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CHAPTER 29 Production and Nutraceutical Properties of Breads Fortified with DHA- and Omega-3- Containing Oils Sergio O. Serna-Saldivar 1 , Ruben Abril 2 1 Department of Biotechnology and Food Engineering, Tecnolo ´gico de Monterrey-Campus Monterrey, Nuevo Leo ´n, Me ´xico 2 Ingredient Formulations & Technical Support, Martek Biosciences Boulder Corporation, Boulder, Colorado, USA CHAPTER OUTLINE List of Abbreviations 313 Introduction 314 Technological Issues and Production of Breads Fortified with DHA and u-3 Oils 314 Fortified bread production and evaluation 315 Baking performance 315 Fatty acid composition 315 Bread color, texture, and sensory evaluations 318 Synthesis of DHA and EPA 318 Metabolic Implications and Health Benefits of DHA, EPA, and u-3 Fatty Acids 318 Summary Points 321 References 322 LIST OF ABBREVIATIONS CVD Cardiovascular disease DHA Docosahexaenoic acid EPA Eicosapentaenoic acid FA Fatty acid(s) PG Prostaglandin PPARa Peroxisome proliferator-activated receptor-a PUFA Polyunsaturated fatty acid SREBP Sterol regulatory element-binding protein SSL Sodium stearoyl-2-lactylate 313 Flour and Breads and their Fortification in Health and Disease Prevention. DOI: 10.1016/B978-0-12-380886-8.10029-7 Copyright Ó 2011 Elsevier Inc. All rights reserved.

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Page 1: Flour and Breads and their Fortification in Health and Disease Prevention || Production and Nutraceutical Properties of Breads Fortified with DHA- and Omega-3-Containing Oils

CHAPTER 29

Production andNutraceutical Propertiesof Breads Fortified withDHA- and Omega-3-Containing Oils

Sergio O. Serna-Saldivar1, Ruben Abril21 Department of Biotechnology and Food Engineering, Tecnologico de Monterrey-CampusMonterrey, Nuevo Leon, Mexico2 Ingredient Formulations & Technical Support, Martek Biosciences Boulder Corporation,Boulder, Colorado, USA

313

Fl

C

CHAPTER OUTLINE

List of Abbreviations 313Introduction 314Technological Issues and Production ofBreads Fortified with DHA and u-3Oils 314

Fortified bread production and

evaluation 315

Baking performance 315

Fatty acid composition 315

our and Breads and their Fortification in Health and Disease Prevention. DOI

opyright � 2011 Elsevier Inc. All rights reserved.

Bread color, texture, and sensory

evaluations 318

Synthesis of DHA and EPA 318Metabolic Implications and HealthBenefits of DHA, EPA, and u-3 FattyAcids 318Summary Points 321References 322

LIST OF ABBREVIATIONSCVD Cardiovascular diseaseDHA Docosahexaenoic acid

EPA Eicosapentaenoic acid

FA Fatty acid(s)PG Prostaglandin

PPARa Peroxisome proliferator-activated receptor-a

PUFA Polyunsaturated fatty acidSREBP Sterol regulatory element-binding protein

SSL Sodium stearoyl-2-lactylate

: 10.1016/B978-0-12-380886-8.10029-7

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314

SECTION 2Fortification of Flour and Breads and their Metabolic Effects

INTRODUCTIONBread is one of the oldest prepared foods, dating back to the Neolithic era. Its origins can be

closely linked to the beginning of agriculture in the area known as the Fertile Crescent.Wheat was probably first eaten as a gruel of crushed grain and water. Then, the gruel or dough

was baked on hot stones into primitive flat breads. Fermentation was the next development

when doughs, exposed to natural yeasts and microflora, fermented before baking. The basicmaterials for bread making have changed little; however, bread has diverged into a wide array

of types (Serna-Saldivar, 2010). Bread continues to be the most widely consumed food and,

with rice, the largest supplier of calories, protein, and certain essential vitamins and mineralsfor the 6.8 billion people that currently inhabit the earth. An average human obtains

approximately 22 and 24% of the daily calories and protein from wheat (Food and Agriculture

Organization, 2010). Flour and bread are commonly fortified with selected essential micro-nutrients; however, the recent trend is to use these to provide fiber, other proteins, and

nutraceuticals that can prevent chronic diseases currently responsible for approximately 60%

of deaths.

