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Abstract

The multienzyme complex cyclooxygenase converts free arachidonic acid predominantly to prostanoids. These prostanoids (prostaglandins F, E2, D2, I2 and thromboxane A2) are not stored in cells but are produced by de novo synthesis following a relevant stimulus (1). In brief, biosynthesis can be subdivided into the following three stages (Figure 1): a) Release of arachidonic acid from membrane phospholipids by phospholipases, the most significant being phospholipase A2. b) Oxygenation of free arachidonic acid by the membrane-bound multi-enzyme complex cyclooxygenase (prostaglandin endoperoxide G/H synthase) to the cyclic endoperoxide PGH2. c) Metabolism of PGH2 to specific biologically active end products (PGF, PGE2, PGI2, PGD2, TXA2) by either a thromboxane or prostacyclin synthase, or PGF reductase, or PGH-PGD2 and PGH-PGE2 isomerases. TXA2 and PGI2 are very unstable and are rapidly, nonenzymatically degraded to TXB2 and 6-keto-PGF respectively. Two additional cyclooxygenase products are malondialdehyde (MDA) and hydroxy-heptadecatrienoic acid (HHT) but both are biologically inert.

Keywords

Airway Smooth Muscle Human Airway Human Airway Smooth Muscle Human Airway Smooth Muscle Cell Late Asthmatic Response 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Birkhäuser Verlag Basel/Switzerland 1995

Authors and Affiliations

  • Phillip J. Gardiner
    • 1
  1. 1.Research Department, Pharmaceutical DivisionBayer plcStoke PogesUK

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