《食品化学》课程教学资源（文献资料）Polyphenol：food sources and bioavailability

Polyphenols:food sources and bioavailability12 Claudine Manach,Augustin Scalbert.Christine Morand.Christian Remesy,and Liliana Jimenez are abundant micronutrients in our diet and evidence es such as existing polyphenols are likely to prov ide the greatest protecti endon the amount and on their bioava ability.In.the nature and of the various poly tion of these compounds in our diet.Such knowledge will allow between the inta of these substances and the risk of develop rption and the influence of chemical structure (eg glycosyla- ively metabolized he d by h he inte in the catabolism of polyphe nols and the roduction of s ome active arget r the various polyphe s are co n the metabolism boeipopeiesorthe TYPES AND DISTRIBUTION OF POLYPHENOLS IN FOODS discus Final dan ups on arom atic rings) severa on Feb 粉 of the hundre generally involved in defense against ultraviolet radiationo that they fh structura that bind th 15.2012 ure 1 The ability flavonoids,which ng of 2 ar that form an o ated hete cle (r INTRODUCTION es as a function of the type of heteroc nce inour diet,an one another. tive stress s.such as cancer r and cular and neurodegen d C.Remes From the Inite des maladies metal ach rch.Pa elle.France found in many ddres ite d tivity of a reprin In th 6312c nra fr biological actions that are as yet poorly understood. :727-47.Printed in USA.004 American Society for Clinical Nutrition 727

Polyphenols: food sources and bioavailability1,2 Claudine Manach, Augustin Scalbert, Christine Morand, Christian Rémésy, and Liliana Jime´nez ABSTRACT Polyphenols are abundant micronutrients in our diet, and evidence for their role in the prevention of degenerative diseases such as cancer and cardiovascular diseases is emerging. The health effects of polyphenols depend on the amount consumed and on their bioavail￾ability. In this article, the nature and contents of the various poly￾phenols present in food sources and the influence of agricultural practices and industrial processes are reviewed. Estimates of dietary intakes are given for each class of polyphenols. The bioavailability of polyphenols is also reviewed, with particular focus on intestinal absorption and the influence of chemical structure (eg, glycosyla￾tion, esterification, and polymerization), food matrix, and excretion back into the intestinal lumen. Information on the role of microflora in the catabolism of polyphenols and the production of some active metabolites is presented. Mechanisms of intestinal and hepatic con￾jugation (methylation, glucuronidation, sulfation), plasma transport, and elimination in bile and urine are also described. Pharmacokinetic data for the various polyphenols are compared. Studies on the iden￾tification of circulating metabolites, cellular uptake, intracellular metabolism with possible deconjugation, biological properties of the conjugated metabolites, and specific accumulation in some target tissues are discussed. Finally, bioavailability appears to differ greatly between the various polyphenols, and the most abundant polyphenols in our diet are not necessarily those that have the best bioavailability profile. A thorough knowledge of the bioavailability of the hundreds of dietary polyphenols will help us to identify those that are most likely to exert protective health effects. Am J Clin Nutr 2004;79:727–47. KEY WORDS Polyphenols, flavonoids, phenolic acids, food sources, dietary intake, intestinal absorption, metabolism, bioavail￾ability INTRODUCTION Over the past 10 y, researchers and food manufacturers have become increasingly interested in polyphenols. The chief reason for this interest is the recognition of the antioxidant properties of polyphenols, their great abundance in our diet, and their probable role in the prevention of various diseases associated with oxida￾tive stress, such as cancer and cardiovascular and neurodegen￾erative diseases (Scalbert A, Manach C, Morand C, Rémésy C, Jime´nez L. Crit Rev Food Sci Nutr, in press). Furthermore, poly￾phenols, which constitute the active substances found in many medicinal plants, modulate the activity of a wide range of en￾zymes and cell receptors (1). In this way, in addition to having antioxidant properties, polyphenols have several other specific biological actions that are as yet poorly understood. Two aims of research are to establish evidence for the effects of polyphenol consumption on health and to identify which of the hundreds of existing polyphenols are likely to provide the greatest protection in the context of preventive nutrition. If these objectives are to be attained, it is first essential to determine the nature and distribu￾tion of these compounds in our diet. Such knowledge will allow evaluation of polyphenol intake and enable epidemiologic anal￾ysis that will in turn provide an understanding of the relation between the intake of these substances and the risk of develop￾ment of several diseases. Furthermore, not all polyphenols are absorbed with equal efficacy. They are extensively metabolized by intestinal and hepatic enzymes and by the intestinal micro￾flora. Knowledge of the bioavailability and metabolism of the various polyphenols is necessary to evaluate their biological activity within target tissues. The types and distribution of poly￾phenols in foods and the bioavailability of polyphenols are the topics of the present review. TYPES AND DISTRIBUTION OF POLYPHENOLS IN FOODS Several thousand molecules having a polyphenol structure (ie, several hydroxyl groups on aromatic rings) have been identified in higher plants, and several hundred are found in edible plants. These molecules are secondary metabolites of plants and are generally involved in defense against ultraviolet radiation or aggression by pathogens. These compounds may be classified into different groups as a function of the number of phenol rings that they contain and of the structural elements that bind these rings to one another. Distinctions are thus made between the phenolic acids, flavonoids, stilbenes, and lignans (Figure 1). The flavonoids, which share a common structure consisting of 2 ar￾omatic rings (A and B) that are bound together by 3 carbon atoms that form an oxygenated heterocycle (ring C), may themselves be divided into 6 subclasses as a function of the type of heterocycle involved: flavonols, flavones, isoflavones, flavanones, antho￾cyanidins, and flavanols (catechins and proanthocyanidins) (Figure 2). In addition to this diversity, polyphenols may be associated with various carbohydrates and organic acids and with one another. 1 From the Unité des Maladies Métaboliques et Micronutriments, INRA, Saint-Genès Champanelle, France (CM, AS, CM, and CR), and Danone Vitapole Research, Palaiseau cedex, France (LJ). 2 Address reprint requests to C Manach, Unité des Maladies Métaboliques et Micronutriments, INRA, 63122 Saint-Genès Champanelle, France. E￾mail: manach@clermont.inra.fr. Received June 3, 2003. Accepted for publication October 17, 2003. Am J Clin Nutr 2004;79:727–47. Printed in USA. © 2004 American Society for Clinical Nutrition 727 by guest on February 15, 2012 www.ajcn.org Downloaded from

728 MANACH ET AL Hydroxybenzoic acids Hydroxycinnamic acids "o R:及8eos 骨 及 尽：传oegm Flavonoids Isoflavones See Flpure 2 。 Stilbenes Lignans R:6:0aee Anthocyanidins R FIGURE 1.Chemical sture of polyphenos. Phenolic acids 及R:8t8 The hvdroxy zoic acid content of edible plants with milligrams Feb allic aci t such asst asp Y15.2012 FIGURE 2.Chemical structures of flavonoids. and are no rations ge rease during the course of ripening but crease as the ftutincrcascsintC ids are r rely found in the free undergone free acid.Catfeircandquimic cid combine to form chlorogenic aci a singl contain 70-350m nic acid and bran is the mn ofpolyphenols(3 loat f tely th the total hydroxycinnamic acid content of most fruit.Hydroxy- acid wheat rn() hough the hihest Cfceteaidclecndnereasandomtidencturs I pa

Phenolic acids Two classes of phenolic acids can be distinguished: deriva￾tives of benzoic acid and derivatives of cinnamic acid (Figure 1). The hydroxybenzoic acid content of edible plants is generally very low, with the exception of certain red fruits, black radish, and onions, which can have concentrations of several tens of milligrams per kilogram fresh weight (2). Tea is an important source of gallic acid: tea leaves may contain up to 4.5 g/kg fresh wt (3). Furthermore, hydroxybenzoic acids are components of complex structures such as hydrolyzable tannins (gallotannins in mangoes and ellagitannins in red fruit such as strawberries, rasp￾berries, and blackberries) (4). Because these hydroxybenzoic acids, both free and esterified, are found in only a few plants eaten by humans, they have not been extensively studied and are not currently considered to be of great nutritional interest. The hydroxycinnamic acids are more common than are the hydroxybenzoic acids and consist chiefly of p-coumaric, caffeic, ferulic, and sinapic acids. These acids are rarely found in the free form, except in processed food that has undergone freezing, sterilization, or fermentation. The bound forms are glycosylated derivatives or esters of quinic acid, shikimic acid, and tartaric acid. Caffeic and quinic acid combine to form chlorogenic acid, which is found in many types of fruit and in high concentrations in coffee: a single cup may contain 70–350 mg chlorogenic acid (5). The types of fruit having the highest content (blueberries, kiwis, plums, cherries, apples) contain 0.5–2 g hydroxycinnamic acids/kg fresh wt (Table 1) (6). Caffeic acid, both free and esterified, is generally the most abundant phenolic acid and represents between 75% and 100% of the total hydroxycinnamic acid content of most fruit. Hydroxy￾cinnamic acids are found in all parts of fruit, although the highest concentrations are seen in the outer parts of ripe fruit. Concen￾trations generally decrease during the course of ripening, but total quantities increase as the fruit increases in size. Ferulic acid is the most abundant phenolic acid found in cereal grains, which constitute its main dietary source. The ferulic acid content of wheat grain is
0.8–2 g/kg dry wt, which may rep￾resent up to 90% of total polyphenols (28, 29). Ferulic acid is found chiefly in the outer parts of the grain. The aleurone layer and the pericarp of wheat grain contain 98% of the total ferulic acid. The ferulic acid content of different wheat flours is thus directly related to levels of sieving, and bran is the main source of polyphenols (30). Rice and oat flours containapproximatelythe same quantity of phenolic acids as wheat flour (63 mg/kg), although the content in maize flour is about 3 times as high (2). Ferulic acid is found chiefly in the transform, which is esterified to arabinoxylans andhemicellulosesinthealeuroneandpericarp.Only10%offerulic acid is found in soluble free form in wheat bran (29). Several dimers of ferulic acid are also found in cereals and form bridge structures between chains of hemicellulose. FIGURE 1. Chemical structures of polyphenols. FIGURE 2. Chemical structures of flavonoids. 728 MANACH ET AL by guest on February 15, 2012 www.ajcn.org Downloaded from

