What Are the Benefits of Beta Glucan Powder?

Feb 28,2025
Category:Product News

Dextran is the most common type of polymeric polysaccharide chain in nature, which is formed by the polymerization of glucose monomers. It uses D-glucose pyranose as its basic unit, and its structure is diverse. There are three types of glycosidic bonds: (1→3), (1→4) and (1→6), divided into α and β types [1-2]. α-glucan has a ribbon-like single-chain structure that extends along the fiber axis without a helix. It is basically not biologically active and represents substances such as starch, which provides the body with its main energy source.

 

The α-glucan series is a polymer formed by the enzymatic catalysis of the synthetic precursor substance uridine diphosphate glucose [3-4]. In recent years, due to its excellent physical and chemical properties, 阝-glucan has become a research hotspot in the food industry. In particular, with the newer applications of research techniques such as isolation and purification, structural identification, and functional characterization, the special physiological activity and medicinal value of 阝-glucan have also been continuously discovered. This paper introduces the current research status of the biological functions of 阝-glucan in recent years, focusing on its regulatory effects on blood glucose and lipids, immunity, neural development and intestinal function, etc., providing theoretical reference for the further development and utilization of β-glucan.

 

1. Sources and structure-activity relationships of β-glucan

β-glucan is widely available, and can be obtained from a variety of natural plants such as seaweed, wheat, oats, barley, and microorganisms such as yeast, alkaligenes, and edible fungi [5]. β-glucan from different sources differs in terms of glycosidic bond type, molecular structure, branching position, etc. (see Table 1). Plant-derived beta-glucans mainly have two types of glycosidic bonds: (1→3) and (1→4). In cereal beta-glucans, glucose residues linked by (1→4) glycosidic bonds are often separated by a single (1→3) glycosidic bond, thus forming the fragments of fiber trisaccharide (DP3) and fiber tetrasaccharide (DP4).

 

The ratio of DP3 and DP4 has also become an important structural characteristic of cereal α-glucan [6]. Microbiologically derived α-glucans are often linked by α-(1→3) and α-(1→6) glycosidic bonds [7]. The curdlan isolated from fungi such as yeast and Hericium erinaceus generally have a similar molecular structure, i.e., a main chain composed of glucose residues linked by α-(1→3) glycosidic bonds and branches formed by α-(1→6) glycosidic bonds; curdlan from Agrobacterium is a linear curdlan a linear α-glucan with only α-(1→3) glycosidic bonds [8]. The content and degree of polymerisation of the glycosidic bonds also affect the physicochemical properties of α-glucan, such as solubility and molecular weight. The ratio of the content of the (1→3) and (1→4) glycosidic bonds in water-soluble 阝-glucan is 1: (2.3~2.6), while the corresponding ratio in non-water-soluble 阝-glucan is about 1:4.2 [9]. The molecular weight of 阝-glucan is usually distributed between about 103 and 106 kDa, and there are certain differences depending on the variety, place of origin, extraction method and measurement method [10].

 

2 Physiological functions of β-glucan

With the improvement of people's living standards and the popularity of Western-style diet cultures with high fat and sugar, the incidence of chronic metabolic diseases is rising, and methods of improving body function through dietary control are receiving increasing attention. In order to promote the construction of a healthy China and improve the health of the people, China's “Healthy China 2030” Plan Outline, proposed in 2016, states that nutritional intervention should be used to gradually solve the problem of undernutrition and overnutrition coexisting in some populations. Studies have shown that beta-glucan can play a key role in improving health and preventing chronic non-communicable diseases (such as diabetes, hypercholesterolemia, obesity, cancer and neurodegenerative diseases) [27]. The US Food and Drug Administration approved beta-glucan as a safe food additive in 2007 [28]. Currently, 45 countries including China, Japan, the United States, and Australia have approved the use of β-glucan [10]. Research on the correlation between the molecular properties of β-glucan and precision nutrition and the development of functional foods have become hot topics in the fields of nutrition and pharmacology in various countries.

