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. Author manuscript; available in PMC: 2015 Aug 21.
Published in final edited form as: Cell Rep. 2014 Aug 14;8(4):1160–1170. doi: 10.1016/j.celrep.2014.07.018

Figure 5. The TSC complex is required for improved hepatic insulin sensitivity upon PR.

Figure 5

(A) Insulin sensitivity as determined by immunoblotting for markers of Akt pathway activation in liver extracts from mice fasted for 6 hrs and then stimulated with 0.5 U/kg insulin by portal vein injection 3 min before harvest.

(B) Akt activation status as determined by immunoblotting of liver extracts 3 hrs after reperfusion from mice preconditioned for 1 wk on the indicated diet prior to induction of hepatic IRI.

(C) Serum insulin levels from tail blood of WT mice preconditioned for 1 wk on the indicated diet taken prior to ischemia (0 hr), at the end of the ischemic period (30 min I, n=3–4), 30 min after reperfusion period (30 min R, n=3) or 3 hrs after reperfusion (3 hrs R, n=11–12). Asterisk indicates the significance of the indicated comparison according to a Kruskal-Wallis test followed by Dunn’s multiple comparisons test; *p < 0.05; ns: not significant.

(D) Blood glucose levels of mice on the indicated diets for 1 wk before hepatic IRI, measured before (0hr) and 3 hrs after reperfusion; n = 8–10 mice/group. Asterisks indicate the significance of the difference between 0 and 3 hr values by student’s t test within diet group; **p < 0.001, ***p < 0.0001.

Data in all panels are shown as means ± SD. See also Figure S5.