Comparisons of Ethanol Extracts of Chinese Propolis (Poplar Type) and Poplar Gums Based on the Antioxidant Activities and Molecular Mechanism

被引:24
|
作者
Zhang, Jianglin [1 ]
Cao, Xueping [1 ]
Ping, Shun [1 ]
Wang, Kai [1 ]
Shi, Jinhu [2 ]
Zhang, Cuiping [1 ]
Zheng, Huoqing [1 ]
Hu, Fuliang [1 ]
机构
[1] Zhejiang Univ, Coll Anim Sci, Hangzhou 310058, Zhejiang, Peoples R China
[2] Husb & Vet Tech Popularizat Ctr Zhejiang Prov, Hangzhou 310020, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
GLUTAMATE CYSTEINE LIGASE; HEME OXYGENASE 1; OXIDATIVE STRESS; IN-VITRO; GLUTATHIONE SYNTHESIS; ENZYME EXPRESSION; GENE-EXPRESSION; UP-REGULATION; INDUCTION; ACTIVATION;
D O I
10.1155/2015/307594
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The biological activities of propolis are varied fromplant sources and the prominent antioxidant effects of Chinese propolis (poplar type) have been extensively reported. Oxidative stress is associated with inflammation and induces many diseases. In the study, to evaluate antioxidant capacities and clarify the underlying molecular mechanisms of ethanol extracts of Chinese propolis (EECP) and ethanol extracts of poplar gums (EEPG), we analyzed their compositions by HPLC, evaluating their free radical scavenging activities and reducing power by chemical analysis methods. Moreover, we studied the roles of EECP and EEPG on the elimination of ROS and expressions of antioxidant genes (HO-1, TrxR1, GCLM, and GCLC) in RAW264.7 cells. We further investigated the effects of MAPKs on the antioxidant genes expression by specific inhibitors. The nucleus translocation effects of Nrf2 were also measured by confocal microscopy analysis. The results indicated that EECP had higher TPC and FDC values but regarding TFC values were not significant. EECP also possessed more contents of 11 compounds than EEPG. Both phytochemical analysis and cell experiment reflected that EECP exerted stronger antioxidant activities than EEPG. EECP and EEPG enhanced endogenous antioxidant defenses by eliminating reactive oxygen species directly and activating Erk-Nrf2-HO1, GCLM, and TrxR1 signal pathways.
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页数:15
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