Traditional and modern natural soluble prebiotics
Publication 3. Oligo- and polysaccharides (soluble dietary fiber)
DOI:
https://doi.org/10.54296/18186173_2025_1_15Keywords:
prebiotics, natural prebiotics, soluble prebiotics, carbohydrate-nature (carbohydrate-based) prebiotics, soluble dietary fiber, polysaccharides, oligosaccharides, fructooligosaccharides, galactooligosaccharides, mannan-oligosaccharides, inulin, pectin, beta-glucans, resistant starch, gut (intestinal) microbiotaAbstract
The physiological functions of various prebiotics (dietary fiber) largely depend on their physico-chemical characteristics, including solubility. Compared to insoluble dietary fiber (PP), soluble PP can be easily absorbed and metabolized by microorganisms that break down fiber in the intestine, and produce a number of useful and functional metabolites.
Our research is devoted to the analysis and systematization of modern scientific ideas about soluble surfactants (oligo- and polysaccharides) as prebiotics of carbohydrate nature. One of our goals is to evaluate the feasibility and expediency of using certain groups of soluble surfactants to develop beverages with prebiotic properties based on the experience of TM. We have established that the most promising natural soluble prebiotics of a carbohydrate nature include such groups of surfactants as short-chain fructooligosaccharides (3-7 monomers), galactooligosaccharides, low molecular weight inulins (average degree of polymerization not higher than 10), mannan hydrolysates, as well as soluble dry extracts from a number of plants and fungi containing soluble surfactants with proven prebiotic, antidiabetic, immunotropic and other types of action.
The identified groups of BAS may be promising micronutrients for creating natural, practically harmless biologically available beverages with prebiotic properties.
References
Исследование пребиотической активности гидролизатов маннана в условиях in vitro / Е.П. Анохина, О.С. Корнеева, П.В. Шуваев, И.В. Черемушкина // Вестник ВГУИТ. – 2013. – №4. – С.219–222.
Аронбаев, С.Д. Биосорбция тяжелых металлов клеточными оболочками дрожжей Saccharomyces cerevisiae / С.Д. Аронбаев, А.М. Насимов, Д.М. Аронбаев // Всероссийский журнал научных публикаций. – 2011. – №1(2). – C.13–15.
Барышева, И.Н. Напитки с повышенным содержанием пектина профилактического питания / И.Н. Барышева, Т.Б. Брикота, Н.Б. Фёдорова // Новая наука: Стратегии и векторы развития. – 2016. – № 3–2 (70). – С.99–103.
Бета-глюкан // Реактив-экспресс. – Электронный ресурс. – Доступ: https://reaktiv-ex4. press.ru/product/b-glyukan . – Дата обращения 12.04.2025 г.
Валышев, А.В. Пребиотическая активность пектинов и их производных / А.В. Валышев, В.В. Головченко // Бюллетень Оренбургского научного центра УрО РАН. – 2012. – №3. – С.5–13.
Вандышев, В.В. Изучение морфологии и липидного комплекса семян Plantago psyllium L. и Plantago ovate Forssk. В сравнительном аспекте / В.В. Вандышев, Е.А. Мирошникова, А.А. Терёхин А.А. // Вестник Российского университета дружбы народов. Серия: Агрономия и животноводство. – 2016. – №3. – С.46–51.
Габдукаева, Л.З. Резистентные крахмалы как функциональный ингредиент при производстве продуктов питания / Л.З. Габдукаева, Е.В. Никитина, О.А. Решетник // Вестник Казанского технологического университета. – 2014. – Т.17. – №23. – С.253–255.
Гематдинова В.М., Канарская З.А., Канарский А.В. Потенциальные возможности промышленного производства и перспективы расширения ассортимента продуктов питания, обогащённых ?-глюканом // Вестник Поволжского государственного технологического университета. Серия: Лес. Экология. Природопользование. – 2021. – № 2 (50). – С.82–100.
Горшкова, Н.А. Высокопористые полиэлектролитные аэрогели на основе альгината бурых водорослей / Н.А. Горшкова // Дисс. канд. хим. наук. – Архангельск, 2020.
Двоеносова, П.А. Разработка технологии пектинсодержащего продукта с сорбциоными и нутритивными свойствами / ПА. Двоеносова // Автореферат диссертации на соискание учёной степени кандидата технических наук. – М., 2009. – 26 с.
Пектин-полимер природного происхождения / Л.Ф. Зидиханова, Е.И. Кулиш, В.В. Чернова, А.С. Шуршина // Доклады Башкирского университета. – 2018. – Том 3. – №6. – С.608–614.
Направления использования альгинатов в пищевой промышленности / А.Л. Ишевский, М.В. Успенская, П.И. Гунькова [и др.] // Известия Санкт-Петербургского государственного технологического института (технического университета). – 2019. – №51 (77). – С.61–69.
Киселева, М.А. Традиционные и современные растворимые пребиотики природного происхождения: Публикация 1. Про- и пребиотики в традиционной медицине и современной концепции питания / М.А. Киселева, Т.Л. Киселева, Е.В. Хлебников // Традиционная медицина. – 2024. – №3 (75). – С.17–50.
Киселева, Т.Л. традиционные и современные растворимые пребиотики природного происхождения: Публикация 2. Моносахариды, дисахариды, сахарные спирты / Т.Л. Киселева, М.А. Киселева, Е.В. Хлебников // Традиционная медицина. – 2024. – №4 (76). – Р.19–62.
Клинические исследования: Применение БАД «Бета Глюкан» в комплексной терапии воспалительных заболеваний верхних Дыхательных путей. – Алматы: ТОО «Медоптик», 2015. – 16 с. [Электронный ресурс]. – Доступ: https://ulife-shop.ru/image/catalog/klinika/metodichka%20betaglukan_14_01_2016.pdf. – Дата обращения 30.03.2025.
Коновалова, М.В. Получение и исследование противоспаечных барьерных материалов на основе биополимеров пектина и хитозана / М.В. Коновалова // Автореферат диссертации на соискание уч. степени кандидата биологических наук. – М., 2017. – 25 с.
Котова, А.А. Анализ препаратов галактоолигосахаридов / А.А. Котова, С.А. Рябцева // Вестник Северо-Кавказского федерального университета. – 2013. – №3 (36). – С.128–131.
Изучение строения дрожжевых ?-D-маннанов спектроскопии С-ЯМР / П. Кочиш, Л. Маслер, Й. Шандула [и др.] // Биоорганическая Химия. – 1994. – Т.10. – №4. – С.536–543.
Курочкина, А.С. Исследование сорбционной способности растворимых форм дрожжевого бета-глюкана / А.С. Курочкина, А.А. Красноштанова // Бутлеровские сообщения. – 2020. – Т.63. – №9. – С.43–50.
Лукьянчук, В.Д. Бета-глюканы как основа создания средств иммуномодулирующего действия / В.Д. Лукьянчук, Е.М. Мищенко, М.Н. Бабенко // Укр. мед. часопис (www.umj.com.ua). – 2011. – №5 (85). – IX/X. – С.92–93. – Электронный ресурс. – Доступ: https://docs.yandex.ru/docs/view?tm=1743330423&tld=ru&lang=ru&name=glukany2.pdf&text=Brown%20G.D.%20et%20al.%2C%202002&url=https%3A%2F%2Fkleemed.com.ua%2Fwp-content%2Fuploads%2Fglukany2.pdf&lr=213&mime=pdf&l10n=ru&sign=119fb95974adfff06ae3fa97a1e98792&keyno=0&nosw=1&serpParams=tm%3D1743330423%26tld%3Dru%26lang%3Dru%26name%3Dglukany2.pdf%26text%3DBrown%2BG.D.%2Bet%2Bal.%252C%2B2002%26url%3Dhttps%253A%2F%2Fkleemed.com.ua%2Fwp-content%2Fuploads%2Fglukany2.pdf%26lr%3D213%26mime%3Dpdf%26l10n%3Dru%26sign%3D119fb95974adfff06ae3fa97a1e98792%26keyno%3D0%26nosw%3D1. – Дата обращения 30.03.2025.
