Arachidonic acid free radical oxygenation

Scheme 3.5. Free radical oxygenation of arachidonic acid.

Free radicals are by-products of prostaglandin metabolism and may even regulate the activity of the arachidonate pathway. Arachidonic acid, released from lipids as a result of activation of phospholipases by tissue injury or by hormones, may be metabolized by the prostaglandin or leu-kotriene pathways. The peroxidase-catalysed conversion of prostaglandin G2 to prostaglandin H2 (unstable prostanoids) and the mechanism of hydroperoxy fatty acid to the hydroxy fatty acid conversion both yield oxygen radicals, which can be detected by e.s.r. (Rice-Evans et al., 1991). 

Kinins, neuropeptides, and histamine are also released at the site of tissue injury, as are complement components, cytokines, and other products of leukocytes and platelets. Stimulation of the neutrophil membranes produces oxygen-derived free radicals. Superoxide anion is formed by the reduction of molecular oxygen, which may stimulate the production of other reactive molecules such as hydrogen peroxide and hydroxyl radicals. The interaction of these substances with arachidonic acid results in the generation of chemotactic substances, thus perpetuating the inflammatory process. 

Sulfasalazine. Salicylazosulfapyridine or Azulfadine [599-79-1] (2-hydroxy-5-[[4[(2-pyridylamino)sulfonyl]-phenyl]azo] benzoic acid) (15) is a light brownish yellow-to-bright yellow fine powder that is practically tasteless and odorless. It melts at ca 255°C with decomposition, is very slightly soluble in ethanol, is practically insoluble in water, diethyl ether, chloroform, and benzene, and is soluble in aqueous solutions of alkali hydroxides. Sulfasalazine may be made by the synthesis described in Reference 13. It is not used as an antidiarrheal as such, but is indicated for the treatment of inflammatory bowel diseases such as ulcerative colitis and Crohn s disease. Its action is purported to result from the breakdown in the colon to 5-aminosalicylic acid [89-57-6] (5-AS A) and sulfapyridine [144-83-2]. It may cause infertility in males, as well as producing idiosyncratic reactions in some patients these reactions have been attributed to the sulfa component of the compound. The mechanism of 5-ASA is attributed to inhibition of the arachidonic acid cascade preventing leukotriene B4 production and the ability to scavenge oxygen free radicals. The active component appears to be 5-aminosalicylic acid. 

Arachidonic acid metabolism through eicosanoid biosynthesis is accompanied by the generation and subsequent utilization of oxygen-derived free radicals. Arachidonic acid, released from lipids as a result... 

Prostaglandin H synthase is the first enzyme involved in the arachidonic acid cascade . The prostaglandins can cause both relaxation and tension in smooth muscle and so have vital physiological roles. Prostaglandin H synthase acts as both a peroxidase and an oxygenase its so-called cyclooxygenase activity involves addition of two equivalents of oxygen to a free radical derived from arachidonic acid to form an endoperoxide... 

There are many studies about the relation between the free oxygen radical scavenging activities of many flavonoids and their effects on the enzymes which take part in the metabolism of arachidonic acid, cyclooxygenase (COX) and lipoxygenase (LOX). Duneic [182] shows that the antiradical action affects the COX activity in several ways. In most of the cases, at high substrate concentrations the enzymatic activity was intensified and at low concentrations it was inhibited. Apparently, the influence of the antiradical properties on the activity of enzymatic metabolism of the arachidonic acid in vitro might also be due to the effect of these agents on the active center of the enzymes. 

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