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. 2016 Jun 16;10(5):507–515. doi: 10.4162/nrp.2016.10.5.507

Fig. 3. Effect of G. procumbens extract (GPE) supplementation on PM-GLUT4, pAMPK, and pAS160 expression in the skeletal muscle.

Fig. 3

Western blotting and signal intensities were determined by densitometric analysis using Multi Gauge V3.1 software. Representative blots of PM-GLUT4, pAMPK, and pAS160 protein expression are shown with protein expression levels quantified relative to the expression level observed in samples from db/db-control mice. Each value is expressed as mean ± SD of experiments performed in triplicate. a-c Values denoted by different letters are significantly different (P < 0.05), as analyzed by Duncan's multiple range test. PM-GLUT4: plasma membrane-glucose transporter type 4, pAMPK: phosphorylated AMP-activated protein kinase, pAS160: phosphorylated Akt substrate of 160 kDa.