DOI QR코드

DOI QR Code

Effects of Dietary β-Glucan on Short Chain Fatty Acids Composition and Intestinal Environment in Rats

식이 베타-글루칸이 흰쥐의 장내 단쇄지방산 조성 및 장내환경 개선에 미치는 영향

  • Hong, Kyung Hee (Dept. of Food Science and Nutrition, Dongseo University) ;
  • Jang, Ki-Hyo (Dept. of Food and Nutrition, Kangwon National University) ;
  • Kang, Soon Ah (Institute of Health Industry, Hoseo University)
  • 홍경희 (동서대학교 식품영양학과) ;
  • 장기효 (강원대학교 식품영양학과) ;
  • 강순아 (호서대학교 보건산업연구소)
  • Received : 2016.03.17
  • Accepted : 2016.03.25
  • Published : 2016.04.30

Abstract

The effects of dietary ${\beta}$-glucan, obtained from bacterial fermentation, on the intestinal mass, short chain fatty acids, lactate production and pH in Sprague-Dawley (SD) rats were evaluated. SD rats fed with 0% (control group), 1% or 5% ${\beta}$-glucan supplemented diets (w/w) for 3 weeks. The presence of ${\beta}$-glucan in the diets resulted in a significant increase in colonic contents in a dose dependent manner. The amount of short chain fatty acids increased in rats fed ${\beta}$-glucan diets. Rats fed the 5% ${\beta}$-glucan diets had higher levels of acetate, propionate and butyrate by 1.8, 1.7 and 3.0 fold of the control group in the cecum, and 2.2, 2.9 and 3.1 fold of the control group in the colon, respectively. The ${\beta}$-glucan diets also significantly increased the levels of cecal and colonic lactate by 1.4~3.4 fold, when compared to the control diet, indicating that dietary ${\beta}$-glucan stimulated the growth of lactic acid bacteria within the intestine. These results suggest that dietary ${\beta}$-glucan, by providing short chain fatty acids and reducing the cecal and colonic pH, may be beneficial in improving gut health, and provide evidence for the use of ${\beta}$-glucan as a dietary supplement for human consumption.

