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草木樨(Melilotus officinalis (Linn.) Pall.)的化学成分及抗氧化、抗炎和抗肿瘤活性

Chemical Constituents and Antioxidant, Anti-Inflammatory and Anti-Tumor Activities of Melilotus officinalis (Linn.) Pall.

机构信息

Department of the Research and Development Center of Traditional Chinese Medicine and Biotechnology, Changchun University of Chinese Medicine, Changchun 130117, China.

State Key Laboratory of Natural and Biomimetic Drugs (Peking University), Department of Natural Medicines, School of Pharmaceutical Sciences, Peking University Health Science Center, Peking University, Beijing 100191, China.

出版信息

Molecules. 2018 Jan 29;23(2):271. doi: 10.3390/molecules23020271.

Abstract

Two new p-hydroxybenzoic acid glycosides, namely p-hydroxybenzoic acid-4--α-d-manopyranosyl-(1 → 3)-α-l-rhamnopyranoside (compound ) and 4--α-l-rhamnopyran-osyl-(1 → 6)-α-d-manopyranosyl-(1 → 3)-α-l-rhamnopyranoside (compound ), and seven known compounds, compound , , (acid components), compound , (flavonoids), compound (a coumarin) and compound (an alkaloid), were isolated from the 70% ethanol aqueous extract of the aerial parts of (Linn.) Pall. The structures of all compounds were elucidated by use of extensive spectroscopic methods Infrared Spectroscopy (IR), High resolution electrospray ionization mass spectrometry (HR-ESI-MS), and ¹H and C-NMR). Sugar residues obtained after acid hydrolysis were identified by high-performance liquid chromatography (HPLC). The antioxidant activity of all the compounds was evaluated by 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS⁺) and 1,1-diphenyl-2-picrylhydrazyl (DPPH). The anti-inflammatory effects of the compounds were also evaluated in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages. All compounds were shown to inhibit LPS-induced nitric oxide (NO) and prostaglandin E 2 (PGE 2) production by suppressing the expression of inducible NO synthase (iNOS) and cyclooxygenase-2 (COX-2), respectively, in LPS-stimulated RAW 264.7 cells. The inhibitory effect of all the compounds on MCF-7 cells was determined by Cell Counting Kit-8 (CCK-8) method. The results showed that compounds , , , , exhibited better antioxidant activity compared to the other compounds. compounds - had different inhibitory effects on the release of NO, TNF-α and IL-6 in LPS-stimulated RAW264.7 cells by LPS, of which compound was the most effective against inflammatory factors. compounds and have better antitumor activity compared to other compounds. Further research to elucidate the chemical composition and pharmacological effects of (Linn.) Pall is of major importance towards the development and foundation of clinical application of the species.

摘要

从紫金牛((Linn.)Pall.)的 70%乙醇水溶液提取物中分离得到了两种新的对羟基苯甲酸糖苷,分别为对羟基苯甲酸-4-O-α-D-吡喃甘露糖苷基-(1 → 3)-α-L-鼠李吡喃糖苷(化合物)和 4-O-α-L-鼠李吡喃糖苷基-(1 → 6)-α-D-吡喃甘露糖苷基-(1 → 3)-α-L-鼠李吡喃糖苷(化合物),以及 7 种已知化合物,即化合物 、 、 (酸成分)、化合物 、 (类黄酮)、化合物 (香豆素)和化合物 (生物碱)。利用红外光谱(IR)、高分辨电喷雾电离质谱(HR-ESI-MS)和 ¹H 和 C-NMR 等广泛的光谱方法阐明了所有化合物的结构。通过高效液相色谱(HPLC)鉴定酸水解得到的糖残基。所有化合物的抗氧化活性均通过 2,2'-联氮双(3-乙基苯并噻唑啉-6-磺酸)(ABTS⁺)和 1,1-二苯基-2-苦基肼(DPPH)进行评估。还在脂多糖(LPS)刺激的 RAW 264.7 巨噬细胞中评估了化合物的抗炎作用。所有化合物均通过抑制诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达,抑制 LPS 诱导的 RAW 264.7 细胞中一氧化氮(NO)和前列腺素 E 2(PGE 2)的产生,从而显示出抗炎作用。通过细胞计数试剂盒-8(CCK-8)法测定了所有化合物对 MCF-7 细胞的抑制作用。结果表明,与其他化合物相比,化合物 、 、 、 、 具有更好的抗氧化活性。化合物 、 、 、 对 LPS 刺激的 RAW264.7 细胞中 NO、TNF-α和 IL-6 的释放具有不同的抑制作用,其中化合物 对炎症因子的抑制作用最为明显。化合物 、 具有比其他化合物更好的抗肿瘤活性。进一步研究紫金牛((Linn.)Pall.)的化学成分和药理作用对于该物种的开发和临床应用具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd4/6017420/20c616b8b614/molecules-23-00271-g001.jpg

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