Effect of ligustilide on oxygen and glucose deprivation/reperfusion-induced mitochondria fission in PC12 cells.
10.19540/j.cnki.cjcmm.20200316.401
- Author:
Qian WU
1
;
Ning WANG
1
;
Jiao LIU
2
;
Zhi-Guo MAO
2
;
Yan-Xiang WANG
2
Author Information
1. Key Laboratory of Chinese Medicinal Formula of Anhui Province, Anhui University of Chinese Medicine Hefei 230012, China Institute for Pharmacodynamics and Safety Evaluation of Chinese Medicine, Anhui Academy of Chinese Medicine Hefei 230012, China.
2. Key Laboratory of Chinese Medicinal Formula of Anhui Province, Anhui University of Chinese Medicine Hefei 230012, China.
- Publication Type:Journal Article
- Keywords:
PC12 cell;
ligustilide;
mitochondria fission;
oxygen and glucose deprivation/reperfusion(OGD/R)
- MeSH:
4-Butyrolactone;
analogs & derivatives;
Animals;
Apoptosis;
Cell Survival;
Glucose;
Mitochondria;
Oxygen;
PC12 Cells;
Rats;
Reactive Oxygen Species;
Reperfusion Injury
- From:
China Journal of Chinese Materia Medica
2020;45(16):3931-3937
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to investigate the effect and mechanism of ligustilide, the main active ingredient in Ligusticum wallichii, on mitochondria fission after PC12 cell injury induced by oxygen and glucose deprivation/reperfusion(OGD/R). In the experiment, an OGD/R model was established in vitro, and PC12 cells were pre-treated with ligustilide for 3 h, and then the cell viability was detected by CCK-8 method. The effect of different concentrations of ligustilide on the morphology of PC12 cells after OGD/R injury was observed under an inverted microscope. Transmission electron microscopy was used to observe the mitochondrial fission of PC12 cells after OGD/R injury. DCFH-DA immunofluorescence staining method was used to detect intracellular reactive oxygen species(ROS) changes. Changes in mitochondria membrane potential(MMP) were detected by flow cytometry. Hochest 33258 was used to observe the apoptosis of PC12 cells. Western blot was used to detect changes in cytochrome C(Cyt C) content in mitochondria and cytoplasm, and mitochondrial fission-related proteins Drp 1 and Fis 1. All results showed that compared with the model group, ligustilide significantly increased the survival rate of PC12 cells and the number of cells. Further experiments showed that ligustilide inhibited the release of ROS and decline of mitochondrial membrane potential in PC12 cells after OGD/R injury. Moreover, ligustilide reduced the release of Cyt C and promoted the expressions of Drp1 and Fis1 in mitochondrial fission proteins. Verification experiments showed that mitochondrial fission inhibitor mdivi-1 decreased cell survival rate and inhibited fission. The results indicated that ligustilide exerted neuro-protective effects by promoting mitochondrial fission and reducing cell damage. It preliminary proves that the mechanism of ligustilide on ischemic brain injury may be related to the promotion of mitochondrial fission and the maintenance of cell homeostasis.