It has been suggested that the typical Western diet, which is relatively high in omega (u)-6

and low in u-3 fatty acids (FA), may not provide the appropriate balance for properbiological function. The imbalance is related to cardiovascular disease (CVD), hyperten-

sion, hyperlipidemia, hypercholesterolemia, inflammatory disorders, and certain disrupted

neurological functions (Newton and Snyder, 1997). The nutritional benefits of incorpo-rating docosahexaenoic acid (DHA) and other u-3 FA into bakery products have gained

interest in recent years. The beneficial role of algal and fish oils, rich in u-3 polyunsaturated

fatty acids (PUFAs) such as DHA and eicosapentaenoic acid (EPA), has been well docu-mented in more than 2000 clinical studies pointing to health improvements of various

human disorders, such as CVD, breast and prostate cancer, rheumatoid arthritis, and

inflammatory diseases (Kumar Rudra et al., 2001; Leitzmann et al., 2004). There is alsoevidence indicating the benefit of slowing the progression of Alzheimer’s disease with

the consumption of DHA/EPA-containing fish (Morris et al., 2003). DHA is considered

the most important u-3 FA because it plays an important role in brain chemistry anddevelopment. It constitutes approximately half of the lipids found in neuron membranes

and in the photoreceptors of the retina (Connor et al., 1992). DHA supplementation is

critical in infants because they are very limited in the conversion of linolenic acid intoDHA. A cross-sectional study conducted with a population of 1613 individuals ranging

from 45 to 70 years of age concluded that consumption of marine u-3 PUFA and fatty fish

was associated with a reduced risk of impaired cognitive function, whereas an increasedintake of cholesterol and saturated FA was associated with an increased risk (Kalmijn et al.,

2004).

TECHNOLOGICAL ISSUES AND PRODUCTION OF BREADSFORTIFIED WITH DHA AND u-3 OILSBread is a convenient vehicle for introducing DHA/EPA and other nutraceuticals because it is

a common staple in most cultures throughout the world. Newton and Snyder (1997)

concluded that bread is an ideal medium for u-3 PUFA because the CO2 produced duringdough fermentation protects the oil from oxidation, especially while it is exposed to high

temperatures during baking. Serna-Saldivar et al. (2006) researched the production of different

breads containingu-3 FA in oils and emulsions. The aimwas to substitute part of the vegetableshortening so as to produce slices of bread (32 g) with 25 or 50 mg DHA or u-3 FA. DHA/EPA-

rich oils were obtained from algae or fish oil, whereas the high-linolenic oil was obtained from

flax.

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CHAPTER 29Production and Nutraceutical Properties of Fortified Breads

315

Fortified bread production and evaluation

Breads were produced following the straight or sponge dough procedures. The first procedure

(method 10-10B; American Association of Cereal Chemists (AACC), 2000) was used in orderto detect possible deleterious effects of the u-3 oil sources and estimate optimum water

absorption and mix times. The formulation included 100 g commercial bread flour, 5.5 g

sugar, 3 g vegetable shortening, 1.5 g salt, and 2 g dry yeast (Saccharomyces cerevisiae). Bakeabsorption, mixing time, proof height, loaf height, oven spring, loaf weight, loaf volume, loaf

apparent density, and crumb grain texture were determined (Serna Saldivar et al., 2006).

Sponge dough breads were manufactured to obtain commercial loaves for sensory and textureanalyses throughout 14 days of storage at room temperature. Sponges were produced from

604 g flour (14% mb), 356 ml water, and 14 g dry yeast. Sponges were fermented for 4.5 h

in a proof cabinet set at 29oC and 85% relative humidity. Resulting sponges were mixed withthe dough-stage ingredients (326 g flour, 56 g sugar, 28 g shortening, 28 g nonfat dry milk,

18.6 g salt, 9.3 g vital gluten, 1.86 g diastatic malt, 1.86 g lecithin, 0.94 g sodium stearoyl-2-

lactylate (SSL), 55.8 mg sodium ascorbate, and 18.6 mg potassium bromate) and 258 ml ofwater until optimum dough development was obtained. Resulting doughs were weighed and

cut into two identical parts before punching, final proofing, baking (28 min at 225oC),

cooling, and slicing. One slice per loaf from 16 different loaves was submitted for determi-nation of its full FA profile using a gas chromatograph flame ionization detector.

