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Genetic loss-of-function of Lipg and plasma triglycerides in mice.

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posted on 2021-09-20, 17:46 authored by Sumeet A. Khetarpal, Cecilia Vitali, Michael G. Levin, Derek Klarin, Joseph Park, Akhil Pampana, John S. Millar, Takashi Kuwano, Dhavamani Sugasini, Papasani V. Subbaiah, Jeffrey T. Billheimer, Pradeep Natarajan, Daniel J. Rader

A. Plasma TC, HDL-C, nonHDL-C, TGs, phospholipids, and nonesterified fatty acids from WT vs. Lipg-/- mice after a 4 hour fast and again after 4 hours of refeeding a chow diet. Lipids were measured by chemical autoanalyzer. B. Percent change in each plasma lipid measure from (A) in 4 hour refed vs fasting measures. C. TG from plasma of fasted mice (left) and four hour-refed mice (right) fractionated by fast-protein liquid chromatography (FPLC) from pools from WT or Lipg-/- mice from groups in (A). D. Total cholesterol, HDL-C, nonHDL-C, TGs, phospholipids, and nonesterified fatty acids in WT and Lipg-/- mice after initiation of feeding adult mice a diet composed of 45% kilocalories fat for the indicated timepoints. Plasma was collected 4 hours after fasting and lipids were measured by autoanalyzer. E. Fasting plasma lipids after 7 weeks of high fat feeding were normalized to the levels at zero weeks of feeding and expressed as a percentage change. F. Triglycerides from fasted (left) and refed (mice) from (D-E) after FPLC-fractionation of plasma. A, B, E: *P<0.05, **P<0.01, ***P<0.001, Student’s unpaired T-test. D: **P<0.01, ***P<0.001, repeated factor 2-way ANOVA compared to WT group. Data is expressed as mean ± S.E.M.

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