 

2.1 Research on the role of β-glucan in regulating blood sugar

The type and strength of the physiological functions of β-glucan are usually attributed to its molecular structure (composition of the main side chain, three-dimensional conformation, molecular weight, etc.) and physicochemical properties (solubility, water retention, swelling, viscosity, fermentability, etc.) [29]. A large number of studies have shown that β-glucan has a good hypoglycemic effect, and the potential mechanism may be: interference with the body's absorption of dietary nutrients:  The interaction of 1,4-glucan with water molecules increases the viscosity of the solution and the thickness of the water layer on the intestinal mucosal surface, reducing the speed of chyme passing through the small intestine and slowing the binding of nutrients (such as sugars, amino acids, etc.) and substrates of digestive enzymes [29-31]. In addition, 1,4-glucan also adsorbs ions such as calcium, iron, and zinc, as well as organic matter, thereby affecting the metabolic level of these substances. The viscosity and concentration of oat-beta-glucan are closely related to its relative molecular weight. The higher the viscosity (the higher the molecular weight), the greater the potential to lower blood sugar [32]. Wood et al. found that oat-beta-glucan with a molecular weight between 1×105 and 8×105 has a stronger effect on blood sugar regulation [33].

 

Oat-derived dextran can also reduce blood glucose by protecting pancreatic islet cells and inhibiting enzymes related to glucose metabolism [34]. Shen et al. found that oat-derived dextran regulates glucose and lipid metabolism by increasing the secretion of insulin and glucagon-like peptide-1, reducing insulin resistance in diabetic model mice [35]. Liu et al. found that oat α-glucan can repair and improve the integrity of islet α-cell and tissue structure, protect hepatic gluconeogenesis, and improve glucose tolerance in type 2 diabetic model mice [36]. In addition, studies by Yokoyama et al. and Juorch et al. showed that 阝-glucan can significantly reduce postprandial blood glucose and insulin levels in healthy people [37-38]. Zheng et al. found that the drug Oatrim (containing oat beta-glucan) can effectively reduce postprandial blood glucose concentrations and insulin levels in patients with type I and type II diabetes, which may be related to the inhibition of beta-glucan on the activities of alpha-amylase, alpha-glucosidase and invertase [39-40]. 


2.2 Research on the role of β-glucan in regulating lipid metabolism

Since 1963, when Dutch scientists Groot and others pointed out that 阝-glucan can effectively reduce cholesterol synthesis in the body, a large number of animal experiments and human clinical studies have confirmed this conclusion [41]. The effect of 阝-glucan on cholesterol is mainly that it can significantly reduce total cholesterol and low-density lipoprotein cholesterol in the blood plasma, while having no significant effect on high-density lipoprotein and triglycerides, and also does not affect the proportion of cholesterol in lipoproteins [42]. The relevant mechanism is currently unclear, and there are five hypotheses: ① Alpha-glucan can bind bile acids and excrete them, thereby promoting the conversion of cholesterol to bile acids and inhibiting the accumulation of cholesterol in the blood [43]; ② Alpha-glucan can be fermented by microorganisms in the intestine to produce short-chain fatty acids (SCFAs), such as acetic acid and butyric acid, which can inhibit cholesterol synthesis in the liver[44]; ③xanthan-glucan can regulate the activity of enzymes related to cholesterol synthesis and metabolism, such as fatty acids and glycerides, regulate lipid metabolism and cholesterol metabolism, and can also promote the breakdown of low-density lipoprotein cholesterol [45]; ④ 阝-glucan forms a highly viscous solution in the small intestine, hindering the emulsifying effect of bile and the reabsorption of bile acids [45]; ⑤ 阝-glucan can regulate cholesterol metabolism by regulating the macrophage-cholesterol axis [46].

 

Drozdowski et al. found that high-viscosity 阝-glucan isolated from oats and waxy barley can reduce intestinal uptake of long-chain fatty acids and cholesterol by downregulating the expression of genes related to fatty acid synthesis and cholesterol metabolism[47]. Wang and Sunberg et al. used 阝-glucanase to demonstrated that β-glucan is the main functional ingredient that reduces plasma cholesterol and low-density lipoprotein levels in rats and hamsters [48]. Thandapilly et al. found that high-molecular-weight barley β-glucan can increase the excretion of bile acids in the feces and the concentration of total SCFAs in patients with mild hypercholesterolemia [49].

