Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
about
Chemistry and antihypertensive effects of tempol and other nitroxidesEndogenous Generation and Signaling Actions of Omega-3 Fatty Acid Electrophilic DerivativesCelastrol prevents atherosclerosis via inhibiting LOX-1 and oxidative stressSelect cyclopentenone prostaglandins trigger glutathione efflux and the role of ABCG2 transportTransgenic fat-1 mouse as a model to study the pathophysiology of cardiovascular, neurological and psychiatric disordersIsoprostane generation and function.Fat-1 transgenic cattle as a model to study the function of ω-3 fatty acidsNitro-fatty acid reaction with glutathione and cysteine. Kinetic analysis of thiol alkylation by a Michael addition reactionPioglitazone inhibition of lipopolysaccharide-induced nitric oxide synthase is associated with altered activity of p38 MAP kinase and PI3K/AktNADPH:quinone oxidoreductase 1 regulates host susceptibility to ozone via isoprostane generation.Human biochemistry of the isoprostane pathway.15-deoxy-Delta12,14-prostaglandin J2 (15d-PGJ2) and ciglitazone modulate Staphylococcus aureus-dependent astrocyte activation primarily through a PPAR-gamma-independent pathway.The fatty acid oxidation product 15-A3t-isoprostane is a potent inhibitor of NFκB transcription and macrophage transformation.Cardiovascular consequences when nitric oxide and lipid signaling converge.Rosiglitazone regulates anti-inflammation and growth inhibition via PTEN.Isoprostanes and asthma.Design of small molecules targeting transcriptional activation by NF-κB: overview of recent advances.Resolution of inflammation: targeting GPCRs that interact with lipids and peptides.PPARgamma1 attenuates cytosol to membrane translocation of PKCalpha to desensitize monocytes/macrophages.Electrophilic cyclopentenone neuroprostanes are anti-inflammatory mediators formed from the peroxidation of the omega-3 polyunsaturated fatty acid docosahexaenoic acid.Accumulation of 15-deoxy-delta(12,14)-prostaglandin J2 adduct formation with Keap1 over time: effects on potency for intracellular antioxidant defence inductionRegulation of lung endothelial permeability and inflammatory responses by prostaglandin A2: role of EP4 receptor.Identification of a novel series of anti-inflammatory and anti-oxidative phospholipid oxidation products containing the cyclopentenone moiety in vitro and in vivo: Implication in atherosclerosis.Release of free F2-isoprostanes from esterified phospholipids is catalyzed by intracellular and plasma platelet-activating factor acetylhydrolases.Ischemic preconditioning reveals that GLT1/EAAT2 glutamate transporter is a novel PPARgamma target gene involved in neuroprotection.
P2860
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P2860
Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
@en
type
label
Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
@en
prefLabel
Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
@en
P2093
P2860
P50
P356
P1476
Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages.
@en
P2093
Dingzhi Wang
Giuseppe Zanoni
Jason D Morrow
M Brett Everhart
Michael G Backlund
Raymond N DuBois
Timothy S Blackwell
P2860
P304
35562-35570
P356
10.1074/JBC.M504785200
P407
P577
2005-08-12T00:00:00Z