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Updated: May 1, 2026

Quantitative Measurement of GLUT4 Translocation to the Plasma Membrane by Flow Cytometry
Published on: November 7, 2010
Expression of Glucose Transporter 4 (GLUT4) is Increased by Cinnamaldehyde in C2C12 Mouse Muscle Cells
Abdolrahim Nikzamir1, Alireza Palangi2, Alireza Kheirollaha3
1Department of Biochemistry, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran ; Endocrinology and Metabolism Research Center (EMRC), Tehran University of Medical Sciences, Tehran, IR Iran.
Background:
In diabetes mellitus because of the absence or insufficient sensitivity to insulin, glucose transporter protein in cell membrane, glucose transporter 4, is decreased. GLUT4 is the major glucose transporter in skeletal muscle and adipose tissue, which is under control of insulin. It remains, however, unclear whether cinnamaldehyde plays a regulatory role(s) or not.
Objectives:
The objective of this study was to investigate the effects of cinnamaldehyde on GLUT4 gene expression.
Materials And Methods:
This study was an experimental trial. Tests were performed in triplicates. This study examined effects of cinnamaldehyde on Glut4 gene expression in C2C12 skeletal muscle cells by using Real Time PCR. C2C12 myoblasts were cultured in DMEM + 10 % FBS. After differentiation of myoblasts to myotubes, the cells were serum deprived for 5 hours and then treated with 10, 20, or 50 µM of cinnamaldehyde for 1 hour.
Results:
Our data revealed a significant increase in the expression of Glut4 in cinnamaldehyde treated cells. In addition, GLUT4 mRNA level was increased in a dose dependent manner. Analyses were performed using the SPSS 16 for Windows software. Differences between the groups were determined by one-way ANOVA.
Conclusions:
These results demonstrate that cinnamaldehyde up regulates the expression of mouse skeletal muscle GLUT4 gene expression.
Insights
Cinnamaldehyde significantly increases glucose transporter 4 (GLUT4) gene expression in skeletal muscle cells. This suggests cinnamaldehyde may play a role in managing glucose uptake, potentially benefiting diabetes mellitus research.
Area of Science:
- Biochemistry
- Molecular Biology
- Diabetes Research
Background:
- Insulin resistance in diabetes mellitus reduces glucose transporter 4 (GLUT4) in cell membranes.
- GLUT4 is crucial for glucose transport in skeletal muscle and adipose tissue, regulated by insulin.
- The regulatory role of cinnamaldehyde on GLUT4 expression was previously unestablished.
Purpose of the Study:
- To investigate the impact of cinnamaldehyde on GLUT4 gene expression.
- To determine if cinnamaldehyde influences the key glucose transporter in skeletal muscle cells.
Main Methods:
- Experimental trial using C2C12 skeletal muscle cells.
- Real-Time PCR to quantify GLUT4 gene expression.
- Treatment of differentiated myotubes with varying concentrations of cinnamaldehyde (10, 20, 50 µM).
Main Results:
- Cinnamaldehyde treatment led to a significant increase in GLUT4 gene expression.
- GLUT4 mRNA levels demonstrated a dose-dependent increase with cinnamaldehyde exposure.
- Statistical analysis confirmed significant differences between treatment groups.
Conclusions:
- Cinnamaldehyde upregulates the expression of the mouse skeletal muscle GLUT4 gene.
- Findings suggest cinnamaldehyde as a potential modulator of glucose transport.
- Further research into cinnamaldehyde's therapeutic potential for glucose metabolism is warranted.
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Glucose Transporters
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Glucose Absorption Into the Small Intestine
Cell Specific Gene Expression
Secondary Active Transport

