Effects of Artemisinin on Anti-Epileptogenic, Antioxidant and Cholinesterase Enzymes in Pentylenetetrazole-Induced Kindling Model in Mice

dc.contributor.author Kocak, Yilmaz
dc.contributor.author Yunusoglu, Oruc
dc.contributor.author Huyut, Zubeyir
dc.contributor.author Turkan, Fikret
dc.date.accessioned 2025-05-10T17:21:42Z
dc.date.available 2025-05-10T17:21:42Z
dc.date.issued 2023
dc.description Kocak, Yilmaz/0000-0002-8364-4826 en_US
dc.description.abstract Background: Artemisinin (ART) is a compound synthesized from the plant Artemisia annua. This compound has various therapeutic effects and is widely used against malaria. However, ART is known to have modulating effects on GABA (gamma-aminobutyric acid) receptors, which are thought to be responsible for epileptic seizures. This study aimed to evaluate the effects of ART on anti-convulsant, antioxidant, and cholinesterase enzyme activities in Pentylenetetrazole (PTZ)-induced kindling model in mice. Materials and Methods: In the experiment, 6 groups were formed, with seven mice in each group. Mice received a total of 11 intraperitoneal injections of PTZ (35 mg/kg). On the last day of the study, a threat dose of PTZ (75 mg/kg) was administered. In addition, behavioral analysis tests (Locomotor activity and rotarod) and biochemical measurements were performed. Results: Compared with the PTZ group, ART attenuated the severity of the kindling, decreasing the seizure score. ART and VPA reversed increased oxidative stress. Decreased cholinesterase enzymes in PTZ-induced brain increased with ART treatment. While the PTZ application impaired locomotor activity in mice, the ART application provided improvement in locomotor activity. However, no significant difference was found between the groups in the motor performance of the mice. Conclusion:The findings show that ART may have the potential to prevent PTZ-induced oxidative stress, neurochemical changes, behavioral disorders, and seizures. en_US
dc.description.sponsorship Biochemistry of Department, Medical Faculty, Van Yuzuncu Yil University en_US
dc.description.sponsorship This study was supported by the Biochemistry of Department, Medical Faculty, Van Yuzuncu Yil University. en_US
dc.identifier.doi 10.5530/ijper.57.3s.93
dc.identifier.issn 0019-5464
dc.identifier.scopus 2-s2.0-85168614568
dc.identifier.uri https://doi.org/10.5530/ijper.57.3s.93
dc.identifier.uri https://hdl.handle.net/20.500.14720/10490
dc.language.iso en en_US
dc.publisher Assoc Pharmaceutical Teachers india en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Anti-Convulsant en_US
dc.subject Antioxidant en_US
dc.subject Cholinesterases en_US
dc.subject Pentylenetetrazole en_US
dc.subject Kindling Model en_US
dc.subject Artemisinin en_US
dc.title Effects of Artemisinin on Anti-Epileptogenic, Antioxidant and Cholinesterase Enzymes in Pentylenetetrazole-Induced Kindling Model in Mice en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Kocak, Yilmaz/0000-0002-8364-4826
gdc.author.scopusid 57216862467
gdc.author.scopusid 57211217097
gdc.author.scopusid 55394375700
gdc.author.scopusid 57115336200
gdc.author.wosid Kocak, Yilmaz/Abg-8344-2021
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Kocak, Yilmaz] Van Yuzuncu Yil Univ, Fac Hlth Sci, Dept Phys Therapy & Rehabil, Van, Turkiye; [Kocak, Yilmaz] Van Yuzuncu Yil Univ, Fac Vet, Dept Pharmacol & Toxicol, Van, Turkiye; [Yunusoglu, Oruc] Bolu Abant Izzet Baysal Univ, Fac Med, Dept Pharmacol, Bolu, Turkiye; [Huyut, Zubeyir] Van Yuzuncu Yil Univ, Fac Med, Dept Biochem, Van, Turkiye; [Turkan, Fikret] Igdir Univ, Fac Dent, Dept Basic Sci, Igdir, Turkiye; [Kocak, Yilmaz] Van Yuzuncu Yil Univ, Fac Hlth Sci, Dept Phys Therapy & Rehabil, TR-65080 Van, Turkiye en_US
gdc.description.endpage S830 en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage S821 en_US
gdc.description.volume 57 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q4
gdc.identifier.wos WOS:001060743500039
gdc.index.type WoS
gdc.index.type Scopus

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