The total antioxidant content of more than 3100 foods, beverages, spices, herbs and supplements used worldwide
- Monica H Carlsen†1,
- Bente L Halvorsen†1,
- Kari Holte1,
- Siv K Bøhn1,
- Steinar Dragland2,
- Laura Sampson3,
- Carol Willey3,
- Haruki Senoo4,
- Yuko Umezono4,
- Chiho Sanada4,
- Ingrid Barikmo5,
- Nega Berhe1,
- Walter C Willett3,
- Katherine M Phillips6,
- David R JacobsJr1, 7 and
- Rune Blomhoff1Email author
© Carlsen et al; licensee BioMed Central Ltd. 2010
Received: 18 August 2009
Accepted: 22 January 2010
Published: 22 January 2010
A plant-based diet protects against chronic oxidative stress-related diseases. Dietary plants contain variable chemical families and amounts of antioxidants. It has been hypothesized that plant antioxidants may contribute to the beneficial health effects of dietary plants. Our objective was to develop a comprehensive food database consisting of the total antioxidant content of typical foods as well as other dietary items such as traditional medicine plants, herbs and spices and dietary supplements. This database is intended for use in a wide range of nutritional research, from in vitro and cell and animal studies, to clinical trials and nutritional epidemiological studies.
We procured samples from countries worldwide and assayed the samples for their total antioxidant content using a modified version of the FRAP assay. Results and sample information (such as country of origin, product and/or brand name) were registered for each individual food sample and constitute the Antioxidant Food Table.
The results demonstrate that there are several thousand-fold differences in antioxidant content of foods. Spices, herbs and supplements include the most antioxidant rich products in our study, some exceptionally high. Berries, fruits, nuts, chocolate, vegetables and products thereof constitute common foods and beverages with high antioxidant values.
This database is to our best knowledge the most comprehensive Antioxidant Food Database published and it shows that plant-based foods introduce significantly more antioxidants into human diet than non-plant foods. Because of the large variations observed between otherwise comparable food samples the study emphasizes the importance of using a comprehensive database combined with a detailed system for food registration in clinical and epidemiological studies. The present antioxidant database is therefore an essential research tool to further elucidate the potential health effects of phytochemical antioxidants in diet.
It is widely accepted that a plant-based diet with high intake of fruits, vegetables, and other nutrient-rich plant foods may reduce the risk of oxidative stress-related diseases [1–6]. Understanding the complex role of diet in such chronic diseases is challenging since a typical diet provides more than 25,000 bioactive food constituents , many of which may modify a multitude of processes that are related to these diseases. Because of the complexity of this relationship, it is likely that a comprehensive understanding of the role of these bioactive food components is needed to assess the role of dietary plants in human health and disease development. We suggest that both their numerous individual functions as well as their combined additive or synergistic effects are crucial to their health beneficial effects, thus a food-based research approach is likely to elucidate more health effects than those derived from each individual nutrient. Most bioactive food constituents are derived from plants; those so derived are collectively called phytochemicals. The large majority of these phytochemicals are redox active molecules and therefore defined as antioxidants. Antioxidants can eliminate free radicals and other reactive oxygen and nitrogen species, and these reactive species contribute to most chronic diseases. It is hypothesized that antioxidants originating from foods may work as antioxidants in their own right in vivo, as well as bring about beneficial health effects through other mechanisms, including acting as inducers of mechanisms related to antioxidant defense [7, 8], longevity [9, 10], cell maintenance and DNA repair .
Several assays have been used to assess the total antioxidant content of foods, e.g. the 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox) equivalent antioxidant capacity (TEAC) assay , the ferric-reducing ability of plasma (FRAP)  and the oxygen radical absorbance capacity assay (ORAC) assay . Based on careful considerations (see Blomhoff 2005 and Halvorsen et al 2002 for discussion [15, 16]) we chose to use a modified version of the FRAP assay by Benzie and Strain  for total antioxidant analysis . Most importantly, the modified FRAP assay is a simple, fast and inexpensive assay with little selectivity. Assay conditions, such as extraction solvents, were optimized regarding detection of both lipophilic and hydrophilic antioxidants . The FRAP assay directly measures antioxidants with a reduction potential below the reduction potential of the Fe3+/Fe2+ couple [16, 17]. Thus, the FRAP assay does not measure glutathione. Most other assays have higher reduction potentials and measures glutathione and other thiols . This may be an advantage when using the FRAP assay, because glutathione is found in high concentrations in foods but it is degraded in the intestine and poorly absorbed by humans . A disadvantage of the FRAP assay is its inability to detect other small molecular weight thiols and sulfur containing molecules of e.g. garlic. Most assays for assessing total antioxidant capacity generally result in similar ranking of foods [20–23]. We have now performed a systematic measurement of the total antioxidant content of more than 3100 foods. This novel Antioxidant Food Table enables us to calculate total antioxidant content of complex diets, identify and rank potentially good sources of antioxidants, and provide the research community with comparable data on the relative antioxidant capacity of a wide range of foods.
There is not necessarily a direct relationship between the antioxidant content of a food sample consumed and the subsequent antioxidant activity in the target cell. Factors influencing the bioavailability of phytochemical antioxidants, include the food matrix, absorption and metabolism [24–27]. Also, the methods measuring total antioxidant capacity do not identify single antioxidant compounds, and they are therefore of limited use when investigating the mechanisms involved. This is however, not the scope of this article. With the present study, food samples with high antioxidant content are identified, but further investigation into each individual food and phytochemical antioxidant compound is needed to identify those which may have biological relevance and the mechanisms involved.
The aim of the present study was to screen foods to identify total antioxidant capacity of fruits, vegetables, beverages, spices and herbs in addition to common everyday foods. In nutritional epidemiologic and intervention studies, the Antioxidant Food Database may be utilized to identify and rank diets and subjects with regard to antioxidant intake and as a tool in planning dietary antioxidant interventions. The database will be available online at the University of Oslo's web site.
