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. Author manuscript; available in PMC: 2013 Feb 1.

Published in final edited form as: J Hepatol. 2011 Jul 23;56(2):433–440. doi: 10.1016/j.jhep.2011.05.030

Fig. 2 — (A) Plasma ceruloplasmin. (B) Plasma copper. (C) Liver copper. Data represent means ± SD (n=5–9). *p<0.05. (D) Hepatic SOD1 expression was determined by Western Blots. Optical density of band was quantified by ImageJ software. The ratio to β-actin was calculated by assigning the value from adequate copper diet controls as one. Data represent means ± SD (n=3). *p<0.05 versus A; ^#p<0.05 versus AF. (E) Plasma ferritin. (F) Liver iron. Data represent means ± SD (n=5–9). *p<0.05. A, adequate copper diet; M, marginal copper deficient diet; AF, adequate copper diet+30% fructose drinking; MF, marginal copper deficient diet+30% fructose drinking.

Fig. 2 — (A) Plasma ceruloplasmin. (B) Plasma copper. (C) Liver copper. Data represent means ± SD (n=5–9). *p<0.05. (D) Hepatic SOD1 expression was determined by Western Blots. Optical density of band was quantified by ImageJ software. The ratio to β-actin was calculated by assigning the value from adequate copper diet controls as one. Data represent means ± SD (n=3). *p<0.05 versus A; ^#p<0.05 versus AF. (E) Plasma ferritin. (F) Liver iron. Data represent means ± SD (n=5–9). *p<0.05. A, adequate copper diet; M, marginal copper deficient diet; AF, adequate copper diet+30% fructose drinking; MF, marginal copper deficient diet+30% fructose drinking.