Маннаны дрожжей // Справочник химика 21. – Электронный ресурс. – Доступ: chem21.info›info/217112/. – Дата обращения 25.11.2020.
Методические рекомендации MP 2.3.1.0253-21 «Нормы физиологических потребностей в энергии и пищевых веществах для различных групп населения Российской Федерации». Утв. Федеральной службой по надзору в сфере защиты прав потребителей и благополучия человека 22 июля 2021 г.) - Введены взамен MP 2.3.1.2432-08.
Анализ перспектив создания функциональных напитков с использованием пектина / М.Ю. Музыка, С.Н. Бутова, Е.Р. Вольнова, Ю.В. Николаева // Colloquium-journal. – 2020. – № 4(56). – С.29–32.
Пищевые загустители, стабилизаторы, гелеобразователи: пектин / А. Аймесон (ред.сост.); перев. с англ. д-ра хим. наук С.В. Макарова. – СПб.: ИД «Профессия», 2012 – 408 с. – Электронный ресурс. – Доступ: https://alternativa-sar.ru/tehnologu/pishchevye-dobavki-i-ingredienty/ajmeson-a-pishchevye-zagustiteli-stabilizatory-geleobrazovateli/2180-13-5-khimicheskie-svojstva. – Дата обращения 12.04.2025.
Постнова, И.В. Формирование и физико-химические свойства гомогенных альгинатных гелей / И.В. Постнова // Дисс. канд. хим. наук. – Владивосток, 2004.
Применение олигофруктозы в мучных кондитерских изделиях – новые идеи для ЗОЖ полки // СОЮЗСНАБ. – 2022. – Электронный ресурс. Доступ: https://ssnab.ru/news/primenenie-oligofruktozy-v-muchnykh-konditerskikh-izdeliyakh-novye-idei-dlya-zozh-polki/ . – Дата обращения 27.02.2025.
Радиф, З.Х. Разработка биотехнологии маннозы и маннозосодержащих гидролизатов из растительного сырья и исследование их биологических функций / З.Х. Радиф // Дисс. канд. техн. наук. – Воронеж, 2018. – 116 с.
Симоненко, С.В. Галактоолигосахариды: технология, анализ рынка и коммерческие перспективы / С.В. Симоненко, Н.А. Шахайло // Молочная промышленность. – 2015. – №7. – С.12–14.
Лактоза и ее производные / Б.М. Синельников, А.Г. Храмцов, И.А. Евдокимов [и др.]. – СПб.: Профессия, 2007. – 786 с.
Стенгель, Б.Ф. Композиция, содержащая маннозный олигосахарид, способ её получения и применения / Б.Ф. Стенгель, Х.Ф. Кюстерс // Заявка на изобретение 2019144988, 14.06.2018. Конвенционный приоритет: 14.06.2017 EP 17175981.4; Дата публ. заявки: 30.06.2021, Бюл. № 19 (DE); Дата начала рассмотр. заявки PCT на нац. фазе: 30.12.2019. Заявка PCT: US 2018/037484 (14.06.2018). Публикация заявки PCT: WO 2018/232078 (20.12.2018). – Электронный ресурс. – Доступ: https://patents.s3.yandex.net/RU2019144988A_20210630.pdf (23.11.2024).
Технические свойства инулина, олигофруктозы Beneo™ и Beneo™Synergy1 // Технические свойства ингредиентов Beneo™. – ORAFTI Active Food Ingredients (www.orafti.com). - Belgium (Tienen). – 15 с. – Дата обращения 15.02.2025 г.
Титова, Л.М. Технология инулина: основные тенденции развития отрасли и спорные вопросы / Л.М. Титова, И.Ю. Алексанян // Пищевая промышленность. – 2016. – №1. – С.46–51.
Свойства D-маннозы: противовоспалительный и противоопухолевый эффекты / И.Ю. Торшин, И.А. Аполихина, А.Н. Громов, О.А. Громова // Экспериментальная и клиническая урология. – 2020. – №2. – С.164–170.
Тенденции развития способов получения галактоолигосахаридов / А.Г. Храмцов, А.Б. Родная, А.Д. Лодыгин, С.А. Рябцева // Известия высших учебных заведений. Пищевая технология. – 2011. – №2–3. – С.5–8.
Пребиотики как функциональные пищевые ингредиенты: терминология, критерии выбора и сравнительной оценки, классификация / А.Г. Храмцов, С.А. Рябцева, Р.О. Будкевич [и др.] // Вопр. питания. – 2018. – Т.87. – №1. – С.5–17.
Антиоксидантная активность продуктов гидролиза природных полимеров (маннана и фукоидана) / Д.А. Черенков, Е.П. Анохина, С.В. Кирьянова, О.С. Корнеева // Вестник ВГУИТ. – 2012. – №1. – С.151–153.
A combination of prebiotic short-and long-chain inulin-type fructans enhances calcium absorption and bone mineralization in young adolescents / S.A. Abrams, I.J. Griffin, K.M. Hawthorne [et al.] // Am. J. Clin. Nutr. – 2005. – Vol. 82. – Р.471–476.
Alcock, J. Is eating behaviour manipulated by the gastrointestinal microbiota? / J. Alcock, C.C. Maley, C.A. Aktipis // Evolutionary pressures and potential mechanisms Bioessays. – 2014. – Vol. 36. – Р.940–949.
Al-Manhel, A.J. Mannan extract from Saccharomyces cerevisiae used as prebiotic in bioyogurt production from buffalo milk / A.J. Al-Manhel, A.K. Niamah // Int Food Res J. – 2017. – Vol.24 (5). – Р.2259–2264.
A unified catalog of 204,938 reference genomes from the human gut microbiome / A. Almeida, S. Nayfach, M. Boland [et al.] // Nat. Biotechnol. – 2021. – Vol.39. – Р.105–114.
Application for the approval of RS4-fibre modified starch (phosphated di-starch phosphate) from high amylose maize starch (final) // Regulation (EC) No 258/97 of the European Parliament and of the Council of 27th January 1997 concerning novel foods and novel food ingredients August 22, 2005. – Электронный ресурс. – Доступ: https://docs.yandex.ru/docs/view?tm=1740595580&tld=ru&lang=en&name=phosphateddistarchphosphate.pdf&text=растворимость%20RS-4&url=https%3A%2F%2Facnfp.food.gov.uk%2Fsites%2Fdefault%2Ffiles%2Fmnt%2Fdrupal_data%2Fsources%2Ffiles%2Fmultimedia%2Fpdfs%2Fphosphateddistarchphosphate.pdf&lr=213&mime=pdf&l10n=ru&sign=400859ca165368dde8ac74660307b77f&keyno=0&nosw=1&serpParams=tm%3D1740595580%26tld%3Dru%26lang%3Den%26name%3Dphosphateddistarchphosphate.pdf%26text%3D%25D1%2580%25D0%25B0%25D1%2581%25D1%2582%25D0%25B2%25D0%25BE%25D1%2580%25D0%25B8%25D0%25BC%25D0%25BE%25D1%2581%25D1%2582%25D1%258C%2BRS-4%26url%3Dhttps%253A%2F%2Facnfp.food.gov.uk%2Fsites%2Fdefault%2Ffiles%2Fmnt%2Fdrupal_data%2Fsources%2Ffiles%2Fmultimedia%2Fpdfs%2Fphosphateddistarchphosphate.pdf%26lr%3D213%26mime%3Dpdf%26l10n%3Dru%26sign%3D400859ca165368dde8ac74660307b77f%26keyno%3D0%26nosw%3D1. – Дата обращения 26.02.2025.
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation / N. Arpaia, C. Campbell, X. Fan [et al.] // Nature. – 2013. – Vol. 504. – Р. 451–455.
Propensity to high-fat diet-induced obesity in rats is associated with changes in the gut microbiota and gut inflammation / C. Barbier de La Serre, C.L., J. Lee [et al.] // Am J. Physiol Gastrointest Liver Physiol. – 2010. – Vol. 299. – Р.G440–G448.