TPTZ (2,4,6-tri-pyridyl-s-triazine) was obtained from Fluka Chemie AG (Deisenhofen, Switzerland), sodium acetate trihydrate and FeSO4 × 7 H2O from Riedel-deHaën AG (Seelze, Germany), acetic acid and hydrochloric acid from Merck (Darmstadt, Germany), FeCl3 × 6H2O from BDH Laboratory Supplies (Dorset, England). MilliQ water (Millipore, Bedford, MA) and methanol of HPLC-grade obtained from Merck was used for all extractions. 2-propanol (HPLC-grade) was obtained from Merck.
Sample collection and sample preparation
The antioxidant measurements have been conducted over a period of eight years, from 2000 to 2008. The samples were procured from local stores and markets in Scandinavia, USA and Europe and from the African, Asian and South American continents. Many of the samples of plant material, like berries, mushrooms and herbs, were handpicked. Commercially procured food samples were stored according to the description on the packing and analyzed within four weeks. Handpicked samples were either stored at 4°C and analyzed within three days or frozen at -20°C and analyzed within four weeks. Products that needed preparation such as coffee, tea, processed vegetables etc. were prepared on the day of analysis. Furthermore, all samples were homogenized, dry samples were pulverized and solid samples were chopped in a food processor. After homogenizing, analytical aliquots were weighed. Included in the database are 1113 of the food samples obtained from the US Department of Agriculture National Food and Nutrient Analysis Program. They were collected, homogenized, and stored as previously described . Three replicates were weighed out for each sample. All samples were extracted in water/methanol, except vegetable oils which were extracted in 2-propanol and some fat-rich samples which were extracted in water/2-propanol. The extracts were mixed, sonicated in ice water bath for 15 min, mixed once more and centrifuged in 1.5 mL tubes at 12.402 × g for 2 min at 4°C. The concentration of antioxidants was measured in triplicate of the supernatant of the centrifuged samples.
Measurements of antioxidant content
The FRAP assay of Benzie and Strain  was used with minor modifications that allowed quantification of most water- and fat-soluble antioxidants [16, 17]. A Technicon RA 1000 system (Technicon instruments corporation, New York, USA) was used for the measurements of absorption changes that appear when the TPTZ-Fe3+ complex reduces to the TPTZ-Fe2+ form in the presence of antioxidants. An intense blue color with absorption maximum at 593 nm develops. The measurements were performed at 600 nm after 4 min incubation. An aqueous solution of 500 μmol/L FeSO4 × 7 H2O was used for calibration of the instrument. Validation of the assay is described in Halvorsen et al. 2002 . Briefly, the within-day repeatability measured as relative standard deviation (RSD) in standard solutions ranged from 0.4% to 6%. The between-day repeatability was < 3%. The variation in the values for replicate food items obtained from the same source were typically between 3 and 10 RSD%.
Organization of the Antioxidant Food Table
The samples were classified into 24 different categories covering products from the plant kingdom, products from the animal kingdom and mixed food products. Information about sample processing (raw, cooked, dried etc), if any, was included, along with all sample specifications, i.e. product name, brand name, where the product/sample was procured and country of origin. The product information in the database was collected from the packing of the product, from supplier or purchaser. When this information was not available or the samples were handpicked, only country of origin is presented. Each sample is assigned to only one category. The classification was done according to information from the supplier or purchaser, or according to common traditional use of the food. Some foods may therefore be categorized otherwise in other food cultures. For products in the categories "Herbal/traditional plant medicine" and "Vitamin and dietary Supplements" some products may rightfully be classified as both an herbal medicine and a supplement, but are still assigned to only one category. All berries, fruits, and vegetables were fresh samples unless otherwise noted in the database. The Antioxidant Food Table contains 3139 samples. About 1300 of these samples have been published before [16, 17, 28] but for comparison and completeness we have included them in the present publication. All individual samples previously published are identified by a comment in the Antioxidant Food Table. The categories and products in the database are presented in alphabetic order. Information about brand names and product trademarks does not imply endorsement by the authors, and are reported as descriptive information for research applications only. The Antioxidant Food Table will in the future be available online as a searchable database. In addition to the products mentioned in this paper, other foods will in the future be analyzed and incorporated into the online version, which will be posted on the University of Oslo's web site.
Statistical descriptives of the Antioxidant Food Table and individual categories.
Antioxidant content in mmol/100 g
Plant based foods a)
Animal based foods b)
Mixed foods c)
1 Berries and berry products
3 Breakfast cereals
4 Chocolates and sweets
5 Dairy products
6 Desserts and cakes
8 Fats and oils
9 Fish and seafood
10 Fruit and fruit juices
11 Grains and grain products
12 Herbal/traditional plant medicine
13 Infant foods and beverages
15 Meat and meat products
16 Miscellaneous ingredients, condiments
17 Mixed food entrees
18 Nuts and seeds
19 Poultry and poultry products
20 Snacks, biscuits
21 Soups, sauces gravies, dressing
22 Spices and herbs
23 Vegetables and vegetable products
24 Vitamin and dietary supplements
Excerpt of the analyses of beverages in the Antioxidant Food Table.
Antioxidant content mmol/100 ga)
Black tea, prepared
Cocoa with milk
Coffee, prepared filter and boiled
Green tea, prepared
Breakfast cereals, grains, legumes, nuts and seeds
Excerpt of the analyses of nuts, legumes and grain products in the Antioxidant Food Table.
Antioxidant content mmol/100 ga)
Barley, pearl and flour
Bread, with fiber/whole meal
Buckwheat, white flour
Buckwheat, whole meal flour
Chestnuts, with pellicle
Crisp bread, brown
Maize, white flour
Peanuts, roasted, with pellicle
Pecans, with pellicle
Walnuts, with pellicle
Wheat bread, toasted
Whole wheat bread, toasted
In the nuts and seeds category we analyzed 90 different products, with antioxidant contents varying from 0.03 mmol/100 g in poppy seeds to 33.3 mmol/100 g in walnuts, with pellicle and purchased with nut shell intact. Pecans with pellicle, sunflower seeds and chestnuts with pellicle, have mean antioxidant content in the range of 4.7 to 8.5 mmol/100 g (Table 3). Walnuts, chestnuts, peanuts, hazelnuts and almonds have higher values when analyzed with the pellicle intact compared to without pellicle.
