Journal Home > Volume 11 , Issue 1

The present work aimed at investigating the effects of soy hull polysaccharide (SHP) in alleviating adverse effects in rats fed a high-fat-high-sucrose diet. After SHP feeding for 4 weeks, the fasting blood glucose (FBG), serum triglyceride (TG), serum high-density lipoprotein cholesterol (HDL-C), short chain fatty acids (SCFAs), and 16S rDNA gene sequence were determined. Administration of SHP significantly decreased body fat content and TG levels, and increased water intake and HDL-C levels after 4 weeks of treatment. The antihyperglycemic effect of SHP at a dose of 400 mg/kg mb had the most significant effects among the three dosage groups. SHP notably restored the FBG in rats fed a high-fat-high-sucrose diet (P < 0.05). Furthermore, SHP at 400 mg/kg mb increased the abundance of Bacteroidetes and decreased that of Firmicutes and Actinobacteria at the phylum level. The polysaccharide treated groups had significantly higher content of total SCFAs, and the main fermentation products were acetic, propionic, n-valeric and i-valeric acids. Thus, SHP restores blood lipid levels in rats fed a high-fat-high sucrose diet through regulation of the gut microbiota.


menu
Abstract
Full text
Outline
About this article

Effects of soy hull polysaccharide on dyslipidemia and pathoglycemia in rats induced by a high-fat-high-sucrose diet

Show Author's information Qian Lina,bLina Yanga,b( )Lin Hana,bZiyi Wanga,bMingshuo Luoa,bDanshi Zhua,bHe Liua,b( )Xin Lia,bYu Fenga,b
College of Food Science and Technology, Bohai University, Jinzhou 121013, China
National & Local Joint Engineering Research Center of Storage, Processing and Safety Control Technology for Fresh Agricultural and Aquatic Products, Jinzhou 121013, China

Peer review under responsibility of KeAi Communications Co., Ltd.

Abstract

The present work aimed at investigating the effects of soy hull polysaccharide (SHP) in alleviating adverse effects in rats fed a high-fat-high-sucrose diet. After SHP feeding for 4 weeks, the fasting blood glucose (FBG), serum triglyceride (TG), serum high-density lipoprotein cholesterol (HDL-C), short chain fatty acids (SCFAs), and 16S rDNA gene sequence were determined. Administration of SHP significantly decreased body fat content and TG levels, and increased water intake and HDL-C levels after 4 weeks of treatment. The antihyperglycemic effect of SHP at a dose of 400 mg/kg mb had the most significant effects among the three dosage groups. SHP notably restored the FBG in rats fed a high-fat-high-sucrose diet (P < 0.05). Furthermore, SHP at 400 mg/kg mb increased the abundance of Bacteroidetes and decreased that of Firmicutes and Actinobacteria at the phylum level. The polysaccharide treated groups had significantly higher content of total SCFAs, and the main fermentation products were acetic, propionic, n-valeric and i-valeric acids. Thus, SHP restores blood lipid levels in rats fed a high-fat-high sucrose diet through regulation of the gut microbiota.

Keywords: Gut microbiota, Soy hull polysaccharide, Antihyperlipidemic, Short-chain fatty acids

References(45)

[1]

Y. Wang, Y.Y. Zhu, K.F. Yuan, et al., MDG-1, a polysaccharide from Ophiopogon japonicus, prevents high fat diet-induced obesity and increases energy expenditure in mice, Carbohydr. Polym. 114 (2014) 183-189. https://doi.org/10.1016/j.carbpol.2014.08.013.

[2]

Y. Zheng, S.H. Ley, F.B. Hu. Global aetiology and epidemiology of type 2 diabetes mellitus and its complications, Nat. Rev. Endocrinol. 14(2) (2018) 88-98. https://doi.org/10.1038/nrendo.2017.151.

[3]

Y. Jiao, X. Wang, X. Jiang, et al., Antidiabetic effects of Morus alba fruit polysaccharides on high-fat diet- and streptozotocin-induced type 2 diabetes in rats, J. Ethnopharmacol. 199 (2017) 119-127. https://doi.org/10.1016/j.jep.2017.02.003.

