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Vitamin E Analog Trolox Attenuates MPTP-Induced Parkinson’s Disease in Mice, Mitigating Oxidative Stress, Neuroinflammation, and Motor Impairment

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dc.contributor.authorAtiq, A.-
dc.contributor.authorLee, H.J.-
dc.contributor.authorKhan, A.-
dc.contributor.authorKang, M.H.-
dc.contributor.authorRehman, I.U.-
dc.contributor.authorAhmad, R.-
dc.contributor.authorTahir, M.-
dc.contributor.authorAli, J.-
dc.contributor.authorChoe, K.-
dc.contributor.authorPark, J.S.-
dc.contributor.authorKim, M.O.-
dc.date.accessioned2023-07-20T06:41:49Z-
dc.date.available2023-07-20T06:41:49Z-
dc.date.issued2023-06-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/59787-
dc.description.abstractTrolox is a potent antioxidant and a water-soluble analog of vitamin E. It has been used in scientific studies to examine oxidative stress and its impact on biological systems. Trolox has been shown to have a neuroprotective effect against ischemia and IL-1β-mediated neurodegeneration. In this study, we investigated the potential protective mechanisms of Trolox against a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinson’s disease mouse model. Western blotting, immunofluorescence staining, and ROS/LPO assays were performed to investigate the role of trolox against neuroinflammation, the oxidative stress mediated by MPTP in the Parkinson’s disease (PD) mouse model (wild-type mice (C57BL/6N), eight weeks old, average body weight 25–30 g). Our study showed that MPTP increased the expression of α-synuclein, decreased tyrosine hydroxylase (TH) and dopamine transporter (DAT) levels in the striatum and substantia nigra pars compacta (SNpc), and impaired motor function. However, Trolox treatment significantly reversed these PD-like pathologies. Furthermore, Trolox treatment reduced oxidative stress by increasing the expression of nuclear factor erythroid-2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1). Lastly, Trolox treatment inhibited the activated astrocytes (GFAP) and microglia (Iba-1), also reducing phosphorylated nuclear factor-κB, (p-NF-κB) and tumor necrosis factor-alpha (TNF-α) in the PD mouse brain. Overall, our study demonstrated that Trolox may exert neuroprotection on dopaminergic neurons against MPTP-induced oxidative stress, neuroinflammation, motor dysfunction, and neurodegeneration. © 2023 by the authors.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleVitamin E Analog Trolox Attenuates MPTP-Induced Parkinson’s Disease in Mice, Mitigating Oxidative Stress, Neuroinflammation, and Motor Impairment-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms24129942-
dc.identifier.scopusid2-s2.0-85163933287-
dc.identifier.wosid001014961400001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.24, no.12-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume24-
dc.citation.number12-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordAuthor1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-
dc.subject.keywordAuthorneurodegeneration-
dc.subject.keywordAuthorneuroinflammation-
dc.subject.keywordAuthoroxidative stress-
dc.subject.keywordAuthorsubstantia nigra pars compacta (SNpc)-
dc.subject.keywordAuthortrolox-
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