Various types of chocolate were analyzed, from milk chocolate to dark chocolate and baking cocoa. The variation of antioxidant content in chocolate ranged from 0.23 in white chocolate to 14.98 mmol/100 g in one individual dark chocolate sample. Mean antioxidant contents increased with increasing content of cocoa in the chocolate product (Pearson correlation r = 0.927, p < 0.001). Chocolate products with cocoa contents of 24-30%, 40-65% and 70-99% had mean antioxidant contents of 1.8, 7.2 and 10.9 mmol/100 g, respectively.
Dairy products, desserts and cakes, eggs, fats and oils
The dairy category included 86 products and the majority of these products were low in antioxidant content, in the range of 0.0 to 0.8 mmol/100 g. Dairy products with added berries or chocolate and cheeses like Brie, Gorgonzola and Roquefort are the most antioxidant rich products in this category.
One hundred and thirty four products are included in the category "Desserts and cakes". In the upper range of this category we find dog rose soup and chocolate cookies. Eggs are almost devoid of antioxidants with the highest antioxidant values found in egg yolk (0.16 mmol/100 g).
Margarine, butter, canola, corn and soybean oil are the highest ranking products in the "Fats and oils" category. Almost half of the fats and oils have antioxidant content between 0.4 and 1.7 mmol/100 g.
Berries, fruit and vegetables
Excerpt of the berries, fruit and vegetable analyses in the Antioxidant Food Table.
Antioxidant content mmol/100 ga)
African baobab tree, leaves dry, crushed
Amla (Indian gooseberry), dried
Chilli, red and green
Dog rose, products of dried hip
Dog rose, wild, dried
Dog rose, wild, fresh
Fruit from the African baobab tree
Moringa Stenopetala, dried leaves, stem
Moringa Stenopetala, fresh leaves, stem
Okra/gumbo from Mali, dry, flour
Zereshk, red sour berries
A total of 278 fruits and fruit products and 303 vegetables and vegetable products were included in the database. In the analyzed vegetables, antioxidant content varied from 0.0 mmol/100 g in blanched celery to 48.1 mmol/100 g in dried and crushed leaves of the African baobab tree. In fruits, procured in 8 different countries, the antioxidant content varies from 0.02 mmol/100 g for watermelon to 55.5 mmol/100 g in the yellow pith of Spanish pomegranate. Examples of antioxidant rich fruits and vegetables were dried apples, flour made of okra, artichokes, lemon skin, dried plums, dried apricots, curly kale, red and green chili and prunes (Table 4). Examples of fruit and vegetables in the medium antioxidant range were dried dates, dried mango, black and green olives, red cabbage, red beets, paprika, guava and plums.
Herbal/traditional plant medicine
This is the most antioxidant rich category in the present study and is also the category with largest variation between products. Half of the products have antioxidant values above the 90th percentile of the complete Antioxidant Food Table and the mean and median values are 91.7 and 14.2 mmol/100 g, respectively. The 59 products included originate from India, Japan, Mexico and Peru. Sangre de Grado (Dragon's Blood) from Peru has the highest antioxidant content of all the products in the database (2897.1 mmol/100 g). Other antioxidant rich products are Triphala, Amalaki and Arjuna from India and Goshuyu-tou, a traditional kampo medicine from Japan, with antioxidant values in the range of 132.6 to 706.3 mmol/100 g. Only four products in this category have values less than 2.0 mmol/100 g.
Infant food and beverages
The category includes 52 products, including European, Scandinavian and American products. The variation in antioxidant content in dinner and dessert products for infants varies from 0.02 to 1.25 mmol/100 g. Interestingly, human breast milk (49 samples from Norwegian mothers) has a mean content of 2.0 mmol/100 g. In addition, the category includes two Norwegian dog rose products for infants with antioxidant contents of 6.7 and 18.5 mmol/100 g.
Spices and herbs
Excerpt of the spices and herbs analyzed in the Antioxidant Food Table.
Antioxidant content mmol/100 ga)
Allspice, dried ground
Bay leaves, dried
Cinnamon sticks and whole bark
Cinnamon, dried ground
Clove, dried, whole and ground
Dill, dried ground
Estragon, dried ground
Mint leaves, dried
Nutmeg, dried ground
Oregano, dried ground
Rosemary, dried ground
Saffron, dried ground
Saffron, dried whole stigma
Sage, dried ground
Thyme, dried ground
Soups, sauces, gravies and dressings
In this broad category, we have analyzed 251 products and found that the products with highest antioxidant content are tomato based sauces, basil pesto, mustard paste, sun dried tomatoes and tomato paste/puree, in the range of 1.0 to 4.6 mmol/100 g.
Vitamin and dietary supplements
The category "Vitamin and dietary supplements" includes 131 commercially available vitamin and dietary supplement products from USA, Norway, Mexico and Japan of which many have high antioxidant scores. Among them are supplements containing anthocyanins, vitamin C, green tea powder and multivitamins and multi-antioxidant tablets.
Meat, poultry, fish and miscellaneous ingredients
The majority of the products in these categories were low in antioxidant content. Nevertheless, products like liver, bacon and some prepared chicken and beef products have antioxidant values between 0.5 and 1.0 mmol/100 g.
With this study we present a comprehensive survey of the total antioxidant capacity in foods. Earlier small-scale studies from other laboratories have included from a few up to a few hundred samples [20–22, 29–31], and in 2007 the U.S. Department of Agriculture presented the Oxygen Radical Absorbance Capacity (ORAC) of Selected Foods report including 277 food samples . These studies have been done using different antioxidant assays for measuring antioxidant capacity making it difficult to compare whole lists of foods, products and product categories. Still, a food that has a high total antioxidant capacity using one antioxidant assay will most likely also be high using another assay [20–22]. Consequently, the exact value will be different but the ranking of the products will be mainly the same whichever assay is used. In the present extensive study, the same validated method has been used on all samples, resulting in comparable measures, thus enabling us to present a complete picture of the relative antioxidant potential of the samples.
