Evaluation of the Neuroprotective Effects of Korean Ginseng Root Extract in an Experimental Model of Multiple Sclerosis

dc.authorscopusid 57463909900
dc.authorscopusid 55662834600
dc.authorscopusid 24067816000
dc.authorscopusid 59942134700
dc.authorscopusid 24079789000
dc.authorscopusid 59942279500
dc.authorscopusid 59942279500
dc.contributor.author Donmez, Muhammet Oguzhan
dc.contributor.author Sener, Goksel
dc.contributor.author Akbay, Tugba Tunali
dc.contributor.author Sivas, Guzin Goksun
dc.contributor.author Akakin, Dilek
dc.contributor.author Unlu, Hilal
dc.contributor.author Goren, Mehmet Zafer
dc.date.accessioned 2025-07-10T20:04:06Z
dc.date.available 2025-07-10T20:04:06Z
dc.date.issued 2025
dc.department Fenerbahçe University en_US
dc.department-temp [Donmez, Muhammet Oguzhan; Goren, Mehmet Zafer] Marmara Univ, Fac Med, Dept Med Pharmacol, Istanbul, Turkiye; [Donmez, Muhammet Oguzhan; Sener, Goksel] Fenerbahce Univ, Fac Pharm, Dept Pharmacol, Istanbul, Turkiye; [Akbay, Tugba Tunali; Sivas, Guzin Goksun] Marmara Univ, Fac Dent, Dept Biochem, Istanbul, Turkiye; [Akakin, Dilek; Unlu, Hilal] Marmara Univ, Fac Med, Dept Histol & Embryol, Istanbul, Turkiye en_US
dc.description.abstract Objective: Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system characterised by demyelination. The aim of this study was to evaluate the neuroprotective effects of Korean ginseng root extract (KGE) using a cuprizone-induced demyelination model. Materials and Methods: C57BL/6 mice were divided into control, demyelination and remyelination groups and each group was treated with KGE. Demyelination was induced with 0.2% cuprizone in the diet for four weeks. KGE (100 mg/kg) was administered by gavage during or after the cuprizone exposure. Body weight, food and water intake, and motor performance parameters were investigated. In addition, glutathione (GSH), glutathione-S-transferase (GST), superoxide dismutase (SOD) malondialdehyde (MDA), oligodendrocyte transcription factor-2 (OLIG2) and myelin basic protein (MBP) levels were measured in brain samples, while MBP and glial fibrillary acidic protein (GFAP) expression was assessed by immunohistochemistry and myelin status was examined using Luxol Fast Blue staining. Results: Korean ginseng root extract prevented myelin loss, promoted remyelination, and improved motor performance. It reduced oxidative stress by increasing GSH, GST, and SOD levels while decreasing MDA. KGE also suppressed demyelination by reducing astrogliosis and restoring OLIG2 and MBP levels. Conclusion: Korean ginseng root extract exhibits neuroprotective properties during demyelination and promotes remyelination, highlighting its therapeutic potential for MS. en_US
dc.description.sponsorship Marmara University Scientific Research Project Committee [TDK-2023-11091] en_US
dc.description.sponsorship Financial Support: This study was financially supported by the Marmara University Scientific Research Project Committee (Project code: TDK-2023-11091) . en_US
dc.description.woscitationindex Emerging Sources Citation Index
dc.identifier.doi 10.5472/marumj.1708769
dc.identifier.endpage 170 en_US
dc.identifier.issn 1309-9469
dc.identifier.issue 2 en_US
dc.identifier.scopus 2-s2.0-105007946914
dc.identifier.scopusquality Q4
dc.identifier.startpage 158 en_US
dc.identifier.uri https://doi.org/10.5472/marumj.1708769
dc.identifier.uri https://hdl.handle.net/20.500.14627/1107
dc.identifier.volume 38 en_US
dc.identifier.wos WOS:001516117100001
dc.identifier.wosquality N/A
dc.language.iso en en_US
dc.publisher Marmara Univ, Fac Medicine en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.scopus.citedbyCount 0
dc.subject Rotarod en_US
dc.subject MBP en_US
dc.subject Olig2 en_US
dc.subject GFAP en_US
dc.subject LFB en_US
dc.subject Demyelination en_US
dc.title Evaluation of the Neuroprotective Effects of Korean Ginseng Root Extract in an Experimental Model of Multiple Sclerosis en_US
dc.type Article en_US
dc.wos.citedbyCount 0
dspace.entity.type Publication

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