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Eicosanoids and Isoeicosanoids: Indices of Cellular Function and Oxidant Stress

Muredach P. Reilly, John A. Lawson, and Garret A. FitzGerald

The Center for Experimental Therapeutics, University of Pennsylvania, Philadelphia, PA 19104

Arachidonic acid (AA) is an unsaturated fatty acid constituent of the phospholipid domain of cell membranes. It is subject to release via mobilization of phospholipases, particularly a cytoplasmic phospholipase A2. Thereafter, it may be metabolized by at least two cyclooxygenase (COX) isoforms to prostaglandins and related compounds, via lipoxygenases to leukotrienes and via p450-catalyzed metabolism to epoxyeicosatrienoic acids. Collectively, these bioactive lipids are termed eicosanoids. All of these lipids express potent bioactivity in vitro. Clinical studies have already demonstrated the importance of COX and lipoxygenase (LOX) products in human disease. The generation of models of COX, LOX and prostaglandin receptor gene inactivation is likely to broaden our insight into the importance of these compounds in vivo. Crystallization of the biosynthetic enzymes is likely to facilitate the development of highly specific inhibitors, as is the case already for COX-2. AA possesses intrinsic biological properties. It is also subject to free radical attack, generating isomeric eicosanoid species, the isoeicosanoids. These compounds may also express biological activity in vitro, although their importance in vivo is unclear. Development of specific assays for these compounds in urine suggests their utility as noninvasive indices of oxidant stress in vivo.

Key words: eicosanoids, isoeicosanoids, oxidant stress, isoprostanes, cyclooxygenase (COX).

The Journal of Nutrition Vol. 128 No. 2 February 1998, pp. 434S-438S
Copyright ©1998 by the American Society for Nutritional Sciences




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H. Jiang, N. Kruger, D. R. Lahiri, D. Wang, J.-M. Vatele, and M. Balazy
Nitrogen Dioxide Induces cis-trans-Isomerization of Arachidonic Acid within Cellular Phospholipids. DETECTION OF TRANS-ARACHIDONIC ACIDS IN VIVO
J. Biol. Chem., June 4, 1999; 274(23): 16235 - 16241.
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Copyright © 1998 by American Society for Nutrition