When classifying the samples into the three main classes the difference in antioxidant content between plant- and animal-based foods become apparent. The results here uncover that the antioxidant content of foods varies several thousand-fold and that antioxidant rich foods originate from the plant kingdom while meat, fish and other foods from the animal kingdom are low in antioxidants. Comparing the mean value of the 'Meat and meat products' category with plant based categories, fruits, nuts, chocolate and berries have from 5 to 33 times higher mean antioxidant content than the mean of meat products. Diets comprised mainly of animal-based foods are thus low in antioxidant content while diets based mainly on a variety of plant-based foods are antioxidant rich, due to the thousands of bioactive antioxidant phytochemicals found in plants which are conserved in many foods and beverages.
Most of the spices and herbs analyzed have particularly high antioxidant contents. Although spices and herbs contribute little weight on the dinner plate, they may still be important contributors to our antioxidant intake, especially in dietary cultures where spices and herbs are used regularly. We interpret the elevated concentration of antioxidants observed in several dried herbs compared to fresh samples, as a normal consequence of the drying process leaving most of the antioxidants intact in the dried end product. This tendency is also seen in some fruits and their dried counterparts. Thus, dried herbs and fruit are potentially excellent sources of antioxidants.
Herbal and traditional plant medicines emerged as many of the highest antioxidant-containing products in our study. We speculate that the high inherent antioxidant property of many plants is an important contributor to the herb's medicinal qualities. In our study we identified Sangre de Grado, the sap from the tree trunk of the species Croton lechleri sampled in Peru to have exceptional high antioxidant content. This sap has a long history of indigenous use in South America for wound healing and as an antifungal, antiseptic, antiviral and antihaemorrhagic medicine. Proanthocyanidins are major constituents of this sap  and studies have shown that Sangre de Grado limits the transcription of a wide range of pro-inflammatory cytokines and mediators and accelerates the healing of stomach ulcers [33, 34] and promotes apoptosis in cancer cells . Other extreme antioxidant rich herbal medicines are Triphala, an Indian Ayurvedic herbal formulation, shown to have anti-inflammatory activity , antibacterial and wound healing properties [37, 38] and cancer chemopreventive potential . Arjuna, another Auyrvedic formula, has been shown to have health beneficial activities [40, 41] while Goshuyu-tou, a traditional Chinese kampo medicine has been shown to significantly reduce the extracellular concentration of NO in the LPS-stimulated Raw 264.7 cells .
With their high content of phytochemicals such as flavonoids, tannins, stilbenoids, phenolic acids and lignans [43–45] berries and berry products are potentially excellent antioxidant sources. The phytochemical content of berries varies with geographical growing condition, and between cultivars [46, 47] explaining the variations found in our study. During the processing of berries to jams, total phenol content is reduced  resulting in lower antioxidant values in processed berry products than in fresh berries.
Nuts are a rich source of many important nutrients and some are also antioxidant-rich. The observed increase in antioxidant content in nuts with pellicle compared to nuts without pellicle is in good agreement with earlier studies showing the flavonoids of many nuts are found in the nut pellicle .
After water, tea and coffee are the two most consumed beverages in the world, although consumption patterns vary between countries. Because of the fairly high content of antioxidants and the frequent use, coffee and tea are important antioxidant sources in many diets. Several different compounds contribute to coffee's antioxidant content, e.g., caffeine, polyphenols, volatile aroma compounds and heterocyclic compounds, [25, 50–52]. Many of these are efficiently absorbed, and plasma antioxidants increase after coffee intake [50, 53]. In green tea, the major flavonoids present are the monomer catechins, epigallocatechin gallate, epigallocatechin, epicatechin gallate and epicatechin. In black tea the polymerized catechins theaflavin and thearubigen predominate in addition to quercetin and flavonols [54, 55].
Interestingly, the antioxidant content in human breast milk is comparable to that in pomegranate juice, strawberries and coffee and on average higher than the antioxidant content observed in the commercially available infant formulas analyzed in our study. Breakfast cereals are also potential important sources of antioxidants; some of these products have antioxidant contents comparable to berries, which are fairly high, compared to other grain products and may be due to antioxidants added to the products in fortification process.
Chocolate have for several years been studied for its possible beneficial health effects . Our results show a high correlation between the cocoa content and the antioxidant content, which is in agreement with earlier studies [30, 57].
As demonstrated in the present study, the variation in the antioxidant values of otherwise comparable products is large. Like the content of any food component, antioxidant values will differ for a wide array of reasons, such as growing conditions, seasonal changes and genetically different cultivars [46, 58], storage conditions [59–61] and differences in manufacturing procedures and processing [62–64]. Differences in unprocessed and processed plant food samples are also seen in our study where processed berry products like jam and syrup have approximately half the antioxidant capacity of fresh berries. On the other hand, processing may also enhance a foods potential as a good antioxidant source by increasing the amount of antioxidants released from the food matrix which otherwise would be less or not at all available for absorption . Processing of tomato is one such example where lycopene from heat-processed tomato sauce is more bioavailable than unprocessed tomato . The large variations in antioxidant capacity observed in the present study emphasize the importance of using a comprehensive antioxidant database combined with a detailed system for food registration in clinical and epidemiological studies.
