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Preventive effect of small‐leaved Kuding tea (Ligustrum robustum) on high‐diet‐induced obesity in C57BL/6J mice

机译:小型叶茶(Ligustrum Robustum)对C57BL / 6J小鼠高饮食诱导肥胖的预防效果

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Small‐leaved Kuding tea (SLKDT; Ligustrum robustum) is a traditional Chinese tea. We systematically investigated the effect of SLKDT extract on obesity. SLKDT‐controlled weight gain in mice fed a high‐fat diet. Tissue specimen results showed that the SLKDT extract alleviated liver damage and fat accumulation. Meanwhile, SLKDT extract improved dyslipidemia by decreasing total cholesterol, triglycerides, and low‐density lipoprotein cholesterol levels and increasing high‐density lipoprotein cholesterol levels. Furthermore, SLKDT extract reduced alanine aminotransferase, alkaline phosphatase, and aspartate transaminase levels in the serum and liver tissues; decreased inflammatory cytokines, including interleukin (IL)‐1β, tumor necrosis factor‐α, interferon‐γ, and IL‐6; and increased the anti‐inflammatory cytokines, IL‐4 and IL‐10. The quantitative PCR results showed that SLKDT extract upregulated the mRNA expressions of peroxisome proliferator‐activated receptor (PPAR)‐α, lipoprotein lipase, carnitine palmitoyltransferase 1, and cholesterol 7 alpha hydroxylase and downregulated PPAR‐γ and CCAAT/enhancer‐binding protein‐alpha mRNA expressions in the obese mouse livers to reduce adipocyte differentiation and fat accumulation, promote fat oxidation, and improve dyslipidemia, thereby inhibiting the immune response and alleviating liver injury. SLKDT shows a potential for preventing obesity and regulating obesity‐related syndrome, so it is possible to be further developed as a novel treatment for fighting obesity.
机译:小型叶子茶(Slkdt; Ligustrum Robustum)是一种传统的中国茶。我们系统地研究了SLKDT提取物对肥胖症的影响。喂养高脂饮食的小鼠的SLKDT控制的体重增加。组织标本结果表明,SLKDT提取物缓解肝损伤和脂肪积累。同时,SLKDT通过减少总胆固醇,甘油三酯和低密度脂蛋白胆固醇水平并增加高密度脂蛋白胆固醇水平,提取改善的血脂血症。此外,SLKDT提取血清和肝组织中的丙氨酸氨基转移酶,碱性磷酸酶和天冬氨酸转氨酶水平降低;减少炎症细胞因子,包括白细胞素(IL)-1β,肿瘤坏死因子-α,干扰素-γ和IL-6;并增加抗炎细胞因子,IL-4和IL-10。定量PCR结果表明,SLKDT提取物上调过氧化物体增殖物激活受体(PPAR)-α,脂蛋白脂肪酶,肉碱棕榈酰转移酶1和胆固醇7α羟基化酶和下调的PPAR-γ和CCAAT /增强剂 - 结合蛋白-α-羟基苯肥胖小鼠肝脏中mRNA表达,以减少脂肪细胞分化和脂肪积聚,促进脂肪氧化,改善血脂血症,从而抑制免疫应答和缓解肝损伤。 SLKDT显示了防止肥胖和调节肥胖相关综合症的可能性,因此可以进一步发展成为对抗肥胖症的新型治疗方法。

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