POLYPHENOLS:FOOD SOURCES AND BIOAVAILABILITY 729 TABLE I s in food Polyphenol conten So urce (rving size) By wt or vol By serving mg/g fresh w (or mg/四 Bla lic acid amic acids (2.5-7) acid le (200 0g1 .oat (75 g) nidin ols (1) 200g t(200g 老 200e20g on February 15.2012 es1-l2,14,18) 22-25) Tof (00 08 5.1.,.**1971.3 00E

TABLE 1 Polyphenols in foods Source (serving size) Polyphenol content By wt or vol By serving mg/kg fresh wt (or mg/L) mg/serving Hydroxybenzoic acids (2, 6) Blackberry (100 g) 80–270 8–27 Protocatechuic acid Raspberry (100 g) 60–100 6–10 Gallic acid Black currant (100 g) 40–130 4–13 p-Hydroxybenzoic acid Strawberry (200 g) 20–90 4–18 Hydroxycinnamic acids (2, 5–7) Blueberry (100 g) 2000–2200 200–220 Caffeic acid Kiwi (100 g) 600–1000 60–100 Chlorogenic acid Cherry (200 g) 180–1150 36–230 Coumaric acid Plum (200 g) 140–1150 28–230 Ferulic acid Aubergine (200 g) 600–660 120–132 Sinapic acid Apple (200 g) 50–600 10–120 Pear (200 g) 15–600 3–120 Chicory (200 g) 200–500 40–100 Artichoke (100 g) 450 45 Potato (200 g) 100–190 20–38 Corn flour (75 g) 310 23 Flour: wheat, rice, oat (75 g) 70–90 5–7 Cider (200 mL) 10–500 2–100 Coffee (200 mL) 350–1750 70–350 Anthocyanins (8–10) Aubergine (200 g) 7500 1500 Cyanidin Blackberry (100 g) 1000–4000 100–400 Pelargonidin Black currant (100 g) 1300–4000 130–400 Peonidin Blueberry (100 g) 250–5000 25–500 Delphinidin Black grape (200 g) 300–7500 60–1500 Malvidin Cherry (200 g) 350–4500 70–900 Rhubarb (100 g) 2000 200 Strawberry (200 g) 150–750 30–150 Red wine (100 mL) 200–350 20–35 Plum (200 g) 20–250 4–50 Red cabbage (200 g) 250 50 Flavonols (11–18) Yellow onion (100 g) 350–1200 35–120 Quercetin Curly kale (200 g) 300–600 60–120 Kaempferol Leek (200 g) 30–225 6–45 Myricetin Cherry tomato (200 g) 15–200 3–40 Broccoli (200 g) 40–100 8–20 Blueberry (100 g) 30–160 3–16 Black currant (100 g) 30–70 3–7 Apricot (200 g) 25–50 5–10 Apple (200 g) 20–40 4–8 Beans, green or white (200 g) 10–50 2–10 Black grape (200 g) 15–40 3–8 Tomato (200 g) 2–15 0.4–3.0 Black tea infusion (200 mL) 30–45 6–9 Green tea infusion (200 mL) 20–35 4–7 Red wine (100 mL) 2–30 0.2–3 Flavones (11–12, 14, 18) Parsley (5 g) 240–1850 1.2–9.2 Apigenin Celery (200 g) 20–140 4–28 Luteolin Capsicum pepper (100 g) 5–10 0.5–1 Flavanones (19–21) Orange juice (200 mL) 215–685 40–140 Hesperetin Grapefruit juice (200 mL) 100–650 20–130 Naringenin Lemon juice (200 mL) 50–300 10–60 Eriodictyol Isoflavones (22–25) Soy flour (75 g) 800–1800 60–135 Daidzein Soybeans, boiled (200 g) 200–900 40–180 Genistein Miso (100 g) 250–900 25–90 Glycitein Tofu (100 g) 80–700 8–70 Tempeh (100 g) 430–530 43–53 Soy milk (200 mL) 30–175 6–35 Monomeric flavanols (6, 17, 26, 27) Chocolate (50 g) 460–610 23–30 Catechin Beans (200 g) 350–550 70–110 Epicatechin Apricot (200 g) 100–250 20–50 Cherry (200 g) 50–220 10–44 Grape (200 g) 30–175 6–35 Peach (200 g) 50–140 10–28 Blackberry (100 g) 130 13 Apple (200 g) 20–120 4–24 Green tea (200 mL) 100–800 20–160 Black tea (200 mL) 60–500 12–100 Red wine (100 mL) 80–300 8–30 Cider (200 mL) 40 8 POLYPHENOLS: FOOD SOURCES AND BIOAVAILABILITY 729 by guest on February 15, 2012 www.ajcn.org Downloaded from

代 MANACH ET AL flavonoids ids content of its man ively low concentrations gfresh wt.and contains between sugar moiety is very often seor rhamnose,but other sugars (catechins)and the may also s of fruit (a re th 6)Thes flay nols accumulate in the outer Table 1).The mg/L. s)becau se their biosynthesis is far the riches me ee and even between dif 381 ta gre zed during heating)of tea leaves to mor expo the cabbage,the glycoside concentrati nis≥l0 times as high n the green outer leaves as in the i ne olored lea ves(14).This atechin epiga cherry tomatoes than of use they have and more im ard ton ain see(7.39) st to other lasses of flav onoids,flavanol are n d to hea 15%ofh The only important edible ances are es of flavones ident vater at pH 5(40) The are dimer oligomers andp mers of catechins that are contain C 32-341 skin of citrus fruit conta arge qu tities of polvme d the mean degre of om dto 4 the for are the most hydrophobic natic plant an and uch as mint but ent in high tea The main agly cho centrations only in citrusfruit nes are naringe nin ingrap ando anpea hen th hes ripene this change has e ge impartsa bitter taste been whic s flavo unts for the apparent redu tion in tannin content that is com a single glass of ora dins are as rating th ery high flav tent, whol olar sap ofthe with struc b 9)7 7 and are not rms,both according to pH. cule. This c a ht H at a likely to d Degra and ester ids (citric products are the main lic acids In addition, citein. a concer are -0-glucosio OL d in red win malonylgluc side derivatives have unpleas and ishes).but they are most abundant in fruit Cvanidin is the most