Baye, K. The unresolved role of dietary fibers on mineral absorption / K. Baye, J.P. Guyot, C. Mouquet-Rivier // Crit. Rev. Food Sci. Nutr. – 2017. – Vol.57. – Р.949–957.
Dynamics of Human Gut Microbiota and Short-Chain Fatty Acids in Response to Dietary Interventions with Three Fermentable Fibers / N.T. Baxter, A.W. Schmidt, A. Venkataraman [et al.] // mBio 2019. – Vol.10. – e02566–18.
Behera, S.S. Nutritional and potential health benefits of konjac glucomannan, a promising polysaccharide of elephant foot yam, Amorphophallus konjac K. Koch: A review / S.S. Behera, R.C. Ray // Food Reviews International. – 2017– Vol. 33, Issue 1. – Pages 22–43. Published online: 09 May 2016.
Benton, D. Reducing Calorie Intake May Not Help You Lose Body Weight / D. Benton, H.A. Young // Perspect. Psychol. Sci. – 2017. – Vol.12. – Р.703–714.
Bile acids as endogenous etiologic agents in gastrointestinal cancer / H. Bernstein, C. Bernstein, C.M. Payne, K. Dvorak // World J. Gastroenterol. – 2009. – Vol.15. – Р.3329–3340.
Pectins that Structurally Differ in the Distribution of Methyl-Esters Attenuate Citrobacter rodentium-Induced Colitis / M. Beukema, R. Akkerman, E. Jermendi [et al.] // Mol. Nutr. Food Res. – 2021. – Vol.65. – Article 2100346.
Beukema, M. The effects of different dietary fiber pectin structures on the gastrointestinal immune barrier: impact via gut microbiota and direct effects on immune cells / M. Beukema, M.M. Faas, P. de Vos // Exp Mol Med. – 2020. – Vol.52. – Р.1364–1376.
The Dietary Fiber Pectin: Health Benefits and Potential for the Treatment of Allergies by Modulation of Gut Microbiota / F. Blanco-P?rez, H. Steigerwald, S. Sch?lke [et al.] // Curr Allergy Asthma Rep. – 2021 Sep 10. – Vol. 21(10). – Article 43.
Bosscher, D. Effect of thickening agents, based on soluble dietary fiber, on the availability of calcium, iron, and zinc from infant formulas / D. Bosscher, M. Van Caillie-Bertrand, H. Deelstra // Nutrition. – 2001. – Vol.17. – Р.614–618.
Bouaziz, M. Chemical Composition, Functional Properties, and Effect of Inulin from Tunisian Agave americana L. Leaves on Textural Qualities of Pectin Gel / M. Bouaziz, R. Rassaoui, S. Besbes // Journal of Chemistry. – 2014. – V.2014 – 11 p.
Brighenti, F. Dietary fructans and serum triacylglycerols: A meta-analysis of randomized controlled trials / F. Brighenti // J. Nutr. – 2007. – Vol.137. – 2552S–2556S.
Brown, M.R. The amino-acid and sugar composition of 16 species of microalgae used in mariculture / M.R. Brown // Journal of Experimental Marine Biology and Ecology. – 1991. – Vol.145. – Р.79–99.
The Orphan G protein-coupled receptors GPR41 and GPR43 are activated by propionate and other short chain carboxylic acids / A.J. Brown, S.M. Goldsworthy, A.A. Barnes [et al.] // J. Biol. Chem. – 2003. – Vol. 278. – Р.11312–11319.
Brown, G.D. Immune reсognition. A new reсeptor for beta-gluсans / G.D. Brown, S. Gordon // Nature. – 2001. – Vol. 413(6851). – Р.36–37.
Dectin-1 is a major beta-glucan receptor on macrophages / G.D. Brown, P.R. Taylor, D.M. Reid [et al.] // J. Exp. Med. – 2002. – Vol. 196(3). – Р.407–412.
Dietary supplement of neosugar alters the fecal flora and decreases activities of some reductive enzymes in human subjects / R.K. Buddington, C.H. Williams, S.C. Chen, S.A. Witherly // The American Journal of Clinical Nutrition. – 1996. – Vol. 63, Issue 5. – Р.709–716.
Burton-Freeman, B. Dietary fiber and energy regulation / B. Burton-Freeman // J. Nutr. – 2000. – Vol. 130. – Р. 272S–275S.
Gum arabic establishes prebiotic functionality in healthy human volunteers in a dose-dependent manner / W. Calame, A.R. Weseler, C. Viebke [et al.] // Br. J. Nutr. – 2008. – Vol. 100. – Р.1269–1275.
Dietary non-digestible carbohydrates promote L-cell differentiation in the proximal colon of rats / P.D. Cani, S. Hoste, Y. Guiot, N.M. Delzenne // Br J Nutr. – 2007. – Vol.98. – Р.32–37.
Gut microbiota fermentation of prebiotics increases satietogenic and incretin gut peptide production with consequences for appetite sensation and glucose response after a meal / P.D. Cani, E. Lecourt, E.M. Dewulf [et al.] // Am J. Clin Nutr. – 2009. – Vol. 90. – Р.1236–1243.
Fruit for thought: anaphylaxis to fruit pectin in foods / P. Capucilli, K. Kennedy, A.M. Kazatsky // J. Allergy Clin Immunol Pract. – 2019. – Vol.7. – Р.719–720.
Chae, H.J. Utilization of brewer’s yeast cells for the production of food-grade yeast extract. Part 1: effects of different enzymatic treatments on solid and protein recovery and flavor characteristics / H.J. Chae, H. Joo, M.J. In // Bioresource technology. – 2001. – Vol.76 (3). – Р.253–258.
The microbial metabolite butyrate regulates intestinal macrophage function via histone deacetylase inhibition / P.V. Chang, L. Hao, S. Offermanns, R. Medzhitov // Proc. Natl. Acad. Sci. USA. – 2014. – Vol.111. – Р.2247–2252.
Chawla, R. Soluble dietary fiber / R. Chawla, G. Patil // Compr. Rev. Food Sci. Food Saf. – 2010. – Vol.9. – Р.178–196.
Structural characterization and antidiabetic potential of a novel heteropolysaccharide from Grifola frondosa via IRS1/PI3K-JNK signaling pathways / Y. Chen, Y. Liu, M.M.R. Sarker [et al.] // Carbohydr. Polym. – 2018. – Vol. 198. – Р.452–461.
Chiang, J.Y. Bile acids: Regulation of synthesis / J.Y. Chiang // J. Lipid Res. – 2009. – Vol. 50. – Р.1955–1966.
Chiang, J.Y.L. Bile Acids as Metabolic Regulators and Nutrient Sensors / J.Y.L. Chiang, J.M. Ferrell // Annu. Rev. Nutr. – 2019. – Vol.39. – Vol.175–200.
?2-1 fructan supplementation alters host immune responses in a manner consistent with increased exposure to microbial components: Results from a double-blinded, randomised, cross-over study in healthy adults / S. Clarke, J. Green-Johnson, S. Brooks [et al.] // Br. J. Nutr. – 2016. – Vol.115. – Р.1748–1759.
Cohen, A.J. Occupational asthma caused by pectin inhalation during the manufacture of jam / A.J. Cohen, M.S. Forse, S.M. Tarlo // Chest. – 1993. – Vol.103. – Р.309–311.
Enterotypes in the landscape of gut microbial community composition / P.I. Costea, F. Hildebrand, M. Arumugam [et al.] // Nat. Microbiol. – 2018. – Vol.3. – Р.8–16.
Effect of soluble or partly soluble dietary fibres supplementation on absorption and balance of calcium, magnesium, iron and zinc in healthy young men / C. Coudray, J. Bellanger.,C. Castiglia Delavaud [et al.] // Eur. J. Clin. Nutr. – 1997. – Vol.51 (6). – Р.375–380.
Cui, S.W. The range of dietary fibre ingredients and a comparison of their technical functionality / S.W. Cui, Y. Wu, H. Ding // In book: Fibre-Rich and Wholegrain Foods. – Woodhead Publishing Series in Food Science, Technology and Nutrition. – 2013. – Р.96–119.
