Oxygen radical absorbance capacity

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Oxygen radical absorbance capacity (ORAC) is a method of measuring antioxidant capacities in biological samples in vitro.[1][2]

A wide variety of foods has been tested using this method, with certain spices, berries and legumes rated highly in extensive tables once published by the United States Department of Agriculture (USDA), but withdrawn in 2012 since no correlation between test results and biological activity could be determined,[3] stating that no physiological proof in vivo existed in support of the free-radical theory.

Although not all have been unilaterally dismissive,[4] the majority position supports the USDA decision.[5] Alternative measurements include the Folin-Ciocalteu reagent, and the Trolox equivalent antioxidant capacity assay.

Method[edit]

The assay measures the oxidative degradation of the fluorescent molecule (either beta-phycoerythrin or fluorescein) after being mixed with free radical generators such as azo-initiator compounds. Azo-initiators are considered to produce the peroxyl radical by heating, which damages the fluorescent molecule, resulting in the loss of fluorescence. Antioxidants are considered to protect the fluorescent molecule from the oxidative degeneration. The degree of protection is quantified using a fluorometer. Fluorescein is currently used most as a fluorescent probe. Equipment that can automatically measure and calculate the capacity is commercially available (Biotek, Roche Diagnostics).

The fluorescent intensity decreases as the oxidative degeneration proceeds, and this intensity is typically recorded for 35 minutes after the addition of the azo-initiator (free radical generator). So far, AAPH (2,2’-azobis(2-amidino-propane) dihydrochloride) is the sole free-radical generator used. The degeneration (or decomposition) of fluorescein is measured as the presence of the antioxidant slows the fluorescence decay. Decay curves (fluorescence intensity vs. time) are recorded and the area between the two decay curves (with or without antioxidant) is calculated. Subsequently, the degree of antioxidant-mediated protection is quantified using the antioxidant trolox (a vitamin E analogue) as a standard. Different concentrations of trolox are used to make a standard curve, and test samples are compared to this. Results for test samples (foods) have been published as "trolox equivalents" or TEs.[6][7]

One benefit of using the ORAC method to evaluate substances' antioxidant capacities is that it takes into account samples with and without lag phases of their antioxidant capacities. This is especially beneficial when measuring foods and supplements that contain complex ingredients with various slow- and fast-acting antioxidants, as well as ingredients with combined effects that cannot be precalculated.

Drawbacks of this method are: 1) only antioxidant activity against particular (probably mainly peroxyl) radicals is measured; however, peroxyl radical formation has never been proven; 2) the nature of the damaging reaction is not characterized; 3) there is no evidence that free radicals are involved in this reaction; and 4) there is no evidence that ORAC values have any biological significance following consumption of any food. Moreover, the relationship between ORAC values and a health benefit has not been established.

Resulting from scientific refutation of the physiological significance of ORAC, the USDA, which had been collating and publishing ORAC data for more than a decade, withdrew its web publication of ORAC values for common American foods in May 2012.[3]

Several modified ORAC methods have been proposed. Most of them employ the same principle (i.e. measurement of AAPH-radical mediated damage of fluorescein); however, ORAC-EPR, electron paramagnetic resonance-based ORAC method directly measures the decrease of AAPH-radical level by the scavenging action of the antioxidant substance.[8]

Regulatory guidance[edit]

In the following discussion, the term "antioxidant" refers mainly to non-nutrient compounds in foods, such as polyphenols, which have antioxidant capacity in vitro, so provide an artificial index of antioxidant strength—the ORAC measurement.

Other than for dietary antioxidant vitamins -- vitamin A, vitamin C and vitamin E -- no food compounds have been proved with antioxidant efficacy in vivo. Accordingly, regulatory agencies such as the Food and Drug Administration of the United States and the European Food Safety Authority (EFSA) have published guidance disallowing food product labels to claim or imply an antioxidant benefit when no such physiological evidence exists.[9][10] This guidance for the United States and European Union establishes it is illegal to imply potential health benefits on package labels of products with high ORAC.