Flavonoids Flavonols are the most ubiquitous flavonoids in foods, and the main representatives are quercetin and kaempferol. They are generally present at relatively low concentrations of
15– 30 mg/kg fresh wt. The richest sources are onions (up to 1.2 g/kg fresh wt), curly kale, leeks, broccoli, and blueberries (Table 1). Red wine and tea also contain up to 45 mg flavonols/L. These compounds are present in glycosylated forms. The associated sugar moiety is very often glucose or rhamnose, but other sugars may also be involved (eg, galactose, arabinose, xylose, glucu￾ronic acid). Fruit often contains between 5 and 10 different fla￾vonol glycosides (6). These flavonols accumulate in the outer and aerial tissues (skin and leaves) because their biosynthesis is stimulated by light. Marked differences in concentration exist between pieces of fruit on the same tree and even between dif￾ferent sides of a single piece of fruit, depending on exposure to sunlight (31). Similarly, in leafy vegetables such as lettuce and cabbage, the glycoside concentration is 10 times as high in the green outer leaves as in the inner light-colored leaves (14). This phenomenon also accounts for the higher flavonol content of cherry tomatoes than of standard tomatoes, because they have different proportions of skin to whole fruit. Flavones are much less common than flavonols in fruit and vegetables. Flavones consist chiefly of glycosides of luteolin and apigenin. The only important edible sources of flavones identi￾fied to date are parsley and celery (Table 1). Cereals such as millet and wheat contain C-glycosides of flavones (32–34). The skin of citrus fruit contains large quantities of polymethoxylated flavones: tangeretin, nobiletin, and sinensetin (up to 6.5 g/L of essential oil of mandarin) (2). These polymethoxylated flavones are the most hydrophobic flavonoids. In human foods, flavanones are found in tomatoes and certain aromatic plants such as mint, but they are present in high con￾centrations only in citrus fruit. The main aglycones are naringe￾nin in grapefruit, hesperetin in oranges, and eriodictyol in lem￾ons. Flavanones are generally glycosylated by a disaccharide at position 7: either a neohesperidose, which imparts a bitter taste (such as to naringin in grapefruit), or a rutinose, which is flavor￾less. Orange juice contains between 200 and 600 mg hesperi￾din/L and 15–85 mg narirutin/L, and a single glass of orange juice may contain between 40 and 140 mg flavanone glycosides (20). Because the solid parts of citrus fruit, particularly the albedo (the white spongy portion) and the membranes separating the segments, have a very high flavanone content, the whole fruit may contain up to 5 times as much as a glass of orange juice. Isoflavones are flavonoids with structural similarities to estro￾gens. Although they are not steroids, they have hydroxyl groups in positions 7 and 4' in a configuration analogous to that of the hy￾droxyls in the estradiol molecule. This confers pseudohormonal properties on them, including the ability to bind to estrogen recep￾tors, and they are consequently classified as phytoestrogens. Isofla￾vones are found almost exclusively in leguminous plants. Soya and its processed products are the main source of isoflavones in the humandiet.Theycontain3mainmolecules:genistein,daidzein,and glycitein, generally in a concentration ratio of 1:1:0.2. These isofla￾vones are found in 4 forms: aglycone, 7-O-glucoside, 6
-O-acetyl- 7-O-glucoside, and 6
-O-malonyl-7-O-glucoside (35). The 6
-O￾malonylglucoside derivatives have an unpleasant, bitter, and astringent taste. They are sensitive to heat and are often hydrolyzed to glycosides during the course of industrial processing, as in the production of soya milk (36). The fermentation carried out during the manufacturing of certain foods, such as miso and tempeh, results in the hydrolysis of glycosides to aglycones. The aglycones are highly resistant to heat. The isoflavone content of soya and its man￾ufactured products varies greatly as a function of geographic zone, growing conditions, and processing. Soybeans contain between 580 and3800mgisoflavones/kgfreshwt,andsoymilkcontainsbetween 30 and 175 mg/L (25, 37). Flavanols exist in both the monomer form (catechins) and the polymer form (proanthocyanidins). Catechins are found in many types of fruit (apricots, which contain 250 mg/kg fresh wt, are the richest source; Table 1). They are also present in red wine (up to 300 mg/L), but green tea and chocolate are by far the richest sources. An infusion of green tea contains up to 200 mg catechins (38). Black tea contains fewer monomer flavanols, which are oxidized during “fermentation” (heating) of tea leaves to more complex condensed polyphenols known as theaflavins (dimers) and thearubigins (polymers). Catechin and epicatechin are the main flavanols in fruit, whereas gallocatechin, epigallocatechin, and epigallocatechin gallate are found in certain seeds of legu￾minous plants, in grapes, and more importantly in tea (27, 39). In contrast to other classes of flavonoids, flavanols are not glyco￾sylated in foods. The tea epicatechins are remarkably stable when exposed to heat as long as the pH is acidic: only
15% of these substances are degraded after 7 h in boiling water at pH 5 (40). Proanthocyanidins, which are also known as condensed tan￾nins, are dimers, oligomers, and polymers of catechins that are bound together by links between C4 and C8 (or C6). Their mean degree of polymerization in foods has rarely been determined. In cider apples, the mean degree of polymerization ranges from 4 to 11 (41). Through the formation of complexes with salivary pro￾teins, condensed tannins are responsible for the astringent char￾acter of fruit (grapes, peaches, kakis, apples, pears, berries, etc) and beverages (wine, cider, tea, beer, etc) and for the bitterness of choc￾olate (42). This astringency changes over the course of maturation andoftendisappearswhenthefruitreachesripeness;thischangehas been well explained in the kaki fruit by polymerization reactions with acetaldehyde (43). Such polymerization of tannins probably accounts for the apparent reduction in tannin content that is com￾monly seen during the ripening of many types of fruit. It is difficult to estimate the proanthocyanidin content of foods because proan￾thocyanidinshaveawiderangeofstructuresandmolecularweights. The only available data concern dimers and trimers, which are as abundant as the catechins themselves (26). Anthocyanins are pigments dissolved in the vacuolar sap of the epidermal tissues of flowers and fruit, to which they impart a pink, red, blue, or purple color (9). They exist in different chem￾ical forms, both colored and uncolored, according to pH. Al￾though they are highly unstable in the aglycone form (anthocya￾nidins), while they are in plants, they are resistant to light, pH, and oxidation conditions that are likely to degrade them. Degra￾dation is prevented by glycosylation, generally with a glucose at position 3, and esterification with various organic acids (citric and malic acids) and phenolic acids. In addition, anthocyanins are stabilized by the formation of complexes with other fla￾vonoids (copigmentation). In the human diet, anthocyanins are found in red wine, certain varieties of cereals, and certain leafy and root vegetables (aubergines, cabbage, beans, onions, rad￾ishes), but they are most abundant in fruit. Cyanidin is the most common anthocyanidin in foods. Food contents are generally proportional to color intensity and reach values up to 2–4 g/kg 730 MANACH ET AL by guest on February 15, 2012 www.ajcn.org Downloaded from

POLYPHENOLS:FOOD SOURCES AND BIOAVAILABILITY 731 fresh wt in blackberries (Table 1).These values wt and dge is often lim ted toone ora few varieties into various complex structures as the wine ages(10,44). particularly some exotic types of fruit and some Lignans include ripeness at the time of harvest.environmental factors. 2phenylpropane units(Figure 1).The e he hol(udry )f in lin s or f 109 1000 times as high as cctabolized to enteroiotand food tagcT degree s conside ncentra tions a our ing anin conc measured inplasmaandurine.Thus,thereare undou he though very few studies directly addressed this issue the poly without stress,such as those grown in conventional or hydro ables (garlic.asparagus.carrots).and fruit (ears.prunes) as minor sources. in theh tica nic effects hav own during oI m in s and which has were 03 ightorcli ate (54) 图 use resverat e Oxidation ctio sult in the tion of more o hanges in the qu with black tea)or harful 15200a VARIABILITY OF POLYPHENOL CONTENT OF FOODS nolic acids in qualitative terms,bu ons.)whe eas 58.A125 results ir a ep nidin B2 namy.chboogsaaxdandmlgnttesooherhndo vegetable cant portion of p ts tha in th may also h The polyp I pro frying(18).Steam cooking of vege les,wh havoids leac

