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Intervention with citrus flavonoids reverses obesity and improves metabolic syndrome and atherosclerosis in obese Ldlr−/− mice

机译:柑橘类黄酮的干预可逆转肥胖并改善肥胖Ldlr-/-小鼠的代谢综合征和动脉粥样硬化

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摘要

Obesity and its associated metabolic dysfunction and cardiovascular disease risk represent a leading cause of adult morbidity worldwide. Currently available pharmacological therapies for obesity have had limited success in reversing existing obesity and metabolic dysregulation. Previous prevention studies demonstrated that the citrus flavonoids, naringenin and nobiletin, protect against obesity and metabolic dysfunction in Ldlr−/− mice fed a high-fat cholesterol-containing (HFHC) diet. However, their effects in an intervention model are unknown. In this report, we show that, in Ldlr−/− mice with diet-induced obesity, citrus flavonoid supplementation to a HFHC diet reversed existing obesity and adipocyte size and number through enhanced energy expenditure and increased hepatic fatty acid oxidation. Caloric intake was unaffected and no evidence of white adipose tissue browning was observed. Reversal of adiposity was accompanied by improvements in hyperlipidemia, insulin sensitivity, hepatic steatosis, and a modest reduction in blood monocytes. Together, this resulted in atherosclerotic lesions that were unchanged in size, but characterized by reduced macrophage content, consistent with a more stable plaque phenotype. These studies further suggest potential therapeutic utility of citrus flavonoids, especially in the context of existing obesity, metabolic dysfunction, and cardiovascular disease.
机译:肥胖及其相关的代谢功能障碍和心血管疾病的风险是全世界成人发病的主要原因。当前用于肥胖症的药物疗法在逆转现有的肥胖症和代谢异常中的成功有限。先前的预防研究表明,柑桔类黄酮,柚皮素和诺比列汀可以预防肥胖和高脂胆固醇(HFHC)日粮喂养的Ldlr -/-小鼠的代谢功能障碍。但是,它们在干预模型中的作用尚不清楚。在本报告中,我们显示,在饮食诱发的肥胖症的Ldlr -/-小鼠中,向HFHC饮食补充柑橘类黄酮可通过增加能量消耗和增加肝脂肪来逆转现有的肥胖症和脂肪细胞的大小和数量。酸氧化。热量摄入不受影响,没有观察到白色脂肪组织褐变的迹象。肥胖的逆转伴随着高脂血症,胰岛素敏感性,肝脂肪变性和血液单核细胞适度减少的改善。在一起,这导致动脉粥样硬化病变的大小没有变化,但特征在于巨噬细胞含量减少,与更稳定的噬菌斑表型一致。这些研究进一步表明了柑桔类黄酮的潜在治疗作用,尤其是在现有的肥胖,代谢功能障碍和心血管疾病的背景下。

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