Kim Kibong, Baek Suji, Ko Solomon, Moon Seungjae, Lee Kang Pa, Ahn Sanghyun
Second Division of Clinical Medicine, School of Korean Medicine, Pusan National University, Gyeongsangnam-do, Republic of Korea.
Research & Development Center, UMUST R&D corporation, Seoul, Republic of Korea.
Phys Act Nutr. 2023 Dec;27(4):60-66. doi: 10.20463/pan.2023.0039. Epub 2023 Dec 31.
One of the urgent research projects in exercise science should focus on sports supplements for obese people who lack exercise and physical activity. In this study, we explored the efficacy in non-alcoholic fatty liver disease (NAFLD) mice models using a Korean herbal medicine Erigeron breviscapus (EB).
Gene ontology analyses of active compounds in EB were performed using the Traditional Chinese Medicine Database and Analysis Platform (TCMSP) and Cytoscape program, respectively. PA-induced acid (PA) induced-lipid droplets in HepG2 cells were analyzed using a 3D-hologram. To analyze the fat-suppressing efficacy of EB in animal experiments, NAFLD was induced through a 24-week high-fat diet. Subsequently, the same diet was continued for an additional 8 weeks, with concurrent co-administration of drugs for efficacy analysis. In the 8-week experiment, mice were administered saline alone, metformin (17 mg/kg/day), or EB (26 mg/kg/day). The mice were sacrificed and the liver tissue was isolated. The liver tissues were stained with H&E and specific antibodies such as sterol regulatory element binding protein 1 (SREBP-1) and peroxisome proliferator-activated receptor- γ (PPAR-γ).
Seventeen EB-active compounds were identified by whole-body analysis. EB downregulated lipid droplets in PA-treated HepG2 cells. EB regulates lipid accumulation in liver tissue of HFD-fed NAFLD mice Metformin and EB significantly reduced the expression of SREBP-1 and PPAR-γ in liver tissue.
We suggest that EB is a candidate for the management of NAFLD and is an effective exercise supplement owing to its ability to inhibit lipid accumulation.
运动科学中紧迫的研究项目之一应聚焦于针对缺乏运动和体育活动的肥胖人群的运动补剂。在本研究中,我们使用韩国草药灯盏花(EB)探究了其在非酒精性脂肪性肝病(NAFLD)小鼠模型中的疗效。
分别使用中药系统药理学数据库与分析平台(TCMSP)和Cytoscape程序对EB中的活性化合物进行基因本体分析。使用三维全息图分析棕榈酸(PA)诱导的HepG2细胞中的脂滴。为了在动物实验中分析EB的减脂功效,通过24周的高脂饮食诱导NAFLD。随后,继续相同饮食8周,并同时联合给药以进行疗效分析。在为期8周的实验中,小鼠分别单独给予生理盐水、二甲双胍(17毫克/千克/天)或EB(26毫克/千克/天)。处死小鼠并分离肝脏组织。肝脏组织用苏木精和伊红染色以及用固醇调节元件结合蛋白1(SREBP-1)和过氧化物酶体增殖物激活受体-γ(PPAR-γ)等特异性抗体染色。
通过全身分析鉴定出17种EB活性化合物。EB下调了PA处理的HepG2细胞中的脂滴。EB调节高脂饮食喂养的NAFLD小鼠肝脏组织中的脂质积累。二甲双胍和EB显著降低了肝脏组织中SREBP-1和PPAR-γ的表达。
我们认为EB是NAFLD管理的候选药物,并且由于其抑制脂质积累的能力,它是一种有效的运动补剂。