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特异性促解决脂质介质:感染中的内源性作用和药理活性。

Specialized Pro-Resolving Lipid Mediators: Endogenous Roles and Pharmacological Activities in Infections.

机构信息

Laboratory of Pain, Inflammation, Neuropathy, and Cancer, Department of Pathology, Center of Biological Sciences, Londrina State University, Londrina 86057-970, Paraná, Brazil.

Vascular Biology Program, Boston Children's Hospital, Department of Surgery, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Molecules. 2023 Jun 27;28(13):5032. doi: 10.3390/molecules28135032.

Abstract

During an infection, inflammation mobilizes immune cells to eliminate the pathogen and protect the host. However, inflammation can be detrimental when exacerbated and/or chronic. The resolution phase of the inflammatory process is actively orchestrated by the specialized pro-resolving lipid mediators (SPMs), generated from omega-3 and -6 polyunsaturated fatty acids (PUFAs) that bind to different G-protein coupled receptors to exert their activity. As immunoresolvents, SPMs regulate the influx of leukocytes to the inflammatory site, reduce cytokine and chemokine levels, promote bacterial clearance, inhibit the export of viral transcripts, enhance efferocytosis, stimulate tissue healing, and lower antibiotic requirements. Metabolomic studies have evaluated SPM levels in patients and animals during infection, and temporal regulation of SPMs seems to be essential to properly coordinate a response against the microorganism. In this review, we summarize the current knowledge on SPM biosynthesis and classifications, endogenous production profiles and their effects in animal models of bacterial, viral and parasitic infections.

摘要

在感染过程中,炎症会动员免疫细胞来消灭病原体并保护宿主。然而,当炎症加剧和/或慢性化时,它可能会产生有害影响。炎症过程的解决阶段是由专门的促解决脂质介质(SPM)积极协调的,这些 SPM 是由 omega-3 和 -6 多不饱和脂肪酸(PUFA)生成的,它们与不同的 G 蛋白偶联受体结合以发挥其活性。作为免疫调节剂,SPM 调节白细胞向炎症部位的流入,降低细胞因子和趋化因子水平,促进细菌清除,抑制病毒转录本的输出,增强细胞吞噬作用,刺激组织愈合,并降低抗生素的需求。代谢组学研究已经评估了感染期间患者和动物的 SPM 水平,而 SPM 的时间调节似乎对于正确协调针对微生物的反应至关重要。在这篇综述中,我们总结了 SPM 生物合成和分类、内源性产生谱及其在细菌、病毒和寄生虫感染动物模型中的作用的最新知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b41e/10343836/f3ae134cc05f/molecules-28-05032-g001.jpg

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