« Previous
Next »
Prostaglandins, Leukotrienes and Essential Fatty Acids
Volume 82, Issue 2
, Pages 71-81
, February 2010
Isoprostane nomenclature: Inherent problems may cause setbacks for the development of the isoprostanoid field
References
- . A nomenclature system for isoprostanes. Prostaglandins. 1997;53:63–67
- . Nomenclature of isoprostanes: a proposal. Prostaglandins. 1997;54:853–873
- . Radically novel prostaglandins in animals and plants: the isoprostanes. Chem. Biol. 1998;5:323–333
- . Prostaglandin nomenclature. J. Med. Chem. 1974;17:911–918
- . Formation of isoprostane-like compounds (neuroprostanes) in vivo from docosahexaenoic acid. J. Biol. Chem. 1998;273:13605–13612
- . Evidence for the formation of dinor isoprostanes E1 from α-linolenic acid in plants. J. Biol. Chem. 1998;273:32650–32655
- . Analysis of oxidative stress and wound-inducible dinor isoprostanes F1 (phytoprostanes F1) in plants. Plant Physiol. 2000;124:1293–1303
- . Biosynthesis of 13,14-dehydro-12-oxo-phytodienoic acid and related cyclopentenones via the phytoprostane D1 pathway. Phytochemistry. 2003;62:351–358
- . Identification of a novel class of endoperoxides from arachidonate autoxidation. J. Biol. Chem. 2004;279:3766–3776
- . Identification and relative quantitation of F2-isoprostane regioisomers formed in vivo in the rat. Free Radic. Biol. Med. 1997;23:943–954
- . Regiochemistry of neuroprostanes generated from the peroxidation of docosahexaenoic acid in vitro and in vivo. J. Biol. Chem. 2005;280:26600–26611
- . Formation of isoprostane F2-like compounds (phytoprostanes F1) from α-linolenic acid in plants. Free Radic. Biol. Med. 2000;28:720–726
- . Isolation and structure of two prostaglandin endoperoxides that cause platelet aggregation. Proc. Natl. Acad. Sci. USA. 1974;71:345–349
- . Isomerization of prostaglandin H2 into prostaglandin D2 in the presence of serum albumin. Biochim. Biophys. Acta. 1976;431:183–189
- . Albumin-catalyzed metabolism of prostaglandin D2. Identification of products formed in vitro. J. Biol. Chem. 1983;258:11713–11718
- . The nature and composition of 15-deoxy-(delta)12,14PGJ2. Prostaglandins Other Lipid Mediat. 2000;62:15–21
- . Molecular mechanisms of diverse actions of prostanoid receptors. Biochim. Biophys. Acta. 1995;1259:109–119
- . A profile of the residues in the second extracellular loop that are critical for ligand recognition of human prostacyclin receptor. FEBS J. 2008;275:128–137
- . Prediction of the 3D structure and dynamics of human DP G-protein coupled receptor bound to an agonist and an antagonist. J. Am. Chem. Soc. 2007;129:10720–10731
- . Key structural features of prostaglandin E(2) and prostanoid analogs involved in binding and activation of the human EP(1) prostanoid receptor. Mol. Pharmacol. 2001;59:1446–1456
- . Beyond prostaglandins—chemistry and biology of cyclic oxygenated metabolites formed by free-radical pathways from polyunsaturated fatty acids. Angew. Chem. Int. Ed. Engl. 2008;47:5894–5955
- . Isomer-specific contractile effects of a series of synthetic f2-isoprostanes on retinal and cerebral microvasculature. Free Radic. Biol. Med. 2004;36:163–172
- . Isoprostanes: generation, pharmacology, and roles in free-radical-mediated effects in the lung. Pulm. Pharmacol. Ther. 2000;13:149–155
- . Involvement of TP and EP3 receptors in vasoconstrictor responses to isoprostanes in pulmonary vasculature. J. Pharmacol. Exp. Ther. 2002;301:1060–1066
- . Cyclopentenone prostaglandins: new insights on biological activities and cellular targets. Med. Res. Rev. 2001;21:185–210
- M. J. Mueller, S. Berger, Reactive electrophilic oxylipins: pattern recognition and signalling. Phytochemistry (2009)
- . 15-deoxy-(delta)12,14PGJ2: an electrophilic trigger of cellular responses. Chem. Res. Toxicol. 2008;21:138–144
- . Structural basis for the activation of PPAR gamma by oxidized fatty acids. Nat. Struct. Mol. Biol. 2008;15:924–931
- . Impact of cyclopentenone–oxylipins on the proteome of Arabidopsis thaliana. Biochim. Biophys. Acta. 2008;1784:1975–1985
- . General detoxification and stress responses are mediated by oxidized lipids through TGA transcription factors in arabidopsis. Plant Cell. 2008;20:768–785
- . B1-phytoprostanes trigger plant defense and detoxification responses. Plant Physiol. 2005;137:328–340
PII: S0952-3278(09)00203-8
doi: 10.1016/j.plefa.2009.11.007
© 2009 Elsevier Ltd. All rights reserved.
« Previous
Next »
Prostaglandins, Leukotrienes and Essential Fatty Acids
Volume 82, Issue 2
, Pages 71-81
, February 2010