The impact of oligofructose on stimulation of gut hormones, appetite regulation and adiposity / N.M. Daud, N.A. Ismail, E.L. Thomas [et al.] // Obesity. – 2014. – Vol.22. – Р.1430–1438.
Prebiotics: Definition, Types, Sources, Mechanisms, and Clinical Applications / D. Davani-Davari, M. Negahdaripour, I. Karimzadeh. [et al.] // Foods. – 2019 Mar. – Vol. 8(3). – Article 92.
Effect of fermentable fructo-oligosaccharides on mineral, nitrogen and energy digestive balance in the rat / N. Delzenne, J. Aertssens, H. Verplaetse [et al.] // Life Sciences. – 1995. – No. 17. – Р.1579–1587.
Insight into the prebiotic concept: Lessons from an exploratory, double blind intervention study with inulin-type fructans in obese women / E.M. Dewulf, P.D. Cani, S.P. Claus [et al.] // Gut. – 2013. – Vol.62. – Р.1112–1121.
Beneficial effect of standardized extracts of Amorphophallus paeoniifolius tuber and its active constituents on experimental constipation in rats / Y.N. Dey, M.M. Wanjari, B. Srivastava [et al.] // Heliyon. – 2020 May 30. – Vol.6(5). – e04023.
Spectroscopic and Biochemical Analysis of Regions of the Cell Wall of the Unicellular «Mannan Weed» / E.K. Dunn, D.A. Shoue, X. Huang [et al.] // Acetabularia acetabulum. – 2007. – Vol. 48 (1). – Р.122–133.
The abundance and variety of carbohydrate-active enzymes in the human gut microbiota / A. El Kaoutari, F. Armougom, J.I. Gordon [et al.] // Nat. Rev. Microbiol. 2013, 11, 497–504. [Google Scholar] [CrossRef]
Eswaran, S. Fiber and functional gastrointestinal disorders / S. Eswaran, J. Muir, W.D. Chey // Am. J. Gastroenterol. – 2013. – Vol.108. – Р.718–727.
Galactoglucomannan oligosaccharide supplementation affects nutrient digestibility, fermentation end-product production, and large bowel microbiota of the dog / T.A. Faber, A.C. Hopkins, I.S. Middelbos [et al.] // J. of Animal Science. – 2011. – Vol.89 (1). – Р.103–112.
Ferdman, R.M. Pectin anaphylaxis and possible association with cashew allergy / R.M. Ferdman, P.Y. Ong, J.A. Church // Ann Allergy Asthma Immunol. – 2006. – Vol.97. – Р.759–760.
Improved humoral immune response to measles vaccine in infants receiving infant cereal with fructooligosaccharides / A. Firmansyah, G. Pramita, A. Carrie Fassler [et al.] // J. Pediatr. Gastroenterol. Nutr. – 2001. – Vol. 31. – A521.
Fishbein, L. Fructooligosaccharides: a review / L. Fishbein, M. Kaplan, M. Gough // Vet Hum Toxicol. – 1988 Apr. – Vol. 30(2). – Р.104–107.
Microbial degradation of complex carbohydrates in the gut / H.J. Flint, K.P. Scott, S.H. Duncan [et al.] // Gut Microbes. – 2012. – Vol. 3. – Р.289–306.
Foley, M.H. The Sus operon: A model system for starch uptake by the human gut Bacteroidetes / M.H. Foley, D.W. Cockburn, N.M. Koropatkin // Cell. Mol. Life Sci. – 2016. – Vol.73. – Р.2603–2617.
Franck, A. Prebiotics stimulate calcium absorption: a review / A. Franck // Milchwissenschaft. – 1998. – V.53 (8). – Р.427–429.
Franco-Robles, E. Implication of Fructans in Health: Immunomodulatory and Antioxidant Mechanisms / E. Franco-Robles, M.G. L?pez // The Scientific World Journal. – Vol. 2015. – Article ID 289267. – 15 p.
Maternal consumption of fructo-oligosaccharide diminishes the severity of skin inflammation in offspring of nc/nga mice / R. Fujiwara, N. Takemura, J. Watanabe, K. Sonoyama // Br. J. Nutr. – 2010. – Vol.103. – Р.530–538.
A review of the potential mechanisms for the lowering of colorectal oncogenesis by butyrate / K.Y. Fung, L. Cosgrove, T. Lockett [et al.] // Br. J. Nutr. 2012. – Vol.108. – Р.820–831.
Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells / Y Furusawa, Y. Obata, S. Fukuda [et al.] // Nature. – 2013. – Vol.504. – Р.446–450.
Causal relationship between diet-induced gut microbiota changes and diabetes: A novel strategy to transplant Faecalibacterium prausnitzii in preventing diabetes / K. Ganesan, S.K. Chung, J.Vanamala, B. Xu // Int. J. Mol. Sci. – 2018. – Vol.19. – Article 3720.
Ganesan, K. Anti-Diabetic Effects and Mechanisms of Dietary Polysaccharides / K. Ganesan, B. Xu // Molecules. – 2019 Jul 13. – Vol.24(14). – Article 2556.
High-esterified pectin reverses metabolic malprogramming, improving sensitivity to adipostatic/adipokine hormones / F. Garc?a-Carrizo, C. Pic?, A.M. Rodr?guez, A. Palou // J. Agric Food Chem. – 2019. – Vol.67. – Р. 3633–3642.
Dietary modulation of the human colonic microbiota: updating the concept of prebiotics / G.R. Gibson, H.M. Prober, J.V. Loo [et al.] // Nutr. Res. Rev. – 2004. – Vol.17. – P.259–275.
Gibson, G.R. Prebiotics: Development and Application / G.R. Gibson, R.A. Rastall. – Chichester: John Wiley and Sons, 2006. – 249 p.
Dietary prebiotics: current status and new definition / G.R. Gibson, K.P. Scott, R.A. Rastall [et al.] // Food Sci. Technol. Bull. Funct. Foods. – 2010. – Vol.7. – P.1–19.
Dietary fibre in gastrointestinal health and disease / S.K. Gill, M. Rossi, B. Bajka, K. Whelan // Nat. Rev. Gastroenterol. Hepatol. – 2021. – Vol.18. – Р.101–116.
Global Prebiotics Industry. – Электронный ресурс. – Доступ: http://www.marketwatch.com/story/global-prebiotics-industry. - 2013-08-06. – Дата обращения 15.01.2025.
The Pros and Cons of Using Algal Polysaccharides as Prebiotics / M. Gotteland, K. Riveros, N. Gasaly [et al.] // Frontiers in Nutrition. – 2020. – Vol.7. – Article 163.
Mannan Molecular Substructures Control Nanoscale Glucan Exposure in Candida Article Mannan Molecular Substructures Control Nanoscale Glucan Exposure in Candida / M.S. Graus, M.J. Wester, D.W. Lowman [et al.] // CellReports. – 2018. – Vol.24 (9). – Р.2432–2442.
Griffin, I. Non-digestible oligosaccharides and calcium absorption in girls with adequate calcium intakes / I. Griffin, P. Davila, S. Abrams // Br. J. Nutr. – 2002. – Vol.87 (suppl. 2). – Р.187–191.
Guan, Z.W. Soluble Dietary Fiber, One of the Most Important Nutrients for the Gut Microbiota / Z.W. Guan, E.Z. Yu, Q. Feng // Molecules. – 2021 Nov 11. – Vol.26(22). – Article 6802.
Guo C., Li R., Zheng N., Xu L., Liang T., He Q. Anti-diabetic effect of ramulus mori polysaccharides, isolated from Morus alba L., on STZ-diabetic mice through blocking inflammatory response and attenuating oxidative stress // International Immunopharmacology. – 2013. – Vol. 16, Issue 1. – P.93–99.
Bioresource Technology Structural characteristics and antioxidant activities of the extracellular polysaccharides produced by marine bacterium Edwardsiella tarda / S. Guo, W. Mao, Y. Han [et al.] // Bioresour Technol. – 2010. – Vol.101 (12). – Р.4729–4732.
