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TOTAL ANTIOXIDANT STATUS (TAS)


Introduction:

Free radicals have been implicated in numerous human diseases including cancer, heart disease, lung disease, eye disorders, inflammatory disease, rheumatoid arthritis and the aging process. Free radicals are formed in the human body during normal cellular metabolism and after exposure to any of the following agents UV light, gamma radiation, environmental pollutants (such as metals and xenobiotics) and cigarette smoke.  For more information on free radicals section of this web site.

Antioxidant systems are capable of removing free radicals, thereby providing protection from free radical attack from such destructive molecules as H2O2 and the RO., ROO. and O2. radicals.  

Three main groups of antioxidants make up the antioxidant defense system. These include the primary, secondary, and tertiary defense. The TAS test measures the total antioxidant effect of these three defense systems in circulation. The three systems are as follows:


References:

  1. Boyce, N, Oxidative Stress Testing: A New Addition to Lab Menus? Clin. Lab News 23:1-2 (1997).
  2. Diaz, MN, et al., Antioxidants and Atherosclerotic Heart Disease, New Engl. J. Med. 337:408-416 (1997).
  3. Halliwell, B & Gutteridge, JMC, The Antioxidants of Human Extracellular Fluids, Archives of Biochemistry and Biophysics 280:1-8 (1990).
  4. Jacob, RA, The Integrated Antioxidant System, Nutrition Research 15:755-766 (1995).
  5. Knoght, JA, Diseases Related to Oxygen-derived Free Radicals, Ann. Clin. Lab. Sci. 25:111-121 (1995).
  6. Martinez-Cayuela, M, Oxygen Free Radicals and Human Disease, Biochimie 77:147-161 (1995).
  7. Rusting, RL, Why Do We Age? Scientific American December:130-141 (1992).

Assay Principle

The test is designed to measure all of the antioxidants present in the specimen by their abilities to inhibit a specific enzymatic oxidation reaction. The assay response is standardized against the antioxidant standard Trolox.


References:

  1. Miller, NJ et al. A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates, Clinical Science 84:407-412 (1993).
  2. Miller, NJ & Rice-Evans, CA, Spectrophotometric determination of antioxidant activity, Redox Report 2:161-171 (1996).
  3. Miller, NJ et al. Serum total antioxidant activity after myocardial infarction, Ann. Clin. Biochem. 34:85-90 (1997).

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Last modified: December 03, 1998