Buckwheat as a Functional Food and Its Effects on Health - Journal of

Aug 13, 2015 - Chengnan Zhang , Rui Zhang , Yuk Man Li , Ning Liang , Yimin Zhao ... Shelf-life extension of semi-dried buckwheat noodles by the ... J...
0 downloads 0 Views 774KB Size
Subscriber access provided by Georgetown University | Lauinger and Blommer Libraries

Review

Buckwheat as a Functional Food and its effects on Health – a Comprehensive Review Henryk Zielinski, and Juan Antonio Gimenez Bastida J. Agric. Food Chem., Just Accepted Manuscript • DOI: 10.1021/acs.jafc.5b02498 • Publication Date (Web): 13 Aug 2015 Downloaded from http://pubs.acs.org on August 20, 2015

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

Journal of Agricultural and Food Chemistry is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 65

Journal of Agricultural and Food Chemistry

254x190mm (96 x 96 DPI)

ACS Paragon Plus Environment

Journal of Agricultural and Food Chemistry

1 2 3

Buckwheat as a Functional Food and its effects on Health – a Comprehensive Review

4 5 6 7

Juan Antonio Giménez-Bastida, Henryk Zieliński*

8 9 10

Division of Food Science, Institute of Animal Reproduction and Food Research of the Polish

11

Academy of Sciences, Tuwima 10, P.O. Box 55, 10-748 Olsztyn 5, Poland

12 13 14 15 16 17 18 19

*Corresponding author: Tel.: +48 89 523 46 82. Fax: +48 89 524 01 24.

20

E-mail:[email protected]

21 22 23 24 1 ACS Paragon Plus Environment

Page 2 of 65

Page 3 of 65

25

Journal of Agricultural and Food Chemistry

ABSTRACT

26

27

Buckwheat (BW) is a gluten-free pseudocereal that belongs to the Polygonaceae family. BW

28

grain is a highly nutritional food component that has been shown to provide a wide range of

29

beneficial effects. Health benefits attributed to BW include plasma cholesterol levels´ reduction,

30

neuroprotection, anticancer, anti-inflammatory, antidiabetic effects, and improvement of

31

hypertension conditions. In addition, BW has been reported to possess prebiotic and antioxidant

32

activities. In vitro and animal studies suggest that BW´s bioactive compounds, such as D-chiro-

33

inositol (DCI), BW proteins (BWP) and BW flavonoids (mainly rutin and quercetin) may be

34

partially responsible for the observed effects. Bearing this in mind, the purpose of this paper is to

35

review the recent research regarding the health benefits of BW, in vitro and in vivo, focusing on

36

the specific the role of its bioactive compounds and on the mechanisms by which these effects

37

are exerted.

38 39 40

KEYWORDS: Common buckwheat; bioactive compounds; Fagopyrum; rutin; buckwheat

41

protein

42 43 44 45 46 47 2 ACS Paragon Plus Environment

Journal of Agricultural and Food Chemistry

48

49

INTRODUCTION The family Polygonaceae is a group of plants composed by 1200 species approximately1.

50

BW, which belongs to this family, is found almost everywhere but grows mainly in the northern

51

hemisphere. Russia and China are the main producers of BW in the world2. Furthermore, the

52

consumption of this product has become increasingly popular in United States, Canada and

53

Europe3. Among the main nine species with agricultural meaning, common BW (Fagopyrum

54

esculentum Moench) and tartary BW (F. tataricum Gaertn) are the most widely grown species.

55

Tartary BW is cultivated in some mountain regions, whereas common BW is grown from

56

temperate Europe to Japan4.

57

BW seeds are the main form of consumption of this pseudocereal. Dehulled seeds (raw

58

groats) are principally used for human consumption as breakfast cereals, or as processed flour for

59

making different bakery products (bread, cookies, snacks and noodles) enriched with BW flour

60

(0.3 – 60%), and BW-enhanced non-bakery products (tea, honey, tarhana, and sprouts)5. Since

61

BW is a gluten-free pseudoceral, these products may be included in gluten-free diets for patients

62

suffering gluten intolerance6.