Extraction of crude Mannan oligosaccharides from yeast and their uses / R. Harbah, E.O. Agembo, T.V. Meledina [et al.] // Вестник Международной академии холода. – 2020. – № 1. – С.46–51.
Mannan: structure, biosynthesis, and methods extraction from yeast saccharomyces cerevisiae / R. Harbah, T.V. Meledina, D.V. Manshin, V.V. Andreev // Вестник МАХ. – 2021. – №1. – С.59–65.
Inulin: Fermentation and microbial ecology in the intestinal tract / R. Havenaar, S. Bonnin-Marol, W. Van Dokkum [et al.] // Food Rev. Int. – 1999. - Vol. 15. – Р. 109–120.
In vitro fermentation profiles, gas production rates, and microbiota modulation as affected by certain fructans, galactooligosaccharides, and polydextrose / D.C. Hernot, T.W. Boileau, L.L. Bauer [et al.] // J. Agric. Food Chem. – 2009. - Vol. 57. – Р.1354–1361.
van den Heuvel, E.G. Transgalactooligosaccharides stimulate calcium absorption in postmenopausal women / E.G. van den Heuvel, M.H. Schoterman, T. Muijs // J. Nutr. – 2000. – Vol.130. – Р.2938–2942.
Effects of a diet based on inulin-rich vegetables on gut health and nutritional behavior in healthy humans / S. Hiel, L.B. Bindels, B.D. Pachikian [et al.] // The American Journal of Clinical Nutrition. – 2019. – Vol.109, Issue 6. – P.1683–1695.
Holscher, H.D. Dietary fiber and prebiotics and the gastrointestinal microbiota / H.D. Holscher // Gut Microbes. – 2017. – Vol.8. – Р.172–184.
Agave Inulin Supplementation Affects the Fecal Microbiota of Healthy Adults Participating in a Randomized, Double-Blind, Placebo-Controlled, Crossover Trial / H.D. Holscher, L.L. Bauer, V. Gourineni [et al.] // J. Nutr. – 2015. – Vol.145. – Р.2025–2032.
Photoprotective effects of galacto-oligosaccharide and/or bifidobacterium longum supplementation against skin damage induced by ultraviolet irradiation in hairless mice / K.-B. Hong, M. Jeong, K.S. Han [et al.] // Int. J. Food Sci. Nutr. – 2015. – Vol.66. – Р.923–930.
Composition and bioactivity of polysaccharides from Inula britannica flower / T. Hong, J. Zhao, M. Dong [et al.] // Int. J. Biol. Macromol. – 2012. – Vol.51. – Р.550–554.
Hooge, D.M. Meta-analysis summary of broiler chicken trials with dietary Actigen® (2009-2011) / D.M. Hooge, A. Kiers, A. Connolly // Int. J. Poultry Sci. – 2013. – Vol.12. – Р.1–8.
Howarth, N.C. Dietary fiber and weight regulation / N.C. Howarth, E. Saltzman, S.B. Roberts // Nutr. Rev. – 2001. – Vol.59. – Р.129–139.
Huang, G.L. Extraction of two active polysaccharides from the yeast cell wall / G.L. Huang // Zeitschrift fur Naturforsch. Sect C J. Bios ci. – 2008. – Vol.63 (11–12). – Р.919–921.
Huang G. L., Yang Q., Wang Z. B. Extraction and deproteiniza tion of mannan oligosaccharide // Zeitschrift fur Naturforsch. – Sect C J Biosci. – 2010. – Vol.65. (5-6). – Р.387–390.
Hume MP, Nicolucci AC, Reimer RA. Prebiotic supplementation improves appetite control in children with overweight and obesity: A randomized controlled trial // Am J. Clin Nutr. – 2017. – Vol.105. – Р.790–799.
Inohara H, Raz A. Effects of natural complex carbohydrate (citrus pectin) on murine melanoma cell properties related to galectin-3 functions // Glycoconj J. – 1994. – Vol.11. – Р.527–532.
Mc Intosh M, Miller C. A diet containing food rich in soluble and insoluble fiber improves glycemic control and reduces hyperlipidemia among patients with type 2 diabetes mellitus // Nutr. Rev. – 2001. – Vol.59. – Р.52–55.
Inulin and inulin-containing crops. Studies in plant science 3 // Edited by A. Fuchs. – Elsevier Science Publishers BV, The Netherlands. – 1993. – 417 p.
Iwamoto A, Inoue Y, Tachibana H, Kawahara H. Alkali-soluble pectin suppresses IgE production in human myeloma cell line in vitro // Cytotechnology. – 2019. – Vol.71. – Р.573–581.
Jaakkola MS, Tammivaara R, Tuppurainen M, Lahdenne L, Tupasela O, Keskinen H. Asthma caused by occupational exposure to pectin // J Allergy Clin Immunol. – 1997. – Vol.100. – Р.575–576.
Jalanka-Tuovinen J, Salonen A, Nikkil? J, Immonen O, Kekkonen R, Lahti L, Palva A, de Vos WM. Intestinal microbiota in healthy adults: Temporal analysis reveals individual and common core and relation to intestinal symptoms // PLoS One. – 2011. – Vol.6. – e23035.
Prebiotic mannooligosaccharides: Synthesis, characterization and bioactive properties / U.K. Jana, R.K. Suryawanshi, B.P. Prajapati, N. Kango // Food Chem. – 2021 Apr 16. – Vol. 342. – Article 128328.
Comparison of physicochemical properties and antidiabetic effects of polysaccharides extracted from three seaweed species / R.-B. Jia, J. Wu, Zh.-R. Li [et al.] // Intern. J. of Biol. Macromol. – 2020. – Vol.149. – P.81–92.
Jia, W. Bile acid-microbiota crosstalk in gastrointestinal inflammation and carcinogenesis / W. Jia, G. Xie, W. Jia // Nat. Rev. Gastroenterol. Hepatol. – 2018. – Vol.15. – Р.111–128.
Jung, A. 10 Foods to Help Relieve Constipation / A. Jung // Diet & Nutrition. – Published: Aug 4, 2020. – Электронный ресурс. – Доступ: https://www.goodhousekeeping.com/health/diet-nutrition/g33492824/foods-that-relieve-constipation/. – Дата обращения 04.10.2024.
Potato powders prepared by successive cooking-process depending on resistant starch content affect the intestinal fermentation in rats / S. Kawakami, K.H. Han, T. Araki [et al.] // Biosci. Biotechnol. Biochem. – 2017. – Vol.81. – Р.359–364.
Dietary galacto-oligosaccharides mixture can suppress serum phenol and p-cresol levels in rats fed tyrosine diet / K. Kawakami, I. Makino, T. Asahara [et al.] // J. Nutr. Sci. Vitaminol. – 2005. – Vol. 51. – Р.182–186.
Kelly, G. Inulin-Type prebiotics: a review (part 2) / G. Kelly // Altern. Med. Rev. – 2009. – Vol.14. – № 1. – P.36–55.
Kim, K.-T. Molecular weight and sulfate content modulate the inhibition of ?-amylase by fucoidan relevant for type 2 diabetes management / K.-T. Kim, L.-E. Rioux, S.L. Turgeon // Pharma. Nutr. – 2015. – Vol.3. – Р.108–114.
The gut microbiota suppresses insulin-mediated fat accumulation via the short-chain fatty acid receptor GPR43 / I. Kimura, K. Ozawa, D. Inoue [et al.] // Nat. Commun. – 2013. – Vol.4. – Article 1829.
Jerusalem artichoke and chicory inulin in bakery products affect faecal microbiota of healthy volunteers / B. Kleessen, S. Schwarz, A. Boehm [et al.] // Br J Nutr. – 2007. – Vol. 98. – Р.540–549.
From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites / A. Koh, F. De Vadder, P. Kovatcheva-Datchary, F. B?ckhed // Cell. – 2016. – Vol.165. – Р.1332–1345.
