Figure 4
Figure 4. Plasma lipids and lipoprotein profiles in P-sel+/+/apoE−/− and P-selΔCT/ΔCT/apoE−/− mice. Plasma was collected from individual mice of both sexes, fasted for 4 hours. (A) Total cholesterol, unesterified cholesterol, phospholipid, and triglyceride levels in plasma from P-sel+/+/apoE−/− (■) and P-selΔCT/ΔCT/apoE−/− (□) mice. Data represent mean ± SEM (n = 6-9). Error bars indicate SEM. (B) Plasma samples from P-sel+/+/apoE−/− (●) and P-selΔCT/ΔCT/apoE−/− (○) individual animals were size fractionated by FPLC, and the total cholesterol content of each fraction was determined. The chromatograms are the average of multiple individually determined profiles (n = 4). Approximate elution positions of native very low density lipoprotein (VLDL), IDL/LDL, and HDL particles are indicated by brackets.

Plasma lipids and lipoprotein profiles in P-sel+/+/apoE−/− and P-selΔCTCT/apoE−/− mice. Plasma was collected from individual mice of both sexes, fasted for 4 hours. (A) Total cholesterol, unesterified cholesterol, phospholipid, and triglyceride levels in plasma from P-sel+/+/apoE−/− (■) and P-selΔCTCT/apoE−/− (□) mice. Data represent mean ± SEM (n = 6-9). Error bars indicate SEM. (B) Plasma samples from P-sel+/+/apoE−/− (●) and P-selΔCTCT/apoE−/− (○) individual animals were size fractionated by FPLC, and the total cholesterol content of each fraction was determined. The chromatograms are the average of multiple individually determined profiles (n = 4). Approximate elution positions of native very low density lipoprotein (VLDL), IDL/LDL, and HDL particles are indicated by brackets.

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