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Kreft, I.; Golob, A.; Vombergar, B.; Germ, M. Interaction among Substances in Buckwheat Groats. Encyclopedia. Available online: https://encyclopedia.pub/entry/42198 (accessed on 17 June 2024).
Kreft I, Golob A, Vombergar B, Germ M. Interaction among Substances in Buckwheat Groats. Encyclopedia. Available at: https://encyclopedia.pub/entry/42198. Accessed June 17, 2024.
Kreft, Ivan, Aleksandra Golob, Blanka Vombergar, Mateja Germ. "Interaction among Substances in Buckwheat Groats" Encyclopedia, https://encyclopedia.pub/entry/42198 (accessed June 17, 2024).
Kreft, I., Golob, A., Vombergar, B., & Germ, M. (2023, March 14). Interaction among Substances in Buckwheat Groats. In Encyclopedia. https://encyclopedia.pub/entry/42198
Kreft, Ivan, et al. "Interaction among Substances in Buckwheat Groats." Encyclopedia. Web. 14 March, 2023.
Interaction among Substances in Buckwheat Groats
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Tartary buckwheat (Fagopyrum tataricum Gaertn.) originates in mountain regions of Western China, and is cultivated in China, Bhutan, Northern India, Nepal, and Central Europe. The content of flavonoids in Tartary buckwheat grain and groats is much higher than in common buckwheat (Fagopyrum esculentum Moench), and depends on ecological conditions, such as UV-B radiation. Buckwheat intake has preventative effects in chronic diseases, such as cardiovascular diseases, diabetes, and obesity, due to its content of bioactive substances. The main bioactive compounds in Tartary buckwheat groats are flavonoids (rutin and quercetin). There are differences in the bioactivities of buckwheat groats obtained using different husking technologies, based on husking raw or pretreated grain. Husking hydrothermally pretreated grain is among the traditional ways of consuming buckwheat grain in Europe and some parts of China and Japan.

Fagopyrum tataricum Fagopyrum esculentum flavonoids

1. Technologies for Husking Buckwheat Grain and Preparing Groats

Due to their robust husk, dormant Tartary buckwheat seeds may remain alive in the soil for several years and, under favorable conditions, can be activated. Tartary buckwheat may appear as a weed in other crops and is often a weed in a crop of common buckwheat (Fagopyrum esculentum Moench) [1].
One method to husk buckwheat is to use non-precooked grain. The raw husked common buckwheat groats are green when newly harvested buckwheat is husked. After some weeks, chlorophyll fades and phenolic substances oxidize, so the older non-precooked buckwheat groats are yellow, and later become reddish. From the green color it is possible to estimate if raw husked groats are fresh and made from newly harvested common buckwheat. By pressing the flat side of the knife, non-precooked groats are broken into floury particles, and when cooking the groats, they become slimy [1][2].
Buckwheat groats obtained by precooking are harder, and break under pressure into larger particles with a vitreous appearance. Precooked buckwheat groats (husked buckwheat grain) cook nicely, and they also have a special taste. Substances of traditional buckwheat groats, important for this distinctive taste, have been studied [3]. Buckwheat groats are popular in Slovenia, Croatia, Poland, Belarus, Ukraine, Russia, some parts of China (Shanxi and Shaanxi), and Japan (Shikoku island) [1][2]. They were also once known in Carinthia, Austria. In Karelia (Finland), buckwheat groats cooked in milk or cream are added on the top of traditional open pierogi (karjalan piirakka) on a base of rye dough [1][2].
For husking, precooked buckwheat grains are firstly soaked in boiling water, and during this treatment, the starch swells. In doing so, the husk bursts on one of the three corners. When ready, the water is removed and the grain is dried at a moderate temperature. In old times, the grain was traditionally dried on canvas in the shade or on a warm top of a wood-burning stove. The grains were repeatedly mixed to dry evenly. They were dried only so that the husk was dry and brittle, and the inside of the grain was elastic, but solid enough not to squeeze or smear when the process continued. Properly dried grain was placed in a husking device called a stope. A stope consists of a stable hollowed trunk with an opening for at least five liters of grain. Above the opening is a fixed beam with a downward-facing iron tip with horizontal ribs. The beam went up several tens of inches and then fell freely into the prepared grain. This was repeated as needed, even a hundred times if necessary. When the grains were struck, the husk was separated from the grain, and groats (kasha) were formed. When most grains were husked, farmers used ventilation to separate light husks from heavier kasha grains. In areas rich in streams, the stopes were powered by water wheels. Stopes were foot-powered in plain landscapes. In Carinthia, Austria, hydrothermally pretreated buckwheat was husked by treading on grain with heavy wooden shoes [4]. Preparing husked buckwheat grain, kasha, is very challenging. The process has been known among Slovenians for a long time, as was described by Valvasor [5].
The modern husking of buckwheat grain is essentially the same as it used to be—cooking, drying, husking, drying again, and blowing off the husks. The details of technology are the intellectual property of each producer, especially in husking technology for Tartary buckwheat, which is because of the significant issue of thick husks. To separate the remaining unhusked grain from the husked grain, producers use photocell-supported equipment. Buckwheat kasha obtained the traditional way by precooking before husking has a special taste and properties, including the composition of bioactive substances. Tartary buckwheat grains have a much higher content of rutin and total flavonoids than common buckwheat grains. In addition, the husked grains of Tartary buckwheat have a much higher content of rutin than the husked grains of common buckwheat. As a result of hydrothermal treatment, husked Tartary buckwheat grains contain much less rutin in comparison to intact grains, but a much higher content of quercetin. This is the result of the enzymatic conversion of rutin to quercetin during hydrothermal treatment.

