Effects of arbutin on glucose uptake by glucose transporter 4 (GLUT4) and its cytoprotective properties in L6 skeletal muscle cell line.
- Resource Type
- Article
- Authors
- Gholami Bahnemiri, Mehdi; Nouri, Hamid Reza; Zabihi, Ebrahim; Sadeghi, Farzin; Pouramir, Mahdi
- Source
- Cell Biochemistry & Function. Jun2022, Vol. 40 Issue 4, p417-425. 9p.
- Subject
- *MUSCLE cells
*SKELETAL muscle
*CELL lines
*GLUCOSE transporters
*REACTIVE oxygen species
*MESSENGER RNA
- Language
- ISSN
- 0263-6484
It has been well known that oxidative stress and increased intracellular reactive oxygen species (ROS) have a pivotal role in disrupting the insulin signaling pathways leading to cellular insulin resistance. In this study, we evaluated arbutin's effects on glucose uptake by GLUT4 and cytoprotective properties in the L6 skeletal muscle cell line. The effect of arbutin and tertiary butyl hydrogen peroxide (t‐BHP) on glucose uptake in cultured L6 cells was investigated by flow cytometry. We also evaluated gene expression levels of GLUT1 and GLUT4 in the L6 cells by quantitative real‐time polymerase chain reaction analysis. The results from the study demonstrated that the optimum ROS generation occurred 3 h after 100 µM t‐BHP treatment and pretreatment with arbutin (500 and 1000 µM) significantly inhibited the t‐BHP induced ROS generation (p <.05). Our result indicated that 3 h pretreatment of L6 cells with 1000 μM of arbutin before 50 μM t‐BHP significantly increased glucose uptake than the 50 μM t‐BHP alone group (p <.05). Our findings may suggest that an increase in the uptake of 2‐NBDG by L6 cells with arbutin pretreatment can be associated with increased expression of GLUT4 and GLUT1 under oxidative stress. Significance statement: Arbutin, as a natural bioactive compound has the potential ability for protecting fibroblasts against oxidative cell damage. Molecular mechanisms of the anti‐hyperglycemic effects of this compound have not been clearly explained. These findings showed that arbutin saved glucose uptake partly by GLUT4 and GLUT1 messenger RNA expression under oxidative Stress Conditions. [ABSTRACT FROM AUTHOR]