Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, South Korea.
Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC.
J Nutr Biochem. 2020 Dec;86:108483. doi: 10.1016/j.jnutbio.2020.108483. Epub 2020 Aug 26.
The aim of this study was to determine whether the atheroprotective phytochemical 23-hydroxy ursolic acid protects against diet-induced obesity and hyperglycemia by preventing nutrient stress-induced monocyte reprogramming. After a two week run-in period on a defined, phytochemical-free low-fat maintenance diet, 12-week old female C57BL/6J mice were either kept on the maintenance diet for additional 13 weeks or switched to either a high-calorie diet, a high-calorie diet supplemented with either 0.05% 23-hydroxy ursolic acid or a high-calorie diet supplemented with 0.2% 23-hydroxy ursolic acid. Dietary supplementation with 23-hydroxy ursolic acid reduced weight gain and adipose tissue mass, prevented hyperglycemia, hyperleptinemia and adipose tissue inflammation, and preserved glucose tolerance. 23-Hydroxy ursolic acid also preserved blood monocyte mitogen-activated protein kinase phosphatase-1 activity, a biomarker of monocyte health, and reduced macrophage content in the adipose tissue. Targeted gene profiling by qRT-PCR using custom-designed TaqMan® Array Cards revealed that dietary 23-hydroxy ursolic acid converts macrophages into a transcriptionally hyperactive phenotype with enhanced antioxidant defenses and anti-inflammatory potential. In conclusion, our findings show that dietary 23-hydroxy ursolic acid exerts both anti-obesogenic effects through multiple mechanisms. These include improving glucose tolerance, preventing hyperleptinemia, maintaining blood monocyte function, reducing recruitment of monocyte-derived macrophages into adipose tissues during nutrient stress, and converting these macrophages into an anti-inflammatory, potentially inflammation-resolving phenotype, all contributing to reduced adipose tissue inflammation. Our data suggest that 23-hydroxy ursolic acid may serve as an oral therapeutic and dietary supplement suited for patients at risk for obesity, impaired glucose tolerance and cardiovascular disease.
本研究旨在探讨具有抗动脉粥样硬化作用的植物化学物 23-羟基乌苏酸是否通过防止营养应激诱导的单核细胞重编程来预防饮食诱导的肥胖和高血糖。12 周龄雌性 C57BL/6J 小鼠在特定的、不含植物化学物的低脂维持饮食中适应两周后,继续维持该饮食(13 周)或切换至高热量饮食、添加 0.05% 23-羟基乌苏酸的高热量饮食或添加 0.2% 23-羟基乌苏酸的高热量饮食。23-羟基乌苏酸的饮食补充可减少体重增加和脂肪组织质量,预防高血糖、高瘦素血症和脂肪组织炎症,并维持葡萄糖耐量。23-羟基乌苏酸还可维持血液单核细胞有丝分裂原激活蛋白激酶磷酸酶-1 活性(单核细胞健康的生物标志物),并减少脂肪组织中的巨噬细胞含量。使用定制的 TaqMan®Array 卡进行的靶向基因表达谱分析显示,饮食中的 23-羟基乌苏酸可将巨噬细胞转化为转录活性增强的表型,增强抗氧化防御和抗炎潜力。总之,我们的研究结果表明,饮食中的 23-羟基乌苏酸通过多种机制发挥抗肥胖作用。这些机制包括改善葡萄糖耐量、预防高瘦素血症、维持血液单核细胞功能、在营养应激期间减少单核细胞衍生的巨噬细胞向脂肪组织的募集、并将这些巨噬细胞转化为抗炎、潜在的炎症消退表型,从而减少脂肪组织炎症。我们的数据表明,23-羟基乌苏酸可能作为一种口服治疗和饮食补充剂,适合肥胖、葡萄糖耐量受损和心血管疾病风险患者。