1.Garcinia xanthochymus extract protects PC12 cells from HO-induced apoptosis through modulation of PI3K/AKT and NRF2/HO-1 pathways.
Jing XU ; Sheng GAN ; Jun LI ; De-Bing WAND ; Yu CHEN ; Xin HU ; Guang-Zhong YANG
Chinese Journal of Natural Medicines (English Ed.) 2017;15(11):825-833
The aim of the present study was to investigate the protective effects and underlying mechanisms of Garcinia xanthochymus, a perennial medicinal plant native to Yunnan, China, against HO-induced oxidative damage in rat pheochromacytoma PC12 cells. Preincubation of PC12 cells with fruit EtOAc fraction (fruit-EFr., 12.5-50 µmol·L) of G. xanthochymus for 24 h prior to HO exposure markedly improved cell viability and increased the activities of antioxidant enzymes (superoxide dismutase, catalase, and heme oxygenase-1 [HO-1]), prevented lactate dehydrogenase release and lipid peroxidation malondialdehyde production, attenuated the decrease of matrix metalloproteinases (MMP), and scavenged reactive oxygen species (ROS). Fruit-EFr. also reduced BAX and cytochrome C expression and improved BCL-2 expression, thereby decreasing the ratio of BAX to BCL-2. Fruit-EFr. activated the nuclear translocation of NRF2 to increase HO-1 and induced the phosphorylation of AKT. Its cytoprotective effect was abolished by LY294002, a specific inhibitor of PI3K. Taken together, the above findings suggested that fruit-EFr.of G. xanthochymus could enhance cellular antioxidant defense capacity, at least in part, through upregulating HO-1 expression and activating the PI3K/AKT pathway and that it could suppress HO-induced oxidative damage via PI3K/AKT and NRF2/HO-1 signaling pathways.
Animals
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Antioxidants
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metabolism
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pharmacology
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Apoptosis
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drug effects
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Biological Transport
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Cell Survival
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Cytochromes c
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metabolism
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Fruit
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Garcinia
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Heme Oxygenase-1
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metabolism
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Hydrogen Peroxide
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NF-E2-Related Factor 2
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metabolism
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Oxidative Stress
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drug effects
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PC12 Cells
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Phosphatidylinositol 3-Kinase
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metabolism
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Phosphatidylinositol 3-Kinases
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Phosphorylation
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Plant Extracts
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pharmacology
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Protective Agents
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pharmacology
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Proto-Oncogene Proteins c-akt
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metabolism
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Proto-Oncogene Proteins c-bcl-2
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metabolism
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Rats
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Signal Transduction
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bcl-2-Associated X Protein
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metabolism