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. 2013 Oct 31;6(1):57–65. doi: 10.1002/emmm.201303183

Figure 2.

Figure 2

Metabolic remodelling induced by HFD is prevented by mTORC1 inhibition.

A  Lower glycolytic (hexokinase) activity but increased oxidative (citrate synthase and β-hydroxy-acyl-CoA dehydrogenase) in HFD-fed AAV controls compared to AAV-PRAS40 mouse hearts. ***p < 0.01 versuscontrol chow; ###p < 0.01 versus control HFD. n = 4 for Chow, n = 5 for HFD group. One-way anova. Values are mean ± SEM.

B  TG content in the heart *p < 0.01 versus control chow; #p < 0.05 versuscontrol HFD. n = 3 for Chow, n = 3 for HFD group. One-way anova. Values are mean ± SEM. Lipid accumulation evidenced by Oil Red O staining. Bar = 100 μm.

C  The expression levels of genes from glucose metabolism and oxidatative phosphorylation were measured by qRT-PCR. *p < 0.05 versus control chow; #p < 0.05 versus control HFD. n = 4 for Chow, n = 5 for HFD group. One-way anova. Values are mean ± SEM.

D  The expression levels of genes from FA metabolism and lipid and sterol biosynthesis were measured by qRT-PCR. Expression levels of HIF1a and SREBP *p < 0.05 versus control chow; #p < 0.05 versus control HFD. n = 4 for Chow, n = 5 for HFD group. One-way anova. Values are mean ± SEM.

E  Glucose uptake, visualized by fluorescence imaging of Xenolight RediJect 2-DG 750 in cardiac and skeletal muscle. ***p < 0.01 versus control chow; ###p < 0.01 versus control HFD. n = 4 for Chow, n = 4 for HFD group. One-way anova. Values are mean ± SEM.

F  Immunoblots of proteins involved in insulin signalling.

G  IRS-1 gene expression levels in the indicated groups.