[4]

H. Zhao, Q. Lai, J. Zhang, et al., Antioxidant and hypoglycemic effects of acidic-extractable polysaccharides from Cordyceps militaris on type 2 diabetes mice, Oxid. Med. Cell Longev. (2018) 9150807. https://doi.org/10.1155/2018/9150807.

[5]

G.P. Lin, T. Jiang, X.B. Hu, et al., Effect of Siraitia grosvenorii polysaccharide on glucose and lipid of diabetic rabbits induced by feeding high fat/high sucrose chow, Exp. Diabetes Res. (2007) 67435. https://doi.org/10.1155/2007/67435.

[6]

Y. Pan, C. Wang, Z. Chen, et al., Physicochemical properties and antidiabetic effects of a polysaccharide from corn silk in high-fat diet and streptozotocin-induced diabetic mice, Carbohydr. Polym. 164 (2017) 370-378. https://doi.org/10.1016/j.carbpol.2017.01.092.

[7]

Q. Nie, J. Hu, H. Gao, et al., Polysaccharide from Plantago asiatica L. attenuates hyperglycemia, hyperlipidemia and affects colon microbiota in type 2 diabetic rats, Food Hydrocoll. 86 (2019) 34-42. https://doi.org/10.1016/j.foodhyd.2017.12.026.

[8]

G. Musso, R. Gambino, M. Cassader, Interactions between gut microbiota and host metabolism predisposing to obesity and diabetes, Annu. Rev. Med. 62 (2011) 361-380. https://doi.org/10.1146/annurev-med-012510-175505.

[9]

D. Artis, Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut, Nat. Rev. Immunol. 8(6) (2008) 411-420. https://doi.org/10.1038/nri2316.

[10]

J.C. Clemente, L.K. Ursell, L.W. Parfrey, et al., The impact of the gut microbiota on human health: an integrative view, Cell 148(6) (2012) 1258-1270. https://doi.org/10.1016/j.cell.2012.01.035.

[11]

L.M. Cox, I. Cho, S.A. Young, et al., The nonfermentable dietary fiber hydroxypropyl methylcellulose modulates intestinal microbiota, FASEB J. 27(2) (2013) 692-702. https://doi.org/10.1096/fj.12-219477.

[12]

E.M. O'Connor, E.A. O'Herlihy, P.W. O'Toole, Gut microbiota in older subjects: variation, health consequences and dietary intervention prospects, Proc. Nutr. Soc. 73 (4) (2014) 441-451. https://doi.org/10.1017/S0029665114000597.

[13]

L. Zhao, The gut microbiota and obesity: from correlation to causality, Nat. Rev. Microbiol. 11(9) (2013) 639-647. https://doi.org/10.1038/nrmicro3089.

[14]

C. Haro, M. Montes-Borrego, O.A. Rangel-Zúñiga, et al., Two healthy diets modulate gut microbial community improving insulin sensitivity in a human obese population, J. Clin. Endocr. Metab. 101(1) (2016) 233-242. https://doi.org/10.1210/jc.2015-3351.

[15]

J.A. Parnell, R.A. Reimer, Weight loss during oligofructose supplementation is associated with decreased ghrelin and increased peptide YY in overweight and obese adults, Am. J. Clin. Nutr. 89(6) (2009) 1751-1759. https://doi.org/10.3945/ajcn.2009.27465.

[16]

X. Yan, C. Yang, G. Lin, et al., Antidiabetic potential of green seaweed Enteromorpha prolifera flavonoids regulating insulin signaling pathway and gut microbiota in type 2 diabetic mice, J. Food Sci. 84(1) (2019) 165-173. https://doi.org/10.1111/1750-3841.14415.

[17]

J.L. Hu, S.P. Nie, M.Y. Xie, High pressure homogenization increases antioxidant capacity and short-chain fatty acid yield of polysaccharide from seeds of Plantago asiatica L, Food Chem. 138(4) (2013) 2338-2345. https://doi.org/10.1016/j.foodchem.2012.12.016.

[18]

S.H. Al-Lahham, M.P. Peppelenbosch, H. Roelofsen, et al., Biological effects of propionic acid in humans; metabolism, potential applications and underlying mechanisms, BBA-Mol. Cell Biol. L. 1801(11) (2010) 1175-1183. https://doi.org/10.1016/j.bbalip.2010.07.007.

