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RETRACTED: The Aminopyridinol Derivative BJ-1201 Protects Murine Hippocampal Cells against Glutamate-Induced Neurotoxicity via Heme Oxygenase-1 (Retracted Article. See vol 21, Art no 1463, 2016)open access

Authors
Lee, Dong-SungNam, Tae-GyuJeong, Byeong-SeonJeong, Gil-Saeng
Issue Date
May-2016
Publisher
MDPI AG
Keywords
aminopyridinol compound BJ-1201; neuroprotection; aminopyridinol HT22; heme oxygenase-1; nuclear transcription factor erythroid-2 related factor 2
Citation
MOLECULES, v.21, no.5, pp.1 - 11
Indexed
SCIE
SCOPUS
Journal Title
MOLECULES
Volume
21
Number
5
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/14023
DOI
10.3390/molecules21050594
ISSN
1420-3049
Abstract
Glutamate is the major excitatory neurotransmitter in the brain. It can cause neuronal cell damage in the context of oxidative stress. BJ-1201 is a derivative of the compound aminopyridinol, which is known for its antioxidant activity. In this study, we examined the effect of BJ-1201, a 6-(diphenylamino)-2,4,5-trimethylpyridin-3-ol compound, on neuroprotection in HT22 cells. Our data showed that BJ-1201 can protect HT22 cells against glutamate-induced cell cytotoxicity. In addition, BJ-1201 upregulated heme oxygenase-1 (HO-1) to levels comparable to those of the CoPP-treated group. BJ-1201 treatment induced phosphorylation of JNK, but not p38-MAPK or ERK. It also increased the signal in the reporter assay based on beta-galactosidase activity driven by the nuclear transcription factor erythroid-2 related factor 2 (Nrf2) promoter harboring antioxidant response elements (AREs) and induced the translocation of Nrf2. These results demonstrate that BJ-1201 may be a good therapeutic platform against neurodegenerative diseases induced by oxidative stress.
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