| Literature DB >> 28314243 |
Jun-Feng Zhang1, Li Zhang1, Li-Li Shi1, Zhao-Hua Zhao1, Hao Xu1, Fei Liang1, Hong-Bo Li1, Yan Zhao1, Xi Xu2, Ke Yang3, Ying-Fang Tian4.
Abstract
Parthenolide (PN), a sesquiterpene lactone isolated from the herbal medicine feverfew (Tanacetum parthenium), was reported to possess neuroprotective activity. However, the neuroprotective effect of PN against cerebral ischemia/reperfusion (I/R) injury remains unclear. Therefore, the aim of the present study was to explore the neuroprotective effects of PN against oxygen-glucose deprivation (OGD)-induced apoptosis in PC12 cells and the underlying mechanisms. Our results demonstrated that PN ameliorated OGD/R-evoked neuronal injury and oxidative stress in PC12 cells. In addition, PN notably decreased HIF-1α expression, as well as inhibited apoptosis in PC12 cells after OGD/R. Furthermore, PN pretreatment significantly enhanced the phosphorylation of Akt and GSK-3β in PC12 cells exposed to OGD/R. In conclusion, the present study demonstrated that PN exhibits a neuroprotective effect against OGD/R through activation of the Akt/GSK-3β signaling pathway. Our findings suggest that PN has the potential to serve as a novel therapeutic agent for cerebral I/R injury.Entities:
Keywords: Apoptosis; Cerebral ischemia/reperfusion (I/R); Oxygen-glucose deprivation (OGD); Parthenolide (PN)
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Year: 2017 PMID: 28314243 DOI: 10.1016/j.biopha.2017.03.009
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529