Bilobalide protects pheochromocytoma cell from oxygen-glucose deprivation/reperfusion induced injury via activating Wnt1/beta catenin pathway
By: Yu, X.
Contributor(s): Hou, Jie.
Publisher: Mumbai Indian Journal of Pharmaceutical Science 2022Edition: Vol.84(5), Sep-Oct.Description: 1323-1327p.Subject(s): PHARMACEUTICSOnline resources: Click here In: Indian journal of pharmaceutical sciencesSummary: To explore the protective effect of bilobalide on the pheochromocytoma cell injury induced by oxygen-glucose deprivation/reperfusion in vitro. To simulate ischemia-reperfusion condition, the pheochromocytoma cell injury was induced by oxygen-glucose deprivation/reperfusion in vitro. The cells were divided into control, oxygen-glucose deprivation/reperfusion and oxygen-glucose deprivation/ reperfusion+bilobalide groups. The cell viability, proliferative capacity, malondialdehyde level, superoxide dismutase level, apoptosis, Wnt1 protein level and nuclear beta-catenin protein level were assayed. Compared with control group, the cell viability, proliferative capacity, superoxide dismutase level, Wnt1 protein level and nuclear beta-catenin protein level decreased in the oxygen-glucose deprivation/ reperfusion group, malondialdehyde level and the percentage of apoptotic cells increased in the oxygen- glucose deprivation/reperfusion group, while the cells were treated with bilobalide in the oxygen-glucose deprivation/reperfusion+bilobalide group, all the above-mentioned observation indicators recovered to a certain extent, but still did not reach the level of the control group. Bilobalide protects pheochromocytoma cell from oxygen-glucose deprivation/reperfusion induced injury in vitro through inhibiting oxidative stress via activating Wnt1/beta-catenin pathway.Item type | Current location | Call number | Status | Date due | Barcode | Item holds |
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Articles Abstract Database | School of Pharmacy Archieval Section | Not for loan | 2023-1145 |
To explore the protective effect of bilobalide on the pheochromocytoma cell injury induced by
oxygen-glucose deprivation/reperfusion in vitro. To simulate ischemia-reperfusion condition, the
pheochromocytoma cell injury was induced by oxygen-glucose deprivation/reperfusion in vitro. The
cells were divided into control, oxygen-glucose deprivation/reperfusion and oxygen-glucose deprivation/
reperfusion+bilobalide groups. The cell viability, proliferative capacity, malondialdehyde level, superoxide
dismutase level, apoptosis, Wnt1 protein level and nuclear beta-catenin protein level were assayed.
Compared with control group, the cell viability, proliferative capacity, superoxide dismutase level,
Wnt1 protein level and nuclear beta-catenin protein level decreased in the oxygen-glucose deprivation/
reperfusion group, malondialdehyde level and the percentage of apoptotic cells increased in the oxygen-
glucose deprivation/reperfusion group, while the cells were treated with bilobalide in the oxygen-glucose
deprivation/reperfusion+bilobalide group, all the above-mentioned observation indicators recovered to a
certain extent, but still did not reach the level of the control group. Bilobalide protects pheochromocytoma
cell from oxygen-glucose deprivation/reperfusion induced injury in vitro through inhibiting oxidative
stress via activating Wnt1/beta-catenin pathway.
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