Koropatkin, N.M. How glycan metabolism shapes the human gut microbiota / N.M. Koropatkin, E.A. Cameron, E.C. Martens // Nat. Rev. Microbiol. – 2012. – Vol.10. – Р.323–335.
Christmas candy maker›s asthma. IgG4-mediated pectin allergy / A. Kraut, Z. Peng, A.B. Becker [et al.] // Chest. – 1992. – Vol.102. – Р.1605–1607.
Probiotics and prebiotic galacto-oligosaccharides in the prevention of allergic diseases: A randomized, double-blind, placebo-controlled trial / K. Kukkonen, E. Savilahti, T. Haahtela [et al.] // J. Allergy Clin. Immunol. – 2007. – Vol.119. – Р.192–198.
Transglycosidase activity of Bifidiobacterium adolescentis DSM 20083 galactosidase / KM. Laere [et al.] // Appl. Microbiol. Biotechnol. – 1999. – V.52. – Р.681–688.
Recent Development of Prebiotic Research – Statement from an Expert Workshop / G. La Fata, R.A. Rastall, C. Lacroix [et al.] // Nutrients. – 2017. – Vol 9 (12). – Article 1376.
Potential of pectins to beneficially modulate the gut microbiota depends on their structural properties / N. Larsen, C. Bussolo de Souza, L. Krych [et al.] // Front Microbiol. – 2019. – Vol.10. – Article 223.
Asian pear pectin administration during pre-sensitization inhibits allergic response to ovalbumin in BALB/c mice / J.C. Lee, S.C. Pak, S.H. Lee [et al.] // J Altern Complement Med. – 2004. – Vol.10. – Р.527–534.
Leenen, C.H. Inulin and oligofructose in chronic inflammatory bowel disease / C.H. Leenen, L.A. Dieleman // J. Nutr. – 2007. – Vol.137. – Р.2572S–2575S.
Leroux O., Leroux F., Bagniewska-Zadworna A., Knox J. P., Claeys M., Bals S., Viane R. L. Ultrastructure and composition of cell wall appositions in the roots of Asplenium (Polypodiales) // Micron. – 2011. – Vol.42. – Р.863–870.
Lew D.B. Use of mannan from saccharomyces cerevisiae for the treatment of asthma / PatentUS-7582620-B2; Priority: 2003.10.14, Grant: 2009.09.01 // National Center for Biotechnology Information (2024). PubChem Patent Summary for US-7582620-B2, Use of mannan from saccharomyces cerevisiae for the treatment of asthma. Retrieved December 2, 2024 from https://pubchem.ncbi.nlm.nih.gov/patent/US-7582620-B2.
Selective colonization of insoluble substrates by human faecal bacteria / E.C. Leitch, A.W. Walker, S.H. Duncan [et al.] // Environ. Microbiol. – 2007. – Vol.9. – Р.667–679.
Mannose-mediated inhibitory effects of PA-MSHA on invasion and metastasis of hepatocellular carcinoma via EGFR/Akt/I?B?/NF-?B pathway / T. Li, Z.R. Dong, Z.Y. Guo [et al.] // Liver Int. – 2015. – Vol.35(4). – Р.1416–1429.
Modified apple polysaccharides could induce apoptosis in colorectal cancer cells / Y. Li, Y. Niu, H. Wu [et al.] // J. Food Sci. – 2010. – Vol.75. – Р.H224–H229.
The beneficial effects of purple yam (Dioscorea alata L.) resistant starch on hyperlipidemia in high-fat-fed hamsters / T. Li, H. Teng, F. An [et al.] // Food Funct. – 2019. – Vol.10. – Р.2642–2650.
Clinical, microbiological, and immunological effects of fructo-oligosaccharide in patients with crohn’s disease / J.O. Lindsay, K. Whelan, A.J. Stagg [et al.] // Gut. – 2006. – Vol.55. – Р.348–355.
Interaction of various pectin formulations with porcine colonic tissues/ L. Liu, M.L. Fishman, K.B. Hicks, M. Kende // Biomaterials. – 2005. – Vol.26. – Р.5907–5916.
Liu, Y. Extraction, characterization and antioxidant activities of mannan from yeast cell wall / Y. Liu, G. Huang, M. Lv // Int J Biol Macromol. – 2018. – Vol.118 (Pt A). – Р.952–956.
Antidiabetic and antinephritic activities of aqueous extract of Cordyceps militaris fruit body in diet-streptozotocin-induced diabetic Sprague Dawley rats / C. Liu, J. Song, M. Teng [et al.] // Oxid. Med. Cell. Longev. – 2016. – Vol.2016. – Р.1–11.
Polymannuronic acid ameliorated obesity and inflammation associated with a high-fat and high-sucrose diet by modulating the gut microbiome in a murine model / F. Liu, X. Wang, H. Shi // Br. J. Nutr. – 2017. – Vol.117. – Р.1332–1342.
?2-1 fructans have a bifidogenic effect in healthy middle-aged human subjects but do not alter immune responses examined in the absence of an in vivo immune challenge: Results from a randomised controlled trial / A.R. Lomax, L.V. Cheung, K.M. Tuohy [et al.] // Br. J. Nutr. – 2012. – Vol.108. – Р.1818–1828.
Role of polysaccharides in food, digestion, and health / A. Lovegrove, C.H. Edwards, I. De Noni [et al.] // Crit. Rev. Food Sci. Nutr. – 2017. – Vol.57. – Р.237–253.
Preparation of the controlled acid hydrolysates from pumpkin polysaccharides and their antioxidant and antidiabetic evaluation / A. Lu, M. Yu, Z. Fang [et al.] // Int. J. Biol. Macromol. – 2019. – Vol.121. – Р.261–269.
Production, fractionation, characterization of extracellular polysaccharide from a newly isolated Trametes gibbosa and its hypoglycemic activity / Y. Ma, D. Mao, L. Geng, [et al.] // Carbohydr. Polym. – 2013. – Vol.96. – Р.460–465.
Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasome / L. Macia, J. Tan, A.T. Vieira [et al.] // Nat. Commun. – 2015. – Vol.6. – Article 6734.
The Impact of Dietary Fiber on Gut Microbiota in Host Health and Disease / K. Makki, E.C. Deehan, J. Walter, F. Backhed // Cell Host Microbe. – 2018. – Vol.23. – Р.705–715.
Mannan // National Center for Biotechnology Information // PubChem Compound Summary for CID 25147451, Mannan. – Электронный ресурс. – Доступ: https://pubchem.ncbi.nlm.nih.gov/compound/Mannan. – Дата обращения 25.11.2024.
Mannan 1526 – Mannan liquid. Homeopathic product // National Library of Medicine. – Электронный ресурс. – Доступ: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=9ddfae02-bba7-4490-a685-cdeb4eb437e4. – Дата обращения 02.12.2014.
Depolymerized RG-I-enriched pectin from citrus segment membranes modulates gut microbiota, increases SCFA production, and promotes the growth of Bifidobacterium spp., Lactobacillus spp. and Faecalibaculum spp. / G. Mao, S. Li, C. Orfila [et al.] // Food Funct. – 2019. – Vol.10. – Р.7828–7843.
Recognition and degradation of plant cell wall polysaccharides by two human gut symbionts / E.C. Martens, E.C. Lowe, H. Chiang [et al.] // PLoS Biol. – 2011. – Vol.9. – e1001221.
Partial Purification and Characterization of Mannan Oligosaccharides from Cell Wall of Saccharomyces cerevisiae / V. Maru, S. Hewale, H. Mantri, V. Ranade // Int J Curr Microbiol Appl Sci. – 2015. – Vol.4 (12). – Р.705–711.
Effect of inulin-type fructans in patients undergoing cancer treatments: A systematic review / R. Mazraeh, F. Azizi-Soleiman, S.M.H.M. Jazayeri, S.M.A. Noori // Pak J Med Sci. – 2019. – Vol.35(2). – Р.575-580.