 

2.3 Research on the immunomodulatory effects of β-glucan

Recent studies have shown that β-glucan, as a natural immunomodulator, can bind and activate immune cells to secrete cytokines, participate in the host's specific and non-specific immunity, and thus improve the body's immune function [50-51]. Jin et al. found that oat β-glucan can regulate the immune response, increase serum immunoglobulin in mice, and stimulate the secretion of anti-inflammatory factors, thereby enhancing the immunity of mice [52]. Yun et al. found that β-glucan can effectively change the cell numbers in the mesenteric lymph nodes and Peyer's patches of mice, thereby enhancing the resistance of mice to infection with Staphylococcus aureus or Escherichia coli [53]. Salah et al. found that β-glucan can regulate the immune-related genes of tilapia to resist infection with Streptococcus fishicola [54]. Golisch et al. found that fungal β-glucan is internalized by macrophages and binds to neutrophils. The resulting activated granulocytes can kill some tumor cells [2].

 

2.4 Research on the effect of β-glucan on improving brain function

A large number of studies have found that dietary fibres such as inulin and fructo-oligosaccharides and their metabolites have potential protective effects on brain function. Haider et al. showed that β-glucan can alleviate scopolamine-induced cognitive deficits in rats by inhibiting the hydrolysis of acetylcholine in the central nervous system [55]. A high-fat, low-fiber diet causes activation of microglia and synaptic damage in mice, while dietary supplementation with β-glucan can optimize synaptic ultrastructure and related signaling pathways in the brain, reducing neuroinflammation and cognitive decline in obese mice [56-57]. Xu et al. showed that yeast β-glucan improved neuroinflammation and brain insulin resistance in a mouse model of dementia [58]. Hu et al. demonstrated that long-term supplementation with β-glucan significantly improved synaptic ultrastructure in the prefrontal cortex and enhanced recognition memory [59]. More importantly, clinical studies have shown that after taking a food supplement containing β-glucan, the behavioral patterns (a significant decrease in the Autism Assessment Scale score) and the expression level of α-synuclein in autistic children aged 3 to 18 years old improved significantly [60].

 

2.5 Research on the effect of β-glucan on the intestinal microenvironment

The large number of symbiotic bacteria in the human intestine forms a microbial barrier that can resist the invasion of pathogenic bacteria and provide important protection. Changes in the intestinal microbiota also significantly affect the physiological functions of the host [27]. As an important prebiotic, β-glucan can have a positive effect on the microbiota in the stomach and intestines. Due to the lack of β-glucanase in the human body, β-glucan cannot be directly digested in the digestive tract, but can be degraded and absorbed by glycosidases secreted by probiotics in the large intestine.

 

Therefore, β-glucan selectively stimulates the vitality and proliferation of probiotics. At the same time, some probiotics produce substances such as lactic acid in their own metabolism, which lowers the pH of the intestine and inhibiting the growth and reproduction of harmful bacteria [61]. On the other hand, SCFAs produced by the catabolism of β-glucan by anaerobic bacteria in the colon provide nutrients for colonic mucosal cells [62] and promote the proliferation of intestinal epithelial cells and intestinal T cells [63]. SCFAs can also inhibit the activity of intestinal cancer-inducing factors such as glucuronidase, uricase and other intestinal cancer-inducing factors, inhibit the conversion of primary bile acids to secondary bile acids, and increase the excretion of secondary bile acids, which has a preventive effect on colon cancer [64-65].

 

Shen Ruiling et al. found that oat β-glucan can promote the proliferation of bifidobacteria and lactobacilli in the mouse intestine, inhibit the reproduction of Escherichia coli, and improve the intestinal environment [66]. Pieper et al. found that a feed containing β-glucan is beneficial for the proliferation of butyric acid-producing probiotics in the intestines of weaned piglets [67]. butyric acid can provide energy for intestinal epithelial cells, help maintain the integrity of the intestinal mucosa, and inhibit the activity of cancer cells in cell experiments [68]. SCFAs can also increase the thickness of the mucus layer in the colon of rats and maintain the normal function of the intestines [69].

