棘肉杆菌提取物对胰岛素受体的激活作用及新型活性化合物肌蓝蛋白A的鉴定

IF 3.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Ayala Wollman, Rania Hasib Afana, Shmuel Carmeli and Tovit Rosenzweig*, 
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引用次数: 0

摘要

棘肉杆菌是一种具有降血糖作用的药用植物。本研究旨在鉴定其有效成分及其作用机制。利用生物引导分离分离活性分子,核磁共振和HRESI质谱对活性分子进行鉴定和结构解析。在体外测定了胰岛素受体(IR)的结合和受体的活化。体内降糖效果得到验证。鉴定出一种新的原花青素三聚体,命名为sarcocyanidin A(1,儿茶素-(4α-8)-表儿茶素-(4β-8)-表儿茶素)。Sarcocyanidin A(1)激活CHO-IR和L6肌管中的胰岛素信号,而IR抑制剂则消除了这一作用。红外自身荧光和基于细胞的热移分析表明,肌青素a(1)与红外有直接的相互作用。在小鼠中,肌青素A(1)也能激活胰岛素信号并降低血糖。Sarcocyanidin A是一种新型的原花青素三聚体,通过激活IR介导SSE至少部分的抗糖尿病特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activation of the Insulin Receptor by Sarcopoterium spinosum Extract and Identification of Sarcocyanidin A as a Novel Active Compound

Sarcopoterium spinosum is a medicinal plant, presenting glucose-lowering properties. The study aimed to identify the active components and their mechanisms of action. Bioguided fractionation was utilized to isolate the active molecules, followed by NMR and HRESI MS for their identification and structural elucidation. Binding to the insulin receptor (IR) and activation of the receptor were measured in vitro. Glucose-lowering effects were validated in vivo. A novel procyanidin trimer, named sarcocyanidin A (1, catechin-(4α-8)-epicatechin-(4β-8)-epicatechin), was identified. Sarcocyanidin A (1) activated insulin signaling in CHO-IR and L6 myotubes, while the IR inhibitor abolished this effect. IR autofluorescence and cell-based thermal shift assays indicate a direct interaction of sarcocyanidin A (1) with IR. Sarcocyanidin A (1) also activated insulin signaling and reduced blood glucose in mice. Sarcocyanidin A, a novel procyanidin trimer, mediates at least part of the antidiabetic properties of SSE, through activation of IR.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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