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Nat Commun ; 8: 15010, 2017 04 19.
Article in English | MEDLINE | ID: mdl-28422089

ABSTRACT

Brown and beige adipocytes combust nutrients for thermogenesis and through their metabolic activity decrease pro-atherogenic remnant lipoproteins in hyperlipidemic mice. However, whether the activation of thermogenic adipocytes affects the metabolism and anti-atherogenic properties of high-density lipoproteins (HDL) is unknown. Here, we report a reduction in atherosclerosis in response to pharmacological stimulation of thermogenesis linked to increased HDL levels in APOE*3-Leiden.CETP mice. Both cold-induced and pharmacological thermogenic activation enhances HDL remodelling, which is associated with specific lipidomic changes in mouse and human HDL. Furthermore, thermogenic stimulation promotes HDL-cholesterol clearance and increases macrophage-to-faeces reverse cholesterol transport in mice. Mechanistically, we show that intravascular lipolysis by adipocyte lipoprotein lipase and hepatic uptake of HDL by scavenger receptor B-I are the driving forces of HDL-cholesterol disposal in liver. Our findings corroborate the notion that high metabolic activity of thermogenic adipocytes confers atheroprotective properties via increased systemic cholesterol flux through the HDL compartment.


Subject(s)
Adipocytes/metabolism , Cholesterol/metabolism , Lipoproteins, HDL/metabolism , Thermogenesis , Animals , Biological Transport , CD36 Antigens/metabolism , Cardiotonic Agents/pharmacology , Cardiotonic Agents/therapeutic use , Cholesterol, HDL/blood , Cholesterol, HDL/metabolism , Cold Temperature , Humans , Hyperlipidemias/drug therapy , Hyperlipidemias/pathology , Lipolysis , Lipoprotein Lipase/metabolism , Liver/metabolism , Male , Metabolome , Mice, Inbred C57BL , Triglycerides/metabolism
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