Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, University of Washington Medicine Diabetes Institute, University of Washington, Box 358062, 750 Republican Street, Seattle, WA 98109, USA.
Department of Medicine, Cardiology, University of Washington, Box 356422, 1959 Pacific Ave NE, Seattle, WA 98195, USA.
Nutrients. 2018 Oct 3;10(10):1416. doi: 10.3390/nu10101416.
The dietary fatty acid 10,12 conjugated linoleic acid (10,12 CLA) promotes weight loss by increasing fat oxidation, but its effects on atherosclerosis are less clear. We recently showed that weight loss induced by 10,12 CLA in an atherosclerosis-susceptible mouse model with characteristics similar to human metabolic syndrome is accompanied by accumulation of alternatively activated macrophages within subcutaneous adipose tissue. The objective of this study was to evaluate whether 10,12 CLA-mediated weight loss was associated with an atheroprotective phenotype. Male low-density lipoprotein receptor deficient (Ldlr) mice were made obese with 12 weeks of a high-fat, high-sucrose diet feeding (HFHS: 36% fat, 36% sucrose, 0.15% added cholesterol), then either continued on the HFHS diet with or without caloric restriction (CR), or switched to a diet with 1% of the lard replaced by either 9,11 CLA or 10,12 CLA for 8 weeks. Atherosclerosis and lipid levels were quantified at sacrifice. Weight loss in mice following 10,12 CLA supplementation or CR as a weight-matched control group had improved cholesterol and triglyceride levels, yet only the 10,12 CLA-treated mice had improved en face and aortic sinus atherosclerosis. 10,12 CLA-supplemented mice had increased lesion macrophage content, with enrichment of surrounding perivascular adipose tissue (PVAT) alternative macrophages, which may contribute to the anti-atherosclerotic effect of 10,12 CLA.
饮食中的脂肪酸 10,12 共轭亚油酸(10,12 CLA)通过增加脂肪氧化促进体重减轻,但它对动脉粥样硬化的影响尚不清楚。我们最近表明,在具有类似于人类代谢综合征特征的易患动脉粥样硬化的小鼠模型中,10,12 CLA 诱导的体重减轻伴随着皮下脂肪组织中选择性激活的巨噬细胞的积累。本研究的目的是评估 10,12 CLA 介导的体重减轻是否与动脉粥样硬化保护表型相关。雄性低密度脂蛋白受体缺陷(Ldlr)小鼠用 12 周高脂肪、高蔗糖饮食喂养(HFHS:36%脂肪、36%蔗糖、0.15%添加胆固醇)使其肥胖,然后继续或不继续 HFHS 饮食加或不加热量限制(CR),或切换到含 1%猪油的饮食,用 9,11 CLA 或 10,12 CLA 代替 8 周。在牺牲时定量测定动脉粥样硬化和血脂水平。在补充 10,12 CLA 或 CR 的小鼠中,体重减轻作为体重匹配的对照组可改善胆固醇和甘油三酯水平,但只有 10,12 CLA 治疗的小鼠改善了正面和主动脉窦动脉粥样硬化。补充 10,12 CLA 的小鼠具有增加的病变巨噬细胞含量,周围血管周脂肪组织(PVAT)选择性巨噬细胞丰富,这可能有助于 10,12 CLA 的抗动脉粥样硬化作用。