Azaphilones from an Endophytic Penicillium sp. Prevent Neuronal Cell Death via Inhibition of MAPKs and Reduction of Bax/Bcl-2 Ratio

被引:8
|
作者
Bang, Sunghee [1 ]
Baek, Ji Yun [2 ]
Kim, Geum Jin [3 ,4 ]
Kim, Jaekyeong [5 ]
Kim, SungJin [5 ]
Deyrup, Stephen T. [6 ]
Choi, Hyukjae [3 ,4 ]
Kang, Ki Sung [2 ]
Shim, Sang Hee [5 ]
机构
[1] Duksung Womens Univ, Coll Pharm, Seoul 01369, South Korea
[2] Gachon Univ, Coll Korean Med, Seongnam 13120, South Korea
[3] Yeungnam Univ, Coll Pharm, Gyongsan 38541, South Korea
[4] Yeungnam Univ, Inst Cell Culture, Gyongsan 38541, South Korea
[5] Seoul Natl Univ, Coll Pharm, Nat Prod Res Inst, Seoul 08826, South Korea
[6] Siena Coll, Dept Chem & Biochem, Loudonville, NY 12211 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2021年 / 84卷 / 08期
基金
新加坡国家研究基金会;
关键词
NATURAL-PRODUCTS; ABSOLUTE-CONFIGURATION; GLUTAMATE NEUROTOXICITY; OXIDATIVE STRESS; FUNGUS; DERIVATIVES; DISEASES;
D O I
10.1021/acs.jnatprod.1c00298
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Fourteen azaphilone-type polyketides (1-14), including nine new ones (1-6 and 8-10), were isolated from cultures of Vitex rotundifolia-associated Penicillium sp. JVF17, and their structures were determined by spectroscopic analysis together with computational methods and chemical reactions. Neuroprotective effects of the isolated compounds were evaluated against glutamate-induced neurotoxicity. Treatment with compounds 3, 6, 7, and 11-14 increased cell viabilities of hippocampal neuronal cells damaged by glutamate, with compound 12 being the most potent. Compound 12 markedly decreased intracellular Ca2+ and nuclear condensation levels. Mechanistically, molecular markers of apoptosis induced by treatment with glutamate, i.e., phosphorylation of MAPKs and elevated Bax/Bcl-2 expression ratio, were significantly lowered by compound 12. The azaphilones with an isoquinoline core structure were more active than those with pyranoquinones, but N-substitution decreased the activity. This study, including the structure-activity relationship, indicates that the azaphilone scaffold is a promising lead toward the development of novel neuroprotective agents.
引用
收藏
页码:2226 / 2237
页数:12
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