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膳食胆固醇会加重肥胖的低密度脂蛋白受体缺陷小鼠的脂肪组织巨噬细胞积聚和动脉粥样硬化。

Dietary cholesterol worsens adipose tissue macrophage accumulation and atherosclerosis in obese LDL receptor-deficient mice.

作者信息

Subramanian Savitha, Han Chang Yeop, Chiba Tsuyoshi, McMillen Timothy S, Wang Shari A, Haw Antonio, Kirk Elizabeth A, O'Brien Kevin D, Chait Alan

机构信息

Department of Medicine, University of Washington, 1959 NE Pacific Street, Seattle, WA 98195-6426, USA.

出版信息

Arterioscler Thromb Vasc Biol. 2008 Apr;28(4):685-91. doi: 10.1161/ATVBAHA.107.157685. Epub 2008 Jan 31.

Abstract

OBJECTIVE

Chronic systemic inflammation accompanies obesity and predicts development of cardiovascular disease. Dietary cholesterol has been shown to increase inflammation and atherosclerosis in LDL receptor-deficient (LDLR(-/-)) mice. This study was undertaken to determine whether dietary cholesterol and obesity have additive effects on inflammation and atherosclerosis.

METHODS AND RESULTS

LDLR(-/-) mice were fed chow, high-fat, high-carbohydrate (diabetogenic) diets without (DD) or with added cholesterol (DDC) for 24 weeks. Effects on adipose tissue, inflammatory markers, and atherosclerosis were studied. Despite similar weight gain between DD and DDC groups, addition of dietary cholesterol increased insulin resistance relative to DD. Adipocyte hypertrophy, macrophage accumulation, and local inflammation were observed in intraabdominal adipose tissue in DD and DDC, but were significantly higher in the DDC group. Circulating levels of the inflammatory protein serum amyloid A (SAA) were 4.4-fold higher in DD animals and 15-fold higher in DDC animals than controls, suggesting chronic systemic inflammation. Hepatic SAA mRNA levels were similarly elevated. Atherosclerosis was increased in the DD-fed animals and further increased in the DDC group.

CONCLUSIONS

Obesity-induced macrophage accumulation in adipose tissue is exacerbated by dietary cholesterol. These local inflammatory changes in adipose tissue are associated with insulin resistance, systemic inflammation, and increased atherosclerosis in this mouse model.

摘要

目的

慢性全身性炎症伴随肥胖,并预示心血管疾病的发生。膳食胆固醇已被证明会增加低密度脂蛋白受体缺陷(LDLR(-/-))小鼠的炎症和动脉粥样硬化。本研究旨在确定膳食胆固醇和肥胖对炎症和动脉粥样硬化是否具有叠加效应。

方法与结果

给LDLR(-/-)小鼠喂食普通饲料、不含胆固醇(DD)或添加胆固醇(DDC)的高脂肪、高碳水化合物(致糖尿病)饮食,持续24周。研究对脂肪组织、炎症标志物和动脉粥样硬化的影响。尽管DD组和DDC组体重增加相似,但相对于DD组,添加膳食胆固醇会增加胰岛素抵抗。在DD组和DDC组的腹内脂肪组织中均观察到脂肪细胞肥大、巨噬细胞聚集和局部炎症,但DDC组显著更高。与对照组相比,DD组动物循环炎症蛋白血清淀粉样蛋白A(SAA)水平高4.4倍,DDC组动物高15倍,提示慢性全身性炎症。肝脏SAA mRNA水平同样升高。喂食DD饮食的动物动脉粥样硬化增加,DDC组进一步增加。

结论

膳食胆固醇会加剧肥胖诱导的脂肪组织中巨噬细胞的聚集。在该小鼠模型中,脂肪组织的这些局部炎症变化与胰岛素抵抗、全身性炎症和动脉粥样硬化增加有关。

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