Initial studies have been carried out to examine the association between intake of antioxidant rich foods and their health effects [67, 70]. Some of these studies describe a beneficial effect on oxidative stress related chronic diseases, e.g. from intake of nuts [49, 69], pomegranates [71–73], tomatoes , coffee , tea [54, 75, 76], red wine [77–79] and cocoa . The highly reactive and bioactive phytochemical antioxidants are postulated to in part explain the protective effect of plant foods. An optimal mixture of different antioxidants with complementary mechanisms of action and different redox potentials is postulated to work in synergistic interactions. Still, it is not likely that all antioxidant-rich foods are good sources and that all antioxidants provided in the diet are bioactive. Bioavailability differs greatly from one phytochemical to another [26, 27, 80], so the most antioxidant rich foods in our diet are not necessarily those leading to the highest concentrations of active metabolites in target tissues. The antioxidants obtained from foods include many different molecular compounds and families with different chemical and biological properties that may affect absorption, transport and excretion, cellular uptake and metabolism, and eventually their effects on oxidative stress in various cellular compartments . Biochemically active phytochemicals found in plant-based foods also have many powerful biological properties which are not necessarily correlated with their antioxidant capacity, including acting as inducers of antioxidant defense mechanisms in vivo or as gene expression modulators. Thus a food low in antioxidant content may have beneficial health effects due to other food components or phytochemicals executing bioactivity through other mechanisms.
The Antioxidant Food Table is a valuable research contribution, expanding the research evidence base for plant-based nutritional research and may be utilized in epidemiological studies where reported food intakes can be assigned antioxidant values. It can also be used to test antioxidant effects and synergy in experimental animal and cell studies or in human clinical trials. The ultimate goal of this research is to combine these strategies in order to understand the role of dietary phytochemical antioxidants in the prevention of cancer, cardiovascular diseases, diabetes and other chronic diseases related to oxidative stress.
This work was funded by the Throne Holst foundation, The Research Council of Norway, and the Norwegian Cancer Society. The authors thank Amrit K. Sakhi, Nasser Bastani, Ingvild Paur and Trude R. Balstad for help procuring samples, the Tsumura Pharmaceutical Company for providing traditional herb medicines and Arcus AS and Norsk Øko-Urt BA for providing samples of beverages and herbs, respectively.
- Johnson IT: New approaches to the role of diet in the prevention of cancers of the alimentary tract. Mutat Res. 2004, 551: 9-28.View ArticleGoogle Scholar
- Joshipura KJ, Ascherio A, Manson JE, Stampfer MJ, Rimm EB, Speizer FE, Hennekens CH, Spiegelman D, Willett WC: Fruit and vegetable intake in relation to risk of ischemic stroke. JAMA. 1999, 282: 1233-1239. 10.1001/jama.282.13.1233.View ArticleGoogle Scholar
- Joshipura KJ, Hu FB, Manson JE, Stampfer MJ, Rimm EB, Speizer FE, Colditz G, Ascherio A, Rosner B, Spiegelman D, Willett WC: The effect of fruit and vegetable intake on risk for coronary heart disease. Ann Intern Med. 2001, 134: 1106-1114.View ArticleGoogle Scholar
- Riboli E, Norat T: Epidemiologic evidence of the protective effect of fruit and vegetables on cancer risk. Am J Clin Nutr. 2003, 78: 559S-569S.Google Scholar
- Stanner SA, Hughes J, Kelly CN, Buttriss J: A review of the epidemiological evidence for the 'antioxidant hypothesis'. Public Health Nutr. 2004, 7: 407-422. 10.1079/PHN2003543.View ArticleGoogle Scholar
- World Cancer Research Fund/American Institute for Cancer Research: Food, Nutrition, Physical Activity and the Prevention of Cancer: a Global Perspective. 2007, American Institute of Cancer Research, Washington DCGoogle Scholar
- Kensler TW, Wakabayashi N, Biswal S: Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway. Annu Rev Pharmacol Toxicol. 2007, 47: 89-116. 10.1146/annurev.pharmtox.46.120604.141046.View ArticleGoogle Scholar
- Jeong WS, Jun M, Kong AN: Nrf2: a potential molecular target for cancer chemoprevention by natural compounds. Antioxid Redox Signal. 2006, 8: 99-106. 10.1089/ars.2006.8.99.View ArticleGoogle Scholar
- Baur JA, Pearson KJ, Price NL, Jamieson HA, Lerin C, Kalra A, Prabhu VV, Allard JS, Lopez-Lluch G, Lewis K, Pistell PJ, Poosala S, Becker KG, Boss O, Gwinn D, Wang M, Ramaswamy S, Fishbein KW, Spencer RG, Lakatta EG, Le CD, Shaw RJ, Navas P, Puigserver P, Ingram DK, de CR, Sinclair DA: Resveratrol improves health and survival of mice on a high-calorie diet. Nature. 2006, 444: 337-342. 10.1038/nature05354.View ArticleGoogle Scholar
- Wood JG, Rogina B, Lavu S, Howitz K, Helfand SL, Tatar M, Sinclair D: Sirtuin activators mimic caloric restriction and delay ageing in metazoans. Nature. 2004, 430: 686-689. 10.1038/nature02789.View ArticleGoogle Scholar