 

3 Summary

Beta-glucan plays an important role in promoting health and preventing disease. It has a positive effect on controlling postprandial blood glucose and reducing insulin response, lowering cholesterol and hyperlipidemia, enhancing the body's immune system and protecting intestinal health, which gives it great potential for development in the health industry, such as functional foods, healthcare, food additives, etc. Recent research has focused on the source of beta-glucan, processing methods, molecular size or viscosity, etc., and the nutritional efficacy has been characterized using in vitro and in vivo experiments in terms of biochemical indicators and metabolic regulation. However, the research on the various biological activity mechanisms of β-glucan is not yet clear. In the future, research can combine new technical methods such as metabolomics, genomics and transcriptomics to further explain its nutritional mechanisms and provide more scientific evidence for the development of new health foods containing β-glucan.

 

Reference:

[1] NAKASHIMA A, YAMADA K, IWATA O, et al. β-Glucan in foods and its physiological functions[J]. Journal of Nutritional Science and Vitaminology (Tokyo), 2018, 64(1):8-17.

[2] GOLISCH  B, LEI Z, TAMURA K, et al. Configured for the human gut microbiota: Molecular mechanisms of dietary 阝-Glucan utilization[J]. ACS Chemical Biology, 2021, 16(11): 2087-2102.

[3] INGLETT G E, NEWMAN R K. Oat beta-glucan-amylodextrins: Preliminary   preparations   and   biological   properties[J].   Plant Foods For Human Nutrition, 1994, 45(1): 53-61.

[4]BEER M U, ARRIGONI E, AMADO R. Extraction of oat gum from oat bran: Effects of process on yield, molecular weight distribution, viscosity and (1→3)(1→4)-阝-D-glucan content of the gum[J]. Cereal Chemistry, 1996, 73(1): 58-62.

[5] WANG S Y. Research progress of 阝-glucan in Oat[J]. Science and Technology of Cereals, Oils and Foods, 2004(6): 47-48.

[6]LIU Y F, ZHAO A J. Research progress of molecular structures, physical  properties  and  applications  of  cereal   阝-D-glucans[J]. Food Industry, 2017, 38(2): 253-256.

[7]     DU  B, MEENU M, LIU H Z et al. A concise review on the molecular  structure  and  function  relationship  of  阝-glucan[J]. International Journal of Molecular Sciences, 2019, 20(16): 4032.

[8]     WAN  Y J, XU X J, GILBERT R G, et al. A review on the structure  and  anti-diabetic  (type  2)  functions  of  阝-glucans[J]. Foods, 2022, 11(57): 57.

[9]     GAJDOSOVA A, PETRULAKOVA Z, HAVRLENTOVA M, et al. The content of water-soluble and water-insoluble 阝-d-glucans in selected oats and barley varieties[J]. Carbohydrate Polymers, 2007, 70(1): 46-52.

[10]   ZHANG  H,   CAI  Q  S.  Research  progress of  阝-glucan  in cereals[J]. Cereals & Oils, 2010(5): 7-11.

[11]   YAO H Y Y. Isolation, purification and structural characterization of 阝-glucan and arabinoxylan from highland barley[D]. Nanchang University, 2016.

[12]   ZHANG   H,   ZHANG  N,  XIONG  Z   Q,  et  al.   Structural characterization andrheological properties of 阝-D-glucan from hull-less barley (Hordeum vulgare L. var. nudum Hook. f.)[J]. Phytochemistry, 2018, 155:155-163.

[13]   HUANG  Z  H.  Study  on  the  effect  of  thermally   induced infiltration   of  barley   阝-glucan   microgel   on   wheat   protein aggregation and the application[D]. Jiangnan University, 2019.

[14]   XIAO  X,  TAN  C,  SUN  X,  et  al. Effects of fermentation on structural characteristics and in vitro physiological activities of barley 阝-glucan[J]. Carbohydrate Polymers, 2020, 231: 115685.

[15]   HUANG Z H, ZHU K X, ZHOU H M. Research progress ingel properties and application of barley 阝-glucan[J]. Journal of Food Science and Technology, 2017, 35(5): 25-31.

[16]   RYU J H, LEE S Y, YOU S G, et al. Effects of barley and oat 阝-glucan  structures on  their  rheological and  thermal characteristics[J]. Carbohydrate Polymers, 2012, 89(4): 1238-1243.

