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              Natural Antioxidants In Foods                                                               339
























































                                     FIGURE 2 Chemical structures of miscellaneous natural antioxidants.


              oxidized glutathione state. Reduced glutathione inhibits  2. Lipoic Acid
              lipid oxidation directly by interacting with free radi-
              cals to form a relatively unstable sulfhydryl radical or  Lipoic (thioctic) acid (Fig. 2) is a thiol cofactor for many
              by providing a source of electrons, which allows glu-  plant and animal enzymes. In biological systems, the two
              tathione peroxidase to enzymically decompose hydrogen  thiol groups of lipoic acid are found in both reduced (dihy-
              and lipid peroxides. Total glutathione concentrations in  drolipoic acid) and oxidized forms (lipoic acid). Both the
              muscle foods range from 0.7–0.9 ug/kg. Oral administra-  oxidized and reduced forms of the molecule are capable
              tion of 3.0 of glutathione to seven healthy adults did not  of acting as antioxidants through their ability to quench
              result in any increases in plasma glutathione or cysteine  singlet oxygen, scavenge free radicals, chelate iron, and,
              concentrations after 270 minutes. The bioavailability of  possibly, regenerate other antioxidants such as ascorbate
              glutathione in rats has also been reported to be low. Lack  and tocopherols. Lipoic and dehydrolipoic acids can pro-
              of, or low absorption of, glutathione may be due to the  tect LDL, erythrocytes, and cardiac muscle from oxidative
              hydrolysis of the tripeptide by gastrointestinal protease.  damage.
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