[19]

Y. Ding, Y. Yan, Y. Peng, et al., In vitro digestion under simulated saliva, gastric and small intestinal conditions and fermentation by human gut microbiota of polysaccharides from the fruits of Lycium barbarum, Int. J Biol. Macromol. 125 (2019) 751-760. https://doi.org/10.1016/j.ijbiomac.2018.12.081.

[20]

M.L. Sleeth, E.L. Thompson, H.E. Ford, et al., Free fatty acid receptor 2 and nutrient sensing: a proposed role for fibre, fermentable carbohydrates and short-chain fatty acids in appetite regulation, Nutr. Res. Rev. 23(1) (2010) 135-145. https://doi.org/10.1017/S0954422410000089.

[21]

H.W. Kim, Y.J. Lee, Y.H.B. Kim, Efficacy of pectin and insoluble fiber extracted from soy hulls as a functional non-meat ingredient, LWT-Food Sci Technol. 64(2) (2015) 1071-1077. https://doi.org/10.1016/j.lwt.2015.07.030.

[22]

L. Yang, H. Zhang, Y. Zhao, et al., Chemical structure, chain conformation and rheological properties of pectic polysaccharides from soy hulls, Int. J. Biol. Macromol. 148 (2020) 41-48. https://doi.org/10.1016/j.ijbiomac.2020.01.047.

[23]

H. Liu, X. Guo, J. Li, et al., The effects of MgSO4, d-glucono-δ-lactone (GDL), sucrose, and urea on gelation properties of pectic polysaccharide from soy hull, Food Hydrocoll. 31(2) (2013) 137-145. https://doi. org/10.1016/j.foodhyd.2012.10.013.

[24]

C.J. Chang, C.S. Lin, C.C. Lu, et al., Ganoderma lucidum reduces obesity in mice by modulating the composition of the gut microbiota, Nat. Commun. 6(1) (2015) 74-89. https://doi.org/10.1038/ncomms8489.

[25]

Y.J. Zhou, D.D, Zhao, H.D. Liu, et al., Cancer killers in the human gut microbiota: diverse phylogeny and broad spectra, Oncotarget 8(30) (2017) 49574-49591. https://doi.org/10.18632/oncotarget.17319.

[26]

A. Everard, V. Lazarevic, M. Derrien, et al., Responses of gut microbiota and glucose and lipid metabolism to prebiotics in genetic obese and diet-induced leptin-resistant mice, Diabetes 60(11) (2011) 2775-2786. https://doi.org/10.2337/db11-0227.

[27]

S. Wang, L. Zhao, Q. Li, et al., Rheological properties and chain conformation of soy hull water-soluble polysaccharide fractions obtained by gradient alcohol precipitation, Food Hydrocoll. 91 (2019) 34-39. https://doi.org/10.1016/j.foodhyd.2018.12.054.

[28]

S. Ou, K. Kwok, Y. Li, et al., In vitro study of possible role of dietary fiber in lowering postprandial serum glucose, J. Agr. Food Chem. 49(2) (2001) 1026-1029. https://doi.org/10.1021/jf000574n.

[29]

G. Kroemer, C. López-Otín, F. Madeo, et al., Carbotoxicity-noxious effects of carbohydrates, Cell 175(3) (2018) 605-614. https://doi.org/10.1016/j.cell.2018.07.044.

[30]

R.E. Ley, P.J. Turnbaugh, S. Klein, et al., Microbial ecology: human gut microbes associated with obesity, Nature 444(7122) (2006) 1022-1023. https://doi.org/10.1038/4441022a.

[31]

J. Yang, P.H. Summanen, S.M. Henning, et al., Xylooligosaccharide supplementation alters gut bacteria in both healthy and prediabetic adults: a pilot study, Front Physiol. 6 (2015) 216. https://doi.org/10.3389/fphys.2015.00216.

[32]

B. Di Luccia, R. Crescenzo, A. Mazzoli, et al., Rescue of fructose-induced metabolic syndrome by antibiotics or faecal transplantation in a rat model of obesity, PLoS One 10(8) (2015) e0134893. https://doi.org/10.1371/journal. pone.0134893.