63

BW is recognized as a good source of nutritionally valuable protein, lipid, dietary fiber

64

and minerals, and in combination with other health-promoting components, such as phenolic

65

compounds and sterols, it has received increasing attention as a potential functional food7.

66

Functional foods are those that exert a scientifically proven specific health benefit (health claim)

67

beyond their nutritional properties, although the consumption of its specific formulation is not

68

essential for human life8.It has been described that the consumption of BW and BW-enriched

69

products is related to a wide range of biological and healthy activities: hypocholesterolemic,

70

hypoglucemic, anticancer, and anti-inflammatory. Buckwheat proteins (BWPs) and phenolic 3 ACS Paragon Plus Environment

Page 4 of 65

Page 5 of 65

Journal of Agricultural and Food Chemistry

71

compounds are presumed to be responsible, at least in part, for these benefits4. It has been

72

recognized that some of these effects may be related to the antioxidant capacity of these

73

compounds, but newly discovered mechanisms of action may be also responsible for the

74

observed healthy effects9, 10. The purpose of this paper is to review the recent literature addressing the health benefits

75 76

of BW, its proteins and phytochemicals, and to describe the mechanisms underlying the

77

beneficial effects attributed to these compounds.

78 79

BIOACTIVE COMPOUNDS IN BUCKWHEAT

80

BW is presently considered a food component of high nutritional value. BW seed is the

81

main form of consumption, although the consumption of BW sprouts is increasingly popular in

82

North America and other parts of the world. The general composition of sprouts and dehulled,

83

unroasted BW seeds or groats from common and tartary BW is described in tables 1A7, 11-15 and

84

1B16.

85

Fagopyritols are mono-, di-, and trigalactosyl derivatives of DCI termed fagopyritols B1,

86

B2, and B3, respectively. Fagopyritols A1, A2 and A3 have also been identified as isomers of

87

B1, B2, and B3, respectively13, 17, 18. Fagopyritols are concentrated in aleurone and embryo cells

88

of the seed being the most abundant the fagopyritol B1 (0.392 mg g-1 d.m. of whole common

89

BW groats)13. DCI, the free form, is present in lower concentration (0.21 – 0.42 mg g-1 dry

90

matter –d.m.-)12. The role of DCI and fagopyritols as molecules exerting insulin-like activity has

91

been previously reported 12, 19, 20. Chemically synthesized DCI has shown to reduce elevated

92

plasma glucose level in an important number of studies21, 22. Although studies investigating the

93

effect of DCI and fagopyritols in humans have not been conducted so far, these compounds may

4 ACS Paragon Plus Environment

Journal of Agricultural and Food Chemistry

94

have positive effects in diabetes treatment. D-fagomine is a minor component detected in

95

common BW groats (1 – 25 mg kg-1 in common BW-based foodstuffs) that exhibits a glucose-

96

lowering effect23, 24. The anthraquinone emodin is present in BW at concentrations between 1.72

97

– 2.71 mg kg-1 d.m. 25. Due to the broad spectrum of biological activities exerted by emodin, it

98

may be an important bioactive factor in BW26.

99

BWPs have a high biological value due to a well-balanced amino acid composition. They

100

are rich in lysine, which is generally the first limiting amino acid in other plant proteins, and

101

arginine. However, the content in glutamine and proline is much lower than in wheat27, and

102

threonine and methionine are the first and the second limiting amino acids, respectively.

103

Thiamin-binding proteins isolated from BW may be used in the care of people who suffer from

104

the lack of thiamin7. Furthermore, many researchers reported that the low digestibility of BWPs

105

and lysine/arginine and methionine/glycine rates are critical factors in determining the

106

cholesterol-lowering effects of the plant proteins7, 28.

107

The contents and composition of flavonoids are dissimilar in different BW species.

