Herpotrichone A Exerts Neuroprotective Effects by Relieving Ferroptosis

被引:1
作者
Deng, Jia-Le [1 ]
Wang, Guo-Yan [2 ]
Zhai, Yi-Jie [1 ]
Feng, Xu-Yao [1 ]
Deng, Lu [2 ]
Han, Wen-Bo [1 ]
Tang, Jiang-Jiang [1 ,3 ]
机构
[1] Northwest A&F Univ, Coll Chem & Pharm, Shaanxi Key Lab Nat Prod & Chem Biol, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Coll Anim Sci & Technol, Yangling 712100, Shaanxi, Peoples R China
[3] Northwest A&F Univ, Shenzhen Res Inst, Shenzhen Virtual Univ Pk Bldg, Shenzhen 518000, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
herpotrichones; neuroprotective effect; ferroptosis; lipidROS; Nrf2; SLC7A11; OXIDATIVE STRESS;
D O I
10.1021/acs.jafc.4c02418
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Inhibition of oxidative stress and ferroptosis is currently considered to be a promising therapeutic approach for neurodegenerative diseases. Herpotrichones, a class of compounds derived from insect symbionts, have shown potential for neuroprotective activity with low toxicity. However, the specific mechanisms through which herpotrichones exert their neuroprotective effects remain to be fully elucidated. In this study, the natural [4 + 2] adducts herpotrichone A (He-A) and its new analogues were isolated from the isopod-associated fungus Herpotrichia sp. SF09 and exhibited significantly protective effects in H2O2-, 6-OHDA-, and RSL3-stimulated PC12 cells and LPS-stimulated BV-2 cells. Moreover, He-A was able to relieve ferroptotic cell death in RSL3-stimulated PC12 cells and 6-OHDA-induced zebrafish larvae. Interestingly, He-A can activate antioxidant elements and modulate the SLC7A11 pathway without capturing oxidic free radical and chelating iron. These findings highlight He-A as a novel hit that protects against ferroptosis-like neuronal damage in the treatment of neurodegenerative diseases.
引用
收藏
页码:17356 / 17367
页数:12
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