[33]

J.P. Furet, L.C. Kong, J. Tap, et al., Differential adaptation of human gut microbiota to bariatric surgery-induced weight loss: links with metabolic and low-grade inflammation markers, Diabetes 59(12) (2010) 3049-3057. https://doi.org/10.2337/db10-0253.

[34]

R. Pedersen, H.C. Ingerslev, M. Sturek, et al., Characterisation of gut microbiota in Ossabaw and Gottingen minipigs as models of obesity and metabolic syndrome, PLoS One 8(2) (2013) e56612. https://doi.org/10.1371/journal.pone.0056612.

[35]

A. Santacruz, M.C. Collado, L. García-Valdés, et al., Gut microbiota composition is associated with body weight, weight gain and biochemical parameters in pregnant women, Br. J. Nutr. 104(1) (2010) 83-92. https://doi.org/10.1017/s0007114510000176.

[36]

C.M. Chiu, W.C. Huang, S.L. Weng, et al., Systematic analysis of the association between gut flora and obesity through high-throughput sequencing and bioinformatics approaches, Biomed. Res. Int. (2014) 906168. https://doi.org/10.1155/2014/906168.

[37]

H.J. Hu, S.G. Park, H.B. Jang, et al., Obesity alters the microbial community profile in korean adolescents, PLoS One 10(7) (2015) e0134333. https://doi.org/10.1371/journal.pone.0134333.

[38]

L. Shi, Y. Li, Y. Wang, et al., MDG-1, an Ophiopogon polysaccharide, regulate gut microbiota in high-fat diet-induced obese C57BL/6 mice, Int. J. Biol. Macromol. 81 (2015) 576-583. https://doi.org/10.1016/j.ijbiomac.2015.08.057.

[39]

X. Xu, P. Xu, C. Ma, et al., Gut microbiota, host health, and polysaccharides, Biotechnol. Adv. 31(2) (2013) 318-337. https://doi.org/10.1016/j.biotechadv.2012.12.009.

[40]

M.S. Desai, A.M. Seekatz, N.M. Koropatkin, et al., A dietary fiber-deprived gut microbiota degrades the colonic mucus barrier and enhances pathogen susceptibility, Cell 167(5) (2016) 1339-1353. https://doi.org/10.1016/j.cell.2016.10.043.

[41]

L. Yang, J. Huang, M. Luo, et al., The influence of gut microbiota on the rheological characterization of soy hull polysaccharide and mucin interactions, RSC Advances 10 (2020) 2830-2840. https://doi.org/10.1039/c9ra09594b.

[42]

A.R. Mackie, A. Macierzanka, K. Aarak, et al. Sodium alginate decreases the permeability of intestinal mucus, Food Hydrocoll. 52 (2016) 749-755. https://doi.org/10.1016/j.foodhyd.2015.08.004.

[43]

X. Wang, X. Wang, H. Jiang, et al., Marine polysaccharides attenuate metabolic syndrome by fermentation products and altering gut microbiota: an overview, Carbohydr Polym. 195 (2018) 601-612. https://doi.org/10.1016/j.carbpol.2018.05.003.

[44]

Y. Wang, Y. Fei, L. Liu, et al., Polygonatum odoratum polysaccharides modulate gut microbiota and mitigate experimentally induced obesity in rats, Int. J. Mol. Sci. 19(11) (2018) 3587. https://doi.org/10.3390/ijms19113587.

[45]

V. Gowd, Z. Jia, and W. Chen, Anthocyanins as promising molecules and dietary bioactive components against diabetes – a review of recent advances, Trends Food Sci. Tech. 68 (2017) 1-13. https://doi.org/10.1016/j.tifs.2017.07.015.

Publication history
Copyright
Acknowledgements
Rights and permissions

Publication history

Received: 13 March 2020
Revised: 28 April 2020
Accepted: 29 May 2020
Published: 11 September 2021
Issue date: January 2022

Copyright

© 2021 Beijing Academy of Food Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.

Acknowledgements

Acknowledgements

This study was supported by the National Natural Science Foundation of China (Grant No. 31901680 and 31972031).

Rights and permissions

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

Return