Breadwas cut into 1-inch-thick slices for determination of texture, color, and sensory properties.Bread firmness throughout 14 days of storage at room temperature was objectively evaluated

according to AACC (2000) method 74-09 with a texture analyzer equipped with a cylindrical

probe. Crumb color was determined with a Minolta color meter. L, a, and b were obtainedand color index Ewas determined by the following equation: E¼ (L2þ a2þ b2)1/2. Between 25

and 30 untrained panelists evaluated the color, flavor, texture, and overall acceptability of the

control bread and breads enriched with 25 or 50 mg DHA/slice throughout 14 days of storage.Breads were evaluated using a 9-point hedonic scale (Serna-Saldivar et al., 2006).

Baking performance

According to the FA composition of all experimental oil sources, the vegetable shortening

was partially substituted to yield 32-g slices of bread containing either 25 or 50mg DHA, 25e50mg totalu-3 in the case of fish oil, or 120mg linolenic acid fromflax oil. The source of the oil did

not significantly affect optimumwater absorptionbut reducedmix timeby 10e15%(Table 29.1).

A similar performance was observed in commercial breads produced by the sponge doughprocedure. The utilization of dough conditioners and improvers such as vital gluten, oxidizing

agents, lecithin, and SSL counteracted the deleterious effects of the u-3-rich oils (Table 29.2).

Fatty acid composition

According to Newton and Snyder (1997), the prehistoric human diet provided a relativelyequal balance of u-6 and u-3 FA. The modern diet in Western societies has dramatically

changed this ratio to approximately 10e25:1. This unbalance is believed to exacerbate chronic

diseases.

Breads fortified with algae and fish oils required the least weight addition of u-3 oils because

they contained relatively high levels of DHA/u-3 FA. The algae oil breads contained approx-imately 25 or 50 mg DHA/serving, whereas the fish oil supplemented bread contained

approximately half of the amount but still maintained the 25e50 mg of total long-chain u-3

FA, namely contributed by EPA and DHA. As expected, the flax oil bread did not contain DHAbut contained the highest level of linolenic acid (Table 29.3). Experimental loaves supple-

mented with the highest amount of algal DHA or DHA/EPA fish oils contained at least four

times more u-3 FA than did the control or flax supplemented bread. Flax oil enriched breads

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TABLE 29.1 Effect of Different Types and Concentrations of DHA/u-3-Rich Oils on Baking PerformanceEstimated with the Straight Dough Procedurea

Sample

WaterAbsorption

(%)Mixing Time(min:sec)

ProofHeight(cm)

BreadHeight(cm)

OvenSpring(cm)b

BreadWeight

(g)

BreadVolume(cm3)

ApparentDensity (g/

cm3)CrumbTexturec

25 mg DHAControl 64 3:43a 7.625a 10.875a 3.250a 143.2a,b 888.3a 0.162c 5.3a,b

Algae oil 64 3:35a,b 7.500a 10.575a 2.975a 144.2a,b 826.3b 0.175b 5.0aec

Emulsion-P 64 3:23b,c 7.525a 10.575a 3.050a 143.4a,b 830.8a,b 0.174b,c 6.0a

Emulsion-L 64 3:28aec 7.700a 10.350a,b 2.725a,b 142.2b 828.3a,b 0.172b,c 5.8a

Flax oil 64 3:20b,c 7.475a 10.325a,b 2.850a,b 142.5b 823.3b,c 0.174b,c 5.8a

Fish oil 64 3:15c 7.550a 10.300a,b 2.750a,b 144.1a,b 823.8b,c 0.175b,c 4.3b,c

50 mg DHAControl 64 3:33a,b 7.700a 10.175a,b 2.475b 140.5bed 841.3a 0.167a,b 4.8bed