2. Impact of Buckwheat Phenolic Substances on Proteins and Cholesterol

During husking and the hydrothermal pretreatment of buckwheat grain, phenolic substances have an impact on protein digestibility [6]. Substantial interactions have been reported between proteins and phenolic substances, and as such, the digestibility of buckwheat proteins is reduced. In any way, microbial processes in the large intestine enhance the digestion of proteins [6]. It was established that phenolic substances in buckwheat grain lower the digestibility of proteins. Ikeda et al. [7] reported that tannic acid and catechin significantly inhibit the in vitro peptic and pancreatic digestion of buckwheat globulin. Ikeda et al. [7] and Ikeda and Kishida [8] studied the impact of secondary buckwheat metabolites on the in vitro digestibility of buckwheat grain proteins. It was established that undigested buckwheat proteins can reduce cholesterol levels in serum by increasing the fecal excretion of steroids, which is induced by the binding of steroids to proteins. Ma and Xiong [9] reported that digestion-resistant peptides are largely responsible for the elimination of bile acids and lowering the risk of the appearance of a high level of cholesterol in human serum. In this way, buckwheat proteins, in their interaction with phenolic substances, protect the human cardiovascular system.

3. Transformation of Phenolic Substances

The treatment of Tartary buckwheat grain with water impacts the transformation of rutin to quercetin by the rutin-degrading enzyme [10][11][12][13]. The activity of the rutin-degrading enzyme is prevented when buckwheat grains are exposed to temperatures at about 80 °C or higher during husking treatment [13].
Ingested quercetin can cross the blood–brain barrier and accumulate in the brain tissue [14]. Indeed, important bioactivities have been established for quercetin and its derivatives, not just in blood vessels, muscle, and the gastrointestinal system, but also in the brain. Quercetin and other phenolic metabolites have been isolated from the stool samples of people who had eaten food rich in phenolic substances [14].
Phenolic compounds are often transformed in the gut before their absorption. The gut microbiota are essential in this process [15]. Large-sized dietary phenolic substances are poorly absorbed, while small-sized products of microbial conversion are more easily absorbed in the colon. It is interesting to note the suitability of buckwheat groats for feeding dogs. There are nutritional differences between buckwheat groats that are husked raw and those that are husked after the precooking of the grain. The first are toxic to dogs and cause them liver damage, and the second can be safely consumed [16]. Carnivores are susceptible to low-molecular-weight tannins, but not to high-molecular-weight tannins. Conversion occurs in the case of precooked buckwheat groats, but not in groats obtained without precooking.