- Astley SB, Elliott RM, Archer DB, Southon S: Evidence that dietary supplementation with carotenoids and carotenoid-rich foods modulates the DNA damage: repair balance in human lymphocytes. Br J Nutr. 2004, 91: 63-72. 10.1079/BJN20031001.View ArticleGoogle Scholar
- Miller NJ, RiceEvans CA: Spectrophotometric determination of antioxidant activity. Redox Report. 1996, 2: 161-171.Google Scholar
- Benzie IF, Strain JJ: The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": the FRAP assay. Anal Biochem. 1996, 239: 70-76. 10.1006/abio.1996.0292.View ArticleGoogle Scholar
- DeLange RJ, Glazer AN: Phycoerythrin fluorescence-based assay for peroxy radicals: a screen for biologically relevant protective agents. Anal Biochem. 1989, 177: 300-306. 10.1016/0003-2697(89)90056-0.View ArticleGoogle Scholar
- Blomhoff R: Dietary antioxidants and cardiovascular disease. Curr Opin Lipidol. 2005, 16: 47-54. 10.1097/00041433-200502000-00009.View ArticleGoogle Scholar
- Halvorsen BL, Holte K, Myhrstad MCW, Barikmo I, Hvattum E, Remberg SF, Wold AB, Haffner K, Baugerod H, Andersen LF, Moskaug JO, Jacobs DR, Blomhoff R: A systematic screening of total antioxidants in dietary plants. J Nutr. 2002, 132: 461-471.Google Scholar
- Halvorsen BL, Carlsen MH, Phillips KM, Bohn SK, Holte K, Jacobs DR, Blomhoff R: Content of redox-active compounds (ie, antioxidants) in foods consumed in the United States. Am J Clin Nutr. 2006, 84: 95-135.Google Scholar
- Buettner GR: The pecking order of free radicals and antioxidants: lipid peroxidation, alpha-tocopherol, and ascorbate. Arch Biochem Biophys. 1993, 300: 535-543. 10.1006/abbi.1993.1074.View ArticleGoogle Scholar
- Stahl W, van den Berg H, Arthur J, Bast A, Dainty J, Faulks RM, Gartner C, Haenen G, Hollman P, Holst B, Kelly FJ, Polidori MC, Rice-Evans C, Southon S, van Vliet T, Vina-Ribes J, Williamson G, Astley SB: Bioavailability and metabolism. Mol Aspects Med. 2002, 23: 39-100. 10.1016/S0098-2997(02)00016-X.View ArticleGoogle Scholar
- Miller HE, Rigelhof F, Marquart L, Prakash A, Kanter M: Antioxidant content of whole grain breakfast cereals, fruits and vegetables. J Am Coll Nutr. 2000, 19: 312S-319S.View ArticleGoogle Scholar
- Pellegrini N, Serafini M, Colombi B, Del Rio D, Salvatore S, Bianchi M, Brighenti F: Total antioxidant capacity of plant foods, beverages and oils consumed in Italy assessed by three different in vitro assays. J Nutr. 2003, 133: 2812-2819.Google Scholar
- Pellegrini N, Serafini M, Salvatore S, Del Rio D, Bianchi M, Brighenti F: Total antioxidant capacity of spices, dried fruits, nuts, pulses, cereals and sweets consumed in Italy assessed by three different in vitro assays. Mol Nutr Food Res. 2006, 50: 1030-1038. 10.1002/mnfr.200600067.View ArticleGoogle Scholar
- Oxygen Radical Absorbance Capacity (ORAC) of Selected Foods - 2007. [http://www.ars.usda.gov/sp2userfiles/place/12354500/data/orac/orac07.pdf]
- Astley SB, Lindsay DG: European Research on the Functional Effects of Dietary Antioxidants - EUROFEDA. Mol Aspects Med. 2002, 23: 1-38. 10.1016/S0098-2997(02)00019-5.View ArticleGoogle Scholar
- Gonthier MP, Verny MA, Besson C, Remesy C, Scalbert A: Chlorogenic acid bioavailability largely depends on its metabolism by the gut microflora in rats. J Nutr. 2003, 133: 1853-1859.Google Scholar
- Manach C, Scalbert A, Morand C, Remesy C, Jimenez L: Polyphenols: food sources and bioavailability. Am J Clin Nutr. 2004, 79: 727-747.Google Scholar
- Manach C, Williamson G, Morand C, Scalbert A, Remesy C: Bioavailability and bioefficacy of polyphenols in humans. I. Review of 97 bioavailability studies. Am J Clin Nutr. 2005, 81: 230S-242S.Google Scholar
- Dragland S, Senoo H, Wake K, Holte K, Blomhoff R: Several culinary and medicinal herbs are important sources of dietary antioxidants. J Nutr. 2003, 133: 1286-1290.Google Scholar
- Kahkonen MP, Hopia AI, Vuorela HJ, Rauha JP, Pihlaja K, Kujala TS, Heinonen M: Antioxidant activity of plant extracts containing phenolic compounds. J Agric Food Chem. 1999, 47: 3954-3962. 10.1021/jf990146l.View ArticleGoogle Scholar
- Lee KW, Kim YJ, Lee HJ, Lee CY: Cocoa has more phenolic phytochemicals and a higher antioxidant capacity than teas and red wine. J Agric Food Chem. 2003, 51: 7292-7295. 10.1021/jf0344385.View ArticleGoogle Scholar
- Richelle M, Tavazzi I, Offord E: Comparison of the antioxidant activity of commonly consumed polyphenolic beverages (coffee, cocoa, and tea) prepared per cup serving. J Agric Food Chem. 2001, 49: 3438-3442. 10.1021/jf0101410.View ArticleGoogle Scholar
- Cai Y, Evans FJ, Roberts MF, Phillipson JD, Zenk MH, Gleba YY: Polyphenolic compounds from Croton Lechleri. Phytochemistry. 1991, 30: 2033-2040. 10.1016/0031-9422(91)85063-6.View ArticleGoogle Scholar
- Miller MJ, MacNaughton WK, Zhang XJ, Thompson JH, Charbonnet RM, Bobrowski P, Lao J, Trentacosti AM, Sandoval M: Treatment of gastric ulcers and diarrhea with the Amazonian herbal medicine sangre de grado. Am J Physiol Gastrointest Liver Physiol. 2000, 279: G192-G200.Google Scholar
- Miller MJ, Vergnolle N, McKnight W, Musah RA, Davison CA, Trentacosti AM, Thompson JH, Sandoval M, Wallace JL: Inhibition of neurogenic inflammation by the Amazonian herbal medicine sangre de grado. J Invest Dermatol. 2001, 117: 725-730. 10.1046/j.0022-202x.2001.01446.x.View ArticleGoogle Scholar