Algae oil 64 3:23b,c 7.625a,b 10.475a,b 2.850a,b 140.4c,d 842.5a 0.167a,b 5.0aec

Emulsion-P 64 3:28aec 7.475b,c 10.500a 3.025a,b 139.8d 853.8a 0.164b 5.8a,b

Emulsion-L 64 3:23b,c 7.525a,b 10.425a,b 2.900a,b 141.6aed 841.3a 0.168a,b 6.3a

Flax oil 64 3:18c 7.475b,c 10.350a,b 2.875a,b 142.0aec 840.0a 0.169a,b 3.8c,d

Fish oil 64 3:28aec 7.550a,b 10.575a 3.025a,b 141.4aed 841.3a 0.168a,b 5.8a,b

Source: From Serna-Saldivar et al. (2006)aMeans with a different letter(s) within column and enrichment level are statistically different (p < 0.05).bOven spring ¼ bread height - proof height.c1, poor; 3, regular; 5, good; 7, excellent.

TABLE 29.2 Effect of Different Types and Concentrations of DHA/u-3-Rich Oils on Baking PerformanceEstimated with the Sponge Dough Procedurea

Sample

WaterAbsorption

(%)

MixingTime

(min:sec)

ProofHeight(cm)

BreadHeight(cm)

OvenSpring(cm)b

DoughWeight

(g)

BreadWeight

(g)

BreadWeight/Dough

Weight (%)CrumbTexturec

25 mg DHAControl 65.5 4:40a 10.53a 12.33a,b 1.80b,c 830.7a 748.1c,d 90.1b,c 7.0a

Algae oil 65.5 4:35a 10.40a 12.23a,b 1.83b,c 836.0a 750.9bed 89.8b,c 6.5a,b

Emulsion-P 65.5 4:32a,b 10.28a 12.80a 2.52a,b 834.0a 752.1b,c 90.2b,c 7.0a

Emulsion-L 65.5 4:40a 10.18a 12.33a,b 2.15aec 832.8a 744.2d,e 89.4c 6.5a,b

Flax oil 65.5 4:40a 10.15a 12.53a,b 2.38a,b 831.5a 756.0b 90.9a,b 6.5a,b

Fish oil 65.5 4:42a 10.60a 11.80b 1.25c 835.5a 768.2a 92.0a 6.0b

50 mg DHAControl 65.5 4:35a 11.05a 12.60a,b 1.55a,b 830.8b,c 742.8b,c 89.4bed 7.0a

Algae oil 65.5 4:33a 11.23a 12.90a,b 1.67a,b 834.2b 739.4c 88.6d 7.0a

Emulsion-P 65.5 4:35a 10.83a,b 12.48a,b 1.65a,b 832.7b,c 740.6c 88.9c,d 6.5a,b

Emulsion-L 65.5 4:35a 10.38b 12.38b 2.00a,b 829.9c 738.9c 89.0c,d 6.0b

Flax oil 65.5 4:30a 10.83a,b 12.83a,b 2.00a,b 834.7b 754.0a 90.3a,b 6.0b

Fish oil 65.5 4:10b 10.80a,b 13.10a 2.30a 832.9b,c 754.6a 90.6a 6.3a,b

Source: From Serna-Saldivar et al. (2006).aMeans with a different letter(s) within column and enrichment level are statistically different (p < 0.05).bOven spring ¼ bread height - proof height.c1, poor; 3, regular; 5, good; 7, excellent.

SECTION 2Fortification of Flour and Breads and their Metabolic Effects

316

contained at least 2.5 times more linolenic acid than did the other experimental counterparts

and were practically free of long-chain FA. The u-6:u-3 FA ratio of the control bread wasapproximately 9 (see Table 29.3). Addition of the different oil sources improved the ratio

to less than 3.5 and 2.2 for the 25- and 50-mg fortified breads, respectively. The most

balanced ratio was observed in the flax oil enriched bread because it was the richest sourceof linolenic acid.