4. Tartary Buckwheat Diet in the Prevention of Diabetes

The complexation of quercetin in Tartary buckwheat materials with molecules of starch has an influence on the in vitro digestibility and physicochemical properties of starch [17]. The effects of quercetin–starch complexation indicate that food products based on Tartary buckwheat have lower starch digestibility. Indeed, quercetin in Tartary buckwheat can reduce body weight, serum triacylglycerols, and low-density lipoprotein. In rats, a diet with 0.1% quercetin was shown to have the significant impact of lowering low-density lipoprotein concentrations in serum, with no such effects on high-density lipoprotein. Tartary buckwheat has also been shown to prevent increases in body weight and fat deposition during high-fat intake in rats, although on the other hand, this was reported to protect against hepatic stenosis [18][19][20]. A buckwheat diet can also reduce insulin and ameliorate glucose intolerance in humans [21].
Rat experiments with common buckwheat have further suggested the complexity of the impact of the gut microbiota. Indeed, Peng et al. [20] suggested that the link between weight gain and the gut microbiota is very complex, with a need for further studies. Luo et al. [22] studied the slow digestion properties of Tartary buckwheat starch treated with ethanol extract. The slow digestibility of this starch appeared to be due to the impact of phenolic substances on starch. In the in vivo experiments, mice showed reduced postprandial glycemic responses. The data of Luo et al. [22] for Tartary buckwheat grain and glycemic responses were similar to those obtained earlier in common buckwheat [21].

5. Buckwheat Groats in a Health-Preserving Diet

In Japan, buckwheat groats are less well known than in Europe [2]. However, soup with buckwheat groats (soba-gome) is served in Tokushima on Shikoku island [23]. In China, Tartary buckwheat groats are known in some regions, for example, in Shanxi and Shaanxi [2].
Many dishes can be made with common or Tartary buckwheat kasha [24][25]. Some attractive dishes can be made simply by replacing white rice or husked barley with common or Tartary buckwheat kasha. It is possible to cook buckwheat kasha one day, preserve it overnight in the refrigerator, and mix it into oil-fried vegetables (sliced pumpkins, tomatoes, etc.) the next day, or mix it with cottage cheese, cream, and/or walnuts, and/or sliced apples for baking in the oven [24]. In addition to rutin, buckwheat dishes, especially Tartary buckwheat dishes, contain metabolites such as tannins and quercetin, which also inhibit starch degradation [1][26][27]. As a food rich in quercetin, Tartary buckwheat groats may hold nutraceutic potential against SARS-CoV-2 due to their ability to inhibit the virus at various stages of its life cycle [28][29].

6. Bioactivity Impact of Metabolites

During the treatment of Tartary buckwheat groat, the concentrations of bioactive substances with strong impacts on human health are altered. This includes the concentration of rutin and quercetin in buckwheat groats.
The supplementation of rutin-rich diets with vitamin C is able to reduce oxidative stress, have an impact on glycemic stress, and reduce fasting blood glucose in patients with type 2 diabetes [18]. A rutin-rich Tartary buckwheat diet may be effective in reducing body weight through its antioxidant effects [19][30]. The fermentation of dietary fiber from Tartary buckwheat helps to improve its solubility, in addition to the impact of flavonoids on countering obesity [30].
Phenolic substances in buckwheat have significant bioactivities in addition to their antioxidative and anti-inflammatory effects [31]. Phenolic substances incorporated in the hydrophilic erythrocyte membranes are barriers against free radicals. This is possible because of the double nature of phenolic substances: a lipophilic phenolic aglycone and a hydrophilic sugar part. Buckwheat flavonoid extracts have an impact on the antioxidant system in the liver and brain [32].
Ingested quercetin and its glycosides are metabolized during human digestion, and are absorbed and transported as conjugates with the blood. A major metabolite of quercetin is quercetin-glucuronide, which is transported to the target tissues. Following the separation of the sugar part of hydrophilic quercetin-glucuronide, the hydrophobic aglycone remains at injured sites to perform the improvement of pathological conditions [14].
High levels of rutin and quercetin in Tartary buckwheat, and high levels of antioxidative impacts, have further effects on the cytotoxic and antigenotoxic impacts [27][33]. A study of the antigenotoxic effects of Tartary buckwheat in human hepatoma cell lines has shown that flavonoid-rich Tartary buckwheat products are more effective for maintaining health in their complexed form than as the single active substances, rutin or quercetin [33]. It has been suggested that the Tartary buckwheat metabolites rutin and quercetin may be effective against cancers, based on experiments in cell lines and animal models for mammary, colon, skin, and other cancers [34][35][36][37][38][39].

