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

Published in final edited form as: Atherosclerosis. 2012 May 16;223(1):137–143. doi: 10.1016/j.atherosclerosis.2012.04.025

Plasma cholesterol (A) and triglyceride levels (B) in diabetic Lias^+/+Apoe⁻^/⁻ mice (open bars) and diabetic Lias^+/⁻Apoe⁻^/⁻ mice (black bars). Results are expressed as means ± SEM. (C) FPLC of plasma from diabetic and non-diabetic Lias^+/⁻Apoe⁻^/⁻ and Lias^+/+Apoe⁻^/⁻ mice. Equal volumes of plasma from the mice at 6 months old were pooled and subjected to gel filtration chromatography. Eluted fractions (0.5 ml) were collected, and cholesterol concentrations were measured as described in methods. VLDL, very-low-density lipoproteins; IDL, intermediate density lipoprotein; LDL, low-density lipoproteins; HDL, high-density lipoproteins.

Plasma cholesterol (A) and triglyceride levels (B) in diabetic Lias^+/+Apoe⁻^/⁻ mice (open bars) and diabetic Lias^+/⁻Apoe⁻^/⁻ mice (black bars). Results are expressed as means ± SEM. (C) FPLC of plasma from diabetic and non-diabetic Lias^+/⁻Apoe⁻^/⁻ and Lias^+/+Apoe⁻^/⁻ mice. Equal volumes of plasma from the mice at 6 months old were pooled and subjected to gel filtration chromatography. Eluted fractions (0.5 ml) were collected, and cholesterol concentrations were measured as described in methods. VLDL, very-low-density lipoproteins; IDL, intermediate density lipoprotein; LDL, low-density lipoproteins; HDL, high-density lipoproteins.