Kim Kyung Eun, Ko Keon-Hee, Heo Rok Won, Yi Chin-ok, Shin Hyun Joo, Kim Jun Young, Park Jae-Ho, Nam Sanghae, Kim Hwajin, Roh Gu Seob
1 Department of Anatomy and Convergence Medical Science, Institute of Health Sciences, Gyeongsang National University School of Medicine , Gyeongnam, Republic of Korea.
2 Gyeongnam Oriental Medicinal Herb Institute , Gyeongnam, Republic of Korea.
J Med Food. 2016 Mar;19(3):290-9. doi: 10.1089/jmf.2015.3527. Epub 2016 Jan 7.
Artemisia annua L. (AA) is a well-known source of the antimalarial drug artemisinin. AA also has an antibacterial and antioxidant activity. However, the effect of AA extract on hepatic steatosis induced by obesity is unclear. We investigated whether AA extract prevents obesity-induced insulin resistance and hepatic steatosis in high-fat diet (HFD)-fed mice. Mice were randomly divided into groups that received a normal chow diet or HFD with or without AA for 12 weeks. We found that AA extract reduced insulin resistance and hepatic steatosis in HFD-fed mice. Western blot analysis showed that HFD-induced expression of nuclear sterol regulatory element-binding protein 1 and carbohydrate-responsive element-binding protein in the livers was decreased by AA extract. In particular, dietary administration of AA extract decreased hepatic high-mobility group box 1 and cyclooxygenase-2 expression in HFD-fed mice. AA extract also attenuated HFD-induced collagen deposition and fibrosis-related transforming growth factor-β1 and connective tissue growth factor. These data indicate that dietary AA extract has beneficial effects on hepatic steatosis and inflammation in HFD-fed mice.
黄花蒿是抗疟药物青蒿素的著名来源。黄花蒿还具有抗菌和抗氧化活性。然而,黄花蒿提取物对肥胖诱导的肝脂肪变性的影响尚不清楚。我们研究了黄花蒿提取物是否能预防高脂饮食(HFD)喂养小鼠的肥胖诱导的胰岛素抵抗和肝脂肪变性。将小鼠随机分为接受正常饲料或高脂饮食(含或不含黄花蒿)12周的组。我们发现黄花蒿提取物降低了高脂饮食喂养小鼠的胰岛素抵抗和肝脂肪变性。蛋白质印迹分析表明,高脂饮食诱导的肝脏中核固醇调节元件结合蛋白1和碳水化合物反应元件结合蛋白的表达被黄花蒿提取物降低。特别是,在高脂饮食喂养的小鼠中,饮食中给予黄花蒿提取物可降低肝脏中高迁移率族蛋白B1和环氧合酶-2的表达。黄花蒿提取物还减弱了高脂饮食诱导的胶原蛋白沉积以及与纤维化相关的转化生长因子-β1和结缔组织生长因子。这些数据表明,饮食中的黄花蒿提取物对高脂饮食喂养小鼠的肝脂肪变性和炎症具有有益作用。