References

  1. Kreft, I. Grenko Seme Tatarske Ajde; Slovenska Akademija Znanosti in Umetnosti: Ljubljana, Slovenia, 2020.
  2. Kreft, I. Bitter Seed Tartary Buckwheat; Kreft, I., Ed.; Slovenian Academy of Sciences and Arts; Fagopyrum–Slovenian Association for Buckwheat Promotion: Ljubljana, Slovenia, 2022.
  3. Janeš, D.; Prosen, H.; Kreft, I.; Kreft, S. Aroma Compounds in Buckwheat (Fagopyrum esculentum Moench) Groats, Flour, Bran, and Husk. Cereal Chem. 2010, 87, 141–143.
  4. Scheucher, S. Buchweizen in Österreich: Geschichtliches und Kulinarisches. In Das Buchweizenbuch; Islek ohne Grenzen: Islek, Luxemburg, 1999.
  5. Valvasor, J.V. Die Ehre Dess Hertzogthums Crain, Das Ist, Wahre, Gründliche, und Recht Eigendliche Belegen- und Beschaffenheit Dieses; Römisch-Keyserlichen herrlichen Erblandes: Ljubljana, Slovenia, 1689.
  6. Škrabanja, V.; Lærke, H.N.; Kreft, I. Protein-Polyphenol Interactions and in Vivo Digestibility of Buckwheat Groat Proteins. Pflugers Arch. Eur. J. Physiol. 2000, 440, R129–R131.
  7. Ikeda, K.; Oku, M.; Kusano, T.; Yasumoto, K. Inhibitory Potency of Plant Antinutrients towards the In Vitro Digestibility of Buckwheat Protein. J. Food Sci. 1986, 51, 1527–1530.
  8. Ikeda, K.; Kishida., M. Digestibility of Proteins in Buckwheat Seed. Fagopyrum 1993, 13, 21–24.
  9. Ma, Y.; Xiong, Y.L. Antioxidant and Bile Acid Binding Activity of Buckwheat Protein in Vitro Digests. J. Agric. Food Chem. 2009, 57, 4372–4380.
  10. Suzuki, T.; Morishita, T.; Takigawa, S.; Noda, T.; Ishiguro, K. Characterization of Rutin-Rich Bread Made with ‘Manten-Kirari’, a Trace-Rutinosidase Variety of Tartary Buckwheat (Fagopyrum tataricum Gaertn.). Food Sci. Technol. Res. 2015, 21, 733–738.
  11. Suzuki, T.; Morishita, T.; Kim, S.J.; Park, S.U.; Woo, S.H.; Noda, T.; Takigawa, S. Physiological Roles of Rutin in the Buckwheat Plant. Japan Agric. Res. Q. JARQ 2015, 49, 37–43.
  12. Suzuki, T.; Morishita, T.; Noda, T.; Ishiguro, K. Acute and Subacute Toxicity Studies on Rutin-Rich Tartary Buckwheat Dough in Experimental Animals. J. Nutr. Sci. Vitaminol. 2015, 61, 175–181.
  13. Germ, M.; Árvay, J.; Vollmannová, A.; Tóth, T.; Golob, A.; Luthar, Z.; Kreft, I. The Temperature Threshold for the Transformation of Rutin to Quercetin in Tartary Buckwheat Dough. Food Chem. 2019, 283, 28–31.
  14. Kawabata, K.; Mukai, R.; Ishisaka, A. Quercetin and Related Polyphenols: New Insights and Implications for Their Bioactivity and Bioavailability. Food Funct. 2015, 6, 1399–1417.
  15. Selma, M.V.; Espín, J.C.; Tomás-Barberán, F.A. Interaction between Phenolics and Gut Microbiota: Role in Human Health. J. Agric. Food Chem. 2009, 57, 6485–6501.