[17]   AHMAD A, ANJUM F M, ZAHOOR T, et al. Extraction and characterization   of   beta-D-glucan from    oat   for    industrial utilization[J]. International Journal of Biological Macromolecules, 2010, 46(3): 304-309.

[18]   YU   S  J,  WANG  J,  LI  Y  X,   et  al.  Structural  studies  of water-insoluble 阝-glucan from oat bran and its effect on improving lipid metabolism in mice fed high-fat diet[J]. Nutrients, 2021, 13(9): 3254.

[19]   SCHMIDT  M.  Cereal  beta-glucans:  An  underutilized  health endorsing food ingredient[J]. Critical Review in Food Science and Nutrition, 2022, 62(12): 3281-3300.

[20]   WOOD  P  J.  Review:  Oat  and  rye  阝-glucan:  Properties  and function[J].   Cereal    Chemistry,   2010,    87(4):    1007210812- 1007210330.

[21]   ZHANG   N,   AI  L  Z,  ZHANG  H.  Research  progress  of structure,function   and   application   of   cereal    阝-glucans[J]. Science and Technology of Food Industry, 2018, 39(9):318-324.

[22]   AVRAMIA I, AMARIEI S. Spent brewer’s yeast as a source of insoluble   阝-glucans[J].   International   Journal    of   Molecular Sciences, 2021, 22(2): 825.

[23]   LIU Y  F,  WANG  Y  T,  ZHOU  S,  et  al.  Structure  and  chain conformation of bioactive 阝-D-glucan purified from water extracts of ganoderma lucidum unbroken spores[J]. International journal of biological macromolecules, 2021, 180: 484-493.

[24]   DONG  Q,  WANG  Y,  SHI  L,  et  al.  A  novel  water-soluble 阝-D-glucan isolated from the spores of ganoderma lucidum[J]. Carbohydrate Research, 2012, 353: 100-105.

[25]  ZHANG  S F.  Structural  identification of Hericium  erinaceus 阝-Glucan and its interaction with starch[D]. Shanghai University of Technology, 2019.

[26]   MCINTOSH M, STONE B A, STANISICH V A. Curdlan and other bacterial (1-->3)-beta-D-glucans[J]. Applied Microbiology and Biotechnology , 2005, 68(2): 163-73.

[27]   JAYACHANDRAN M, CHEN J L, CHUANG S S M, et al. A critical review on the impacts of 阝-glucans on gut microbiota and human health[J]. Journal of Nutritional Biochemistry, 2018, 61: 101-110.

[28]   MATHEWS R, KAMIL A, CHU Y F. Global review of heart health claims for oat beta-glucan products[J]. Nutrition Reviews, 2020, 78(Supplement 1): 78-97.

[29]   LAZARIDOU  A,  BILIADERIS  C  G.  Molecular  aspects  of cereal 阝-glucan functionality: Physical properties, technological applications  and  physiological  effects[J].  Journal  of  Cereal Science, 2007, 46(2): 101-118.

[30]   FERAL,  TEMELLI.  Extraction  and  functional  properties  of barley 阝-Glucan as affected by temperature and pH[J]. Journal of Food Science, 1997, 62(6): 1194-1201.

[31]   BARBARA  A  W,  LUCAS  J  G,  MICHAEL J  G,  et  al.  Gut fermentation of dietary fibres: Physico-chemistry of plant cell walls  and  implications  for  health[J].  International Journal  of Molecular Sciences, 2017, 18(10): 2203.

[32]   WANG  H,  XU  Q,  LIU  D,  et  al.  Rheological  properties  of 阝-glucans from oats[J]. Transactions of the Chinese Society of Agricultural Engineering, 2008, 24(5):31-36.

[33]   WOOD P J, BEER M U, BUTLER G, et al. 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[J]. British Journal of nutrition, 2000, 84(1): 19-23.

[34]   JENKINS  A L,  JENKINS D J A, ZDRAVKOVIC U, et al. Depression of the glycemic index by high levels of beta-glucan fiber  in  two  functional  foods  tested  in  type  2  diabetes[J]. European Journal of Clinical Nutrition, 2002, 56(7): 622-628.