fresh wt in blackcurrants or blackberries (Table 1). These values increase as the fruit ripens. Anthocyanins are found mainly in the skin, except for certain types of red fruit, in which they also occur in the flesh (cherries and strawberries). Wine contains
200– 350 mg anthocyanins/L, and these anthocyanins are transformed into various complex structures as the wine ages (10, 44). Lignans Lignans are formed of 2 phenylpropane units (Figure 1). The richest dietary source is linseed, which contains secoisolaricir￾esinol (up to 3.7 g/kg dry wt) and low quantities of matairesinol. Other cereals, grains, fruit, and certain vegetables also contain traces of these same lignans, but concentrations in linseed are
1000 times as high as concentrations in these other food sources (45). Lignans are metabolized to enterodiol and en￾terolactone by the intestinal microflora. The low quantities of secoisolariciresinol and matairesinol that are ingested as part of our normal diet do not account for the concentrations of the metabolites enterodiol and enterolactone that are classically measured in plasma and urine. Thus, there are undoubtedly other lignans of plant origin that are precursors of enterodiol and en￾terolactone and that have not yet been identified (46). Thompson et al (47) used an in vitro technique involving the fermentation of foods by human colonic microflora to quantitatively evaluate precursors of enterodiol and enterolactone. They confirmed that oleaginous seeds (linseed) are the richest source and identified algae, leguminous plants (lentils), cereals (triticale and wheat), vegetables (garlic, asparagus, carrots), and fruit (pears, prunes) as minor sources. Stilbenes Stilbenes are found in only low quantities in the human diet. One of these, resveratrol, for which anticarcinogenic effects have been shown during screening of medicinal plants and which has been extensively studied, is found in low quantities in wine (0.3–7 mg aglycones/L and 15 mg glycosides/L in red wine) (48–50). However, because resveratrol is found in such small quantities in the diet, any protective effect of this molecule is unlikely at normal nutritional intakes. VARIABILITY OF POLYPHENOL CONTENT OF FOODS Fruit and beverages such as tea and red wine constitute the main sources of polyphenols. Certain polyphenols such as quer￾cetin are found in all plant products (fruit, vegetables, cereals, leguminous plants, fruit juices, tea, wine, infusions, etc), whereas others are specific to particular foods (flavanones in citrus fruit, isoflavones in soya, phloridzin in apples). In most cases, foods contain complex mixtures of polyphenols, which are often poorly characterized. Apples, for example, contain flavanol monomers (epicatechin mainly) or oligomers (procyanidin B2 mainly), chlorogenic acid and small quantities of other hydroxy￾cinnamic acids, 2 glycosides of phloretin, several quercetin gly￾cosides, and anthocyanins such as cyanidin 3-galactoside in the skin of certain red varieties. Apples are one of the rare types of food for which fairly precise data on polyphenol composition are available. Differences in polyphenol composition between vari￾eties of apples have notably been studied. The polyphenol pro￾files of all varieties of apples are practically identical, but con￾centrations may range from 0.1 to 5 g total polyphenols/kg fresh wt and may be as high as 10 g/kg in certain varieties of cider apples (41, 51). For many plant products, the polyphenol composition is much less known, knowledge is often limited to one or a few varieties, and data sometimes do not concern the edible parts. Some foods, particularly some exotic types of fruit and some cereals, have not been analyzed yet. Furthermore, numerous factors other than variety may affect the polyphenol content of plants; these factors include ripeness at the time of harvest, environmental factors, processing, and storage. Environmental factors have a major effect on polyphenol con￾tent. These factors may be pedoclimatic (soil type, sun exposure, rainfall) or agronomic (culture in greenhouses or fields, biolog￾ical culture, hydroponic culture, fruit yield per tree, etc). Expo￾sure to light has a considerable effect on most flavonoids. The degree of ripeness considerably affects the concentrations and proportions of the various polyphenols (6). In general, phenolic acid concentrations decrease during ripening, whereas anthocy￾anin concentrations increase. Many polyphenols, especially phe￾nolic acids, are directly involved in the response of plants to different types of stress: they contribute to healing by lignifica￾tion of damaged areas, they possess antimicrobial properties, and their concentrations may increase after infection (2, 6, 52). Al￾though very few studies directly addressed this issue, the poly￾phenol content of vegetables produced by organic or sustainable agriculture is certainly higher than that of vegetables grown without stress, such as those grown in conventional or hydro￾ponic conditions. This was shown recently in strawberries, blackberries, and corn (53). With the current state of knowledge, it is extremely difficult to determine for each family of plant products the key variables that are responsible for the variability in the content of each polyphenol and the relative weight of those variables. A huge amount of analysis would be required to obtain this information. For example, determination of the p-coumaric acid content of 500 red wines showed that genetic factors were more important than was exposure to light or climate (54). Storage may also affect the content of polyphenols that are easily oxidized. Oxidation reactions result in the formation of more or less polymerized substances, which lead to changes in the quality of foods, particularly in color and organoleptic characteristics. Such changes may be beneficial (as is the case with black tea) or harmful (browningoffruit)toconsumeracceptability.Storageofwheatflour results in marked loss of phenolic acids (28). After 6 mo of storage, flours contained the same phenolic acids in qualitative terms, but their concentrations were 70% lower. Cold storage, in contrast, did not affect the content of polyphenols in apples (55, 56), pears (57), or onions (58). At 25 °C, storage of apple juice for 9 mo results in a 60% loss of quercetin and a total loss of procyanidins, despite the fact that polyphenols are more stable in fruit juices than is vita￾min C (59, 60). Methods of culinary preparation also have a marked effect on the polyphenol content of foods. For example, simple peeling of fruit and vegetables can eliminate a significant portion of poly￾phenols because these substances are often present in higher concentrations in the outer parts than in the inner parts. Cooking may also have a major effect. Onions and tomatoes lose between 75% and 80% of their initial quercetin content after boiling for 15 min, 65% after cooking in a microwave oven, and 30% after frying (18). Steam cooking of vegetables, which avoids leaching, is preferable. Potatoes contain up to 190 mg chlorogenic acid/kg, mainly in the skin (61). Extensive loss occurs during cooking, POLYPHENOLS: FOOD SOURCES AND BIOAVAILABILITY 731 by guest on February 15, 2012 www.ajcn.org Downloaded from

732 MANACH ET AL fruit is practically the sole source of flavanones.in stion of nol content As with fruit peeling.dehulling of legume als can res in a loss of som don average.although sult of cellular dec on and co etween cythe of soya in the Asian counries. 00m22327374 Europeans,soya consumeony a fewmilligramsof This kin sper day.Neverth s,the i nt corporation of e in isoflavone intake.Women unde ing pet oes have low flavonoid content.The pectinolytic enzymes used dur- extract capsules(75). the main sources are apple gra and red wine(76) (63)and is also higher than that(64) apples,and pears(27) sted (42)but there are still no rence food-composition tables (as theyxs partial data and hins,and s0 ished on as much as 500- pilations(37,65).Sir e March2003.a database i n w hich the also eat small quantities of fruit and veg ables do not inge d contents mg/d(54).AGerman e aily co culture website (66).A co eive table ipa of 599 ofp-coumaric acid)(65). 图 V15. in the 90 ntile 2014 DIETARY INTAKE OF POLYPHENOLS sumed up to 100mg/d(6).The main reason for thes d as the ined t the consumption the total i976Khnu()caouaiedthadicat oid intake ake.Ifm an values are diheahonothemakesoi and davano and and 459 Although these figures were 150 to which must be de he nins and nth nidins Finally the total no more precise ning the intake nt e probab com nly rea es I g/d in people w d in the United Sta mean value was 35(0).The intake of flavanones is similar useful.A few studies have tried to correlate flavonol.flavanone

and no remaining phenolic acids were found in French fries or freeze-dried mashed potatoes (54). Industrial food processing also affects polyphenol content. As with fruit peeling, dehulling of legume seeds and decortication and bolting of cereals can result in a loss of some polyphenols. Grinding of plant tissues may lead to oxidative degradation of polyphenols as a result of cellular decompartmentation and con￾tact between cytoplasmic polyphenol oxidase and phenolic sub￾strates present in the vacuoles. Polyphenols are then transformed into brown pigments that are polymerized to different degrees. This unwanted process can occur, for example, during the pro￾cess of making jam or compote from fruit. Production of fruit juice often involves clarification or stabilization steps specifi￾cally aimed at removing certain flavonoids responsible for dis￾coloration and haze formation. Manufactured fruit juices thus have low flavonoid content. The pectinolytic enzymes used dur￾ing such processing also hydrolyze the esters of hydroxycin￾namic acid (62). Conversely, maceration operations facilitate diffusion of polyphenols in juice, as occurs during vinification of red wine. This maceration accounts for the fact that the polyphe￾nol content of red wines is 10 times as high as that of white wines (63) and is also higher than that of grape juice (64). Because of the wide range of existing polyphenols and the considerable number of factors that can modify their concentra￾tion in foods, no reference food-composition tables (as they exist for other micronutrients such as vitamins) have yet been drawn up. Only partial data for certain polyphenols, such as flavonols and flavones, catechins, and isoflavones, have been published on the basis of direct food analysis (11, 27) or bibliographic com￾pilations (37, 65). Since March 2003, a database in which the flavonoid contents of 225 selected foods were compiled from 97 bibliographic sources has been available on the US Department of Agriculture website (66). A comprehensive composition table for polyphenols is essential; it should allow daily polyphenol consumption to be calculated from dietary questionnaires. Poly￾phenol intake could then be correlated with the incidence of certain diseases or early markers for these diseases in epidemi￾ologic studies, which would permit investigations of the protec￾tive role of these micronutrients. DIETARY INTAKE OF POLYPHENOLS Only partial information is available on the quantities of poly￾phenols that are consumed daily throughout the world. These data have been obtained through analysis of the main aglycones (after hydrolysis of their glycosides and esters) in the foods most widely consumed by humans. In 1976 Kuhnau (8) calculated that dietary flavonoid intake in the United States was
1 g/d and consisted of the following: 16% flavonols, flavones, and flavanones; 17% anthocyanins; 20% catechins; and 45% “biflavones.” Although these figures were obtained under poorly detailed conditions, they continue to serve as reference data. Certain studies have subsequently provided more precise individual data concerning the intake of various classes of polyphenols. Flavonols have been more extensively studied. Consumption of these substances has been estimated at
20–25 mg/d in the United States, Denmark, and Holland (67– 69). In Italy, consumption ranged from 5 to 125 mg/d, and the mean value was 35 mg/d (70). The intake of flavanones is similar to or possibly higher than that of flavonols, with a mean con￾sumption of 28.3 mg hesperetin/d in Finland (71). Because citrus fruit is practically the sole source of flavanones, ingestion of these substances is probably greater in regions where these fruits are produced, such as southern Europe. Anthocyanin consump￾tion was studied only in Finland, where high amounts of berries are eaten, and was found to be 82 mg/d on average, although some intakes exceeded 200 mg/d (72). Consumption of soya in the Asian countries is
10–35 g/d, which is equivalent to a mean intake of 25–40 mg isoflavones/d, with a maximum intake of 100 mg/d (23, 73, 74). Americans and Europeans, who eat little soya, consume only a few milligrams of isoflavones per day. Nevertheless, the incorporation of growing quantities of soya extracts into manufactured food products could result in an increase in isoflavone intake. Women under￾going phytoestrogen replacement therapy for menopause con￾sume between 30 and 70 mg isoflavones/d in the form of soya extract capsules (75). In Spain the total consumption of catechins and proanthocya￾nidin dimers and trimers has been estimated at 18–31 mg/d, and the main sources are apples, pears, grapes, and red wine (76). Consumption of monomer flavonols in Holland is significantly higher (50 mg/d), and the principal sources are tea, chocolate, apples, and pears (27). Ingestion of more highly polymerized proanthocyanidins could be as high as several hundred milli￾grams per day as previously suggested (42), but there are still no reliable data. Consumption of hydroxycinnamic acids may vary highly ac￾cording to coffee consumption. Some persons who drink several cups per day may ingest as much as 500–800 mg hydroxycin￾namic acids/d, whereas subjects who do not drink coffee and who also eat small quantities of fruit and vegetables do not ingest 25 mg/d (54). A German study estimated daily consumption of hydroxycinnamic acids and hydroxybenzoic acids at 211 and 11 mg/d, respectively. Caffeic acid intake alone was 206 mg/d, and the principal sources were coffee (which provides 92% of caffeic acid) and fruit and fruit juices combined (source of 59% of p-coumaric acid) (65). Various authors have noted a high variability in polyphenol intake. Intake of phenolic acids ranged from 6 to 987 mg/d in Germany (65). The mean consumption of flavonols and flavones in the Dutch population was 23 mg/d; values at the 10th and 90th percentiles were 4 and 46 mg/d, respectively; and some subjects consumed up to 100 mg/d (69). The main reason for these vari￾ations is individual food preferences. When polyphenol content is expressed as the amount provided by a food serving, as in Table 1, the consumption of one particular food, such as berries for anthocyanins or coffee for hydroxycinnamic acids, clearly ap￾pears to be capable of markedly changing the total polyphenol intake. If mean values are required, the addition of the intakes of flavonols, flavanones, flavanols (monomers, dimers, and tri￾mers), and isoflavones gives a total daily consumption of 100– 150 mg in Western populations, to which must be added the considerably variable intake of hydroxycinnamic acids, antho￾cyanins, and proanthocyanidins. Finally, the total polyphenol intake probably commonly reaches 1 g/d in people who eat sev￾eral servings of fruit and vegetables per day. Note that it is really difficult to follow a diet totally free of polyphenols. Because polyphenol intake is difficult to evaluate by using dietary ques￾tionnaires, biomarkers for polyphenol exposure would be very useful. A few studies have tried to correlate flavonol, flavanone, and isoflavone intakes with plasma concentrations or urinary excretion of metabolites (77–82), but we are not yet able to 732 MANACH ET AL by guest on February 15, 2012 www.ajcn.org Downloaded from

