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Abstract


Objective : This study investigated the anti-diabetic effects of DM1, a herbal mixture with Atractylodis Rhizoma, Anemarrhenae Rhizoma, and Cinnamomi Cortex in high fat diet (HFD)-induced diabetic mice and the mechanism in C2C12 mouse skeletal muscle cells.

Methods : The C57B/6 mice were fed high fat for 12 weeks, and then administrated DM1 extract (500 §·/§¸, p.o.) for 4 weeks. The changes of body weight, calorie and water intakes, fasting blood glucose levels and the serum levels of glucose, insulin, triglyceride, HDL-cholesterol, AST and ALT were measured in mice. The histological changes of liver and pancreas tissues were also observed by H&E stain. C2C12 myoblasts were differentiated into myotubes and then treated with DM1 extract (0.5, 1, and 2 §·/§¢) for 24 hr. The expression of myosin heavy chain (MHC), PGC1¥á, Sirt1 and NRF1, and the AMPK phosphorylation were determined in the myotubes by western blot, respectively.

Results : The DM1 extract administration significantly decreased the calorie and water intakes, glucose, triglyceride, AST and ALT levels and increased insulin and HDL-cholesterol in HFD-induced diabetic mice. DM1 extract inhibited lipid accumulation in liver tissue and improved glucose tolerance. In C2C12 myotubes, DM1 treatment increased the expression of MHC, PGC1¥á, Sirt-1, NRF-1 and the AMPK phosphorylation.

Conclusion : In our results indicate that DM1 can improve diabetic symptoms by decreasing the obesity, glucose tolerance and fatty liver in HFD-induced diabetic mice, and responsible mechanism is might be related with energy enhancement.

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Antidiabetic Effect; Atractylodis Rhizoma; Anemarrhenae Rhizoma; Cinnamomi Cortex; C2C12 cell; High Fat Diet; Obesity; Skeletal Muscle

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