Berbée Jimmy F P, Boon Mariëtte R, Khedoe P Padmini S J, Bartelt Alexander, Schlein Christian, Worthmann Anna, Kooijman Sander, Hoeke Geerte, Mol Isabel M, John Clara, Jung Caroline, Vazirpanah Nadia, Brouwers Linda P J, Gordts Philip L S M, Esko Jeffrey D, Hiemstra Pieter S, Havekes Louis M, Scheja Ludger, Heeren Joerg, Rensen Patrick C N
1] Division of Endocrinology, Department of Medicine, Leiden University Medical Center, Albinusdreef 2, Leiden 2333 ZA, The Netherlands [2] Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Albinusdreef 2, Leiden 2333 ZA, The Netherlands.
1] Division of Endocrinology, Department of Medicine, Leiden University Medical Center, Albinusdreef 2, Leiden 2333 ZA, The Netherlands [2] Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Center, Albinusdreef 2, Leiden 2333 ZA, The Netherlands [3] Department of Pulmonology, Leiden University Medical Center, Albinusdreef 2, Leiden 2333 ZA, The Netherlands.
Nat Commun. 2015 Mar 10;6:6356. doi: 10.1038/ncomms7356.
Brown adipose tissue (BAT) combusts high amounts of fatty acids, thereby lowering plasma triglyceride levels and reducing obesity. However, the precise role of BAT in plasma cholesterol metabolism and atherosclerosis development remains unclear. Here we show that BAT activation by β3-adrenergic receptor stimulation protects from atherosclerosis in hyperlipidemic APOE*3-Leiden.CETP mice, a well-established model for human-like lipoprotein metabolism that unlike hyperlipidemic Apoe(-/-) and Ldlr(-/-) mice expresses functional apoE and LDLR. BAT activation increases energy expenditure and decreases plasma triglyceride and cholesterol levels. Mechanistically, we demonstrate that BAT activation enhances the selective uptake of fatty acids from triglyceride-rich lipoproteins into BAT, subsequently accelerating the hepatic clearance of the cholesterol-enriched remnants. These effects depend on a functional hepatic apoE-LDLR clearance pathway as BAT activation in Apoe(-/-) and Ldlr(-/-) mice does not attenuate hypercholesterolaemia and atherosclerosis. We conclude that activation of BAT is a powerful therapeutic avenue to ameliorate hyperlipidaemia and protect from atherosclerosis.
棕色脂肪组织(BAT)燃烧大量脂肪酸,从而降低血浆甘油三酯水平并减轻肥胖。然而,BAT在血浆胆固醇代谢和动脉粥样硬化发展中的具体作用仍不清楚。在此,我们表明,通过β3-肾上腺素能受体刺激激活BAT可保护高脂血症APOE*3-莱顿.CETP小鼠免受动脉粥样硬化影响,这是一种成熟的类人脂蛋白代谢模型,与高脂血症Apoe(-/-)和Ldlr(-/-)小鼠不同,它表达功能性载脂蛋白E(apoE)和低密度脂蛋白受体(LDLR)。BAT激活增加能量消耗,并降低血浆甘油三酯和胆固醇水平。从机制上讲,我们证明BAT激活增强了富含甘油三酯脂蛋白中脂肪酸向BAT的选择性摄取,随后加速了富含胆固醇残粒的肝脏清除。这些作用依赖于功能性肝脏apoE-LDLR清除途径,因为在Apoe(-/-)和Ldlr(-/-)小鼠中激活BAT并不能减轻高胆固醇血症和动脉粥样硬化。我们得出结论,激活BAT是改善高脂血症和预防动脉粥样硬化的有效治疗途径。