POLYPHENOLS:FOOD SOURCES AND BIOAVAILABILITY 733 me that the long-term intake of the various polyphenols BIOAVAILABILITY OF POLYPHENOLS It is important to realize that the polyphenols that are the most s questio tivityor because they are poorly absorbed from the intestine because ofa smaller exchange areaand a lower density of trans port systems.as ageneral geosidcsTmisthsbendleatyhonnnar ercetin of the bioavailability of glycos ab tial if their nd e 01 health effects are to be under 00d quantity of rutin( 3B-ruti form o than after ing on of ap the colonic microffora ore they can be ab orption oc rs in the small intest and the that i leSecsgndprodiurcS5wernoussimplearomatrcacid cetin ab orption has been partly cidated.Hollman et al su This is methylation, could then be inside the cells that restricts their potential agluc the aglycones are gen nt in the brush border (9).Both enz are r nvolyed bu on for the various d de nols are olic R.ol s certainly absorbec ey are m inchydrolasc,atlfS st in hydrolys 粉 tigated.Polyph nd the vatives are e 81 namofdcgt vlati the ypre the are subiected to the nila on of This enterohepatic recvcling may lead to a onger presence of B-gluc polyphenols within the body. cone sent in fermented Intestinal absorption and metabolisn du wn to be bette Much about the intestinal mechanisms of the gastrointestinal matr x effect may exp absorption pure but ane carriers that ld be involved in ministered orally to healthy that has he d f rable transpor mechanism involved in cin- 294 54 52 and 4.95 h/mL for daid n foods all fla e found in e ingestion than aft stomach showed that c level is pos ble for cones in a soy drink dnot ch inge the bic bilit中yo in humans.but note that in of

propose a reliable measurement in urine or plasma samples that could reflect the long-term intake of the various polyphenols. BIOAVAILABILITY OF POLYPHENOLS It is important to realize that the polyphenols that are the most common in the human diet are not necessarily the most active within the body, either because they have a lower intrinsic ac￾tivity or because they are poorly absorbed from the intestine, highly metabolized, or rapidly eliminated. In addition, the me￾tabolites that are found in blood and target organs and that result from digestive or hepatic activity may differ from the native substances in terms of biological activity. Extensive knowledge of the bioavailability of polyphenols is thus essential if their health effects are to be understood. Metabolism of polyphenols occurs via a common pathway (83). The aglycones can be absorbed from the small intestine. However, most polyphenols are present in food in the form of esters, glycosides, or polymers that cannot be absorbed in their native form. These substances must be hydrolyzed by intestinal enzymes or by the colonic microflora before they can be ab￾sorbed. When the flora is involved, the efficiency of absorption is often reduced because the flora also degrades the aglycones that it releases and produces various simple aromatic acids in the process. During the course of absorption, polyphenols are con￾jugated in the small intestine and later in the liver. This process mainly includes methylation, sulfation, and glucuronidation. This is a metabolic detoxication process common to many xe￾nobiotics that restricts their potential toxic effects and facilitates their biliary and urinary elimination by increasing their hydro￾philicity. The conjugation mechanisms are highly efficient, and aglycones are generally either absent in blood or present in low concentrations after consumption of nutritional doses. Circulat￾ing polyphenols are conjugated derivatives that are extensively bound to albumin. Polyphenols are able to penetrate tissues, particularly those in which they are metabolized, but their ability to accumulate within specific target tissues needs to be further investigated. Polyphenols and their derivatives are eliminated chiefly in urine and bile. Polyphenols are secreted via the biliary route into the duodenum, where they are subjected to the action of bacterial enzymes, especially
-glucuronidase, in the distal segments of the intestine, after which they may be reabsorbed. This enterohepatic recycling may lead to a longer presence of polyphenols within the body. Intestinal absorption and metabolism Much about the intestinal mechanisms of the gastrointestinal absorption of polyphenols remains unknown. Most polyphenols are probably too hydrophilic to penetrate the gut wall by passive diffusion, but the membrane carriers that could be involved in polyphenol absorption have not been identified. To date, the unique active transport mechanism that has been described is a Na-dependent saturable transport mechanism involved in cin￾namic and ferulic acid absorption in the rat jejunum (84). In foods, all flavonoids except flavanols are found in glyco￾sylated forms, and glycosylation influences absorption. The fate of glycosides in the stomach is not clear. Experiments using surgically treated rats in which absorption was restricted to the stomach showed that absorption at the gastric level is possible for some flavonoids, such as quercetin and daidzein, but not for their glycosides (85, 86). Most of the glycosides probably resist acid hydrolysis in the stomach and thus arrive intact in the duodenum (87). Only aglycones and some glucosides can be absorbed in the small intestine, whereas polyphenols linked to a rhamnose moi￾ety must reach the colon and be hydrolyzed by rhamnosidases of the microflora before absorption (88, 89). The same probably applies to polyphenols linked to arabinose or xylose, although this question has not been specifically studied. Because absorp￾tion occurs less readily in the colon than in the small intestine because of a smaller exchange area and a lower density of trans￾port systems, as a general rule, glycosides with rhamnose are absorbed less rapidly and less efficiently than are aglycones and glucosides. This has been clearly shown in humans for quercetin glycosides: maximum absorption occurs 0.5–0.7 h after inges￾tion of quercetin 4'-glucoside and 6–9 h after ingestion of the same quantity of rutin (quercetin-3
-rutinoside). The bioavail￾ability of rutin is only 15–20% of that of quercetin 4'-glucoside (90, 91). Similarly, absorption of quercetin is more rapid and efficient after ingestion of onions, which are rich in glucosides, than after ingestion of apples containing both glucosides and various other glycosides (92). In the case of quercetin glucosides, absorption occurs in the small intestine, and the efficiency of absorption is higher than that for the aglycone itself (93, 94). The underlying mechanism by which glucosylation facilitates quer￾cetin absorption has been partly elucidated. Hollman et al sug￾gested that glucosides could be transported into enterocytes by the sodium-dependent glucose transporter SGLT1 (93). They could then be hydrolyzed inside the cells by a cytosolic
-glucosidase (95). Another pathway involves the lactase phlo￾ridzine hydrolase, a glucosidase of the brush border membrane of the small intestine that catalyzes extracellular hydrolysis of some glucosides, which is followed by diffusion of the aglycone across the brush border (96). Both enzymes are probably involved, but their relative contribution for the various glucosides remains to be clarified. Quercetin 3-glucoside, which is not a substrate for cytosolic
-glucosidase, is certainly absorbed after hydrolysis by lactase phloridzine hydrolase, at least in rats, whereas hydrolysis of quercetin 4'-glucoside seems to involve both pathways (97, 98). In humans, whatever the mechanism of deglucosylation, the kinetics of plasma concentrations are similar after ingestion of quercetin 3-glucoside or quercetin 4'-glucoside (99). Isoflavone glycosides present in soya products can also be deglycosylated by
-glucosidases from the human small intestine (95, 96). How￾ever, the effect of glucosylation on absorption is less clear for isoflavones than for quercetin. Aglycones present in fermented soya products were shown to be better absorbed than were the glucosides ingested from soybeans (100). However, a dose or matrix effect may explain the difference in absorption observed in this first study. Setchell et al (101) showed that when pure daidzein, genistein, or their corresponding 7-glucosides were administered orally to healthy volunteers, a tendency toward greater bioavailability was observed with the glucosides, as mea￾sured from the area under the curve of the plasma concentrations: 2.94, 4.54, 4.52, and 4.95 g · h/mL for daidzein, genistein, daidzin, and genistin, respectively. However, in another human study, peak plasma concentrations were markedly higher after aglycone ingestion than after glucoside ingestion, and this effect was observed with low or high single doses and after long-term intakes (102). In addition, hydrolysis of isoflavone glycosides into aglycones in a soy drink did not change the bioavailability of the isoflavones in humans (103). No data are available for other polyphenols in humans, but note that in rats, no enhancement of POLYPHENOLS: FOOD SOURCES AND BIOAVAILABILITY 733 by guest on February 15, 2012 www.ajcn.org Downloaded from

