Phenylethanoid glycosides from Paraboea martinii protect rat pheochromocytoma (PC12) cells from hydrogen peroxide-induced cell injury

被引:11
作者
Gong, Xue [1 ]
Xu, Yan [2 ]
Ren, Kai [3 ]
Bai, Xiaorong [4 ]
Zhang, Chunhong [1 ]
Li, Minhui [1 ,3 ,5 ,6 ]
机构
[1] Baotou Med Coll, Dept Pharm, Baotou, Peoples R China
[2] Inner Mongolia Univ Sci & Technol, Affiliated Hosp 1, Baotou Med Coll, Baotou, Peoples R China
[3] Inner Mongolia Autonomous Reg Hosp Tradit Chinese, Intens Care Unit, Hohhot, Peoples R China
[4] Xilinggol Vocat Coll, Dept Med, Inner Mongolia, Peoples R China
[5] Guangxi Bot Garden Med Plants, Guangxi Key Lab Med Resources Protect & Genet Imp, Nanning, Peoples R China
[6] Inner Mongolia Inst Tradit Chinese Med, Pharmaceut Lab, Hohhot, Peoples R China
关键词
Paraboea martinii; phenylethanoid glycosides; neuroprotective effects; zinc protoporphyrin; HO-1; OXIDATIVE STRESS; IDENTIFICATION; EXPRESSION; APOPTOSIS; PATHWAY; CANCER;
D O I
10.1080/09168451.2019.1654359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we isolated eight phenylethanoid glycosides from Paraboea martinii for the first time, and evaluated the mechanism underlying their neuroprotective effects against H2O2-induced injury in PC12 cells. The MTS method was utilized to screen the phenylethanoid glycosides for protective ability. Next, qRT-PCR and western blotting analysis were used to detect the transcription levels of HO-1 and GCLC, which are regulated by Nrf2. The inhibitor ZnPP was used to analyze the involvement of Nrf2 in HO-1 expression. Analyses showed that caleolarioside B, paraboside B, and paraboside II also upregulated the expression of HO-1, but showed no obvious effect on GCLC. Pretreatment with ZnPP significantly reduced the neuroprotective effects. Thus, phenylethanoid glycosides isolated from P. martinii protected PC12 cells from H2O2-induced damage by upregulating HO-1. The results provided evidence that P. martinii might be a potential therapeutic agent for the treatment of neurodegenerative diseases.
引用
收藏
页码:2202 / 2212
页数:11
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