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长叶轮钟藤中环六烷及六烷达玛烷三萜的胰岛素模拟活性。

Insulin Mimetic Activity of 3,4- Seco and Hexanordammarane Triterpenoids Isolated from Gynostemma longipes.

机构信息

Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy , Seoul National University , Seoul 08826 , Republic of Korea.

Department of Botany , Hanoi University of Pharmacy , Hanoi , Vietnam.

出版信息

J Nat Prod. 2018 Nov 26;81(11):2470-2482. doi: 10.1021/acs.jnatprod.8b00524. Epub 2018 Nov 2.

DOI:10.1021/acs.jnatprod.8b00524
PMID:30387350
Abstract

As part of ongoing research to find new antidiabetic agents from medicinal plants, the chemical composition of Gynostemma longipes, an ethnomedicinal plant used to treat type 2 diabetes mellitus by local communities in Vietnam, was investigated. Ten new dammarane triterpenes, including two 3,4- seco-dammarane analogues, secolongipegenins S1 and S2 (1 and 2), a 3,4- seco-hexanordammarane, secolongipegenin S3 (3), two hexanordammarane glycosides, longipenosides ND1 and ND2 (4 and 5), and five other dammarane glycosides, longipenosides GL1-GL5 (6-10), were isolated from a 70% EtOH extract of the whole G. longipes plant. The structures of the new compounds were elucidated using diverse spectroscopic methods. All of the isolates were evaluated for their stimulatory activities on glucose uptake in differentiated 3T3-L1 adipocyte cells using 2-[ N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-d-glucose as a fluorescent-tagged glucose probe. The stimulant activities on glucose uptake by the test compounds were mediated via the activation of the AMPK pathway using differentiated mouse C2C12 skeletal myoblasts. Consequently, compounds 1, 2, and 4 enhanced glucose uptake and GLUT4 translocation significantly by regulating the AMPK signaling pathway.

摘要

作为从药用植物中寻找新型抗糖尿病药物的持续研究的一部分,对越南当地社区用于治疗 2 型糖尿病的传统药用植物绞股蓝的化学成分进行了研究。从绞股蓝全草的 70%乙醇提取物中分离得到了 10 种新的达玛烷三萜,包括两种 3,4- 裂环达玛烷类似物,即 secolongipegenin S1 和 S2(1 和 2)、一种 3,4- 裂环己烷达玛烷,secolongipegenin S3(3)、两种己烷达玛烷糖苷,longipenosides ND1 和 ND2(4 和 5)以及另外 5 种达玛烷糖苷,longipenosides GL1-GL5(6-10)。利用多种光谱学方法阐明了这些新化合物的结构。所有分离物均采用 2-[N-(7-硝基苯并-2-氧代-1,3-二唑-4-基)氨基]-2-脱氧-d-葡萄糖作为荧光标记葡萄糖探针,在分化的 3T3-L1 脂肪细胞中评估了它们对葡萄糖摄取的刺激活性。测试化合物对葡萄糖摄取的刺激活性是通过使用分化的小鼠 C2C12 骨骼肌成肌细胞激活 AMPK 途径介导的。结果表明,化合物 1、2 和 4 通过调节 AMPK 信号通路显著增强了葡萄糖摄取和 GLUT4 易位。

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