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及其成分苍术素通过激活AMPK改善代谢功能障碍相关的脂肪性肝病。

and Its Constituent, Atractylodin, Ameliorates Metabolic Dysfunction-Associated Steatotic Liver Disease via AMPK Activation.

作者信息

Song Ga Yeon, Kim Sun Myoung, Back Seungil, Yang Seung-Bo, Yang Yoon Mee

机构信息

Department of Pharmacy, Kangwon National University, Chuncheon 24341, Republic of Korea.

KNU Innovative Drug Development Research Team for Intractable Diseases (BK21 Four), Kangwon National University, Chuncheon 24341, Republic of Korea.

出版信息

Biomol Ther (Seoul). 2024 Nov 1;32(6):778-792. doi: 10.4062/biomolther.2024.083. Epub 2024 Oct 11.

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD), which encompasses a spectrum of conditions ranging from simple steatosis to hepatocellular carcinoma, is a growing global health concern associated with insulin resistance. Since there are limited treatment options for MASLD, this study investigated the therapeutic potential of , a traditional herbal remedy for digestive disorders in East Asia, and its principal component, atractylodin, in treating MASLD. Following 8 weeks of high-fat diet (HFD) feeding, mice received oral doses of 30, 60, or 120 mg/kg of . In HFD-fed mice, treatment reduced the body weight; serum triglyceride, total cholesterol, and alanine aminotransferase levels; and hepatic lipid content. Furthermore, significantly ameliorated fasting serum glucose, fasting serum insulin, and homeostatic model assessment of insulin resistance levels in response to HFD. Additionally, a glucose tolerance test demonstrated improved glucose homeostasis. Treatment with 5 or 10 mg/kg atractylodin also resulted in anti-obesity, anti-steatosis, and glucose-lowering effects. Atractylodin treatment resulted in the downregulation of key lipogenic genes (, , , and ) and the upregulation of genes regulated by peroxisome proliferator-activated receptor-α. Notably, the molecular docking model suggested a robust binding affinity between atractylodin and AMP-activated protein kinase (AMPK). Atractylodin activated AMPK, which contributed to SREBP1c regulation. In conclusion, our results revealed that and atractylodin activated the AMPK signaling pathway, leading to improvements in HFD-induced obesity, fatty liver, and glucose intolerance. This study suggests that the phytochemical, atractylodin, can be a treatment option for MASLD.

摘要

代谢功能障碍相关脂肪性肝病(MASLD)涵盖了从单纯性脂肪变性到肝细胞癌的一系列病症,是一个与胰岛素抵抗相关且日益受到全球关注的健康问题。由于MASLD的治疗选择有限,本研究调查了东亚一种用于治疗消化系统疾病的传统草药及其主要成分苍术素醇治疗MASLD的潜力。在高脂饮食(HFD)喂养8周后,小鼠口服30、60或120mg/kg的[草药名称未给出]。在HFD喂养的小鼠中,[草药名称未给出]治疗降低了体重、血清甘油三酯、总胆固醇和丙氨酸转氨酶水平以及肝脏脂质含量。此外,[草药名称未给出]显著改善了空腹血清葡萄糖、空腹血清胰岛素以及对HFD的胰岛素抵抗稳态模型评估水平。另外,葡萄糖耐量试验表明葡萄糖稳态得到改善。用5或10mg/kg苍术素醇治疗也产生了抗肥胖、抗脂肪变性和降血糖作用。苍术素醇治疗导致关键脂肪生成基因([具体基因未给出])的下调以及过氧化物酶体增殖物激活受体-α调控基因的上调。值得注意的是,分子对接模型表明苍术素醇与AMP激活的蛋白激酶(AMPK)之间具有强大的结合亲和力。苍术素醇激活了AMPK,这有助于对固醇调节元件结合蛋白1c(SREBP1c)进行调控。总之,我们的结果表明[草药名称未给出]和苍术素醇激活了AMPK信号通路,从而改善了HFD诱导的肥胖、脂肪肝和葡萄糖不耐受。本研究表明植物化学物质苍术素醇可以作为MASLD的一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/547b/11535289/4c0ed172e0d9/bt-32-6-778-f1.jpg

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