Detailed Information

Cited 28 time in webofscience Cited 28 time in scopus
Metadata Downloads

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

Authors
Atiq, A.Lee, H.J.Khan, A.Kang, M.H.Rehman, I.U.Ahmad, R.Tahir, M.Ali, J.Choe, K.Park, J.S.Kim, M.O.
Issue Date
Jun-2023
Publisher
MDPI
Keywords
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP); neurodegeneration; neuroinflammation; oxidative stress; substantia nigra pars compacta (SNpc); trolox
Citation
International Journal of Molecular Sciences, v.24, no.12
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
24
Number
12
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/59787
DOI
10.3390/ijms24129942
ISSN
1661-6596
1422-0067
Abstract
Trolox 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.
Files in This Item
There are no files associated with this item.
Appears in
Collections
ETC > Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Kim, Myeong Ok photo

Kim, Myeong Ok
대학원 (응용생명과학부)
Read more

Altmetrics

Total Views & Downloads

BROWSE