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咖啡酸甲酯从(L.)巴特希的花中分离出来,可增强葡萄糖刺激的胰岛素分泌。

Methyl Caffeate Isolated from the Flowers of (L.) Batsch Enhances Glucose-Stimulated Insulin Secretion.

机构信息

College of Korean Medicine, Gachon University, Seongnam 13120, Korea.

Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul 02447, Korea.

出版信息

Biomolecules. 2021 Feb 14;11(2):279. doi: 10.3390/biom11020279.

Abstract

Phenolic compounds from natural products are considered effective enhancers of insulin secretion to prevent and treat type 2 diabetes (T2DM). The flowers of (L.) Batsch also contain many phenolic compounds. In this study, the extract of flowers of (PRPE) exhibited an insulin secretion effect in a glucose-stimulated insulin secretion (GSIS) assay, which led us to isolate and identify the bioactive compound(s) responsible for these effects. Compounds isolated from PRPE were screened for their efficacy in INS-1 rat pancreatic β-cells. Among them, caffeic acid (5), methyl caffeate (6), ferulic acid (7), chlorogenic acid (8), naringenin (11), nicotiflorin (12), and astragalin (13) isolated from PRPE increased GSIS without inducing cytotoxicity. Interestingly, the GSIS effect of methyl caffeate (6) as a phenolic compound was similar to gliclazide, an antidiabetic sulfonylurea drug. Western blot assay showed that methyl caffeate (6) enhanced the related signaling proteins of the activated pancreatic and duodenal homeobox-1 (PDX-1) and peroxisome proliferator-activated receptor-γ (PPAR-γ), but also the phosphorylation of the total insulin receptor substrate-2 (IRS-2), phosphatidylinositol 3-kinase (PI3K), and Akt, which influence β-cell function and insulin secretion. This study provides evidence that methyl caffeate (6) isolated from PRPE may aid in the management of T2DM.

摘要

从天然产物中提取的酚类化合物被认为是有效增强胰岛素分泌的物质,可用于预防和治疗 2 型糖尿病(T2DM)。 (L.)Batsch 的花也含有许多酚类化合物。在这项研究中,(PRPE)花的提取物在葡萄糖刺激的胰岛素分泌(GSIS)试验中显示出胰岛素分泌作用,这促使我们分离和鉴定负责这些作用的生物活性化合物。从 PRPE 中分离出的化合物在 INS-1 大鼠胰腺β细胞中进行了功效筛选。其中,咖啡酸(5)、甲基咖啡酸(6)、阿魏酸(7)、绿原酸(8)、柚皮苷(11)、野漆树苷(12)和杨梅素(13)均能在不诱导细胞毒性的情况下增强 GSIS。有趣的是,作为酚类化合物的甲基咖啡酸(6)的 GSIS 作用类似于治疗糖尿病的磺酰脲类药物格列齐特。Western blot 分析表明,甲基咖啡酸(6)增强了胰腺十二指肠同源盒-1(PDX-1)和过氧化物酶体增殖物激活受体-γ(PPAR-γ)的相关信号蛋白,同时还增强了胰岛素受体底物-2(IRS-2)、磷酸肌醇 3-激酶(PI3K)和 Akt 的总磷酸化,这些蛋白影响β细胞功能和胰岛素分泌。这项研究为 PRPE 中分离出的甲基咖啡酸(6)可能有助于 T2DM 的管理提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/def4/7917615/a02831d23589/biomolecules-11-00279-g001.jpg

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