| Literature DB >> 33672606 |
Seulah Lee1, Yeon Ji Suh1, Seonguk Yang1, Dong Geun Hong1, Akihito Ishigami2, Hangun Kim3, Jae-Seoun Hur4, Seung-Cheol Chang5, Jaewon Lee1.
Abstract
Oxidative stress, mitochondrial dysfunction, and neuroinflammation are strongly associated with the pathogenesis of Parkinson's disease (PD), which suggests that anti-oxidative and anti-inflammatory compounds might provide an alternative treatment for PD. Here, we evaluated the neuroprotective effects of evernic aid (EA), which was screened from a lichen library provided by the Korean Lichen Research Institute at Sunchon National University. EA is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. However, the neuroprotective effects of EA have not been studied. We found that EA protected primary cultured neurons against 1-methyl-4-phenylpyridium (MPP+)-induced cell death, mitochondrial dysfunction, and oxidative stress, and effectively reduced MPP+-induced astroglial activation by inhibiting the NF-κB pathway. In vivo, EA ameliorated MPTP-induced motor dysfunction, dopaminergic neuronal loss, and neuroinflammation in the nigrostriatal pathway in C57BL/6 mice. Taken together, our findings demonstrate that EA has neuroprotective and anti-inflammatory effects in PD models and suggest that EA is a potential therapeutic candidate for PD.Entities:
Keywords: 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Parkinson’s disease; anti-inflammation; evernic acid; neuroinflammation; neuroprotection
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Year: 2021 PMID: 33672606 PMCID: PMC7924051 DOI: 10.3390/ijms22042098
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923