Physiological context[edit]

Although research in vitro indicates polyphenols are good antioxidants and probably influence the ORAC value, antioxidant effects in vivo are probably negligible or absent.[3][11] By non-antioxidant mechanisms still undefined, flavonoids and other polyphenols may reduce the risk of cardiovascular disease and cancer.[12]

As interpreted by the Linus Pauling Institute, EFSA and the USDA, dietary polyphenols have little or no direct antioxidant food value following digestion.[3][11][10][13] Not like controlled test tube conditions, the fate of polyphenols in vivo shows they are poorly conserved (less than 5%), with most of what is absorbed existing as chemically modified metabolites destined for rapid excretion.[14]

The increase in antioxidant capacity of blood seen after the consumption of polyphenol-rich (ORAC-rich) foods is not caused directly by the polyphenols, but most likely results from increased uric acid levels derived from metabolism of flavonoids.[13][14] According to Frei, "we can now follow the activity of flavonoids in the body, and one thing that is clear is that the body sees them as foreign compounds and is trying to get rid of them."[14]

Food sources[edit]

Values are expressed as the sum of the lipid soluble (e.g. carotenoid) and water-soluble (e.g. phenolic) antioxidant fractions (i.e., “total ORAC”) reported as in micromoles trolox equivalents (TE) per 100 gram sample, and are compared to assessments of total polyphenol content in the samples.

These values are considered biologically irrelevant by the EFSA and USDA.[10][3]

Food ORAC scores - USDA
Food Serving size ORAC, Trolox equiv., μmol per 100 g
Prune 1 cup 14,582
Small Red Bean ½ cup dried beans 13,727
Wild blueberry 1 cup 13,427
Red kidney bean ½ cup dried beans 13,259
Pinto bean ½ cup 11,864
Cranberry 1 cup raw (whole berries) 9,584
Blueberry 1 cup raw (cultivated berries) 9,019
Artichoke hearts 1 cup, cooked 7,904
Raw unprocessed Cocoa bean 1 oz 7.840
Blackberry 1 cup raw (cultivated berries) 7,701
Raspberry 1 cup 6,058
Strawberry 1 cup 5,938
Red Delicious apple 1 apple 5,900
Granny Smith apple 1 apple 5,381
Pecan oz 5,095
Sweet cherry 1 cup 4,873
Black plum 1 plum 4,844
Russet potato 1, cooked 4,649
Chokeberry 1 oz 4,497
Black bean ½ cup dried beans 4,181
Plum 1 plum 4,118
Gala apple 1 apple 3,903
Pomegranate 100 grams 2,860

With nearly all vegetables, conventional boiling can reduce the ORAC value by up to 90%, while steaming retains more of the antioxidants.[15]

Comparisons of ORAC values[edit]

The United States Department of Agriculture, previously a publisher of ORAC data, withdrew its web publication of ORAC values for common American foods in 2012 due to absence of scientific evidence that ORAC has any biological significance.[3]

When comparing ORAC data, care must be taken to ensure the units and food being compared are similar. Some evaluations will compare ORAC units per gram of dry weight of the intact food or its milled powder, others will evaluate ORAC units in fresh or frozen wet weight, and still others will look at ORAC units per serving. Under each evaluation, different foods can appear to have higher ORAC values. For example, although a raisin has no more antioxidant potential than the grape from which it was dried, raisins will appear to have a higher ORAC value per gram of wet weight than grapes due to their reduced water content. Likewise, the large water content in watermelon can make it appear as though this fruit is low in ORAC. Similarly, the typical quantity of food used should be considered; herbs and spices may be high in ORAC, but are applied in much smaller quantities compared to intact whole foods.[16]

Numerous health food and beverage companies and marketers have erroneously capitalized on the ORAC rating by promoting products claimed to be "high in ORAC". As most of these ORAC values have not been independently validated or subjected to peer review for publication in scientific literature, they remain unconfirmed, are not scientifically credible, and may mislead consumers.

See also[edit]

References[edit]