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TABLE 29.3 Effect of Different Types and Concentrations of DHA/Omega-3-Rich Oils on Fatty AcidComposition of Breads (Expressed Per 32-g Serving)a

Fatty Acid (mg/Serving) Control Algae Oil Emulsion-L Emulsion-P Flax Oil Fish Oil

Low Enrichment Level

Dodecanoate 20 20 23 19 21 21Myristate 24 27 24 22 18 32Myristoleate 6 5 5 4 4 6Palmitate 149 153 129 129 147 154Palmitoleate 22 20 17 17 18 29Stearate 95 91 70 69 90 93Oleate 156 150 118 117 146 154Linoleate 138 135 128 129 149 135Arachidate 2 2 2 2 3 3Linolenate 14 14 12 13 93 18Eicosenoate-11 4 3 3 3 3 6Eicosapentaenoate 1 2 2 2 0 11Lignocerate 0 2 2 2 0 1Docosapentaenoate n-6 0 11 12 12 0 0Docosahexaenoate 0 26 29 29 0 16Omega-6 138 146 140 141 149 138Omega-3 15 42 43 44 93 46Omega-6:omega-3 9.20 3.47 3.25 3.20 1.60 3.00Saturated 290 295 250 243 279 305Monounsaturated 178 178 143 141 171 196Polyunsaturated 153 188 183 185 242 184Saturated:monounsaturated:polyunsaturated

47:29:25 45:27:28 43:25:22 43:25:33 40:25:35 45:29:27

High Enrichment Level

Dodecanoate 19 21 21 20 21 20Myristate 25 30 21 19 11 29Myristoleate 6 5 2 0 3 5Palmitate 162 153 100 103 108 148Palmitoleate 24 20 12 11 13 27Stearate 104 82 34 36 52 82Oleate 167 138 70 69 112 141Linoleate 138 136 119 124 153 132Arachidate 3 2 0 0 3 2Linolenate 16 14 12 3 172 18Eicosenoate-11 4 3 3 0 0 6Eicosapentaenoate 0 4 4 4 0 18Lignocerate 1 2 2 3 2 0Docosapentaenoate n-6 0 20 24 23 0 2Docosahexaenoate 0 51 59 58 0 27Omega-6 138 156 143 147 153 136Omega-3 16 71 77 67 172 65Omega-6:omega-3 8.63 2.20 1.86 2.19 0.89 2.09Saturated 313 290 178 181 197 281Monounsaturated 201 166 87 80 128 179Polyunsaturated 154 227 220 214 325 201Saturated:monounsaturated:polyunsaturated

47:30:23 42:24:33 36:18:45 38:17:45 30:20:50 42:27:30

Source: From Serna-Saldivar et al. (2006).aValues are means of three observations. The standard deviations of the fatty acid determinations were less than 0.05 mg/g.

CHAPTER 29Production and Nutraceutical Properties of Fortified Breads

317

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SECTION 2Fortification of Flour and Breads and their Metabolic Effects

318

Bread color, texture, and sensory evaluations

Within enrichment concentration, addition of different sources of algae oils did not signifi-

cantly affect lightness (L), a, b, and color indexes (E) determined at the center portion of thecrumb. The color remained the same throughout 14 days of storage at room temperature

(Serna-Saldivar et al., 2006). Sensory evaluations of 25- and 50-mg enriched breads indicated

that all breads were equally preferred compared to the control bread. Objective color valueswere similar in terms of lightness and color scores. As expected, panelists graded with lower

scores bread texture stored for longer periods of time. However, they considered that experi-

mental breads had similar texture or firmness throughout storage compared with the controlbread. The flavor and overall acceptability of all breads were rated similarly during the first

6 days storage. However, the 14-day-old bread enriched with the highest level of fish oil had

a significantly lower flavor score and overall acceptability compared to the rest of the treat-ments. Presumably, the high PUFA oil became rancid and/or its flavor reverted, negatively

affecting organoleptic properties. This bread was the only one rated as “neither like or dislike”

or worse after 14 days of storage at ambient temperature (Serna-Saldivar et al., 2006).

SYNTHESIS OF DHA AND EPAHumans are only capable of synthesizing EPA and DHA from a-linolenic acid, although theconversion has been reported to be extremely limited (John-Bjarne et al., 1998). Therefore, the

diet should either provide the precursor or these PUFA or these two FA. However, several

plants, fungi, and fish have the capacity to produce EPA and DHA from other FA. Thebiosynthetic pathway starts when stearic acid (18:0) is elongated to a 20-carbon chain and

desaturated in the 5, 8, 11, 14, and 17 positions to yield EPA. DHA is produced similarly, but

the chain is elongated to 22 carbons with six insaturations in positions 4, 7, 10, 13, 16, and 19.These reactions occur in the endoplasmic reticulum. Key enzymes for the production of these

FA are the 2-carbon elongases and D4, -6, -9, -12, and -15 desaturases (Figure 29.1).