Mcanalley B.H., Carpenter R.H., Mcdaniel H.R. Use of acetylated mannan (acemannan) for the regulation of blood cholesterol levels and for removing plaques in blood vessels / Patent / EP-0611304-B1; European Patent Office; Priority: 1991.11.05, Grant: 1999.09.15 // National Center for Biotechnology Information (2024). PubChem Patent Summary for EP-0611304-B1. Retrieved December 2, 2024. – Электронный ресурс. – Доступ: https://pubchem.ncbi.nlm.nih.gov/patent/EP-0611304-B1. – Дата обращения 15.11.2024.
McRorie, J. Clinical data support that psyllium is not fermented in the gut / J. McRorie // Am. J. Gastroenterol. – 2013. – Vol.108. – Article 1541.
Psyllium is superior to docusate sodium for treatment of chronic constipation / J.W. McRorie, B.P. Daggy, J.G. Morel [et al.] // Aliment. Pharmacol. Ther. – 1998. – Vol.12. – Р.491–497.
Merheb, R. Immunomodulatory effect of natural and modified Citrus pectin on cytokine levels in the spleen of BALB/c mice / R. Merheb, R.M. Abdel-Massih, M.C. Karam // Int J. Biol Macromol. – 2019. – Vol.121. – Р.1–5.
Behavioural and cognitive effects of oligofructose-enriched inulin in rats / M. Messaoudi, P. Rozan, A. Nejdi [et al.] // Br. J. Nutr. – 2005. – Vol. 93. – Р.S27–S30.
Genomic encyclopedia of type strains of the genus Bifidobacterium / C. Milani, G.A. Lugli, S. Duranti [et al.] // Appl. Environ. Microbiol. – 2014. – Vol.80. – Р.6290–6302.
Biological activity and pharmacological application of pectic polysaccharides: A Review / S.T. Minzanova, V.F. Mironov, D.M. Arkhipova [et al.] // Polymers (Basel). – 2018. – Vol. 10(12). – Article 1407.
Consecutive intake of fermented milk containing bifidobacterium breve strain yakult and galacto-oligosaccharides benefits skin condition in healthy adult women / K. Mitsuyoshi, N. Masuoka, K. Chiaki [et al.] // Biosci. Microbiot. Food Health. – 2013. – Vol.32. – Р.33–39.
Bifidobacterium fermented milk and galacto-oligosaccharides lead to improved skin health by decreasing phenols production by gut microbiota / K. Miyazaki, N. Masuoka, M. Kano, R. Iizuka // Benef. Microbes. – 2013. – Vol.5. – Р.121–128.
Oligosaccharides and probiotic bacteria / H.W. Modler, I. Birlouez, S. Holland [et al.] // Bull. IDF. – 1996. – Vol.313. – P.58-65.
Moreira, L.R. An overview of mannan structure and mannan-degrading enzyme systems / L.R. Moreira, E.X. Filho // Appl Microbiol Biotechnol. – 2008. – Vol.79. – Р.165–178.
Murari, S. Fructooligosaccharides – type prebiotic: A Review / S. Murari // Journal of Pharmacy Research. – 2014. – Vol.8 (3). – Р.321–330.
Inhibitory effects of laminaran and alginate on production of putrefactive compounds from soy protein by intestinal microbiota in vitro and in rats / Nakata T, Kyoui D, Takahashi H, [et al.] // Carbohydr Polym. – 2016. – Vol.143. – Р.61–69.
Butyrate produced by commensal bacteria potentiates phorbol esters induced AP-1 response in human intestinal epithelial cells / M. Nepelska, A. Cultrone, F. Beguet-Crespel [et al.] // PLoS ONE. – 2012. – Vol.7. – e52869.
Prebiotic reduces body fat and alters intestinal microbiota in children with overweight or obesity / A.C. Ficolucci, M.P. Hume, I. Mart?nez [et al.] // Gastroenterology. – 2017. – Vol.153. – Р.711–722.
Review article: Dietary fibre in the era of microbiome science / J. O’Grady, E.M. O’Connor, F. Shanahan // Aliment. Pharmacol. Ther. – 2019. – Vol.49. – Р.506–515.
Structure-activity relationship of (1–>3)-beta-D-glucans in the induction of cytokine production from macrophages, in vitro / M. Okazaki, Y. Adachi, N. Ohno, T. Yadomae // Biol. Pharm. Bull. – 1995. – Vol.18(10). – Р.1320–1327.
Prebiotic galacto-oligosaccharides mitigate the adverse effects of iron fortification on the gut microbiome: A randomised controlled study in Kenyan infants / D. Paganini, M.A. Uyoga, G.A.M. Kortman [et al.] // Gut. – 2017. – Vol.66. – Р.1956–1967.
The effects of regular consumption of short-chain fructo-oligosaccharides on digestive comfort of subjects with minor functional bowel disorders / D. Paineau, F. Payen, S. Panserieu, [et al.] // Br. J. Nutr. – 2008. – Vol.99. – Р.311–318.
The binding of lead by a pectic polyelectrolyte / A.J. Paskins-Hurlburt, Y. Tanaka, S.C. Skoryna [et al.] // Environ Res. – 1977. – Vol.14. – Р.128–140.
Effects of heat treatment and pectin addition on beta-lactoglobulin allergenicity / S. Peyron, J. Mou?coucou, S. Fr?mont [et al.] // J Agric Food Chem. – 2006. – Vol.54. – Р.5643–5650.
Modulation of the lung colonization of B16–F1 melanoma cells by citrus pectin / D. Platt, A. Raz // J. Natl Cancer Inst. – 1992. – Vol.84. – Р.438–442.
Galacto-oligosaccharides and other products derived from lactose / M.J. Playne // Advanced Dairy Chemistry. – 2009. – P.15–26.
Galactoglucomannan Extracted from Spruce (Picea abies) as a Carbohydrate Source for Probiotic Bacteria / L. Polari, P. Ojansivu, S. Makela [et al.] // Agric. Food Chem. – 2012. – Vol.60. – Р.11037–11043.
A matrix effect in pectin-rich fruits hampers digestion of allergen by pepsin in vivo and in vitro / N. Polovic, M. Blanusa, M. Gavrovic-Jankulovic [et al.] // Clin Exp Allergy. – 2007. – Vol.37. – Р.764–771.
Pool-Zobel, B.L. Inulin-type fructans and reduction in colon cancer risk: Review of experimental and human data / B.L. Pool-Zobel // Br. J. Nutr. – 2005. – Vol.93. – Р.S73–S90.
Popov, S.V. Polypotency of the immunomodulatory effect of pectins / S.V. Popov, Y.S. Ovodov // Biochemistry Mosc. – 2013. – Vol.78. – Р.823–835.
Study of prebiotic properties of selected banana species in Thailand / P. Powthong, B. Jantrapanukorn, P. Suntornthiticharoen, K. Laohaphatanalert // J. Food Sci. Technol. – 2020 Jul. – Vol.57(7). – Р.2490–2500.
Schols, H.A. Pectin interaction with immune receptors is modulated by ripening process in papayas / S.B.R. Prado, M. Beukema, E. Jermendi [et al.] // Sci Rep. – 2020. – Vol.10. – Article 1690.
R?s?nen, L. Pectin and cashew nut allergy: cross-reacting allergens? / L. R?s?nen, S. M?kinen-Kiljunen,R.J. Harvima // Allergy. – 1998. – Vol.53. – Р.626–628.
Review: Effects of fibre, grain starch digestion rate and the ileal brake on voluntary feed intake in pigs / V. Ratanpaul, B.A. Williams, J.L. Black, M.J. Gidley // Animal. – 2019. – Vol.13. – Р.2745–2754.
Manipulation of Gut Microbiota Using Acacia Gum Polysaccharide / M.H. Rawi, A. Abdullah, A. Ismail, S.R. Sarbini // ACS Omega. – 2021. – Vol.6. – Р.17782–17797.
Inulin-type fructans and whey protein both modulate appetite but only fructans alter gut microbiota in adults with overweight/obesity: A randomized controlled trial / R.A. Reimer, H.J. Willis, J.M. Tunnicliffe [et al.] // Mol Nutr Food Res. – 2017. – Vol.61. – Р.1–12.
