Blueberry attenuates liver injury in metabolic dysfunction-associated liver disease by promoting the expression of mitofilin/Mic60 in human hepatocytes and inhibiting the production of superoxide.
- Author:
Ya REN
1
;
Houmin FAN
2
;
Lili ZHU
2
;
Tao LIN
3
;
Tingting REN
4
Author Information
1. Department of Clinical Biochemistry, School of Medical Laboratory, Guizhou Medical University, Guiyang 550004, China.
2. Department of Blood Transfusion Affiliated Hospital, Guizhou Medical University, Guiyang 550004, China.
3. Department of Hematology and Body Fluids, Clinical Laboratory Center of the Hospital Affiliated to Guizhou Medical University, Guiyang 550004, China.
4. Department of Clinical Biochemistry, School of Medical Laboratory, Guizhou Medical University, Guiyang 550004, China. *Corresponding author, E-mail: 2529719067@qq.com.
- Publication Type:Journal Article
- MeSH:
Humans;
Blueberry Plants/chemistry*;
Hepatocytes/metabolism*;
Liver/metabolism*;
Liver Diseases/metabolism*;
Reactive Oxygen Species/metabolism*;
Superoxide Dismutase/metabolism*;
Superoxides/metabolism*;
Mitochondrial Membranes/metabolism*;
Mitochondrial Proteins/metabolism*;
Plant Extracts/pharmacology*
- From:
Chinese Journal of Cellular and Molecular Immunology
2023;39(4):318-324
- CountryChina
- Language:Chinese
-
Abstract:
Objective To study the effect and mechanism of blueberry on regulating the mitochondrial inner membrane protein mitofilin/Mic60 in an in vitro model of metabolic dysfunction-associated liver disease (MAFLD). Methods L02 human hepatocytes were induced by free fatty acids (FFA) to establish MAFLD cell model. A normal group, a model group, an 80 μg/mL blueberry treatment group, a Mic60 short hairpin RNA (Mic60 shRNA) transfection group, and Mic60 knockdown combined with an 80 μg/mL blueberry treatment group were established. The intracellular lipid deposition was observed by oil red O staining, and the effect of different concentrations of blueberry pulp on the survival rate of L02 cells treated with FFA was measured by MTT assay. The levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), total cholesterol (TC), superoxide dismutase (SOD) activity, glutathione (GSH) and malondialdehyde (MDA) contents were measured by visible spectrophotometry. The expression of reactive oxygen species (ROS) in hepatocytes was observed by fluorescence microscopy, and the mRNA and protein expression of Mic60 were detected by real-time quantitative PCR and Western blot analysis, respectively. Results After 24 hours of FFA stimulation, a large number of red lipid droplets in the cytoplasm of L02 cells was observed, and the survival rate of L02 cells treated with 80 μg/mL blueberry was higher. The results of ALT, AST, TG, TC, MDA and the fluorescence intensity of ROS in blueberry treated group were lower than those in model group, while the levels of SOD, GSH, Mic60 mRNA and protein in blueberry treated group were higher than those in model group. Conclusion Blueberry promotes the expression of Mic60, increases the levels of SOD and GSH in hepatocytes, and reduces the production of ROS, thus alleviating the injury of MAFLD hepatocytes and regulating the disorder of lipid metabolism.
