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Resolvins: Natural agonists for resolution of pulmonary inflammation

期刊

PROGRESS IN LIPID RESEARCH
卷 50, 期 1, 页码 75-88

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.plipres.2010.09.002

关键词

Catabasis; Lipid mediators; Lung; Neutrophils; Omega-3; Polyunsaturated fatty acids

资金

  1. US National Institutes of Health [AI068084, HL68669, P50-DE016191]
  2. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL068669] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI068084, R56AI068084] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF DENTAL &CRANIOFACIAL RESEARCH [P50DE016191] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Inappropriate or excessive pulmonary inflammation can contribute to chronic lung diseases. In health, the resolution of inflammation is an active process that terminates inflammatory responses. The recent identification of endogenous lipid-derived mediators of resolution has provided a window to explore the pathobiology of inflammatory disease and structural templates for the design of novel pro-resolving therapeutics. Resolvins (resolution-phase interaction products) are a family of pro-resolving mediators that are enzymatically generated from essential omega-3 polyunsaturated fatty acids. Two molecular series of resolvins have been characterised, namely E- and D-series resolvins which possess distinct structural, biochemical and pharmacological properties. Acting as agonists at specific receptors (CMKLR1, BLT1, ALX/FPR2 and GPR32), resolvins can signal for potent counter-regulatory effects on leukocyte functions, including preventing uncontrolled neutrophil swarming, decreasing the generation of cytokines, chemokines and reactive oxygen species and promoting clearance of apoptotic neutrophils from inflamed tissues. Hence, resolvins provide mechanisms for cytoprotection of host tissues to the potentially detrimental effects of unresolved inflammation. This review highlights recent experimental findings in resolvin research, and the impact of these stereospecific molecules on the resolution of pulmonary inflammation and tissue catabasis. (C) 2010 Elsevier Ltd. All rights reserved.

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