734 MANACH ET AL absorption was observed with gluco ylation of naringenin and compounds are rapidly absorbed from the small intestine and are nd.the me Glycosylation does not nuence the nature of the n nlan Intact glycosides of quercetin,daidzein, and mplex food (107-110).For fla- nts of acid (12-1).This has also been observed in rats (15,126 com pound noid gly ted by ed().Con of th may spec mechanismof 128).In patients who have undergone colonic ablatio was chlor doses leve have bee shown to be good ligands for this ompound a ir ing o n,an from mos ndition were 100-fold tho of the met lites s ol or acids the nlasm rtions were ma nents using single lavers of Caco-2 cells as a model of hich absoptioninthesmnalintcstm owedthtoattpn oge idin B2 is ver ed in rat free caffeic a d the procya 331s1 16 The poss tha k D a s and dimers in acidic ted by of coffee that nic acid ents However.pur only ofhe bound affeic .Thu a pos sible explan of polyme ation in th of administration us oth stud h intuba tion n the rat study stion of c e by colon and lain the rap However,the dies raise loubt about th minor hs es to The ed charid centra in e mp alent intake of hin (004 rted to he ra com 119).P rbed (up to 25% anthoc from tomatoes in humans(130),its ab ngestion of acid n in the tract or vity phenoli acids produced through bolite esent only 3%ofthe ingested do e when ferulic acid is pro e the ir ing 1131 gents and may be and numer tudy showed that ferloyl este are ghout the reach several hundred per liter ()and partcularly in the intestinal mucos d in the segments of the intestine. intestine (26).However.the roe of ases se ems to studies perform rption oc in the colon a

absorption was observed with glucosylation of naringenin and phlorizin (104, 105). Furthermore, diglucosylation of the lignan secoisolariciresinol decreases its absorption (106). Glycosylation does not influence the nature of the circulating metabolites. Intact glycosides of quercetin, daidzein, and genistein were not recovered in plasma or urine after ingestion as pure compounds or from complex food (107–110). For fla￾vanones, only trace amounts of glycosides have been detected in human urine, corresponding to 0.02% of the administered dose of naringin (111). But a very high dose (500 mg) of the pure com￾pound was administered in this study, and some metabolic pro￾cesses may have been saturated by this nonnutritional intake. Anthocyanins constitute an exception, because intact glycosides are the major circulating forms. The explanation for this may lie in the instability of these molecules in the aglycone form or in a specific mechanism of absorption or metabolism for anthocya￾nins. Passamonti et al (112) have proposed that glycosides of anthocyanins may be transported by bilitranslocase at the gastric level, bacause they have been shown to be good ligands for this carrier. They could also be directly converted into glucuronides by a UDP glucose dehydrogenase as suggested by Wu et al (113). Proanthocyanidins differ from most other plant polyphenols because of their polymeric nature and high molecular weight. This particular feature should limit their absorption through the gut barrier, and oligomers larger than trimers are unlikely to be absorbed in the small intestine in their native forms. In vitro experiments using single layers of Caco-2 cells as a model of absorption in the small intestine showed that only the dimers and trimers of flavanols are able to cross the intestinal epithelium (114). Procyanidin B2 is very poorly absorbed in rats, whereas procyanidin B3 is not absorbed (115, 116). The possibility that procyanidin oligomers are hydrolyzed to mixtures of flavanol monomers and dimers in acidic conditions was suggested by Spencer et al from in vitro experiments (117). However, purified procyanidin dimer B3, as well as grapeseed proanthocyanidins having a higher degree of polymerization, are not degraded to more readily absorbable monomers in rats (116). The stability of proanthocyanidins was investigated in humans by regular anal￾ysis of gastric juice sampled with a gastric probe after ingestion of a proanthocyanidin-rich cocoa beverage (118). This study confirmed that proanthocyanidins are not degraded in the acidic conditions of the stomach in vivo. A minor absorption of some procyanidin dimers seems possible in humans. The procyanidin dimer B2 was detected in the plasma of volunteers after ingestion of a cocoa beverage; however, the maximal plasma concentra￾tion that was reached 2 h after ingestion was much lower than that reached after a roughly equivalent intake of epicatechin (0.04 compared with 6.0mol/L) (119). Proanthocyanidins, which are among the most abundant dietary polyphenols, are very poorly absorbed and may exert only local activity in the gastrointestinal tract or activity mediated by phenolic acids produced through microbial degradation. Their local action may nevertheless be important because the intestine is particularly exposed to oxidiz￾ing agents and may be affected by inflammation and numerous diseases such as cancer (120). Polyphenol concentrations in the colon can reach several hundred micromoles per liter (83), and together with a few carotenoids, polyphenols constitute the only dietary antioxidants present in the colon, because vitamins C and E are absorbed in the upper segments of the intestine. Despite the scarcity of studies performed on the bioavailability of hydroxycinnamic acids, when ingested in the free form, these compounds are rapidly absorbed from the small intestine and are conjugated and, in particular, glucuronidated in the same way that flavonoids are (54, 121). However these compounds are naturally esterified in plant products, and this impairs their ab￾sorption. Human tissues (intestinal mucosa, liver) and biological fluids (plasma, gastric juice, duodenal fluid) do not possess es￾terases capable of hydrolyzing chlorogenic acid to release caffeic acid (122–124). This has also been observed in rats (125, 126). Only the colonic microflora would be capable of carrying out this hydrolysis, and some of the bacterial strains involved have been identified (127). Consequently, as observed for flavonoid gly￾cosides that must be hydrolyzed by the microflora, the efficiency of absorption of phenolic acids is markedly reduced when they are present in the esterified form rather than in the free form (123, 125, 128). In patients who have undergone colonic ablation, caffeic acid was much better absorbed than was chlorogenic acid: 11% and 0.3% of the ingested doses were excreted in urine, respectively (123). Similarly, when chlorogenic acid was given by gavage to rats, no intact compound was detected in plasma in the following 6 h, and the maximum concentrations of metabo￾lites obtained after administration of caffeic acid in the same conditions were 100-fold those of the metabolites (various glu￾curonidated or sulfated derivatives of caffeic and ferulic acids) obtained after chlorogenic acid administration (125). Surpris￾ingly, the plasma concentrations were maximal only 30 min after gavage, which may seem inconsistent with hydrolysis of chlo￾rogenic acid in the cecum. The same observation was made in a human study. When volunteers ingested coffee containing high amounts of esterified phenolic acids but no free caffeic acid, the peak plasma concentration of caffeic acid was observed only 1 h after ingestion of the coffee (129). In this study, the alkaline hydrolysis of coffee showed that chlorogenic acid represented only 30% of the bound caffeic acid. Thus, a possible explanation is that other forms of caffeic acid present in coffee may have been hydrolyzed in the upper part of the gut. Furthermore, the modes of administration used in both studies, ie, direct stomach intuba￾tion in the rat study and ingestion of coffee alone by fasted volunteers in the second study, might allow a rapid transit to the colon and explain the rapid kinetics of appearance of plasma metabolites. However, these 2 studies raise doubt about the total inability of the tissues to hydrolyze esterified phenolic acids. In addition to being esterified to simple acids, hydroxycin￾namic acids may be bound to polysaccharides in plant cell walls; the main example of this is esterification of ferulic acid to arabi￾noxylans in the outer husks of cereals. Although free ferulic acid is reported to be rapidly and efficiently absorbed (up to 25%) from tomatoes in humans (130), its absorption after ingestion of cereals is expected to be much lower because of this esterifica￾tion. Ferulic acid metabolites recovered in the urine of rats rep￾resent only 3% of the ingested dose when ferulic acid is provided as wheat bran, whereas the metabolites represent 50% of the dose when ferulic acid is provided as a pure compound (131). Another study showed that feruloyl esterases are present throughout the entire gastrointestinal tract, particularly in the intestinal mucosa, and that some of the ester bonds between ferulic acid and poly￾saccharides in cell walls may thus be hydrolyzed in the small intestine (126). However, the role of feruloyl esterases seems to be very limited, and absorption occurs mainly in the colon after hydrolysis by enzymes of bacterial origin. Xylanases degrade the 734 MANACH ET AL by guest on February 15, 2012 www.ajcn.org Downloaded from

