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云芝提取物可降低高脂饮食喂养小鼠的肥胖程度,并减少脂肪负荷小鼠对甘油三酯的吸收。

A Phellinus baumii extract reduces obesity in high-fat diet-fed mice and absorption of triglyceride in lipid-loaded mice.

机构信息

Animal Model Center, Korea Research Institute of Bioscience and Biotechnology, Iksan, Jeonbuk, Republic of Korea.

出版信息

J Med Food. 2011 Mar;14(3):209-18. doi: 10.1089/jmf.2010.1152.

Abstract

This study evaluated the anti-obesity effects of Phellinus baumii extract (PBE) in high-fat diet (HFD)-fed mice. Male 8-week-old C57BL/6 mice were randomly divided into four groups: control, normal chow diet plus vehicle; HFD-control, high-fat plus vehicle; HFD plus orlistat (Xenical(®), Roche, Basel, Switzerland) (50 mg/kg); and HFD plus PBE (500 mg/kg). PBE was administered daily by oral gavage for 12 weeks. Oral administration of PBE (500 mg/kg) significantly reduced body weight gain, hepatic lipid concentrations, and fat accumulation in epididymal adipocytes compared with mice fed HFD alone (P < .05). mRNA expression of genes related to triglyceride (TG) synthesis was suppressed in the PBE groups, and fatty acid synthase activity was also significantly inhibited (P < .05). Furthermore, we evaluated the effect of PBE on TG absorption and detected marked reduction in TG absorption in Xenical- and PBE-treated mice compared with the control group (P < .05). To determine the active compound of PBE, fractionation was conducted, and interfungin A, davallialactone, and hypholomine B were identified as the main compounds. Among the three identified compounds, as a representative compound, davallialactone was also shown to suppress fat accumulation in an in vitro model system. These anti-obesity and hypolipidemic effects appear to be partly mediated by suppressing plasma and hepatic fat accumulation through the inhibition of enzymes associated with hepatic and intestinal lipid absorption and synthesis.

摘要

本研究评估了鲍氏木层孔菌提取物(PBE)在高脂饮食(HFD)喂养小鼠中的抗肥胖作用。雄性 8 周龄 C57BL/6 小鼠被随机分为四组:对照组,普通饲料加载体;HFD-对照组,高脂肪加载体;HFD 加奥利司他(Xenical®,罗氏,巴塞尔,瑞士)(50mg/kg);和 HFD 加 PBE(500mg/kg)。PBE 通过口服灌胃给药,每天一次,共 12 周。与单独给予 HFD 的小鼠相比,口服 PBE(500mg/kg)显著降低了体重增加、肝脂质浓度和附睾脂肪细胞中的脂肪堆积(P<.05)。PBE 组与 TG 合成相关的基因的 mRNA 表达受到抑制,脂肪酸合酶活性也显著受到抑制(P<.05)。此外,我们评估了 PBE 对 TG 吸收的影响,并发现与对照组相比,Xenical 和 PBE 治疗的小鼠的 TG 吸收明显减少(P<.05)。为了确定 PBE 的活性化合物,进行了分级分离,鉴定出 interfungin A、da vallialactone 和 hypholomine B 为主要化合物。在鉴定出的三种化合物中,作为代表性化合物,da vallialactone 也显示出在体外模型系统中抑制脂肪积累的作用。这些抗肥胖和降血脂作用部分可能是通过抑制与肝和肠脂质吸收和合成相关的酶来抑制血浆和肝脂肪积累介导的。

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