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.
The inferior epigastric artery flap can be applied to microsurgical flap transfer, potentially in breast reconstruction, hemifacial atrophy, phalloplasty, or when extremely large amounts of skin coverage are required.
Twenty one male Holstein calves were used to evaluate the effects of vanilla flavour added to starter on preweaning and postweaning calf performance. Following 3 d of colostrum and transition milk feeding, calves were assigned in a completely randomized design to two treatments including: 1. unflavoured starter and 2. flavoured starter. Calves were fed whole milk at 10% of the initial body weight daily and had free access to starter and water. The weaning criterion was defined as the calf age at a daily intake of 0.80 kg of starter for 2 days, consecutively. Calves fed flavoured starter weighed more at weaning and at the end of experiment and the preweaning average daily gains increased significantly compared with calves fed unflavoured starter. The starter consumption during the preweaning but not postweaning period was significantly higher in calves fed flavoured starter. The calves fed flavoured starter met weaning criteria at a younger age, so that they had 2 to 3 days shorter preweaning period (P<0.03). These findings demonstrate that supplementing starter with vanilla as a flavour agent is advantageous to calf performance.
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