- Sandoval M, Okuhama NN, Clark M, Angeles FM, Lao J, Bustamante S, Miller MJ: Sangre de grado Croton palanostigma induces apoptosis in human gastrointestinal cancer cells. J Ethnopharmacol. 2002, 80: 121-129. 10.1016/S0378-8741(02)00013-2.View ArticleGoogle Scholar
- Rasool M, Sabina EP: Antiinflammatory effect of the Indian Ayurvedic herbal formulation Triphala on adjuvant-induced arthritis in mice. Phytother Res. 2007, 21: 889-894. 10.1002/ptr.2183.View ArticleGoogle Scholar
- Kumar MS, Kirubanandan S, Sripriya R, Sehgal P: Triphala promotes healing of infected full-thickness dermal wound. J Surg Res. 2008, 144: 94-101. 10.1016/j.jss.2007.02.049.View ArticleGoogle Scholar
- Srikumar R, Parthasarathy NJ, Shankar EM, Manikandan S, Vijayakumar R, Thangaraj R, Vijayananth K, Sheeladevi R, Rao UA: Evaluation of the growth inhibitory activities of Triphala against common bacterial isolates from HIV infected patients. Phytother Res. 2007, 21: 476-480. 10.1002/ptr.2105.View ArticleGoogle Scholar
- Deep G, Dhiman M, Rao AR, Kale RK: Chemopreventive potential of Triphala (a composite Indian drug) on Benzo(a)pyrene induced forestomach tumorigenesis in murine tumor model system. J Exp Clin Cancer Res. 2005, 24: 555-563.Google Scholar
- Manna P, Sinha M, Sil PC: Phytomedicinal activity of Terminalia arjuna against carbon tetrachloride induced cardiac oxidative stress. Pathophysiology. 2007, 14: 71-78. 10.1016/j.pathophys.2007.05.002.View ArticleGoogle Scholar
- Devi RS, Narayan S, Vani G, Shyamala Devi CS: Gastroprotective effect of Terminalia arjuna bark on diclofenac sodium induced gastric ulcer. Chem Biol Interact. 2007, 167: 71-83. 10.1016/j.cbi.2007.01.011.View ArticleGoogle Scholar
- Okayasu H, Suzuki F, Satoh K, Shioda S, Dohi K, Ikeda Y, Nakashima H, Komatsu N, Fujimaki M, Hashimoto K, Maki J, Sakagami H: Comparison of cytotoxicity and radical scavenging activity between tea extracts and Chinese medicines. Vivo. 2003, 17: 577-581.Google Scholar
- Kahkonen MP, Hopia AI, Heinonen M: Berry phenolics and their antioxidant activity. J Agric Food Chem. 2001, 49: 4076-4082. 10.1021/jf010152t.View ArticleGoogle Scholar
- Maatta-Riihinen KR, Kamal-Eldin A, Mattila PH, Gonzalez-Paramas AM, Torronen AR: Distribution and contents of phenolic compounds in eighteen Scandinavian berry species. J Agric Food Chem. 2004, 52: 4477-4486. 10.1021/jf049595y.View ArticleGoogle Scholar
- Maatta-Riihinen KR, Kamal-Eldin A, Torronen AR: Identification and quantification of phenolic compounds in berries of Fragaria and Rubus species (family Rosaceae). J Agric Food Chem. 2004, 52: 6178-6187. 10.1021/jf049450r.View ArticleGoogle Scholar
- Scalzo J, Politi A, Pellegrini N, Mezzetti B, Battino M: Plant genotype affects total antioxidant capacity and phenolic contents in fruit. Nutrition. 2005, 21: 207-213. 10.1016/j.nut.2004.03.025.View ArticleGoogle Scholar
- Wang SY, Lin HS: Antioxidant activity in fruits and leaves of blackberry, raspberry, and strawberry varies with cultivar and developmental stage. J Agric Food Chem. 2000, 48: 140-146. 10.1021/jf9908345.View ArticleGoogle Scholar
- Amakura Y, Umino Y, Tsuji S, Tonogai Y: Influence of jam processing on the radical scavenging activity and phenolic content in berries. J Agric Food Chem. 2000, 48: 6292-6297. 10.1021/jf000849z.View ArticleGoogle Scholar
- Chen CY, Milbury PE, Lapsley K, Blumberg JB: Flavonoids from almond skins are bioavailable and act synergistically with vitamins C and E to enhance hamster and human LDL resistance to oxidation. J Nutr. 2005, 135: 1366-1373.Google Scholar
- Illy E: The complexity of coffee. Sci Am. 2002, 286: 86-91. 10.1038/scientificamerican0602-86.View ArticleGoogle Scholar
- Nawrot P, Jordan S, Eastwood J, Rotstein J, Hugenholtz A, Feeley M: Effects of caffeine on human health. Food Addit Contam. 2003, 20: 1-30. 10.1080/0265203021000007840.View ArticleGoogle Scholar
- Yanagimoto K, Lee KG, Ochi H, Shibamoto T: Antioxidative activity of heterocyclic compounds found in coffee volatiles produced by Maillard reaction. J Agric Food Chem. 2002, 50: 5480-5484. 10.1021/jf025616h.View ArticleGoogle Scholar
- Olthof MR, Hollman PC, Katan MB: Chlorogenic acid and caffeic acid are absorbed in humans. J Nutr. 2001, 131: 66-71.Google Scholar
- McKay DL, Blumberg JB: The role of tea in human health: an update. J Am Coll Nutr. 2002, 21: 1-13.View ArticleGoogle Scholar
- McKay DL, Blumberg JB: Roles of epigallocatechin gallate in cardiovascular disease and obesity: an introduction. J Am Coll Nutr. 2007, 26: 362s-365s.View ArticleGoogle Scholar
- Cooper KA, Donovan JL, Waterhouse AL, Williamson G: Cocoa and health: a decade of research. Br J Nutr. 2008, 99: 1-11. 10.1017/S0007114507795296.View ArticleGoogle Scholar
- Vinson JA, Proch J, Zubik L: Phenol antioxidant quantity and quality in foods: cocoa, dark chocolate, and milk chocolate. J Agric Food Chem. 1999, 47: 4821-4824. 10.1021/jf990312p.View ArticleGoogle Scholar
- Imeh U, Khokhar S: Distribution of conjugated and free phenols in fruits: antioxidant activity and cultivar variations. J Agric Food Chem. 2002, 50: 6301-6306. 10.1021/jf020342j.View ArticleGoogle Scholar