  1. ^ Cao G, Alessio H, Cutler R (1993). "Oxygen-radical absorbance capacity assay for antioxidants". Free Radic Biol Med 14 (3): 303–11. doi:10.1016/0891-5849(93)90027-R. PMID 8458588. 
  2. ^ Ou B, Hampsch-Woodill M, Prior R (2001). "Development and validation of an improved oxygen radical absorbance capacity assay using fluorescein as the fluorescent probe". J Agric Food Chem 49 (10): 4619–26. doi:10.1021/jf010586o. PMID 11599998. 
  3. ^ a b c d e f "Withdrawn: Oxygen Radical Absorbance Capacity (ORAC) of Selected Foods, Release 2 (2010)". United States Department of Agriculture, Agricultural Research Service. 16 May 2012. Retrieved 13 June 2012. 
  4. ^ Jonny Bowden, PhD, C.N.S. (16 Dec 2012). "ORAC no more!". Huffington Post. Retrieved 12 Dec 2012. 
  5. ^ Gross, P (2009). "New Roles for Polyphenols. A 3-Part report on Current Regulations & the State of Science". Nutraceuticals World. Rodman Media. Retrieved April 11, 2013. 
  6. ^ Huang D, Ou B, Prior R (2005). "The chemistry behind antioxidant capacity assays". J. Agric. Food Chem. 53 (6): 1841–56. doi:10.1021/jf030723c. PMID 15769103. 
  7. ^ Garrett, Andrew R.; Murray, Byron K.; Robison, Richard A.; O'Neill, Kim L. (2010). Armstrong, Donald, ed. Measuring antioxidant capacity using the ORAC and TOSC assays. Advanced Protocols in Oxidative Stress II. Methods in Molecular Biology 594. pp. 251–62. doi:10.1007/978-1-60761-411-1_17. ISBN 978-1-60761-410-4. PMID 20072922. 
  8. ^ Kohri S, Fujii H, Oowada S, Endoh N, Sueishi Y, Kusakabe M, Shimmei M, Kotake Y (2009). "An oxygen radical absorbance capacity-like assay that directly quantifies the antioxidant's scavenging capacity against AAPH-derived free radicals". Anal. Biochem. 386 (2): 167–71. doi:10.1016/j.ab.2008.12.022. PMID 19150323. 
  9. ^ Guidance for Industry, Food Labeling; Nutrient Content Claims; Definition for "High Potency" and Definition for "Antioxidant" for Use in Nutrient Content Claims for Dietary Supplements and Conventional Foods U.S. Department of Health and Human Services, Food and Drug Administration, Center for Food Safety and Applied Nutrition, June 2008
  10. ^ a b c EFSA Panel on Dietetic Products, Nutrition and Allergies (2010). "Scientific Opinion on the substantiation of health claims related to various food(s)/food constituent(s) and protection of cells from premature aging, antioxidant activity, antioxidant content and antioxidant properties, and protection of DNA, proteins and lipids from oxidative damage pursuant to Article 13(1) of Regulation (EC) No 1924/20061". EFSA Journal 8 (2): 1489. doi:10.2903/j.efsa.2010.1489 (inactive 2014-03-23). 
  11. ^ a b Williams RJ, Spencer JP, Rice-Evans C (April 2004). "Flavonoids: antioxidants or signalling molecules?". Free Radical Biology & Medicine 36 (7): 838–49. doi:10.1016/j.freeradbiomed.2004.01.001. PMID 15019969. 
  12. ^ Arts, IC; Hollman, PC (2005). "Polyphenols and disease risk in epidemiologic studies". The American journal of clinical nutrition 81 (1 Suppl): 317S–325S. PMID 15640497. 
  13. ^ a b Lotito SB, Frei B (2006). "Consumption of flavonoid-rich foods and increased plasma antioxidant capacity in humans: cause, consequence, or epiphenomenon?". Free Radic. Biol. Med. 41 (12): 1727–46. doi:10.1016/j.freeradbiomed.2006.04.033. PMID 17157175. 
  14. ^ a b c "Studies force new view on biology of flavonoids", by David Stauth, EurekAlert!. Adapted from a news release issued by Oregon State University
  15. ^ Ninfali, Paolino; Mea, Gloria; Giorgini, Samantha; Rocchi, Marco; Bacchiocca, Mara (2007). "Antioxidant capacity of vegetables, spices and dressings relevant to nutrition". British Journal of Nutrition 93 (2): 257–66. doi:10.1079/BJN20041327. PMID 15788119. 
  16. ^ Tapsell, LC; Hemphill, I; Cobiac, L; Patch, CS; Sullivan, DR; Fenech, M; Roodenrys, S; Keogh, JB et al. (2006). "Health benefits of herbs and spices: The past, the present, the future". The Medical journal of Australia 185 (4 Suppl): S4–24. PMID 17022438. 

External links[edit]

  • Xu, Baojun; Chang, Sam K.C. (2008). "Effect of soaking, boiling, and steaming on total phenolic contentand antioxidant activities of cool season food legumes". Food Chemistry 110: 1. doi:10.1016/j.foodchem.2008.01.045.