Keywords

References

  1. AbuMweis SS, Jew S, Ames NP. 2010. ${\beta}$-Glucan from barley and its lipid-lowering capacity: A meta-analysis of randomized, controlled trials. Eur J Clin Nutr 64:1472-1480 https://doi.org/10.1038/ejcn.2010.178
  2. Adam CL, Williams PA, Dalby MJ, Garden K, Thomson LM, Richardson AJ, Gratz SW, Ross AW. 2014. Different types of soluble fermentable dietary fibre decrease food intake, body weight gain and adiposity in young adult male rats. Nutr Metab 14;11:36 https://doi.org/10.1186/1743-7075-11-36
  3. Babi'cek K, Cechova' I, Simon RR. 2007. Toxicological assessment of a particulate yeast (1,3/1,6)-beta-D-glucan in rats. Food Chem Toxicol 45:1719-1730 https://doi.org/10.1016/j.fct.2007.03.013
  4. Campbell JM, Fahey GC Jr, Wolf BW. 1997. Selected indigestible oligosaccharides affect large bowel mass, cecal and fecal short-chain fatty acids, pH and microflora in rats. J Nutr 127:130-136 https://doi.org/10.1093/jn/127.1.130
  5. CIntosh M, Stone BA, Stanisich VA. 2005. Curdlan and other bacterial (1(3)-beta-D-glucans". Appl Microbiol Biotechnol 68:163-173 https://doi.org/10.1007/s00253-005-1959-5
  6. Cook SI, Sellin JH. 1998. Short chain fatty acids in health and disease. Aliment Pharmacol Ther 12:499-507 https://doi.org/10.1046/j.1365-2036.1998.00337.x
  7. Delaney B, Nicolosi RJ, Wilson TA. 2003. Beta-glucan fractions from barley and oats are similarly antiatherogenic in hypercholesterolemic Syrian golden hamsters. J Nutr 133:468-475 https://doi.org/10.1093/jn/133.2.468
  8. Dijkgraff GJ, Li PH, Bussey J. 2002. Biopolymers, Vol 6. Cell-wall ${\beta}$-glucan of Saccharomyces cerevisiae. pp.179-205. Wiley-VCH Verlag Gmbh, Germany
  9. Fedel JG, Newman RK, Newman CW, Barns AE. 1987. Hypocholesterolemic effects of ${\beta}$-glucans in different barley diets fed to broiler chicks. Nutr Rep Int 35:1049-1058
  10. Flint HJ. 2012. The impact of nutrition on the human microbiome. Nutr Rev 70 Suppl 1:S10-3 https://doi.org/10.1111/j.1753-4887.2012.00499.x
  11. Gibson GR, Roberfroid MB. 1995. Dietary modulation of the human colonic microbiota: Introducing the concept of prebiotics. J Nutr 25:1401-1412
  12. Hague A, Elder DJ, Hicks DJ, Paraskeva C. 1995. Apoptosis in colorectal tumour cells: induction by the short chain fatty acids butyrate, propionate and acetate and by the bile salt deoxycholate. Int J Cancer 60:400-406 https://doi.org/10.1002/ijc.2910600322
  13. Han MD, Kim YH, Kim WJ. 2014. In vivo growth inhibition of Sarcoma-180 cells by a ${\beta}$-glucan from the mushroom Ganoderma lucidu. J Life Sci 24:721-727 https://doi.org/10.5352/JLS.2014.24.7.721
  14. Hijova E, Chmelarova A. 2007. Short chain fatty acids and colonic health. Bratisl Lek Listy 108:354-358
  15. Jakobsdottir G, Jädert C, Holm L, Nyman ME. 2013. Propionic and butyric acids, formed in the caecum of rats fed highly fermentable dietary fibre, are reflected in portal and aortic serum. Br J Nutr 110:1565-1572 https://doi.org/10.1017/S0007114513000809
  16. Jenkins DJ, Wolever TM, Jenkins A, Brighenti F, Vuksan V, Rao AV, Cunnane SC, Ocana A, Corey P, Vezina C. 1991. Specific types of colonic fermentation may raise low-densitylipoprotein-cholesterol concentrations. Am J Clin Nutr 54:141-147 https://doi.org/10.1093/ajcn/54.1.141
  17. Kang SA, Jan KH, Hong KH, Choi WA, Jung KH, Lee IY. 2002. Effects of dietary ${\beta}$-glucan on adiposity and serum lipids levels in obese rats induced by high fat diet. J Korean Soc Food Nutr 31:1052-1057 https://doi.org/10.3746/jkfn.2002.31.6.1052
  18. Khoury D El, Cuda C, Luhovyy BL, Anderson GH. 2012. Beta glucan: Health benefits in obesity and metabolic syndrome. J Nutr Metab 2012(851362)
  19. Kim DH, Han MJ. 1995. Inhibition of intestinal bacterial enzyme by lactic acid bacteria. Yakhak Hoeji 38:169-174
  20. Kim MK, Ryu KE, Choi WA, Rhee YH, Lee IY. 2002. Enhanced production of (1,3)-${\beta}$-D-glucan by a mutant strain of Agrobacterium species. Biochemical Engineering J 16:163-168
  21. Kimura K, McCartney AL, McConnell MA, Tannock GW. 1997. Analysis of fecal populations of bifidobacteria and lactobacilli and investigation of the immunological responses of their human hosts to the predominant strains. Appl Environ Microbiol 63:3394-3398
  22. Kumar V, Sinha AK, Makkar HP, de Boeck G, Becker K. 2012. Dietary roles of non-starch polysaccharides in human nutrition. Crit Rev Food Sci Nutr 52:899-935 https://doi.org/10.1080/10408398.2010.512671
  23. Le Blay G, Michel C, Blottière HM, Cherbut C. 1999. Prolonged intake of fructo-oligosaccharides induces a short-term elevation of lactic acid-producing bacteria and a persistent increase in cecal butyrate in rats. J Nutr 129:2231-2235 https://doi.org/10.1093/jn/129.12.2231
  24. Lim BO, Lee CJ, Kim JD. 2004. Study on immunoregulatory function of dietary fiber. Food Ind Nutr 9:26-30
  25. Lobo AR, Filho JM, Alvares EP, Cocato ML, Colli C. 2009. Effects of dietary lipid composition and inulin-type fructans on mineral bioavailability in growing rats. Nutrition 25:216-225 https://doi.org/10.1016/j.nut.2008.08.002
