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10.3892/ijmm.2015.2258

http://scihub22266oqcxt.onion/10.3892/ijmm.2015.2258
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C4501663!4501663!26101183
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suck abstract from ncbi


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pmid26101183      Int+J+Mol+Med 2015 ; 36 (2): 345-54
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  • Puerarin attenuates glucocorticoid-induced apoptosis of hFOB1 19 cells through the JNK-and Akt-mediated mitochondrial apoptotic pathways #MMPMID26101183
  • YU D; MU S; ZHAO D; WANG G; CHEN Z; REN H; FU Q
  • Int J Mol Med 2015[Aug]; 36 (2): 345-54 PMID26101183show ga
  • Puerarin is an active component of Pueraria lobata, which is a commonly used Chinese herbal medicine for the treatment of osteoporosis. The present study aimed to evaluate the osteoprotective effect of puerarin on glucocorticoid (GC)-induced apoptosis of osteoblasts in vitro. The effects of puerarin on dexamethasone (DEX)-induced cell apoptosis were assessed using enzyme-linked immunosorbent assay and a terminal deoxynucleotidyl transferase dUTP nick-end labeling assay, and found that the viability of hFOB1.19 cells was significantly increased following exposure to between 10?6 and 10?10 M puerarin, with a maximal anti-apoptotic effect at a concentration of 10?8 M. In addition, compared with the control group, puerarin upregulated the transcription and protein levels of B-cell lymphoma-2 and downregulated B-cell-associated X protein in the hFOB1.19 cells. Puerarin attenuated the DEX-induced release of cytochrome c and cleavage of caspase-3, and treatment with puerarin inhibited the c-Jun N-terminal kinase (JNK) pathway and activated the phosphoinositide 3-kinase (PI3K)/Akt pathway in the hFOB1.19 cells. Furthermore, the Akt inhibitor, LY294002, partly eliminated the protective effect of puerarin on DEX-induced apoptosis, and puerarin combined with the JNK inhibitor, SP600125, suppressed DEX-induced apoptosis to a lesser extent than in the cells treated with SP600125 alone. These results suggested that the JNK and PI3K/Akt signaling pathways mediate the inhibitory effects of puerarin on apoptosis in the hFOB1.19 cells. In conclusion, puerarin prevented DEX-induced apoptosis of hFOB1.19 cells via inhibition of the JNK pathway and activation of the PI3K/Akt signaling pathway in the cells, dependent on the mitochondrial apoptotic pathway. These results support puerarin as a promising target in the treatment of GC-induced osteoporosis.
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