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1.
Lipids ; 41(7): 663-8, 2006 Jul.
Article in English | MEDLINE | ID: mdl-17069350

ABSTRACT

Dyslipoproteinemia of the Nagase analbuminemic rat (NAR) is characterized by elevated concentrations of VLDL and LDL attributed to increased rates of liver lipoprotein synthesis. Increased lysophosphatidylcholine (LPC) in NAR HDL has been attributed to high plasma LCAT activity. We show here that, as compared with Sprague-Dawley rats (SDR), NAR plasma triacylglycerol (TAG), total cholesterol (TC), HDL TAG, protein, total phospholipids (PL), LPC, and PS are increased. These alterations rendered the NAR HDL particle more susceptible to the activity of the enzyme hepatic lipoprotein lipase (HL), which otherwise was unaltered in our study. Fractional catabolic rates in blood of the autologous 125I-apoHDL (median and lower quartile values), were, respectively, 0.231 and 1.645 (n = 10) in NAR as compared with 0.140 and 0.109 (n = 10) in SDR (P = 0.012), corresponding to synthesis rates of HDL protein of 89.8 +/- 33.7 mg/d in NAR and 17.4 +/- 6.5 mg/d in SDR (P = 0.0122). Furthermore, Swiss mouse macrophage free-cholesterol (FC) efflux rates, measured as the percent [14C]-cholesterol efflux/6 h, were 8.2 +/- 2.3 (n = 9) in NAR HDL and 11.2 +/- 3.2 (n = 10) in SDR HDL (P = 0.03). Therefore, in NAR the modification of the HDL composition slows down the cell FC efflux rate, and together with the increased rate of plasma HDL metabolism influences the reverse cholesterol transport system.


Subject(s)
Apolipoproteins/metabolism , Cholesterol/metabolism , Hyperlipoproteinemias/metabolism , Lipoproteins, HDL/metabolism , Macrophages/metabolism , Serum Albumin/deficiency , Animals , Apolipoproteins/blood , Apolipoproteins/pharmacokinetics , Biological Transport/genetics , Cholesterol/blood , Hyperlipoproteinemias/blood , Hyperlipoproteinemias/genetics , Iodine Radioisotopes , Lipoproteins, HDL/blood , Mice , Rats , Rats, Mutant Strains , Rats, Sprague-Dawley , Triglycerides/blood
2.
J Lipid Res ; 44(4): 727-32, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12562870

ABSTRACT

This study aimed at measuring the influence of a low salt diet on the development of experimental atherosclerosis in moderately hyperlipidemic mice. Experiments were carried out on LDL receptor (LDLR) knockout (KO) mice, or apolipoprotein E (apoE) KO mice on a low sodium chloride diet (LSD) as compared with a normal salt diet (NSD). On LSD, the rise of the plasma concentrations of TG and nonesterified fatty acid (NEFA) was, respectively, 19% and 34% in LDLR KO mice, and 21% and 35% in apoE KO mice, and that of plasma cholesterol was limited to the LDLR KO group alone (15%). Probably due to the apoE KO severe hypercholesterolemia, the arterial inner-wall fat storage was not influenced by the diet salt content and was far more abundant in the apoE KO than in the LDLR KO mice. However, in the less severe hypercholesterolemia of the LDLR KO mice, lipid deposits on the LSD were greater than on the NSD. Arterial fat storage correlated with NEFA concentrations in the LDLR KO mice alone (n = 14, P = 0.0065). Thus, dietary sodium chloride restriction enhances aortic wall lipid storage in moderately hyperlipidemic mice.


Subject(s)
Aorta/metabolism , Lipids/blood , Receptors, LDL/deficiency , Sodium Chloride, Dietary/pharmacology , Animals , Apolipoproteins E/deficiency , Apolipoproteins E/genetics , Arteriosclerosis/etiology , Fatty Acids/blood , Hyperlipidemias/blood , Lipid Metabolism , Mice , Mice, Knockout , Receptors, LDL/genetics , Triglycerides/blood
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