Page 119 - Natural Antioxidants, Applications in Foods of Animal Origin
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98                 Natural Antioxidants: Applications in Foods of Animal Origin
  VetBooks.ir     free radicals present in the system (Masuda et al., 2002; Amakura et


                  al., 2000). (b) The second mechanism involves the removal of reac-
                  tive oxygen species (ROS) and reactive nitrogen species (RNS) initi-
                  ators by quenching the chain initiator catalyst (Hamid et al., 2010).
                  Examples of antioxidants which scavenge free radicals are phenolic
                  compounds (tocopherols,  butylated  hydroxytoluene  (BHT), butyl-
                  ated hydroxyanisole (BHA), tert-butylhydroquinone (TBHQ), propyl
                  gallate  (PG), lignans, flavonoids, and phenolic  acids, carotenoids,
                  and so forth.
               •  Antioxidants that react with transition metals to form complexes, and
                  thus avoid the catalytic effect of the metals in the oxidation process.
                  Metal chelators decrease oxidation by preventing metal redox cycling,
                  forming insoluble metal  complexes, or providing steric  hindrance
                  between metals and food components or their oxidation intermedi-
                  ates (Graf & Eaton, 1990). The most common metal chelators used
                  in foods contain multiple carboxylic acid (e.g., ethylene diamine tetra
                  acetic acid (EDTA) and citric acid) or phosphate groups (e.g., poly-
                  phosphates and phytate). Chelators are typically water soluble but
                  many also exhibit lipid solubility (e.g., citric acid), thus allowing it
                  to inactivate metals in the lipid phase. Lignans, polyphenols, ascorbic
                  acid, and amino acids such as carnosine and histidine can also chelate
                  metals (Decker et al., 2001). Phenolics, which possess hydroxyl and
                  carboxyl groups are able to bind particularly well with metals like Fe
                  or Cu (Jung et al., 2003).
               •  Antioxidants that decompose peroxides and produce stable substances
                  which are unable to produce radicals, such as selenium (Se) containing
                  glutathione  peroxidase, an antioxidative  enzyme,  which inactivate
                  free radicals and other oxidants, particularly hydrogen peroxide.
               •  Antioxidants which inactivate  the singlet form of oxygen: In the
                  presence  of a  photosensitizer, such as chlorophylls  and  pheophy-
                  tins, singlet oxygen may be formed from ordinary triplet oxygen by
                  the action of light. This singlet form of oxygen is very reactive; it
                  is extremely important to deactivate it back to the triplet form very
                  rapidly to prevent the photo-oxidation process. Tocopherols, carot-
                  enoids, curcumin, phenolics, urate, and ascorbate can quench singlet
                  oxygen (Das & Das, 2002; Choe & Min, 2005).
               •  Antioxidants which prevent the enzymatic activity required for auto-
                  oxidation.  Examples  are  flavonoids,  phenolic  acids,  and  gallates,
                  which deactivate the lipoxygenase.
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