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西方饮食中的胆固醇含量在高密度脂蛋白胆固醇的反常增加中起着主要作用,并上调了巨噬细胞逆向胆固醇转运途径。

The cholesterol content of Western diets plays a major role in the paradoxical increase in high-density lipoprotein cholesterol and upregulates the macrophage reverse cholesterol transport pathway.

机构信息

Institut d'Investigacions Biomèdiques Sant Pau, Barcelona, Spain.

出版信息

Arterioscler Thromb Vasc Biol. 2011 Nov;31(11):2493-9. doi: 10.1161/ATVBAHA.111.236075.

Abstract

OBJECTIVE

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.

METHODS AND RESULTS

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.

CONCLUSION

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.

摘要

目的

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。

方法和结果

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。

结论

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。

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