values(p<0.05);. SUR1 and KIR6.1 gene expression levels were considerably lower in the epilepsy pinacidil group compared to the other groups. The gene expression levels in the hippocampus were found to be considerably higher than in the cortex group, according to this study. The fact that HCN1 gene expression levels are significantly greater in both the brain and the hippocampus 24 hours following the commencement of epileptic convulsions suggests that preventive medication may be possible.
Keywords : Epilepsy, Kir 6 1, SUR1, HCN1, KCNT1, gene expressions

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