  16. Lineva, A.; Benković, E.T.; Kreft, S.; Kienzle, E. Remarkable Frequency of a History of Liver Disease in Dogs Fed Homemade Diets with Buckwheat. Tierarztl. Prax. Ausg. K Kleintiere. Heimtiere 2019, 47, 242–246.
  17. Li, Y.; Gao, S.; Ji, X.; Liu, H.; Liu, N.; Yang, J.; Lu, M.; Han, L.; Wang, M. Evaluation Studies on Effects of Quercetin with Different Concentrations on the Physicochemical Properties and in Vitro Digestibility of Tartary Buckwheat Starch. Int. J. Biol. Macromol. 2020, 163, 1729–1737.
  18. Ragheb, S.R.; El Wakeel, L.M.; Nasr, M.S.; Sabri, N.A. Impact of Rutin and Vitamin C Combination on Oxidative Stress and Glycemic Control in Patients with Type 2 Diabetes. Clin. Nutr. ESPEN 2020, 35, 128–135.
  19. Nishimura, M.; Ohkawara, T.; Sato, Y.; Satoh, H.; Suzuki, T.; Ishiguro, K.; Noda, T.; Morishita, T.; Nishihira, J. Effectiveness of Rutin-Rich Tartary Buckwheat (Fagopyrum tataricum Gaertn.) ‘Manten-Kirari’ in Body Weight Reduction Related to Its Antioxidant Properties: A Randomised, Double-Blind, Placebo-Controlled Study. J. Funct. Foods 2016, 26, 460–469.
  20. Peng, L.; Zhang, Q.; Zhang, Y.; Yao, Z.; Song, P.; Wei, L.; Zhao, G.; Yan, Z. Effect of Tartary Buckwheat, Rutin, and Quercetin on Lipid Metabolism in Rats during High Dietary Fat Intake. Food Sci. Nutr. 2020, 8, 199–213.
  21. Škrabanja, V.; Liljeberg Elmståhl, H.G.M.; Kreft, I.; Björck, I.M.E. Nutritional Properties of Starch in Buckwheat Products: Studies in Vitro and in Vivo. J. Agric. Food Chem. 2000, 49, 490–496.
  22. Luo, K.; Zhou, X.; Zhang, G. The Impact of Tartary Buckwheat Extract on the Nutritional Property of Starch in a Whole Grain Context. J. Cereal Sci. 2019, 89, 102798.
  23. Ikeda, K.; Ikeda, S. Buckwheat in Japan. In Ethnobotany of Buckwheat; Kreft, I., Chang, K.J., Choi, Y.S., Park, C.H., Eds.; Jinsol Publishing Co.: Seoul, Republic of Korea, 2003; pp. 54–69.
  24. Vombergar, B.; Tašner, L.; Horvat, M.; Vorih, S.; Pem, N.; Golob, S.; Kovač, T. Buckwheat–Challenges in Nutrition and Technology. Fagopyrum 2022, 39, 33–42.
  25. Vombergar, B.; Luthar, Z. Starting Points for the Study of the Effects of Flavonoids, Tannins and Crude Proteins in Grain Fractions of Common Buckwheat (Fagopyrum esculentum Moench) and Tartary Buckwheat (Fagopyrum tataricum Gaertn.). Folia Biol. Geol. 2018, 59, 101.
  26. Ikeda, K.; Ishida, Y.; Ikeda, S.; Asami, Y.; Lin, R. Tartary, but Not Common, Buckwheat Inhibits α-Glucosidase Activity: Its Nutritional Implications. Fagopyrum 2017, 34, 13–18.
  27. Kreft, M. Buckwheat Phenolic Metabolites in Health and Disease. Nutr. Res. Rev. 2016, 29, 30–39.
  28. Gasmi, A.; Mujawdiya, P.K.; Lysiuk, R.; Shanaida, M.; Peana, M.; Gasmi Benahmed, A.; Beley, N.; Kovalska, N.; Bjørklund, G. Quercetin in the Prevention and Treatment of Coronavirus Infections: A Focus on SARS-CoV-2. Pharmaceuticals 2022, 15, 1049.