POLYPHENOLS:FOOD SOURCES AND BIOAVAILABILITY 735 acids(8,142).Aglycones are split by the opening of the hetero- (132) the bioavailability of poly es mainly produce hy phenols have not been examined in much detail.Dire t int cid.These acids are further me h atives of ben☑ interac indirec fate The clea s are well estab parameters of gut(pH lished in animals,and the chemical structure on tects the npound fromcleay age an in po 3).HG cron tnientsorxenobiotics.lnteractionswMithnmilk ition and of inietal(133)reporte was observed when tea was ned withou urinary excretionof microbialm ns can be ever, than those 1 cetin,or kaempferol in humans(.135) Some investigator hus.the iden ntification and gua icro im i、 thei solubility.Ethan a hown to er nce the a ion acids hib rations of cat were si de biomarkers for polyphenol intake An ass een poly 20 metabolit tea or a crude extract from red win ch 147, 148)H hippu is not a nh mination perhaps On the other thar nolynhenols such as auinic acid and the aromati ich is a major organic acid ino ac) am data donot Aanarkedeiectofhevariolsdhe biom arker (124) The ption re prod ed by the colo m 密 to be broad equivalent when these polyphenols we 140 rding to 150 ch (141). nd diet or type o y food nor the prese e of 40g nic properties equiv he apparent a vone (15 52).There is -ial ae fibe phenols eidenaPeopieceiesgicantqanticsofcap afte ind these ons are c equo 152153)1Th6 tion of polyphe ua food matr ted that be as high as administered to fasted volu nteers in e form o emain the ame for at (15)The com a complex meal col s th and that high plasma concentrations would be ohtained only if supplements were taken separately from meals olasma from are fed soy-based fo hich The role of the colonie microflora Polyphenols that are not absorbed in the small intestine reack bac ia are reportedly able to convert pure daidzein toequol in

parietal polymers to small, soluble feruloyl oligosaccharides, and then esterases release free ferulic acid. Note that diferulic acids from cereal brans have been shown to be absorbed in rats (132). The effects of the food matrix on the bioavailability of poly￾phenols have not been examined in much detail. Direct interac￾tions between polyphenols and some components of food, such as binding to proteins and polysaccharides, can occur, and these interactions may affect absorption. Furthermore, more indirect effects of the diet on various parameters of gut physiology (pH, intestinal fermentations, biliary excretion, transit time, etc) may have consequences on the absorption of polyphenols. Enzymes and carriers involved in polyphenol absorption and metabolism may also be induced or inhibited by the presence of some mi￾cronutrients or xenobiotics. Interactions with milk proteins were considered first because Serafini et al (133) reported that addition of milk to black tea abolished the increase in antioxidant potential that was observed when tea was consumed without milk. How￾ever, subsequent studies showed that addition of milk to black or green tea had no effect on the bioavailability of catechins, quer￾cetin, or kaempferol in humans (134, 135). Some investigators have speculated that the presence of alcohol in red wine could improve the intestinal absorption of polyphenols by increasing their solubility. Ethanol was shown to enhance the absorption of quercetin in rats, but only when present at a concentration too high to be attained in the diet (30%, by vol) (136). In humans, plasma concentrations of catechin metabolites were similar after consumption of red wine or dealcoholized red wine (137). Yet, 20% more catechin metabolites were excreted in urine after red wine intake than after dealcoholized red wine intake, which in￾dicates a possible role of ethanol in enhancing the rate of poly￾phenol elimination, perhaps by a diuretic effect (138). On the other hand, tartaric acid, which is a major organic acid in wine, was shown to enhance the absorption of catechin in rats (139). Existing data do not suggest a marked effect of the various diet components on polyphenol bioavailability. The absorption of quercetin, catechin, and resveratrol in humans was recently shown to be broadly equivalent when these polyphenols were administered in 3 different matrices: white wine, grape juice, and vegetable juice (140). According to Hendrich (141), neither the background diet or type of soy food nor the presence of 40 g wheat fiber significantly alters the apparent absorption of isofla￾vones. However, more studies are needed, especially on dietary fiber. Dietary fiber is generally associated with polyphenols in plant foods and stimulates intestinal fermentation, which could influence the production of particular microbial metabolites. Ad￾ministration of polyphenols without a food matrix could mark￾edly affect their bioavailability. With regard to flavonols, much higher plasma concentrations were achieved when quercetin glu￾cosides were administered to fasted volunteers in the form of a water-alcohol solution (up to 5mol/L) (99) than when an equiv￾alent quantity was ingested with foods such as onions, apples, or a complex meal (0.3–0.75 nmol/L) (92, 107). This suggests that the consumption of any food may limit polyphenol absorption and that high plasma concentrations would be obtained only if supplements were taken separately from meals. The role of the colonic microflora Polyphenols that are not absorbed in the small intestine reach the colon. The microflora hydrolyzes glycosides into aglycones and extensively metabolizes the aglycones into various aromatic acids (8, 142). Aglycones are split by the opening of the hetero￾cycle at different points depending on their chemical structure: flavonols mainly produce hydroxyphenylacetic acids, flavones and flavanones mainly produce hydroxyphenylpropionic acids, and flavanols mainly produce phenylvalerolactones and hy￾droxyphenylpropionic acids. These acids are further metabo￾lized to derivatives of benzoic acid. The microbial metabolites are absorbed and conjugated with glycine, glucuronic acid, or sulfate. The cleavage and metabolic pathways are well estab￾lished in animals, and the influence of chemical structure on degradation is known. For example, the absence of a free hy￾droxyl in position 5, 7, or 4' protects the compound from cleavage (143). However, data are still limited in humans, so it is possible that new microbial metabolites will be identified. Interindividual variations and the influence of the microflora composition and of the usual diet on microbial metabolite production have to be evaluated. Recent studies have shown that plasma concentrations and urinary excretion of microbial metabolites in humans can be higher than those of tissular metabolites, especially for polyphe￾nols such as wine polyphenols that are not easily absorbed (128, 144, 145). Thus, the identification and quantification of micro￾bial metabolites constitute an important field of research. Some microbial metabolites may have a physiologic effect; for exam￾ple, hydroxyphenylacetic acids have been suggested to inhibit platelet aggregation (146). Besides, among the wide array of aromatic acids with low molecular weight, some may be used as biomarkers for polyphenol intake. An association between poly￾phenol intake and the amount of excreted hippuric acid was found after consumption of black tea or a crude extract from Equisenum arvense (147, 148). However, hippuric acid is not a degradation product of catechin and can be derived from sources other than polyphenols, such as quinic acid and the aromatic amino acids; thus, it is not a suitable biomarker of polyphenol intake (144). 3-Hydroxyhippuric acid may be a more valid biomarker (124). Specific active metabolites are produced by the colonic mi￾croflora. This is the case with lignans from linseed, which are metabolized to enterolactone and enterodiol, which have agonis￾tic or antagonistic effects on estrogens (149, 150). Similarly, equol produced from soya daidzein appears to have phytoestro￾genic properties equivalent to or even greater than those of the original isoflavone (151, 152). There is a great interindividual variability in the capacity to produce equol. Only 30-40% of the occidental people excrete significant quantities of equol after consumption of isoflavones, and these persons are called “equol producers” (152, 153). The corresponding percentage among Asian populations is unknown, but a recent study suggested that the percentage in Japanese men could be as high as 60% (154). The ability or inability of persons to produce equol seems to remain the same for at least several years (152, 155). The com￾position of the intestinal flora plays a major role. Inoculation of germ-free rats with human flora from equol producers confers on these rats the capacity to produce this metabolite, whereas col￾onization with flora from non–equol producers leaves the rats incapable of producing equol (156). Equol is not recovered in plasma from infants who are fed soy-based formulas, which suggests that the bacteria responsible for its production are not developed in the first months of life (157). Three strains of bacteria are reportedly able to convert pure daidzein to equol in vitro: Streptococcus intermedius ssp., Ruminococcus productus spp., and Bacteroides ovatus spp. (158). The possibility of con￾POLYPHENOLS: FOOD SOURCES AND BIOAVAILABILITY 735 by guest on February 15, 2012 www.ajcn.org Downloaded from