[35]   SHEN R L, CAI F L, DONG J L, et al. Hypoglycemic effects and biochemical mechanisms of oat products on streptozotocin- induced  diabetic  mice[J].  Journal   of  Agricultural  and  Food Chemistry, 2011, 59(16): 8895-900.

[36]   LIU M, ZHANG Y, ZHANG H, et al. The anti-diabetic activity of oat 阝-D-glucan in streptozotocin-nicotinamide induced diabetic mice[J].  International  Journal  of  Biological   Macromolecules, 2016, 91: 1170-1176.

[37]   TOSH   S   M.   Review   of  human   studies   investigating   the post-prandial blood-glucose lowering ability of oat and barley food products[J]. European Journal of Clinical Nutrition, 2013, 67(4): 310-317.

[38]   HALLFRISCH  J,  BEHALL K M. Physiological responses of men and women to barley and oat extracts (Nu-trimX). I. Breath hydrogen,  methane,  and  gastrointestinal  symptoms[J].  Cereal Chemistry, 2003, 80(1): 76-79.

[39]   ZHENG J X. Functional dietary fiber[M]. Beijing: Chemical Industry Press, 2005: 106-109.

[40]   XU  C,  QIN  N  B,  YAN  C  Y,  et  al.  Isolation,  purification, characterization and bioactivities of a glucan from the root of pueraria lobata[J]. Food & Function, 2018, 09(5): 2644-2652.

[41]   GROOT AD, LUYKEN R, PIKAARN A. Cholesterol-lowering effect of rolled oats[J]. The Lancet, 1963, 282(7302): 303-304.

[42]   CHEN J S, PAN WH, TONG WL, et al. Effect of barley 阝-glucans on serum lipid in mice[J]. Barley science, 2002(3): 23-25.

[43]  RONG  Y  X.  Preparation,   structure  analysis  and  hypidemic activity   of  阝    -glucan   from   highland    barley[D].    Suzhou University, 2019.

[44]   THEUWISSEN E, MENSINK R P. Water-soluble dietary fibers and  cardiovascular  disease[J].  Physiology  &  Behavior,  2008, 94(2): 285-292.

[45]   ZHANG F, YANG Y, ZHAO G H, et al. Advance on beta-glucan from hull-less barley[J]. Cereals & Oils, 2003(12): 3-5.

[46]   VETVICKA  V,    VETVICKOVA  J.  Effects  of  yeast-derived beta-glucans on blood cholesterol and macrophage functionality[J]. Immunotoxicol, 2009, 6(1): 30-35.

[47]   DROZDOWSKI  L  A,  REIMER  R  A,  TEMELLI  F,  et  al. Beta-glucan  extracts  inhibit  the  in  vitro  intestinal  uptake  of long-chain fatty acids and cholesterol and down-regulate genes involved in lipogenesis and lipid transport in rats[J]. Journal of Nutritional Biochemistry, 2010, 21(8): 695-701.

[48]   YANG Z J, ZHANG W G. Application of barley glucan in health food[J]. Barley science, 2000(3): 8-10.

[49]   THANDAPILLY  S J, NDOU  S P, WANG Y N, et al. Barley 阝-glucan increases fecal bile acid excretion and short chain fatty acid levels in mildly hypercholesterolemic individuals[J]. Food Function, 2018, 09(6): 3092-3096.

[50]   DAVIS J M, MURPHY E A, BROWN A S, et al. Effects of oat beta-glucan  on  innate  immunity  and  infection  after  exercise stress[J]. Medicine & Science in Sports & Exercise, 2004, 36(8): 1321-1327.

[51]   LEGENTIL   L,   PARIS  F,  BALLET  C,  et  al.  Molecular interactions of 阝-(1→3)-glucans with their receptors[J]. Molecules, 2015, 20(6): 9745-9766.

[52]   JIN Y, LI P, WANG F. 阝-glucans as potential immunoadjuvants: A review on the adjuvanticity, structure-activity relationship and receptor   recognition   properties[J].    Vaccine,   2018,    36(35): 5235-5244.

[53]   YUN  C  H, ESTRADA A, KESSEL A V, et al. Beta-glucan, extracted from oat, enhances disease resistance against bacterial and  parasitic  infections[J].  FEMS  Immunology  and  Medical Microbiology, 2003, 35(1): 67-75.

