Institut d'Investigacions Biomèdiques Sant Pau, Barcelona, Spain.
Arterioscler Thromb Vasc Biol. 2011 Nov;31(11):2493-9. doi: 10.1161/ATVBAHA.111.236075.
A high-saturated fatty acid- and cholesterol-containing (HFHC) diet is considered to be a major risk factor for cardiovascular disease. The present study aimed to determine the effects of this Western-type diet on high-density lipoprotein (HDL) metabolism and reverse cholesterol transport (RCT) from macrophages to feces.
Experiments were carried out in mice fed a low-fat, low-cholesterol diet, an HFHC diet, or an HFHC diet without added cholesterol (high-saturated fatty acid and low-cholesterol [HFLC]). The HFHC diet caused a significant increase in plasma cholesterol, HDL cholesterol, and liver cholesterol and enhanced macrophage-derived [(3)H]cholesterol flux to feces by 3- to 4-fold. These effects were greatly reduced in mice fed the HFLC diet. This HFHC diet-mediated induction of RCT was sex independent and was not associated with obesity or insulin resistance. The HFHC diet caused 1.4- and 3-fold increases in [(3)H]cholesterol efflux to plasma and HDL-derived [(3)H]tracer fecal excretion, respectively. Unlike a low-fat, low-cholesterol and HFLC diets, the HFHC diet increased liver ABCG5/G8 expression. The effect of the HFHC diet on fecal macrophage-derived [(3)H]cholesterol excretion was totally blunted in ABCG5/G8-deficient mice.
Despite its deleterious effects on atherosclerosis, the HFHC diet promoted a sustained compensatory macrophage-to-feces RCT. Our data provide direct evidence of the crucial role of dietary cholesterol signaling through liver ABCG5/G8 upregulation in the HFHC diet-mediated induction of macrophage-specific RCT.
高饱和脂肪酸和高胆固醇含量的(HFHC)饮食被认为是心血管疾病的主要危险因素。本研究旨在确定这种西式饮食对高密度脂蛋白(HDL)代谢和从巨噬细胞到粪便的胆固醇逆向转运(RCT)的影响。
在喂食低脂、低胆固醇饮食、HFHC 饮食或不添加胆固醇的 HFHC 饮食(高饱和脂肪酸和低胆固醇[HFLC])的小鼠中进行了实验。HFHC 饮食导致血浆胆固醇、HDL 胆固醇和肝脏胆固醇显著增加,并使巨噬细胞来源的[(3)H]胆固醇向粪便的通量增加 3 至 4 倍。在喂食 HFLC 饮食的小鼠中,这些影响大大降低。这种 HFHC 饮食介导的 RCT 诱导与性别无关,与肥胖或胰岛素抵抗无关。HFHC 饮食导致[(3)H]胆固醇向血浆和 HDL 衍生的[(3)H]示踪剂粪便排泄的分别增加 1.4 倍和 3 倍。与低脂、低胆固醇和 HFLC 饮食不同,HFHC 饮食增加了肝脏 ABCG5/G8 的表达。在 ABCG5/G8 缺陷小鼠中,HFHC 饮食对粪便巨噬细胞来源的[(3)H]胆固醇排泄的影响完全减弱。
尽管 HFHC 饮食对动脉粥样硬化有不良影响,但它促进了持续的代偿性巨噬细胞向粪便的 RCT。我们的数据提供了直接证据,证明饮食胆固醇信号通过肝脏 ABCG5/G8 的上调在 HFHC 饮食介导的巨噬细胞特异性 RCT 诱导中起关键作用。