108

Generally, the flavonoid content in F. tataricum (40 mg g-1) is higher than in F. esculentum (10

109

mg g-1) reaching concentrations of 100 mg g-1 in tartary BW flowers, leaves and stems2. BW

110

seeds (groats and hull) and sprouts are important sources of rutin (quercetin-3-rutinoside) and

111

their content depends on the variety and growth conditions29, 30. Tartary BW groats (BWG)

112

contain more rutin (80.94 mg g-1 d.m.) than common BW (0.20 mg g-1 d.m.)31, 32, while tartary

113

BW sprouts (BWS) possess 2.2 fold-time rutin than common BWS33. Rutin has attracted

114

increasing attention mainly due to its numerous beneficial effects observed in vitro and in vivo:

115

anti-inflammatory, antidiabetic, hypocholesterolemic, anti-atherosclerotic, and

116

anticarcinogenic34. Its activity has been associated with its antioxidant capacity, although the

5 ACS Paragon Plus Environment

Page 6 of 65

Page 7 of 65

Journal of Agricultural and Food Chemistry

117

precise mechanism of protection is not known. Quercitrin (quercetin-3-rhamnoside) is another

118

glycoside present in BW at concentrations ranging from 0.01 – 0.05% d.m. in tartary BW, and

119

from 0.54 – 1.80% d.m. in common BW31, 35. Isoquercetin (quercetin-3-glucoside) is present in

120

BW hypocotyls (1.4 µM g-1 d.m.)36, and it has been shown to exert antidiabetic and anticancer

121

activity37-39. The aglycone quercetin is present in BWG (0.001 mg g-1 d.m.) and BW hull (0.009

122

– 0.029 mg g-1 d.m.) at lower concentration than rutin12, 32. The flavone C-glycosides present in

123

BW seedlings (vitexin, isovitexin, orientin and homoorientin), the content of anthocyanins and

124

proanthocyanins36, and the presence of squalene, epicatechin and vitamin E (tocopherols)40 make

125

BW a good antioxidant source in human diet.

126

Phenolic acids of BW also contribute to its antioxidant capacity. 4-hydroxybenzoic (p-

127

Hydroxybenzoic), 3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid (ferulic) and 3,4-

128

dihydroxybenzoic (protocatechuic) acids are prominent in the seeds of different cultivars of

129

tartary BW, and other phenolics, including 4-hydroxycinnamic (p-coumaric), 3,4,5-

130

trihydroxybenzoic (gallic), 3,4-dihydroxycinnamic (caffeic), 4-hydroxy-3-methoxybenzoic

131

(vanillic) and 3,5-dimethoxy-4-hydroxybenzoic (syringic) acids have been detected41. Several

132

phenolic acids were described in the inflorescences of different varieties of BW: 3-(3,4-

133

dihydroxycinnamoyl)quinic (chlorogenic), 4-methoxybenzoic (p-anisic), 2-hydroxybenzoic

134

(salicylic) and methoxycinnamic acid42. The most abundant phytosterol in BW flour (BWF) is β-

135

sitosterol (0.86 mg g-1 d.m.) followed by campesterol (0.11 mg g-1 d.m.) and stigmasterol (0.02

136

mg g-1 d.m.)43.

137

BW is also an important source of vitamins. Total vitamin B content, including B1

138

(thiamin, 2.2 – 3.3 µg g-1 d.m.), B2 (riboflavin, 10.6 µg g-1 d.m.), B3 (niacin, 18 µg g-1), B5

139

(pantothenic acid, 11 µg g-1) and B6 (piridoxine, 1.5 µg g-1), is higher in tartary BW than in 6 ACS Paragon Plus Environment

Journal of Agricultural and Food Chemistry

140

common BW, and the levels of vitamic C have been reported as 50 µg g-1 d.m., reaching up to

141

250 µg g-1 d.m. in sprouts5, 44, 45. Along with vitamins, other compounds such as glutathione

142

(1.10 mmol g-1 d.m. in BWG), phytic acid (35 - 38 mg g-1 d.m. in BW bran), carotenoids (2.10

143

mg g-1 d.m. in BW seeds), and melatonin (470 pg g-1 d.m. in BWG) have been detected and may

144

contribute to the antioxidant activity of BW4, 32.