  26. Macfarlane S, Macfarlane GT. 2003. Regulation of short-chain fatty acid production. Proc Nutr Soc 62:67-72 https://doi.org/10.1079/PNS2002207
  27. Manning TS, Gibson GR. 2004. Microbial-gut interactions in health and disease. Prebiotics. Best Pract Res Clin Gastroenterol 18:287-298 https://doi.org/10.1016/j.bpg.2003.10.008
  28. Metzler-Zebeli BU, Hooda S, Mosenthin R, Gänzle MG, Zijlstra RT. 2010. Bacterial fermentation affects net mineral flux in the large intestine of pigs fed diets with viscous and fermentable nonstarch polysaccharides. J Anim Sci 88:3351-3362 https://doi.org/10.2527/jas.2010-2906
  29. Metzler-Zebeli BU, Zijlstra RT, Mosenthin R, Gänzle MG. 2011. Dietary calcium phosphate content and oat ${\beta}$-glucan influence gastrointestinal microbiota, butyrate-producing bacteria and butyrate fermentation in weaned pigs. FEMS Microbiol Ecol 75:402-413 https://doi.org/10.1111/j.1574-6941.2010.01017.x
  30. Mitsou EK, Panopoulou N, Turunen K, Spiliotis V, Kyriacou A. 2010. Prebiotic potential of barley-derived ${\beta}$-glucan at low intake levels: A randomized, double-blinded, placebo-controlled clinical study. Food Res Int 43:1086-1092 https://doi.org/10.1016/j.foodres.2010.01.020
  31. Rose DJ. 2014. Impact of whole grains on the gut microbiota: the next frontier for oats? Br J Nutr 112 Suppl 2:S44-49 https://doi.org/10.1017/S0007114514002244
  32. Scholz-Ahrens KE, Schaafsma G, van den Heuvel EG, Schrezenmeir J. 2001. Effects of prebiotics on mineral metabolism. Am J Clin Nutr 73(2 Suppl):459S-464S https://doi.org/10.1093/ajcn/73.2.459s
  33. Shen RL, Dang XY, Dong JL, Hu XZ. 2012. Effects of oat ${\beta}$- glucan and barley ${\beta}$-glucan on fecal characteristics, intestinal microflora, and intestinal bacterial metabolites in rats. J Agric Food Chem 14;60:11301-11308 https://doi.org/10.1021/jf302824h
  34. Snart J, Bibiloni R, Grayson T, Lay C, Zhang H, Allison GE, Laverdiere JK, Temelli F, Vasanthan T, Bell R, Tannock GW. 2006. Supplementation of the diet with high-viscosity beta-glucan results in enrichment for lactobacilli in the rat cecum. Appl Environ Microbiol 72:1925-1931 https://doi.org/10.1128/AEM.72.3.1925-1931.2006
  35. Sweeney T, Collins CB, Reilly P, Pierce KM, Ryan M, O'Doherty JV. 2012. Effect of purified ${\beta}$-glucans derived from Laminaria digitata, Laminaria hyperborea and Saccharomyces cerevisiae on piglet performance, selected bacterial populations, volatile fatty acids and pro-inflammatory cytokines in the gastrointestinal tract of pigs. Br J Nutr 108:1226-1234 https://doi.org/10.1017/S0007114511006751
  36. Tosh SM, Brummer Y, Wolever TM S, Wood PJ. 2008. Glycemic response to oat bran muffins treated to vary molecular weight of ${\beta}$-glucan. Cereal Chemistry 85:211-217 https://doi.org/10.1094/CCHEM-85-2-0211
  37. Turunen K, Tsouvelakidou E, Nomikos T, Mountzouris KC, Karamanolis D, Triantafillidis J, Kyriacou A. 2011. Impact of beta-glucan on the faecal microbiota of polypectomized patients: A pilot study. Anaerobe 17:403-406 https://doi.org/10.1016/j.anaerobe.2011.03.025
  38. Vetvicka V, Vetvickova J. 2009. Effects of yeast-derived betaglucans on blood cholesterol and macrophage functionality. J Immunotoxicol 6:30-35 https://doi.org/10.1080/15476910802604317
  39. Whitehead A, Beck EJ, Tosh S, Wolever TM. 2014. Cholesterollowering effects of oat ${\beta}$-glucan: A meta-analysis of randomized controlled trials. Am J Clin Nutr 100:1413-1421 https://doi.org/10.3945/ajcn.114.086108
  40. Wong JM, de Souza R, Kendall CW, Emam A, Jenkins DJ. 2006. Colonic health: fermentation and short chain fatty acids. J Clin Gastroenterol 40:235-243 https://doi.org/10.1097/00004836-200603000-00015
  41. Wood PJ, Beer MU, Butler G. 2000. Evaluation of role of concentration and molecular weight of oat beta-glucan in determining effect of viscosity on plasma glucose and insulin following an oral glucose load. Br J Nutr 84:19-23
  42. Zhong Y, Marungruang N, Fåk F, Nyman M. 2015. Effects of two whole-grain barley varieties on caecal SCFA, gut microbiota and plasma inflammatory markers in rats consuming lowand high-fat diets. Br J Nutr 28;113:1558-1570 https://doi.org/10.1017/S0007114515000793
  43. Zhou M, Pu C, Xia L, Yu X, Zhu B, Cheng R, Xu L, Zhang J. 2014. Salecan diet increases short chain fatty acids and enriches beneficial microbiota in the mouse cecum. Carbohydr Polym 15;102:772-779 https://doi.org/10.1016/j.carbpol.2013.10.091

Cited by

  1. Effect of Barley Flour Addition on Quality Characteristics of Vegetable Pancake vol.33, pp.3, 2017, https://doi.org/10.9724/kfcs.2017.33.3.333
  2. Quality Characteristics and Acceptability of Hotteok with Barley Flour for Development of Representative Foods of Traditional Market vol.34, pp.3, 2018, https://doi.org/10.9724/kfcs.2018.34.3.279
  3. 인간 단핵구 THP-1 세포에서 β-glucan으로 인한 TNF-α 분비 증가 효과 vol.27, pp.11, 2017, https://doi.org/10.5352/jls.2017.27.11.1256
  4. Cereal β‐glucan: a promising prebiotic polysaccharide and its impact on the gut health vol.56, pp.5, 2016, https://doi.org/10.1111/ijfs.14971