  29. Pawar, A.; Pal, A.; Goswami, K.; Squitti, R.; Rongiolettie, M. Molecular Basis of Quercetin as a Plausible Common Denominator of Macrophage-Cholesterol-Fenofibrate Dependent Potential COVID-19 Treatment Axis. Results Chem. 2021, 3, 100148.
  30. Huang, Y.; Zhang, K.; Guo, W.; Zhang, C.; Chen, H.; Xu, T.; Lu, Y.; Wu, Q.; Li, Y.; Chen, Y. Aspergillus Niger Fermented Tartary Buckwheat Ameliorates Obesity and Gut Microbiota Dysbiosis through the NLRP3/Caspase-1 Signaling Pathway in High-Fat Diet Mice. J. Funct. Foods 2022, 95, 105171.
  31. Włoch, A.; Strugała, P.; Pruchnik, H.; Żyłka, R.; Oszmiański, J.; Kleszczyńska, H. Physical Effects of Buckwheat Extract on Biological Membrane In Vitro and Its Protective Properties. J. Membr. Biol. 2016, 249, 155–170.
  32. Sadauskiene, I.; Liekis, A.; Bernotiene, R.; Sulinskiene, J.; Kasauskas, A.; Zekonis, G. The Effects of Buckwheat Leaf and Flower Extracts on Antioxidant Status in Mouse Organs. Oxid. Med. Cell. Longev. 2018, 2018, 6712407.
  33. Vogrinčič, M.; Kreft, I.; Filipič, M.; Žegura, B. Antigenotoxic effect of Tartary (Fagopyrum tataricum) and common (Fagopyrum esculentum) buckwheat flour. J. Med. Food 2013, 16, 944–952.
  34. Kayashita, J.; Shimaoka, I.; Nakajoh, M.; Kishida, N.; Kato, N. Consumption of a buckwheat protein extract retards 7,12-dimethylbenzanthracene-induced mammary carcinogenesis in rats. Biosci. Biotechnol. Biochem. 1999, 63, 1837–1839.
  35. Valido, E.; Stoyanov, J.; Gorreja, F.; Stojic, S.; Niehot, C.; Kiefte-de Jong, J.; Llanaj, E.; Muka, T.; Glisic, M. Systematic Review of Human and Animal Evidence on the Role of Buckwheat Consumption on Gastrointestinal Health. Nutrients 2023, 15, 1.
  36. Dziedzic, K.; Górecka, D.; Szwengiel, A.; Olejnik, A.; Rychlik, J.; Kreft, I.; Drozdzynska, A.; Walkowiak, J. The cytotoxic effect of artificially digested buckwheat products on HT-29 colon cancer cells. J. Cereal Sci. 2018, 83, 68–73.
  37. Zhou, X.-L.; Chen, Z.-D.; Zhou, Y.-M.; Shi, R.-H.; Li, Z.-J. The Effect of Tartary Buckwheat Flavonoids in Inhibiting the Proliferation of MGC80-3 Cells during Seed Germination. Molecules 2019, 24, 3092.
  38. Nouri, Z.; Fakhri, S.; Nouri, K.; Wallace, C.E.; Farzaei, M.H.; Bishayee, A. Targeting Multiple Signaling Pathways in Cancer: The Rutin Therapeutic Approach. Cancers 2020, 12, 2276.
  39. Mansi, K.; Kumar, R.; Narula, D.; Kumar Pandey, S.; Vinod Kumar, V.; Kulvinder Singh, K. Microwave-Induced CuO Nanorods: A Comparative Approach between Curcumin, Quercetin, and Rutin to Study Their Antioxidant, Antimicrobial, and Anticancer Effects against Normal Skin Cells and Human Breast Cancer Cell Lines MCF-7 and T-47D. ACS Appl. Bio. Mater. 2022, 5, 5762–5778.
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