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

被引:11
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
相关论文
共 40 条
[1]   ISOCHROMOPHILONES-III-VI, INHIBITORS OF ACYL-COA - CHOLESTEROL ACYLTRANSFERASE PRODUCED BY PENICILLIUM-MULTICOLOR-FO-3216 [J].
ARAI, N ;
SHIOMI, K ;
TOMODA, H ;
TABATA, N ;
YANG, DJ ;
MASUMA, R ;
KAWAKUBO, T ;
OMURA, S .
JOURNAL OF ANTIBIOTICS, 1995, 48 (07) :696-702
[2]   Glutamate neurotoxicity, oxidative stress and mitochondria [J].
Atlante, A ;
Calissano, P ;
Bobba, A ;
Giannattasio, S ;
Marra, E ;
Passarella, S .
FEBS LETTERS, 2001, 497 (01) :1-5
[3]   Neuroprotective Glycosylated Cyclic Lipodepsipeptides, Colletotrichamides A-E, from a Halophyte-Associated Fungus, Colletotrichum gloeosporioides JS']JS419 [J].
Bang, Sunghee ;
Lee, Changyeol ;
Kim, Soonok ;
Song, Ji Hoon ;
Kang, Ki Sung ;
Deyrup, Stephen T. ;
Nam, Sang-Jip ;
Xia, Xuekui ;
Shim, Sang Hee .
JOURNAL OF ORGANIC CHEMISTRY, 2019, 84 (17) :10999-11006
[4]   Neuroprotective Secondary Metabolite Produced by an Endophytic Fungus, Neosartorya fischeri JS']JS0553, Isolated from Glehnia littoralis [J].
Bang, Sunghee ;
Song, Ji Hoon ;
Lee, Dahae ;
Lee, Changyeol ;
Kim, Soonok ;
Kang, Ki Sung ;
Lee, Jong Hun ;
Shim, Sang Hee .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2019, 67 (07) :1831-1838
[5]   Neuroprotective Effect of Natural Alkaloid Fangchinoline Against Oxidative Glutamate Toxicity: Involvement of Keap1-Nrf2 Axis Regulation [J].
Bao, Fengxia ;
Tao, Lingxue ;
Zhang, Haiyan .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2019, 39 (08) :1177-1186
[6]   Why Are the Majority of Active Compounds in the CNS Domain Natural Products? A Critical Analysis [J].
Bharate, Sonali S. ;
Mignani, Serge ;
Vishwakarma, Ram A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2018, 61 (23) :10345-10374
[7]   Sclerotiorin, a novel inhibitor of lipoxygenase from Penicillium frequentans [J].
Chidananda, C. ;
Sattur, A. P. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (08) :2879-2883
[8]   GLUTAMATE NEUROTOXICITY AND DISEASES OF THE NERVOUS-SYSTEM [J].
CHOI, DW .
NEURON, 1988, 1 (08) :623-634
[9]   Mechanism of reversible fluorescent staining of protein with epicocconone [J].
Coghlan, DR ;
Mackintosh, JA ;
Karuso, P .
ORGANIC LETTERS, 2005, 7 (12) :2401-2404
[10]  
Frisch M. J., 2016, Gaussian 16, RevisionA.03