Shikonin inhibits neuronal apoptosis induced by OGD through targeting PI3K/Akt signaling pathway |
| |
Authors: | CHEN Meng-yue CHEN Wei-dong LIU Yi-min XIANG Si-cheng YIN Hui-ling ZHANG Zhi-feng |
| |
Affiliation: | 1. First Clinical College, Hubei University of Medicine, Shiyan 442000, China;2. Department of Physiology, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan 442000, China |
| |
Abstract: | AIM: To explore the effect of shikonin on rat primary cortical neurons in oxygen-glucose deprivation (OGD)-induced injury model.METHODS: The neurons were pretreated with shikonin at different concentrations (0.02, 0.2, 2 and 20 μmol/L) followed by treatment with OGD. Lactate dehydrogenase (LDH) release assay and fluorescein diacetate/propidium iodide (FDA/PI) double staining were used to detect neuronal viability and apoptosis, and then the optimal concentration of shikonin was determined. LY294002 (PI3K/Akt signaling pathway inhibitor, 1 μmol/L) was added before the addition of shikonin, and the protein level of p-Akt (Ser473) in the neurons was determined by Wes-tern blot. LDH release assay and FDA/PI double staining were also used to detect neuronal viability and apoptosis.RESULTS: A certain concentration (0.2~20 μmol/L) of shikonin increased the viability of impaired neurons (P<0.05) and the protein level of p-Akt (Ser473) in the neurons (P<0.05). The effect of shikonin on neuronal p-Akt (Ser473) levels and the cell death were blocked by LY294002 (P<0.05).CONCLUSION: A certain concentration of shikonin reduces OGD-induced apoptosis of rat primary cortical neurons by activating PI3K/Akt signaling pathway. |
| |
Keywords: | Shikonin Neurons Oxygen-glucose deprivation PI3K/Akt signaling pathway Apoptosis |
|
| 点击此处可从《园艺学报》浏览原始摘要信息 |
|
点击此处可从《园艺学报》下载全文 |
|