MANACH ET AL erting nonproducers to producers by food must be investigated substrate specificities and different tissue distributior 15 The sub 160.Co nof dietary fiber has be ected to affec roe in the first-pass metabolism of equol zymes have a wi omen(159,. mice m to diffe olyph (173 on e diet (1).Butthi human micros mesin the intestine and the liver showed tha even f the ear. d the ability to pro o be a site duc ol after cor uming soymilk for 2 wk(153).But Lampe onides that are formed in th et al 06 rve any with ad su intestind more compreh ensive kn dge of the fact that may )or the P-glycoprotein may be invol ed in this et al (152)convincingly p sed that ea ain more benefits from soya consumption than ferulic acid which indicates that this is not a mechanism o Conjugation a and nature of metabalite 168 82 ation teRoPn in the intestine is not vet clear Cate catalyzes the transfer of a methy 7-glucuronide and -sulfation (183 quercetnCatchincatecacidandlieolin,andWuetalg me que nide is no idin in humans.The methylation generally occurs predom es fo the polyph substrate. omple se of conjugating enzyme stantial amount of f 4'-methy r ous polyphenol olites by nges 164, ee ytes,as s hown ther conjugates vis highest in the iver and the kidney( enc 15. the to impo rences in to The relati tive importance of the s.poly types of n(meth generally a higher-affinity.lower-capacity pathway than ye the liver 169).UDP (186)The hala ronosyltra erases are me rane-bound enzy t ar sulfation of polyphenols Mo olyphen ls.and tho nds of metab glucuronides toward sulfation in the me and polyphenols in the all intestine ofrats shows that acity or co ugation is high The conce humans.humans the s has been ol erve m kedly higher than that by microsomes from the liver (173) polyphenols by age (166 170)Competitive inhibition of e of va ave

verting nonproducers to producers by food must be investigated. Equol producers tend to consume less fat and more carbohydrates as percentages of energy than do non–equol producers (159, 160). Consumption of dietary fiber has been suspected to affect equol production by favoring the growth of certain bacterial species. However, supplementation with 16 g wheat bran/d did not increase equol production in young women (159). In mice, equol production increased with the addition of fructooligosac￾charides in the diet (161). But this result needs to be confirmed in humans because of obvious interspecies differences, which are shown by the fact that rats are constitutive equol producers. The effect of adaptation of the intestinal flora to the consumption of isoflavones is not clear. Lu et al (162) observed an increase in equol production after 1 mo of isoflavone consumption. Some non-equol-producing women even acquired the ability to pro￾duce equol after consuming soymilk for 2 wk (153). But Lampe et al (163) did not observe any effect on equol production of a 1-mo adaptation in comparison with a 4-d supplementation. A more comprehensive knowledge of the factors that may influ￾ence equol production is all the more essential because Setchell et al (152) convincingly proposed that equol producers might gain more benefits from soya consumption than would nonpro￾ducers. Conjugation and nature of metabolites Once absorbed, polyphenols are subjected to 3 main types of conjugation: methylation, sulfation, and glucuronidation. Catechol-O-methyl transferase catalyzes the transfer of a methyl group from S-adenosyl-L-methionine to polyphenols having an o-diphenolic (catechol) moiety. Such a reaction is well known for quercetin, catechin, caffeic acid, and luteolin, and Wu et al (113) recently showed for the first time the methylation of cyanidin to peonidin in humans. The methylation generally occurs predom￾inantly in the 3' position of the polyphenol, but a minor propor￾tion of 4'-O-methylated product is also formed. Note that a sub￾stantial amount of 4'-methylepigallocatechin was detected in human plasma after ingestion of tea (164, 165). Catechol-O￾methyl transferase is present in a wide range of tissues. Its ac￾tivity is highest in the liver and the kidneys (166, 167) although significant methylation was reported for catechin in the small intestine of rats (168). Sulfotransferases catalyze the transfer of a sulfate moiety from 3'-phosphoadenosine-5'-phosphosulfate to a hydroxyl group on various substrates (steroids, bile acids, poly￾phenols, etc). Neither the isoforms that are specifically involved in the conjugation of polyphenols nor the positions of sulfation for the various polyphenols have yet been clearly identified, but sulfation clearly occurs mainly in the liver (166, 169). UDP￾glucuronosyltransferases are membrane-bound enzymes that are located in the endoplasmic reticulum in many tissues and that catalyze the transfer of a glucuronic acid from UDP-glucuronic acid to steroids, bile acids, polyphenols, and thousands of dietary constituents and xenobiotics. The presence of glucuronidated metabolites in the mesenteric or portal blood after perfusion of polyphenols in the small intestine of rats shows that glucuronida￾tion of polyphenols first occurs in the enterocytes before further conjugation in the liver (170–172). This is probably the case in humans as well, because in humans the in vitro glucuronidation of quercetin and luteolin by microsomes from the intestine is markedly higher than that by microsomes from the liver (173). About 15 isoforms of UDP-glucuronosyltransferases have been identified in humans, and these isoforms have broad and over￾lapping substrate specificities and different tissue distribution (174). The subfamily of UDP-glucuronosyltransferases called UGT1A that is localized in the intestine probably plays a major role in the first-pass metabolism of polyphenols. These isoen￾zymes have a wide polymorphic expression pattern that could result in a high interindividual variability in polyphenol glucu￾ronidation. The active isoenzymes of the 1A class seem to differ according to the polyphenol considered (173, 175). In vitro glu￾curonidation of quercetin, luteolin, or isorhamnetin by rat or human microsomes in the intestine and the liver showed that, even if the nature of the glucuronides formed is constant, the proportion of the various metabolites varies widely depending on the species and organ (173, 176, 177). The highest rate of con￾jugation is observed at the 7-position, and the 5-position does not appear to be a site for glucuronidation. For most flavonoids, a significant proportion of the glucuronides that are formed in the intestinal mucosa are secreted back to the gut lumen, which reduces net absorption (178, 179). The transporter multiresistant protein 2 (MRP2) or the P-glycoprotein may be involved in this efflux (180, 181). The proportion of glucuronides that are se￾creted toward the mucosal side depends markedly on the struc￾ture of the polyphenol (0–52% of the initial dose) (182). Intes￾tinal excretion of glucuronides does not occur with catechin and ferulic acid, which indicates that this is not a mechanism of elimination for all polyphenols (131, 168, 182). The metabolic fate in the liver of the conjugates that are pro￾duced in the intestine is not yet clear. After penetration into HepG2 cells, quercetin 7-glucuronide and quercetin 3-O￾glucuronide undergo 2 types of metabolism: methylation of the catechol and deglucuronidation followed by 3'-sulfation (183). However, in the same conditions, quercetin 4'-glucuronide is not metabolized. This could result from a lower rate of penetration into the cells or a lower affinity of the metabolizing enzymes for this substrate. A complex set of conjugating enzymes and carrier systems is probably involved in the regulation of uptake and the production and release of the various polyphenol metabolites by the hepatocytes, as shown for other conjugates (184, 185). The activity of these enzymes and carrier systems may depend on the nature of the polyphenol and may be influenced by genetic poly￾morphisms that lead to important interindividual differences in the capacity to metabolize polyphenols. The relative importance of the 3 types of conjugation (meth￾ylation, sulfation, and glucuronidation) appears to vary accord￾ing to the nature of the substrate and the dose ingested. Sulfation is generally a higher-affinity, lower-capacity pathway than is glucuronidation, so that when the ingested dose increases, a shift from sulfation toward glucuronidation occurs (186). The balance between sulfation and glucuronidation of polyphenols also seems to be affected by species, sex, and food deprivation (187). Moreover, inhibition of methylation by a specific inhibitor shifts metabolism of quercetin glucuronides toward sulfation in HepG2 cells (183). Regardless of the respective contributions of methylation, sulfation, and glucuronidation, in general, the ca￾pacity for conjugation is high. The concentration of free aglycone is usually very low in plasma after the intake of a nutritional dose, except for tea catechins (up to 77% for epigallocatechin gallate) (164). Saturation of the conjugation processes has been observed in rats administered high doses and rats given an acute supply of polyphenols by gavage (166, 170). Competitive inhibition of conjugation could also occur in the presence of various polyphe￾nols and xenobiotics in the intestine, but it has never been studied. 736 MANACH ET AL by guest on February 15, 2012 www.ajcn.org Downloaded from