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首页> 外文期刊>Arteriosclerosis, thrombosis, and vascular biology >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.
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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.

机译: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主要作用,并上调巨噬细胞的反向胆固醇转运途径。

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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.
机译:目的:高饱和脂肪酸和胆固醇(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)代谢和胆固醇从巨噬细胞向粪便的逆向运输(RCT)的影响。方法和结果:实验是在喂养低脂,低胆固醇饮食,HFHC饮食或不添加胆固醇(高饱和脂肪酸和低胆固醇[HFLC])的HFHC饮食的小鼠中进行的。 HFHC饮食导致血浆胆固醇,HDL胆固醇和肝胆固醇显着增加,并使巨噬细胞衍生的[(3)H]胆固醇排泄的粪便增加了3至4倍。在喂了HFLC饮食的小鼠中,这些作用大大降低了。 HFHC饮食介导的RCT诱导与性别无关,并且与肥胖或胰岛素抵抗无关。 HFHC饮食分别导致[(3)H]胆固醇对血浆和HDL衍生的[(3)H]示踪剂粪便排泄增加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缺陷型小鼠中,HFHC饮食对粪便巨噬细胞衍生的[(3)H]胆固醇排泄的影响完全减弱。结论:HFHC饮食尽管对动脉粥样硬化具有有害作用,但仍促进了持续性代偿性巨噬细胞到粪便的随机对照试验。我们的数据提供了通过肝脏ABCG5 / G8上调饮食胆固醇信号传导在HFHC饮食介导的巨噬细胞特异性RCT诱导中的关键作用的直接证据。

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