- Kalt W, Forney CF, Martin A, Prior RL: Antioxidant capacity, vitamin C, phenolics, and anthocyanins after fresh storage of small fruits. J Agric Food Chem. 1999, 47: 4638-4644. 10.1021/jf990266t.View ArticleGoogle Scholar
- Mullen W, Stewart AJ, Lean ME, Gardner P, Duthie GG, Crozier A: Effect of freezing and storage on the phenolics, ellagitannins, flavonoids, and antioxidant capacity of red raspberries. J Agric Food Chem. 2002, 50: 5197-5201. 10.1021/jf020141f.View ArticleGoogle Scholar
- Xianquan S, Shi J, Kakuda Y, Yueming J: Stability of lycopene during food processing and storage. J Med Food. 2005, 8: 413-422. 10.1089/jmf.2005.8.413.View ArticleGoogle Scholar
- Gil-Izquierdo A, Gil MI, Ferreres F: Effect of processing techniques at industrial scale on orange juice antioxidant and beneficial health compounds. J Agric Food Chem. 2002, 50: 5107-5114. 10.1021/jf020162+.View ArticleGoogle Scholar
- Hartmann A, Patz CD, Andlauer W, Dietrich H, Ludwig M: Influence of processing on quality parameters of strawberries. J Agric Food Chem. 2008, 56: 9484-9489. 10.1021/jf801555q.View ArticleGoogle Scholar
- Ismail A, Lee WY: Influence of cooking practice on antioxidant properties and phenolic content of selected vegetables. Asia Pac J Clin Nutr. 2004, 13: S162-Google Scholar
- Lindsay DG, Astley SB: European research on the functional effects of dietary antioxidants - EUROFEDA. Mol Aspects Med. 2002, 23: 39-100. 10.1016/S0098-2997(02)00005-5.View ArticleGoogle Scholar
- Unlu NZ, Bohn T, Francis DM, Nagaraja HN, Clinton SK, Schwartz SJ: Lycopene from heat-induced cis-isomer-rich tomato sauce is more bioavailable than from all-trans-rich tomato sauce in human subjects. Br J Nutr. 2007, 98: 140-146. 10.1017/S0007114507685201.View ArticleGoogle Scholar
- Aviram M, Rosenblat M, Gaitini D, Nitecki S, Hoffman A, Dornfeld L, Volkova N, Presser D, Attias J, Liker H, Hayek T: Pomegranate juice consumption for 3 years by patients with carotid artery stenosis reduces common carotid intima-media thickness, blood pressure and LDL oxidation. Clin Nutr. 2004, 23: 423-433. 10.1016/j.clnu.2003.10.002.View ArticleGoogle Scholar
- Mullen W, Marks SC, Crozier A: Evaluation of phenolic compounds in commercial fruit juices and fruit drinks. J Agric Food Chem. 2007, 55: 3148-3157. 10.1021/jf062970x.View ArticleGoogle Scholar
- Ros E, Nunez I, Perez-Heras A, Serra M, Gilabert R, Casals E, Deulofeu R: A walnut diet improves endothelial function in hypercholesterolemic subjects: a randomized crossover trial. Circulation. 2004, 109: 1609-1614. 10.1161/01.CIR.0000124477.91474.FF.View ArticleGoogle Scholar
- Wang Y, Chang CF, Chou J, Chen HL, Deng X, Harvey BK, Cadet JL, Bickford PC: Dietary supplementation with blueberries, spinach, or spirulina reduces ischemic brain damage. Exp Neurol. 2005, 193: 75-84. 10.1016/j.expneurol.2004.12.014.View ArticleGoogle Scholar
- Adhami VM, Mukhtar H: Anti-oxidants from green tea and pomegranate for chemoprevention of prostate cancer. Mol Biotechnol. 2007, 37: 52-57. 10.1007/s12033-007-0047-8.View ArticleGoogle Scholar
- Malik A, Afaq F, Sarfaraz S, Adhami VM, Syed DN, Mukhtar H: Pomegranate fruit juice for chemoprevention and chemotherapy of prostate cancer. Proc Natl Acad Sci USA. 2005, 102: 14813-14818. 10.1073/pnas.0505870102.View ArticleGoogle Scholar
- Malik A, Mukhtar H: Prostate cancer prevention through pomegranate fruit. Cell Cycle. 2006, 5: 371-373.View ArticleGoogle Scholar
- Andersen LF, Jacobs DR, Carlsen MH, Blomhoff R: Consumption of coffee is associated with reduced risk of death attributed to inflammatory and cardiovascular diseases in the Iowa Women's Health Study. Am J Clin Nutr. 2006, 83: 1039-1046.Google Scholar
- Cabrera C, Artacho R, Gimenez R: Beneficial effects of green tea--a review. J Am Coll Nutr. 2006, 25: 79-99.View ArticleGoogle Scholar
- Lee W, Min WK, Chun S, Lee YW, Park H, Lee DH, Lee YK, Son JE: Long-term effects of green tea ingestion on atherosclerotic biological markers in smokers. Clin Biochem. 2005, 38: 84-87. 10.1016/j.clinbiochem.2004.09.024.View ArticleGoogle Scholar
- Cordova AC, Jackson LS, Berke-Schlessel DW, Sumpio BE: The cardiovascular protective effect of red wine. J Am Coll Surg. 2005, 200: 428-439. 10.1016/j.jamcollsurg.2004.10.030.View ArticleGoogle Scholar
- Klinge CM, Wickramasinghe NS, Ivanova MM, Dougherty SM: Resveratrol stimulates nitric oxide production by increasing estrogen receptor alpha-Src-caveolin-1 interaction and phosphorylation in human umbilical vein endothelial cells. FASEB J. 2008, 22: 2185-2197. 10.1096/fj.07-103366.View ArticleGoogle Scholar
- Sacanella E, Vazquez-Agell M, Mena MP, Antunez E, Fernandez-Sola J, Nicolas JM, Lamuela-Raventos RM, Ros E, Estruch R: Down-regulation of adhesion molecules and other inflammatory biomarkers after moderate wine consumption in healthy women: a randomized trial. Am J Clin Nutr. 2007, 86: 1463-1469.Google Scholar
- Williamson G, Manach C: Bioavailability and bioefficacy of polyphenols in humans. II. Review of 93 intervention studies. Am J Clin Nutr. 2005, 81: 243S-255S.Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.