METABOLIC IMPLICATIONS AND HEALTH BENEFITS OF DHA, EPA,AND u-3 FATTY ACIDSDietary EPA and DHA are packaged and transported through chylomicrons produced in theintestinal epithelial cells. The most relevant tissues that contain u-3 PUFA are hepatic, lung,

kidney, spleen, plasma, heart, retina, and the vascular endothelium. EPA concentrates in the

hepatic, renal, and blood cells, whereas DHA concentrates in the heart, retina, and brain. ThesePUFAs have three major roles: cell membrane structure, precursors of eicosanoids, and effectors

of protein activity (enzymes, receptors, and ionic channels). EPA is preferably incorporated

associated with phosphatidyl choline (67%) and ethanolamine (13%) in platelets, whereasDHA accumulates with phosphatidyl ethanolamine (45%) and choline (37%). DHA is also

incorporated into cardiolipin, a phospholipid only found associated with the cardiac muscle.Eicosanoides are hormones synthesized from 20-carbon FA, mainly araquidonic and EPA, and

the enzymes cyclooxygenases and lipooxygenases (Figure 29.2). EPA is precursor of series 3

prostaglandins (PGs) and thromboxanes and series 5 leukotrienes. These are known to affectinflammatory response, vasodilatation, platelet aggregation, nerve stimulation, atherosclerosis,

asthma, arthritis, diabetes, psoriasis, and possibly cancer tumors (Table 29.4). In addition, their

presence in semen favors the contraction of the uterus and the movement of the spermatozoidsthrough the fallopian tubes. In females, PGs are liberated during menstruation, favoring the

detachment and elimination of the endometrial epithelial cells.

Platelet aggregation requires fibrinogen and is stimulated by thromboxane A2, whereasprostacycline (PG-I) decreases aggregation and stimulates vasodilatation. Both thromboxane

A2 and prostacycline are produced by cyclooxygenase of endothelial cells. EPA reduces the

synthesis of thromboxane A2; produces thromboxane A3 (weak platelet aggregator);

Page 7: Flour and Breads and their Fortification in Health and Disease Prevention || Production and Nutraceutical Properties of Breads Fortified with DHA- and Omega-3-Containing Oils

stearic18:0

oleic18:1 (9c)

animalsdesaturation

towards carboxyl

terminus

desaturation towards

methyl terminus

CO-SR

CO-SR

CO-SR R = SCoA in animal/fungiR = ACP in plants

stearidonic18:4 (6c, 9c, 12c, 15c)

+ C2 (malonate)+ C2 (malonate)

+ C2 (malonate)

CO-SR

CO-SR

CO-SR

CO-SR

dihomo–g–linolenic20:3 (8c, 11c, 14c)

CO-SR

eicosatetraenoic20:4 (8c, 11c, 14c, 17c)

CO-SR

CO-SR

docosapentaenoic (DPA)22:5 (7c, 10c, 13c, 16c, 19c)

docosahexaenoic (DHA)22:6 (4c, 7c, 10c, 13c, 16c, 19c)

Note: the names givenare for the appropriatefatty acid; the structuresshown are actually thethioesters involved inthe conversions

prostaglandins2–series

arachidonic20:4 (5c, 8c, 11c, 14c)

prostaglandins3–series

eicosapentaenoic (EPA)20:5 (5c, 8c, 11c, 14c, 17c)

prostaglandins1–series

plantsfungi

plantsfungiCO-SR CO-SR

18:2 (6c,9c)

chain extension by Claisen

reaction with malonate; chain

length increase by 2

carbons

–linolenic18:3 (6c, 9c, 12c)

animals

linoleic18:2 (9c, 12c)

–linolenic18:3 (9c, 12c, 15c)

animals

CO-SR

FIGURE 29.1Synthesis of EPA and DHA from stearic acid in plants, fungi, and animals. Source: Reproduced with permission from Dewick, P. M. (2001). Medicinal Natural

Products. A Biosynthetic Approach, 2nd edn. Wiley, West Sussex, UK.

