Antioxidant activities and molecular mechanisms of the ethanol extracts of Baccharis propolis and Eucalyptus propolis in RAW64.7 cells
Autor: | Xiaoge Shen, Huoqing Zheng, Jiang-Lin Zhang, Xueping Cao, Kai Wang, Cui-Ping Zhang, Fuliang Hu |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Antioxidant Cell Survival NF-E2-Related Factor 2 medicine.medical_treatment Pharmaceutical Science High-performance liquid chromatography p38 Mitogen-Activated Protein Kinases Antioxidants Propolis 03 medical and health sciences chemistry.chemical_compound Mice 0302 clinical medicine Chlorogenic acid Western blot Phenols Drug Discovery medicine Animals Extracellular Signal-Regulated MAP Kinases Chromatography High Pressure Liquid Pharmacology Eucalyptus Traditional medicine medicine.diagnostic_test biology Dose-Response Relationship Drug Ethanol Baccharis Macrophages General Medicine biology.organism_classification Oxidative Stress 030104 developmental biology RAW 264.7 Cells Complementary and alternative medicine chemistry Biochemistry Gene Expression Regulation 030220 oncology & carcinogenesis Kaempferide Solvents Molecular Medicine Reactive Oxygen Species Signal Transduction |
Zdroj: | Pharmaceutical biology. 54(10) |
ISSN: | 1744-5116 |
Popis: | Context Numerous studies have reported that propolis possesses strong antioxidant activities. However, their antioxidant molecular mechanisms are unclear. Objective We utilize ethanol extracts of Chinese propolis (EECP) as a reference to compare ethanol extracts of Eucalyptus propolis (EEEP) with ethanol extracts of Baccharis propolis (EEBGP) based on their antioxidant capacities and underlying molecular mechanisms. Materials and methods HPLC and chemical analysis are utilized to evaluate compositions and antioxidant activities. ROS-eliminating effects of EEBGP (20-75 μg/mL), EEEP (1.25-3.75 μg/mL) and EECP (1.25-5 μg/mL) are also determined by flow cytometry analysis. Moreover, we compared antioxidant capacities by determining their effects on expressions of antioxidant genes in RAW264.7 cells with qRT-PCR, western blot and confocal microscopy analysis. Results EEBGP mainly contains chlorogenic acid (8.98 ± 0.86 mg/g), kaempferide (11.18 ± 8.31 mg/g) and artepillin C (107.70 ± 10.86 mg/g), but EEEP contains 10 compositions, whereas EECP contains 17 compositions. Meantime, although EEEP shows DPPH (IC50 19.55 ± 1.28), ABTS (IC50 20.0 ± 0.31) and reducing power (2.70 ± 0.08 mmol TE/g) better than EEBGP's DPPH (IC50 43.85 ± 0.54), ABTS (IC50 38.2 ± 0.33) and reducing power (1.53 ± 0.05 mmol TE/g), EEBGP exerts much higher ROS inhibition rate (40%) than EEEP (under 20%). Moreover, EEBGP strengthen antioxidant system by activating p38/p-p38 and Erk/p-Erk kinase via accelerating nucleus translocation of Nrf2. EEEP and EECP improve antioxidant gene expression only via Erk/p-Erk kinase-Nrf2 signalling pathway. Discussion and conclusion EEBGP and EEEP exert antioxidant activities via different molecular mechanisms, which may depend on chemical compositions. |
Databáze: | OpenAIRE |
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