Chung Soonkyu, Cuffe Helen, Marshall Stephanie M, McDaniel Allison L, Ha Jung-Heun, Kavanagh Kylie, Hong Cynthia, Tontonoz Peter, Temel Ryan E, Parks John S
From the Department of Pathology, Sections on Lipid Sciences (S.C., H.C., S.M.M., A.L.M., R.E.T., J.S.P.) and Comparative Medicine (K.K.), and Department of Biochemistry (J.S.P.), Wake Forest School of Medicine, Winston-Salem, NC; Department of Nutrition and Health Sciences, University of Nebraska, Lincoln (S.C.); Department of Food Science and Human Nutrition, University of Florida, Gainesville (S.C., J.-H.H.); and Department of Pathology and Laboratory Medicine, Howard Hughes Medical Institute, University of California, Los Angeles (C.H., P.T.).
Arterioscler Thromb Vasc Biol. 2014 Sep;34(9):1880-7. doi: 10.1161/ATVBAHA.114.303896. Epub 2014 Jun 26.
Excessive caloric intake is associated with obesity and adipose tissue dysfunction. However, the role of dietary cholesterol in this process is unknown. The aim of this study was to determine whether increasing dietary cholesterol intake alters adipose tissue cholesterol content, adipocyte size, and endocrine function in nonhuman primates.
Age-matched, male African Green monkeys (n=5 per group) were assigned to 1 of 3 diets containing 0.002 (low [Lo]), 0.2 (medium [Med]), or 0.4 (high [Hi]) mg cholesterol/kcal. After 10 weeks of diet feeding, animals were euthanized for adipose tissue, liver, and plasma collection. With increasing dietary cholesterol, free cholesterol (FC) content and adipocyte size increased in a stepwise manner in visceral, but not in subcutaneous fat, with a significant association between visceral adipocyte size and FC content (r(2)=0.298; n=15; P=0.035). In visceral fat, dietary cholesterol intake was associated with (1) increased proinflammatory gene expression and macrophage recruitment, (2) decreased expression of genes involved in cholesterol biosynthesis and lipoprotein uptake, and (3) increased expression of proteins involved in FC efflux.
Increasing dietary cholesterol selectively increases visceral fat adipocyte size, FC and macrophage content, and proinflammatory gene expression in nonhuman primates. Visceral fat cells seem to compensate for increased dietary cholesterol by limiting cholesterol uptake/synthesis and increasing FC efflux pathways.
热量摄入过多与肥胖及脂肪组织功能障碍有关。然而,膳食胆固醇在此过程中的作用尚不清楚。本研究的目的是确定增加膳食胆固醇摄入量是否会改变非人灵长类动物的脂肪组织胆固醇含量、脂肪细胞大小和内分泌功能。
将年龄匹配的雄性非洲绿猴(每组5只)分配到三种饮食中的一种,饮食中胆固醇含量分别为0.002(低[Lo])、0.2(中[Med])或0.4(高[Hi])mg/千卡。经过10周的饮食喂养后,对动物实施安乐死以收集脂肪组织、肝脏和血浆。随着膳食胆固醇的增加,内脏脂肪而非皮下脂肪中的游离胆固醇(FC)含量和脂肪细胞大小呈逐步增加,内脏脂肪细胞大小与FC含量之间存在显著相关性(r²=0.298;n=15;P=0.035)。在内脏脂肪中,膳食胆固醇摄入量与以下情况相关:(1)促炎基因表达增加和巨噬细胞募集;(2)参与胆固醇生物合成和脂蛋白摄取的基因表达降低;(3)参与FC流出的蛋白质表达增加。
增加膳食胆固醇选择性地增加了非人灵长类动物内脏脂肪的脂肪细胞大小、FC和巨噬细胞含量以及促炎基因表达。内脏脂肪细胞似乎通过限制胆固醇摄取/合成和增加FC流出途径来补偿膳食胆固醇的增加。