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人参抗炎镇痛活性糖肽结构的研究。

Study on the Structure of Ginseng Glycopeptides with Anti-Inflammatory and Analgesic Activity.

机构信息

Changchun University of Chinese Medicine, Changchun 130117, China.

Jilin Jice Inspection Technology Co., Ltd., Changchun 130117, China.

出版信息

Molecules. 2018 May 31;23(6):1325. doi: 10.3390/molecules23061325.

Abstract

is well known for its medicinal functions. As a class of important compound of ginseng, ginsenoside is widely studied around the world. In addition, ginseng glycopeptides also showed good biological activity, but researches in this field are rarely reported. In this study, ginseng glycopeptides (Gg) were first prepared from by reflux extracted with 85% ethanol and the following purification with Sephadex G-15 column. Then, the inflammatory pain models induced by carrageenan and the rat pain models induced by Faure Marin were established for research on mechanism of analgesic activities. It is showed that Gg had an obvious inhibiting effect on inflammation and a significant reduction on the Malondialdehyde (MDA) of inflammatory foot tissue. And there were significant differences between moderate to high dose of Gg and model group in Interleukin 1β (IL-1β), Interleukin 2 (IL-2), Interleukin 4 (IL-4), Tumor necrosis factor α (TNF-α) and Histamine. The two models can be preliminarily determined that the analgesic effect of Gg may be peripheral, which mechanism may be related to the dynamic balance between proinflammatory cytokines (TNF-α, IL-1β) and anti-inflammatory cytokines (IL-2, IL-4, and Interleukin 10 (IL-10)). A series of methods were used to study Gg in physical-chemical properties and linking mode of glycoside. The high-resolution mass spectrometry was used for identification of the structure of Gg. Moreover, the structure of 20 major Gg were investigated and identified. The structural analysis of Gg was benefit for the next study on structure-activity relationship.

摘要

为人熟知,具有药用功能。作为人参的一类重要化合物,人参皂苷在世界范围内得到了广泛的研究。此外,人参糖肽也表现出良好的生物活性,但这一领域的研究很少有报道。在本研究中,首次通过 85%乙醇回流提取并通过 Sephadex G-15 柱进行后续纯化,从 中制备了人参糖肽(Gg)。然后,建立了卡拉胶诱导的炎症痛模型和 Faure Marin 诱导的大鼠痛模型,以研究其镇痛活性的机制。结果表明,Gg 对炎症有明显的抑制作用,可显著降低炎症足组织的丙二醛(MDA)。Gg 中、高剂量组与模型组比较,白细胞介素 1β(IL-1β)、白细胞介素 2(IL-2)、白细胞介素 4(IL-4)、肿瘤坏死因子α(TNF-α)和组氨酸均有显著性差异。两种模型可初步判断 Gg 的镇痛作用可能为外周性,其作用机制可能与促炎细胞因子(TNF-α、IL-1β)和抗炎细胞因子(IL-2、IL-4、IL-10)的动态平衡有关。采用一系列方法对 Gg 的理化性质和糖苷键连接方式进行了研究。采用高分辨质谱法鉴定 Gg 的结构。此外,还对 20 种主要 Gg 的结构进行了研究和鉴定。Gg 的结构分析有利于下一步进行结构-活性关系研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4428/6099564/5182c9ed2797/molecules-23-01325-g001.jpg

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