[54]   SALAH A S, NAHAS AF E, MAHMOUD S. Modulatory effect of  different  doses  of  阝-1,3/1,6-glucan  on  the   expression   of antioxidant, inflammatory, stress and immune-related genes of oreochromis  niloticus  challenged  with  streptococcus  iniae[J]. Fish Shellfish Immunology, 2017, 70: 204-213.

[55]   HAIDER A, INAM W, KHAN  S A, et al. 阝-glucan attenuated scopolamine  induced  cognitive  impairment  via   hippocampal acetylcholinesterase inhibition in rats[J]. Brain Research, 2016, 5(17): 141-148.

[56]   SHI H L, YU Y H, LIN D H, et al. 阝-glucan attenuates cognitive impairment via the gut-brain axis in diet-induced obese mice[J]. Microbiome, 2020, 8(1): 143.

[57]   PAN W, JIANG P F, ZHAO J X, et al. 阝-Glucan from lentinula edodes prevents cognitive impairments in high-fat diet-induced obese  mice:  involvement  of  colon-brain  axis[J].  Journal  of Translational Medicine, 2021, 19(1): 54.

[58]   XU M, MO X X, HUANG H, et al. Yeast  阝-glucan  alleviates cognitive deficit by regulating gut microbiota and metabolites in A阝(1)(-)(42)-induced AD-like mice[J]. International Journal of Biological Macromolecules, 2020, 161: 258-270.

[59]   HU M M, ZAHNG P, WANG R Q, et al. Three different types of 阝-glucans enhance cognition: The role of the gut-brain axis[J]. Frontiers in nutrition, 2022, 9: 848930.

[60]   RAGHAVAN K, et al. Improvement of behavioural pattern and alpha-synuclein   levels in autism spectrum disorder after consumption of a beta-glucan food supplement in a randomised, parallel-group  pilot  clinical  study[J].  BMJ  neurology  open, 2022, 4(1): e000203.

[61]   BRENNAN C S, CLEARY L J. The potential use of cereal (1 leads to 3,1 leads to 4)-阝-D-glucans as functional food ingredients[J]. Journal of Cereal Science, 2005, 42(1): 1-13.

[62]   BENGMARK   S.  Colonic  food:  Pre-  and  probiotics[J].  The American Journal of Gastroenterology, 2000, 95(1 Suppl): S5-S7.

[63]   CAVAGLIERI C R, MARTINS E F, COLLEONE V. Fiber-rich diets  alter  rat  intestinal  leukocytes  metabolism[J].  Journal of Nutritional Biochemistry, 2000, 11(11-12): 555-561.

[64]   AHMED  R,  SEGAL I,  HASSAN H. Fermentation of dietary starch  in  humans[J].  American  Journal   of  Gastroenterology, 2000, 95(4): 1017-1020.

[65]    LV  Y  C.   Development  and  utilization   of  阝-glucan   in  bare Barley[J]. Barley Science, 1998(2): 43-45.

[66]   SHEN R L, CHEN W W. Current research progress of cereal 阝-glucan as an important dietary fiber component in whole cereal foods[J]. Science and  Technology  of Cereals,  Oils  and  Foods, 2022, 30(2): 31-40.

[67]   PIEPER R, JHA R, ROSSNAGEL B, et al. Effect of barley and oat  cultivars  with  different  carbohydrate  compositions  on  the intestinal  bacterial  communities  in  weaned  piglets[J].  FEMS Microbiology Ecology, 2008, 66(3): 556-66.

[68]   JACOBS   L   R.   Effect   of   dietary   fiber   on   colonic   cell proliferation  and  its  relationship  to  colon  carcinogenesis[J]. Preventive Medicine, 1987, 16(4): 566-571.

[69]   HEDEMANN  M  S,  THEIL  P  K,  KNUDSEN  K  E  B.  The thickness of the intestinal mucous layer in the colon of rats fed various  sources  of  non-digestible  carbohydrates  is positively correlated with the pool of SCFA but negatively correlated with the proportion of butyric acid in digesta[J]. British Journal of Nutrition, 2009, 102(1): 117-125.  

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