Actichinone是一种从猕猴桃根中提取的新型三萜,可通过AMPK和NF-κB途径改善NAFLD。

IF 4.2 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Xinhua Li , Yuanlong Zhang , Leiqing Chen , Xiao Xu , Xiaohong Ma , Shuying Lou , Ziqiang Zou , Chenjing Wang , Bing Jiang , Yunrui Cai , Yu Qi , Yiyuan Xi , Min Zhao , Pengcheng Yan
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引用次数: 0

摘要

从猕猴桃植物猕猴桃(Actinidia chinensis Planch)的根部分离到一个新的熊类三萜actichinone (3-oxo-2α,24- dihydroxyours -12-en-28-oic acid, 1),并分离到18个已知的三萜(2-19)。通过广泛的光谱分析确定了actichinone(1)的结构。Actichinone(1)在油酸(OA)诱导的小鼠原代肝细胞中表现出最强的降脂活性,并对其构效关系(SARs)进行了分析。通过选择性氧化主要化合物2,实现了actichinone(1)的化学半合成。Actichinone(1)可能通过AMPK/SREBP-1c/PPAR-α和IKK/ i -κB /NF-κB信号通路调节脂质积累和炎症反应,在高脂肪蛋氨酸和胆碱缺乏饮食(HFMCD)喂养的小鼠模型中显示出非酒精性脂肪性肝病(NAFLD)的显著缓解。本研究为基于五环三萜家族的新型抗nafld药物的开发提供了有前景的先导化合物和新思路,有望促进金合藤植物的高附加值综合应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Actichinone, a new ursane triterpenoid from Actinidia chinensis roots, ameliorates NAFLD via the AMPK and NF-κB pathways

Actichinone, a new ursane triterpenoid from Actinidia chinensis roots, ameliorates NAFLD via the AMPK and NF-κB pathways
A new ursane triterpenoid, actichinone (3-oxo-2α,24-dihydroxyurs-12-en-28-oic acid, 1), was isolated from the roots of a kiwi plant Actinidia chinensis Planch, together with 18 known triterpenoids (219). The structure of actichinone (1) was established by extensive spectroscopic analysis. Actichinone (1) showed the most potent lipid-lowering activity in the oleic acid (OA)-induced primary mouse hepatocytes and the structure-activity relationships (SARs) were analyzed. Chemical semi-synthesis of actichinone (1) was achieved by selective oxidation of the major compound 2. Actichinone (1) exhibited significant alleviation of non-alcoholic fatty liver disease (NAFLD) in a high-fat with methionine and choline deficiency diet (HFMCD)-fed mice model, by regulating lipid accumulation and inflammatory response probably via the AMPK/SREBP-1c/PPAR-α and IKK/IκB/NF-κB signaling pathways. This study provides a promising lead compound and a new insight into the development of novel anti-NAFLD agents based on the pentacyclic triterpenoid family, and is expected to promote the high value-added comprehensive application of the A. chinensis plants.
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来源期刊
CiteScore
9.00
自引率
0.00%
发文量
572
审稿时长
34 days
期刊介绍: The European Journal of Pharmacology publishes research papers covering all aspects of experimental pharmacology with focus on the mechanism of action of structurally identified compounds affecting biological systems. The scope includes: Behavioural pharmacology Neuropharmacology and analgesia Cardiovascular pharmacology Pulmonary, gastrointestinal and urogenital pharmacology Endocrine pharmacology Immunopharmacology and inflammation Molecular and cellular pharmacology Regenerative pharmacology Biologicals and biotherapeutics Translational pharmacology Nutriceutical pharmacology.
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