期刊
ACTA PHARMACOLOGICA SINICA
卷 31, 期 5, 页码 540-545出版社
ACTA PHARMACOLOGICA SINICA
DOI: 10.1038/aps.2010.28
关键词
geniposide; glucagon-like peptide 1 receptor; heme oxygenase 1; oxidative stress; PC12 cells
资金
- National Natural Science Foundation of China [30701020, 30600813]
- Program for New Century Excellent Talents in University [NCET-07-0913]
- Chongqing Science & Technology Commission (CSTC) [2007AA5029]
- Chongqing Municipal Education Committee [KJ0707009]
Aim: To explore the role of activation of glucagon-like peptide 1 receptor (GLP-1R) and its relative cell signaling pathway in the cytoprotection of geniposide. Methods: Cell viability was determined by MTT assay. Knockdown of the Glp-1r gene was carried out with shRNA. The levels of HO-1 protein and cAMP response element binding protein (CREB) phosphorylation were measured by Western blotting. Results: Geniposide protected PC12 cells from oxidative damage induced by 3-morpholinosydnonimine hydrochloride (SIN-1) by enhancing the expression of heme oxygenase 1 (HO-1) via the cAMP-PKA-CREB signal pathway. After transfecting PC12 cells with the AB1 enhancer from the HO-1 gene, luciferase activity induced by geniposide increased in a dose-dependent manner, but not in the PC12 cells whose Glp-1r gene was disrupted. Additionally, inhibition of HO-1 activity by Sn-protoporphyrin IX (SnPP) or shRNA-mediated knockdown of Glp-1r decreased the neuroprotection of geniposide in PC12 cells. Conclusion: GLP-1R plays a critical role in geniposide-induced HO-1 expression to attenuate oxidative insults in PC12 cells.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据