CHAPTER 29Production and Nutraceutical Properties of Fortified Breads

319

maintains the production of prostacycline; and yields PG-I3, which prevents platelet aggre-

gation (Nettleton, 1995).

EPA and DHA lower serum triglycerides and cholesterol because they bind to peroxisome

proliferator-activated receptors (PPARs), which act as transcription factors of specific genes.

These receptors control cell differentiation and development related to carbohydrate, lipid, andprotein metabolism (Torrejon et al., 2007). The other two receptors (alpha and gamma) have

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TABLE 29.4 Metabolic Effects and Health Implications of DHA and EPA

Health Implication Metabolic and Health Effects

Hyperlipidemia andcholesterolemia

Both EPA and DHA reduce serum TG levels. However, only DHA increases HDL andimproves the LDL:HDL ratio (Egert et al., 2009). Jump et al. (2008) found that the keytranscription factors PPARa and SREBP-1 are regulated by u-3 PUFA. DHA activatesPPARa (lipid oxidation gene) and suppresses the nucleus expression of SREBP-1 (lipidsynthesis gene). As a result, it promotes FA oxidation and suppresses lipogenesis; however,EPA is a more potent activator of PPARa compared to DHA

CVD DHA and EPA lower total cholesterol, VLDL, HDL, and TG by inhibiting the synthesis of VLDLand apoprotein B-100. The u-3 FAs also affect atherogenesis because they are precursorsof PG that interfere with blood coagulation. Both FA inhibit sodium channels that decreaseintracellular calcium transport affecting the electric behavior of the cardiac muscle and heartrate. An epidemiological study indicated that u-3 PUFA reduced levels of C-reactive protein(29%), interleukin-6 (23%), E-selectin (10%), the intracellular adhesion molecule-1 orsICAM-1 (7%), and the vascular adhesion molecule or sVCAM-1 (8%). As a result, thesereduced endothelial inflammation and CVD (Lopez-Garcia et al., 2004). Studies indicate thatthe daily supplementation of 250e500 mg of EPA þ DHA reduces the risk of CVD, cardiacarrhythmia, and mortality in approximately 35% (Harris et al., 2009). Dewailly et al. (2003)compared the effect of fish consumption of three ethnic groups in Quebec, Canada.Interestingly, the Inuit (Indigenous Canadians) people who regularly consumed fish hada lower risk of CVD, despite their high obesity rate and the habit of smoking

Immune response DHA and EPA stimulate the immune response due to the increment of these FA in cellmembranes (Kew et al., 2003). EPA inhibits cytokines and the enzymes involved in thedegradation of connective tissue, which are the main enzymes responsible for rheumatoidarthritis (Simopoulos, 2002). Weldon et al. (2007) indicated that DHA is more effective thanEPA in reducing pro-inflammatory cytokine production by macrophages

Diabetes Hu et al. (2003) prospectively examined the association between intake of fish andu-3 PUFAand risk of CVD and total mortality among 5103 female nurses with diagnosed type-2diabetes but who were free of CVD or cancer. Compared with women who seldomconsumed fish (<1 serving/month), the relative risks of CVD adjusted for age, smoking, andother established coronary risk factors were 0.70 for fish consumption one to three times permonth, 0.60 for consumption once per week, 0.64 for consumption two to four times perweek, and 0.36 for consumption five or more times per week. Higher consumption of fishwas also associated with a significantly lower total mortality

Cancer Consumption of u-3 PUFA is related to lower cancer risk. The mechanism is unknown, but itmay be related to the synthesis of PG, activation of the immune system, peroxy lipidradicals, membrane fluidity, hormone secretion, activity of growth factor, and intracellularsignaling. Animal studies concluded that the consumption of fish oil rich in EPA and DHAreduces the synthesis of PG and thromboxanes-2 in tumor tissues. The changes ineicosanoids also affect the immune system, PG-2 of macrophages increases tumordissemination and induces the production of interleukin-1 by monocytes and the tumornecrotic factor. EPA and DHA inhibit mammary cancer cell growth, whereas u-6 FAs inducein vivo and in vitro growth (Hammamieh et al., 2007)

