首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Kiwifruit seed oil prevents obesity by regulating inflammation, thermogenesis, and gut microbiota in high-fat diet-induced obese C57BL/6 mice
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Kiwifruit seed oil prevents obesity by regulating inflammation, thermogenesis, and gut microbiota in high-fat diet-induced obese C57BL/6 mice

机译:通过在高脂肪饮食诱导的肥胖C57BL / 6小鼠中调节炎症,热生成和肠道微生物来防止肥胖的肥胖籽油

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摘要

Obesity is considered as a chronic disease which seriously affecting people's health and daily life. Kiwifruit (Actinidia chinensis Planch) seed oil (KSO), as a by-product of kiwifruit processing, is rich in fatty acids. Conventional wisdom holds that KSO has many health benefits, but there is no scientific basis. Here, the relieving effects of KSO on obesity and its potential mechanism were investigated in high-fat diet (HFD)-induced C57BL/6 mice. Mice were divided into four groups: ND (normal diet); HFD; L-KSO and H-KSO (HFD supplemented with 1.0 and 3.0 mL/kg.bw of KSO per day, respectively). Results showed that continuous supplementation KSO for 12 weeks significantly decreased bodyweight, inguinal fat tissue weight, blood glucose, and HOMA-IR index and ameliorated serum lipids accumulation (TC, TG, HDL-C, and LDL-C). Relative mRNA expression of inflammatory cytokines(TN-alpha IL-6, IL-beta, COX-2, and iNOS) was down-regulated and expression of thermogenesis-related genes (PPAR-gamma, UCP1, PGC1-alpha, and PRDM16) was up-regulated in the inguinal fat tissue of KSO treated mice. Principal component analysis showed that the microbial community compositions of four groups were different. KSO supplementation dramatically decreased the Firmicutes-to-Bacteroidetes ratio. Together, our findings demonstrated that long-term supplementation KSO ameliorates obesity by reducing inflammation, adipose thermogenesis and gut microbiota dysbiosis.
机译:肥胖被认为是一种严重影响人们健康和日常生活的慢性疾病。 Kiwifruit(Actinidia chinensis Planch)种子油(KSO),作为普韦特加工的副产物,富含脂肪酸。传统智慧认为,KSO有许多健康益处,但没有科学的基础。这里,研究了KSO对肥胖症及其潜在机制的缓解效果,高脂饮食(HFD)诱导C57BL / 6小鼠。小鼠分为四组:Nd(正常饮食); HFD; L-KSO和H-KSO(HFD分别补充了每天1.0和3.0毫升/ kg.bw)。结果表明,12周的连续补充KSO显着降低体重,腹股沟脂肪组织重量,血糖和HOMA-IR指数和改善血清脂质积累(TC,TG,HDL-C和LDL-C)。炎性细胞因子(TN-αIL-6,IL-BETA,COX-2和INOS)的相对mRNA表达被下调和表达热生成相关基因(PPAR-GAMMA,UCP1,PGC1-α和PRDM16)在KSO处理的小鼠的腹股沟脂肪组织中上调。主要成分分析表明,四组的微生物群落组成不同。 KSO补充显着降低了对致细胞比率的差异。我们的研究结果表明,通过减少炎症,脂肪生成和肠道微生物症消除症来改善肥胖的长期补充。

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