藻类类胡萝卜素对炎症信号通路影响的研究进展

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-11-01 DOI:10.1016/j.ejmech.2024.117020
Yudi Wang , Xinrong Geng , Song Qin , Tuanjie Che , Libo Yan , Biao Yuan , Wenjun Li
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引用次数: 0

摘要

炎症的发展对人体的自我保护具有不可或缺的重要意义。然而,过度炎症会损害人体健康,而炎症通路和炎性体对炎症的发生有重要影响。因此,如何通过炎症通路或炎症小体来制约炎症的发展成为研究热点。类胡萝卜素是一种天然色素,也是藻类中的一种活性物质,具有抗炎和抗氧化作用。许多研究表明,类胡萝卜素对炎症通路和炎症体具有抑制作用。在这篇综述中,我们从p38 MAPK、IL-6/JAK/STAT3和PI3K等几种炎症通路的角度探讨了类胡萝卜素靶向那些重要炎症通路的机制及其对常见炎症体NLRP3和炎症相关疾病的影响,重点讨论了类胡萝卜素对不同炎症信号通路的靶点和靶向作用,最后提出了可能的抗炎靶点。
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Advance on the effects of algal carotenoids on inflammatory signaling pathways
The development of inflammation has an indispensable importance in the self-protection of the human body. However, over-inflammation may damage human health, and inflammatory pathways and inflammasomes have a significant impact on the onset of inflammation. Therefore, how to constrain the development of inflammation through inflammatory pathways or inflammasomes becomes a hot research issue. Carotenoids are a natural pigment and an active substance in algae, with anti-inflammatory and antioxidant effects. Many studies have shown that carotenoids have inhibitory effects on the inflammatory pathways and inflammasomes. In this review, we discussed the mechanism of carotenoids targeting those important inflammatory pathways and their effects on common inflammasome NLRP3 and inflammation-related diseases from the perspective of several inflammatory pathways, including p38 MAPK, IL-6/JAK/STAT3, and PI3K, with a focus on the targets and targeting effects of carotenoids on different inflammatory signaling pathways, and at last proposed possible anti-inflammatory targets.
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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