The effect of the HMGB1/RAGE/TLR4/NF-?B signalling pathway in patients with idiopathic epilepsy and its relationship with toxoplasmosis

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dc.authoridKILIÇ, Ümit/0000-0001-9917-0648en_US
dc.authoridTurkoglu, Sule/0000-0001-8616-832Xen_US
dc.authoridSoyturk, Hayriye/0000-0002-0000-3768en_US
dc.authorscopusid57219390008en_US
dc.authorscopusid57204184451en_US
dc.authorscopusid57194432176en_US
dc.authorscopusid16445142100en_US
dc.authorscopusid23048475600en_US
dc.authorwosidKILIÇ, Ümit/KEJ-4241-2024en_US
dc.authorwosidTurkoglu, Sule/ABC-4645-2022en_US
dc.contributor.authorSoyturk, Hayriye
dc.contributor.authorOnal, Cansu
dc.contributor.authorKilic, Umit
dc.contributor.authorTurkoglu, Sule Aydin
dc.contributor.authorAyaz, Erol
dc.date.accessioned2024-08-23T16:04:15Z
dc.date.available2024-08-23T16:04:15Z
dc.date.issued2024en_US
dc.departmentDüzce Üniversitesien_US
dc.description.abstractThis study aims to investigate the relationship between toxoplasmosis and this pathway, which may be effective in the formation of epilepsy by acting through the HMGB1/RAGE/TLR4/NF-kappa B signalling pathway in patients with idiopathic epilepsy. In the study, four different experimental groups were formed by selecting Toxoplasma gondii IgG positive and negative patients with idiopathic epilepsy and healthy controls. Experimental groups were as follows: Group 1: Epilepsy+/Toxo- (E+, T-) (n = 10), Group 2: Epilepsy-/Toxo- (E-, T-) (n = 10), Group 3: Epilepsy-/Toxo+ (E-, T+) (n = 10), Group 4: Epilepsy+/Toxo+ (E+, T+) (n = 10). HMGB1, RAGE, TLR4, TLR1, TLR2, TLR3, IRAK1, IRAK2, IKBKB, IKBKG, BCL3, IL1 beta, IL10, 1 L8 and TNF alpha mRNA expression levels in the HMGB/RAGE/TLR4/NF-kappa B signalling pathway were determined by quantitative simultaneous PCR (qRT-PCR) after collecting blood samples from all patients in the groups. Statistical analysis was performed by one-way ANOVA followed by LSD post-hoc tests, and p < 0.05 was considered to denote statistical significance. The gene expression levels of HMGB1, TLR4, IL10, IL1B, IL8, and TLR2 were significantly higher in the G1 group than in the other groups (p < 0.05). In the G3 group, RAGE and BCL3 gene expression levels were significantly higher than in the other groups (p < 0.05). In the G4 group, however, IRAK2, IKBKB, and IKBKG gene expression levels were significantly higher than in the other groups (p < 0.05). HMGB1, TLR4, IRAK2, IKBKB, IL10, IL1B, IL1B, and IL8 in this signalling pathway are highly expressed in epilepsy patients in G1 and seizures occur with the stimulation of excitatory mechanisms by acting through this pathway. The signalling pathway in epilepsy may be activated by HMGB1, TLR4, and TLR2, which are considered to increase the level of proinflammatory cytokines. In T. gondii, this pathway is activated by RAGE and BCL3.en_US
dc.description.sponsorshipTurkiye Bilimsel ve Teknolojik Arastirma Kurumu [317S052]en_US
dc.description.sponsorshipTurkiye Bilimsel ve Teknolojik Arastirma Kurumu, Grant/Award Number: 317S052en_US
dc.identifier.doi10.1111/jcmm.18542
dc.identifier.issn1582-1838
dc.identifier.issn1582-4934
dc.identifier.issue14en_US
dc.identifier.pmid39046369en_US
dc.identifier.scopus2-s2.0-85199350691en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.urihttps://doi.org/10.1111/jcmm.18542
dc.identifier.urihttps://hdl.handle.net/20.500.12684/14129
dc.identifier.volume28en_US
dc.identifier.wosWOS:001275558600001en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofJournal of Cellular And Molecular Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectepilepsyen_US
dc.subjectgene expressionen_US
dc.subjectHMGB/RAGE/TLR4/NF-kappa B signalling pathwayen_US
dc.subjectinflammationen_US
dc.subjectQ-PCRen_US
dc.subjecttoxoplasmosisen_US
dc.subjectNf-Kappa-Ben_US
dc.subjectTemporal-Lobe Epilepsyen_US
dc.subjectToll-Like Receptorsen_US
dc.subjectRat Modelen_US
dc.subjectCryptogenic Epilepsyen_US
dc.subjectGondii Infectionen_US
dc.subjectToxocara-Canisen_US
dc.subjectExpressionen_US
dc.subjectDiseaseen_US
dc.subjectHmgb1en_US
dc.titleThe effect of the HMGB1/RAGE/TLR4/NF-?B signalling pathway in patients with idiopathic epilepsy and its relationship with toxoplasmosisen_US
dc.typeArticleen_US

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