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朝鲜槲寄生(Viscum album coloratum)提取物具有抗肥胖作用,并可预防高脂饮食诱导肥胖小鼠的肝脂肪变性。

The Korean Mistletoe (Viscum album coloratum) Extract Has an Antiobesity Effect and Protects against Hepatic Steatosis in Mice with High-Fat Diet-Induced Obesity.

机构信息

School of Life and Food Sciences, Handong Global University, Pohang, Gyeongbuk 791-708, Republic of Korea ; Research and Development Team, Pohang Center for Evaluation of Biomaterials, Pohang, Gyeongbuk 790-834, Republic of Korea ; Division of Integrative Biosciences and Biotechnology (IBB), POSTECH (WCU), Pohang, Gyeongbuk 790-784, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2013;2013:168207. doi: 10.1155/2013/168207. Epub 2013 Jul 11.

Abstract

This study investigates the inhibitory effects of Korean mistletoe extract (KME) on adipogenic factors in 3T3-L1 cells and obesity and nonalcoholic fatty liver disease (NAFLD) in mice fed a high-fat diet. Male C57Bl/6 mice fed a high-fat diet were treated with KME (3 g/kg/day) for 15 weeks for the antiobesity and NAFLD experiments. Body weight and daily food intake were measured regularly during the experimental period. The epididymal pad was measured and liver histology was observed. The effects of KME on thermogenesis and endurance capacity were measured. The effects of KME on adipogenic factors were examined in 3T3-L1 cells. Body and epididymal fat pad weights were reduced in KME-treated mice, and histological examination showed an amelioration of fatty liver in KME-treated mice, without an effect on food consumption. KME potently induces mitochondrial activity by activating thermogenesis and improving endurance capacity. KME also inhibited adipogenic factors in vitro. These results demonstrate the inhibitory effects of KME on obesity and NAFLD in mice fed a high-fat diet. The effects appear to be mediated through an enhanced mitochondrial activity. Therefore, KME may be an effective therapeutic candidate for treating obesity and fatty liver caused by a high-fat diet.

摘要

本研究旨在探讨韩国槲寄生提取物(KME)对高脂肪饮食喂养的小鼠脂肪生成因子及肥胖和非酒精性脂肪性肝病(NAFLD)的抑制作用。雄性 C57Bl/6 小鼠给予高脂肪饮食,并接受 KME(3g/kg/天)治疗 15 周,进行抗肥胖和 NAFLD 实验。在实验期间定期测量体重和每日食物摄入量。测量附睾垫的重量并观察肝脏组织学变化。测量 KME 对产热和耐力的影响。在 3T3-L1 细胞中检查 KME 对脂肪生成因子的影响。KME 处理组小鼠的体重和附睾脂肪垫重量减轻,组织学检查显示 KME 处理组小鼠的脂肪肝得到改善,而食物摄入量没有影响。KME 通过激活产热和提高耐力来强烈诱导线粒体活性。KME 还在体外抑制脂肪生成因子。这些结果表明 KME 可抑制高脂肪饮食喂养的小鼠肥胖和 NAFLD。这些作用似乎是通过增强线粒体活性介导的。因此,KME 可能是治疗高脂肪饮食引起的肥胖和脂肪肝的有效治疗候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd44/3725881/11a30be19069/ECAM2013-168207.001.jpg

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