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. Author manuscript; available in PMC: 2020 Apr 1.
Published in final edited form as: Hepatology. 2019 Mar 6;69(4):1535–1548. doi: 10.1002/hep.30364

FIG. 4.

FIG. 4.

Effects of CB1R blockade on HFD-induced oxidative stress and mitochondrial disfunction in WT and Sirt1-LKO mice.

JD5037 reversed HFD-induced mitochondrial ROS production, as indicated by 4-HNE adducts in liver (A) and white adipose tissue (B) in WT but not Sirt1-LKO mice. Same pattern observed for JD5037 reversal of pAkts473 in adipose tissue (B). Western blot bands were quantified and analyzed by densitometry as indicate above. (C) Mitochondrial complex I activity was measured in freshly prepared liver mitochondria as described in Supplementary Methods. (D) Total antioxidant capacity was measured in serum. Data are mean ± SEM, n=5. *p<0.05 compared to STD group, #p<0.05 compared to HFD Veh group, or same age group in (D).