Neurological and retina DHA is the most abundant lipid in the nervous system, especially the brain. It is incorporatedinto the phospholipidic membrane of neuron cells and retina. DHA is mainly associated withthe synaptosomes, and myelin. It accumulates in brain, retina, liver, and adipose tissueduring the third trimester of pregnancy. DHA and fish oil supplementation helps patients withneurological disorders such as attention deficit disorder syndrome, schizophrenia, andAlzheimer’s disease (Ross et al., 2007; Sorgi et al., 2007)

Fetus and childdevelopment

DHA/EPA have an important and critical role in fetus and newborn development becausethey help enhance proper neuron synaptic connections and cognitive and visualdevelopment (Jacobson et al., 2008; Sorgi et al., 2007). DHA supplementation duringlactation increases plasma levels and promotes a higher Bailey psychomotor developmentin 30-month-old infants (Jensen et al., 2005)

CVD, cardiovascular disease; DHA, docosahexaenoic acid; EPA, eicosapentaenoic acid; FA, fatty acid(s); HDL, high-density lipoprotein; LDL, low-density

lipoprotein; PG, prostaglandins; PPARa, peroxisome proliferator-activated receptors-a; PUFA, polyunsaturated fatty acid; SREBP-1, sterol regulatory element

binding protein-1; TG, triglyceride; VLDL, very low-density lipoprotein.

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α-Linolenic acid

EPA

Cyclooxygenase Lipooxygenase

Anti-inflammatory

eicosanoids

Series 3 prostaglandins(TXA3, PGE3, PGI3)

Anti-inflammatory

eicosanoids

Series 4 leucotrienes(LTB5, LTC5, LTE5)

FIGURE 29.2Synthesis of eicosanoids from a-linolenic acid and EPA.

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affinity for EPA andDHA, enhancing b-oxidation and adipogenesis. These FA also inhibit other

important transcription factors known as sterol regulatory element-binding proteins (SREBPs),

which enhances gene expression responsible for sterol and cholesterol synthesis (Larsson et al.,2004). EPA and DHA affect the activity of acyl-CoA:cholesterol acyltransferase, which esterifies

cholesterol and avoids its accumulation in the cytosol (Deckelbaum et al., 2006).

The consumption of EPA and/or DHA contributes more significantly than the consumption of

a-linolenic acid to the prevention of CVD, thrombosis, hypertension, and death (Kumar Rudra

et al., 2001; Torrejon et al., 2007). Their positive effects are related to the alteration of theeicosonoids’ metabolism and the inhibition of proteins involved in cardiomyocytes sodium

transport, which reduces heart rate. In addition, they help to maintain calcium “L” channels,

avoiding the cytosolic saturation, especially during ischemic stress. The beneficial effect againstthrombosis is associated with the liberation of nitric oxide, which improves vascular health via

the inhibition of vasoactive protanoids.

SUMMARY POINTSl Baking tests demonstrated that it was feasible to produce DHA/u-3 fortified breads

containing 25 or 50 mg DHA/slice (32 g). Enriched breads had similar properties as thoseof the control. The flax oil bread contained the highest amount of linolenic acid but lacked

the important long-chain EPA and DHA. The fish oil bread had adequate baking properties

but lost flavor and overall acceptability during the last stages of storage.l Consumption of three slices of bread enriched with algae oil can provide almost all of the

recommended daily amount of DHA (160 mg). The supplementation of 32 mg DHA/

serving of a particular food (20% of the recommendation) allows the nutritional claim thatthe food is enriched with DHA.

l EPA and DHA play an important role in cell membrane structure and integrity, are

precursors of eicosanoids, and are involved in gene regulation affecting the activity ofimportant enzymes, receptors, and ionic channels. Both FA reduce the risk of CVD

(arrhythmias, thrombosis, atherosclerosis, and hypertension) and diabetes, and they

modulate the synthesis of eicosanoids involved in inflammatory/immune (psoriasis,asthma, cancer cell proliferation, and inflammatory intestinal disease) mechanisms and in

the regulation of transcription factors that affect lipid metabolism (PPARa and SREBP-1).

In addition, these FA affect neuron development in fetuses and neonates andphotoreceptors present in retina.

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