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药用及食用同源中药多糖抗炎活性及构效关系研究进展。

Progress on the Anti-Inflammatory Activity and Structure-Efficacy Relationship of Polysaccharides from Medical and Edible Homologous Traditional Chinese Medicines.

机构信息

School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, China.

Key Laboratory for Quality Evaluation of Bulk Herbs of Hunan Province, Hunan University of Chinese Medicine, Changsha 410208, China.

出版信息

Molecules. 2024 Aug 14;29(16):3852. doi: 10.3390/molecules29163852.

DOI:10.3390/molecules29163852
PMID:39202931
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11356930/
Abstract

Medicinal food varieties developed according to the theory of medical and edible homologues are effective at preventing and treating chronic diseases and in health care. As of 2022, 110 types of traditional Chinese medicines from the same source of medicine and food have been published by the National Health Commission. Inflammation is the immune system's first response to injury, infection, and stress. Chronic inflammation is closely related to many diseases such as atherosclerosis and cancer. Therefore, timely intervention for inflammation is the mainstay treatment for other complex diseases. However, some traditional anti-inflammatory drugs on the market are commonly associated with a number of adverse effects, which seriously affect the health and safety of patients. Therefore, the in-depth development of new safe, harmless, and effective anti-inflammatory drugs has become a hot topic of research and an urgent clinical need. Polysaccharides, one of the main active ingredients of medical and edible homologous traditional Chinese medicines (MEHTCMs), have been confirmed by a large number of studies to exert anti-inflammatory effects through multiple targets and are considered potential natural anti-inflammatory drugs. In addition, the structure of medical and edible homologous traditional Chinese medicines' polysaccharides (MEHTCMPs) may be the key factor determining their anti-inflammatory activity, which makes the underlying the anti-inflammatory effects of polysaccharides and their structure-efficacy relationship hot topics of domestic and international research. However, due to the limitations of the current analytical techniques and tools, the structures have not been fully elucidated and the structure-efficacy relationship is relatively ambiguous, which are some of the difficulties in the process of developing and utilizing MEHTCMPs as novel anti-inflammatory drugs in the future. For this reason, this paper summarizes the potential anti-inflammatory mechanisms of MEHTCMPs, such as the regulation of the Toll-like receptor-related signaling pathway, MAPK signaling pathway, JAK-STAT signaling pathway, NLRP3 signaling pathway, PI3K-AKT signaling pathway, PPAR-γ signaling pathway, Nrf2-HO-1 signaling pathway, and the regulation of intestinal flora, and it systematically analyzes and evaluates the relationships between the anti-inflammatory activity of MEHTCMPs and their structures.

摘要

根据药食同源理论开发的食药物质在防治慢性病和保健方面具有良好的效果。截至 2022 年,国家卫生健康委员会已发布 110 种同源中药。炎症是免疫系统对损伤、感染和应激的第一反应。慢性炎症与动脉粥样硬化和癌症等许多疾病密切相关。因此,及时干预炎症是治疗其他复杂疾病的主要方法。然而,市场上一些传统的抗炎药通常会引起许多不良反应,严重影响患者的健康和安全。因此,深入开发新的安全、无害且有效的抗炎药已成为研究热点和临床迫切需求。多糖是药食同源中药(MEHTCMs)的主要活性成分之一,大量研究证实其具有通过多种靶点发挥抗炎作用的特性,被认为是潜在的天然抗炎药。此外,药食同源传统中药多糖(MEHTCMPs)的结构可能是决定其抗炎活性的关键因素,这使得多糖的抗炎作用及其结构-功效关系成为国内外研究的热点。然而,由于当前分析技术和工具的限制,多糖的结构尚未完全阐明,结构-功效关系也相对模糊,这是未来将 MEHTCMPs 开发为新型抗炎药时面临的一些困难。为此,本文综述了 MEHTCMPs 的潜在抗炎机制,如 Toll 样受体相关信号通路、MAPK 信号通路、JAK-STAT 信号通路、NLRP3 信号通路、PI3K-AKT 信号通路、PPAR-γ 信号通路、Nrf2-HO-1 信号通路和肠道菌群的调节,并系统地分析和评价了 MEHTCMPs 的抗炎活性与其结构之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/a46c0ef3ddcd/molecules-29-03852-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/6be93ccfb659/molecules-29-03852-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/8ce0bb525651/molecules-29-03852-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/c97691704bd5/molecules-29-03852-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/4dc9fecd8c97/molecules-29-03852-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/483408c16f56/molecules-29-03852-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/f656962eaabc/molecules-29-03852-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/6cb785242354/molecules-29-03852-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/e19b35a35808/molecules-29-03852-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/a46c0ef3ddcd/molecules-29-03852-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/6be93ccfb659/molecules-29-03852-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/8ce0bb525651/molecules-29-03852-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/c97691704bd5/molecules-29-03852-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/4dc9fecd8c97/molecules-29-03852-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/483408c16f56/molecules-29-03852-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/f656962eaabc/molecules-29-03852-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/6cb785242354/molecules-29-03852-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/e19b35a35808/molecules-29-03852-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/546b/11356930/a46c0ef3ddcd/molecules-29-03852-g009.jpg

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