145

Recently, γ-aminobutyric acid (GABA) and 2”-hydroxynicotianamine (2HN) have been found to

146

serve as functional compounds in BW. Seeds and sprouts contain GABA, while 2HN has been

147

recently identified in BWF. These compounds have been reported to reduce blood pressure in

148

humans, and to inhibit the angiotensin I converting enzyme (ACE) activity46-48.

149

HEALTH BENEFITS AND BUCKWHEAT

150 151

Antioxidant activity

152

Increasing appreciation of the nutritional and functional properties of BW has also

153

encouraged some investigations about its antioxidant properties. The antioxidant features of BW

154

pseudocereals appear reflected in human intervention studies. There have been reported increases

155

in the total antioxidant capacity of plasma samples from healthy donors after consuming 1.5 g of

156

BW honey kg-1 (single dose, n=37)49, or when BW honey was added to water or black tea (160 g

157

honey L-1, n=25)50 as well as after BW-enriched wheat bread consumption51.

158

The biological antioxidant capacity of BW is further supported by in vivo experimental models

159

fed a BWH-containing diet (0.75% in diet, 14 days)52, a BW by-product-enriched diet (15% for 4

160

weeks)53 and 100 and 200 mg of BW kg-1 day-1 for 20 days54. The results showed increased

161

activity of antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT),

162

gluthatione peroxidase (GSH-Px), reduced lipid peroxidation parameters such as thiobarbituric

7 ACS Paragon Plus Environment

Page 8 of 65

Page 9 of 65

Journal of Agricultural and Food Chemistry

163

acid reactive substances (TBARS), malondialdehyde (MDA), and fluorescent substance (FLS) in

164

plasma samples, red blood cells, and several different organs (heart, kidney, liver and brain). In

165

contrast, total plasma antioxidant status and the activities of SOD and GSH-Px were unaltered in

166

healthy rats fed a normal diet containing 30% expanded BW seeds or 5% of BWS for 4 weeks55.

167

In vitro antioxidant activity of BW has been assessed in relation to its phenolic content and

168

composition41, 42, 56-59 and compared to that of other cereals and pseudocereals60-63. In this sense,

169

Zieliński and Kozłowska established the following hierarchy of antioxidant activity: BW >

170

barley > oat > wheat ~ rye64. The high antioxidant capacity of BW is connected with high

171

polyphenol content, especially rutin65, 66. Liu et al. described the antioxidant effects of BWS in

172

human hepatoma HepG2 cells, revealing that tartary and common BW had a positive effect on

173

the production of intracellular peroxide and superoxide anions. Tartary BW was more effective

174

than common BW and this effect was associated with the higher concentration of rutin16. Studies

175

by Zhou et al. also reported that BW honey showed protective effects on hydroxyl radicals-

176

induced DNA damage through is antioxidant activity67. These studies seem to indicate that BW

177

may exert its beneficial effects through its antioxidant activity.

178 179

Hypocholesterolemic activity

180

Increased cholesterol intake can induce oxidative stress and cause an increase in blood

181

cholesterol level, leading to the up-regulation of low density lipoproteins (LDL) and oxidized

182

LDL (oxLDL), contributing to the development of chronic diseases such as atheroclerosis68. In

183

vitro and in vivo studies have proposed that BW’s protective effect against cardiovascular

184

diseases may come from its ability to modulate cholesterol (Ch) level.

8 ACS Paragon Plus Environment

Journal of Agricultural and Food Chemistry

185

The number of studies investigating the cholesterol-lowering activity of BW in humans is

186

scarce (Table 2). The investigation carried out by Zhang et al. in 2007 is one of the biggest

187

studies in relation to the consumption of BW and health. 3542 Mongolians in two adjacent

188

countries of Inner Mongolia (China) were randomly sampled in a cross-sectional study to assess

189

the association of hypertension, dyslipidaemia, and hyperglycaemia with lifetime consumption of

190

BW seed as a staple food. The authors described a reduction of total cholesterol (TCh) (4%;

191

p0.05) and LDL (9.05%; p