A polysaccharide extract of mulberry leaf ameliorates hepatic glucose metabolism and insulin signaling in rats with type 2 diabetes induced by high fat-diet and streptozotocin / Ch. Ren, Y. Zhang, W. Cui [et al.] // Intern. J. Biol. Macromol. – 2015. – Vol.72. – P.951–959.
Ridlon, J.M. Bile salt biotransformations by human intestinal bacteria / J.M. Ridlon, D.J. Kang, P.B. Hylemon // J. Lipid Res. – 2006. – Vol.47. – Р.241–259.
Some dietary fibers reduce the absorption of carotenoids in women / J. Riedl, J. Linseisen, J. Hoffmann, G. Wolfram // J. Nutr. – 1999. – Vol.129. – Р.2170–2176.
Roberfroid, M.B. Introducing inulin-type fructans / M.B. Roberfroid // Br. J. Nutr. – 2005. – Vol.93. – P.13–25.
Roberfroid, M.B. Dietary chicory inulin increases whole-body bone mineral density in growing male rats / M.B. Roberfroid, J. Cumps, J.P. Devogelaer // J. of Nutrition. – 2002. – V.132 (12). – P.3599–3602.
Prebiotic concept and health / M. Roberfroid, G.R. Gibson, L. Hoyles [et al.] // British Journal of Nutrition. – 2010, August. – Vol.104, Suppl. 2. – Р.1–3.
The effect of various dietary fibres on tissue concentration and chemical form of mercury after methylmercury exposure in mice / I.R. Rowland, A.K. Mallett, J. Flynn, R.J. Hargreaves [et al.] // Arch Toxicol. – 1986. – Vol.59. – Р. 94–98.
Inulin-enriched pasta affects lipid profile and lp (a) concentrations in italian young healthy male volunteers / F. Russo, G. Chimienti, G. Riezzo [et al.] // Eur. J. Nutr. – 2008. – Vol.47. – Р.453–459.
Inulin-enriched pasta improves intestinal permeability and modifies the circulating levels of zonulin and glucagon-like peptide 2 in healthy young volunteers / F. Russo, M. Linsalata, C. Clemente [et al.] // Nutr Res. – 2012. – Vol.32. – Р.940–946.
Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41 / B.S. Samuel, A. Shaito, T. Motoike [et al.] // Proc. Natl. Acad. Sci. USA. – 2008. – Vol.105. – Р.16767–16772.
Probiotics and prebiotics in intestinal health and disease: From biology to the clinic / M.E. Sanders, D.J. Merenstein, G. Reid [et al.] // Nat. Rev. Gastroenterol. Hepatol. – 2019. – Vol.16. – Р.605–616.
Sandula, J. (1995) Mitogenic activity of particulate yeast beta-(1–>3)-D-glucan and its water-soluble derivatives / J. Sandula, E. Machov?, V. Hr?balov? // Int. J. Biol. Macromol. – 1995 Dec. – Vol.17(6) – Р.323–326.
Sangeetha, P.T. Recent trends in the microbial production, analysis and applications of fructooligosaccharides / P.T. Sangeetha, M.N. Ramesh, S.G. Prapulla // Trends Food Sci. Technol. – 2005. – Vol.16. – P.442–457.
Galacto-oligosaccharides: novel components of designer foods / V. Sangwan, S.K. Tomar, R.R. Singh [et al.] // J. Food Sci. – 2011. – Vol.76. – P.103–111.
Scheller, H.V. Hemicelluloses / H.V. Scheller, P. Ulvskov // Annu. Rev. Plant Biol. – 2010. – Vol.61. – Р.263–289.
Effects of galactooligosaccharide and long-chain fructooligosaccharide supplementation during pregnancy on maternal and neonatal microbiota and immunity – A randomized, double-blind, placebo-controlled study / Shadid R., Haarman M., Knol J., [et al.] // Am. J. Clin. Nutr. – 2007. – Vol.86. – Р.1426–1437.
Effects of oat ?-glucan and barley ?-glucan on fecal characteristics, intestinal microflora, and intestinal bacterial metabolites in rats / R.L. Shen, X.Y. Dang, J.L. Dong, X.Z. Hu // J. Agric. Food Chem. – 2012. – Vol. 60. – Р.11301–11308.
MDG-1, an Ophiopogon polysaccharide, regulate gut microbiota in high-fat diet-induced obese C57BL/6 mice / L.-l. Shi, Y. Li, Y. Wang, Y. Feng // International Journal of Biological Macromolecules. – 2015. – Vol.81. – P.576-583.
Systematic review of the effects of the intestinal microbiota on selected nutrients and non-nutrients / C. Shortt, O. Hasselwander, A. Meynier [et al.] // Eur. J. Nutr. – 2018. – Vol.57. – Р.25–49.
Clinical trial: The effects of a trans-galactooligosaccharide prebiotic on faecal microbiota and symptoms in irritable bowel syndrome / D.B. Silk, A. Davis, J. Vulevic [et al.] // Aliment. Pharmacol. Ther. – 2009. – Vol.29. – Р.508–518.
Singh, R.P. Glycan utilisation system in Bacteroides and Bifidobacteria and their roles in gut stability and health / R.P. Singh // Appl. Microbiol. Biotechnol. – 2019. – Vol.103. – Р.7287–7315.
Activation of Gpr109a, receptor for niacin and the commensal metabolite butyrate, suppresses colonic inflammation and carcinogenesis / N. Singh, A. Gurav, S. Sivaprakasam [et al.] // Immunity. – 2014. – Vol.40. – Р.128–139.
Singh, S. Mannans: An overview of properties and application in food products / S. Singh, G. Singh, S.K. Arya // Int J Biol Macromol. – 2018 Nov. – Vol.119. – Р.79–95.
Blockade of dendritic cell development by bacterial fermentation products butyrate and propionate through a transporter (Slc5a8)-dependent inhibition of histone deacetylases / N. Singh, M. Thangaraju, P.D. Prasad [et al.] // J. Biol. Chem. – 2010. – Vol.285. – Р.27601–27608.
Dysregulated Microbial Fermentation of Soluble Fiber Induces Cholestatic Liver Cancer / V. Singh, B.S. Yeoh, B. Chassaing [et al.] // Cell. – 2018. – Vol.175. – Р.679–694.
An investigation of the acute effects of oligofructose-enriched inulin on subjective wellbeing, mood and cognitive performance / A.P. Smith, D. Sutherland, P. Hewlett // Nutrients. – 2015. – Vol.7. – Р.8887–8896.
Gut microbiota mediated hypoglycemic effect of Astragalus membranaceus polysaccharides in db/db mice / Q. Song, S.W. Cheng, D. Li [et al.] // Front Pharmacol. – 2022 Nov 14. – Vol.13. – Article 1043527.
Inulin Can Alleviate Metabolism Disorders in ob/ob Mice by Partially Restoring Leptin-related Pathways Mediated by Gut Microbiota / X. Song, L. Zhong, N. Lyu [et al.] // Genom. Proteom. Bioinform. – 2019. – Vol.17. – Р.64–75.
A review of 733 published trials on Bio-Mos®, a mannan oligosaccharide, and Actigen®, a second generation mannose rich fraction, on farm and companion animals / P. Spring, C. Wenk, A. Connolly, A. Kiers // J. Appl. Animal Nutr. – 2015. – Vol.3. – Р.1–11.
Srinivasan, K. Fenugreek (Trigonella foenum-graecum): A Review / K. Srinivasan // Food Reviews International. – 2015. – Vol.22 (2). – Р.203–224.
Increased Long-Term Dietary Fiber Intake Is Associated with a Decreased Risk of Fecal Incontinence in Older Women / K. Staller, M. Song, F. Grodstein [et al.] // Gastroenterology. – 2018. – Vol.155. – Р.661–667.
Dietary fibre in Europe: Current state of knowledge on definitions, sources, recommendations, intakes and relationships to health / A.M. Stephen, M.M. Champ, S.J. Cloran [et al.] // Nutr. Res. Rev. – 2017. – Vol.30. – Р.149–190.
Steinbach, W.J. Principles and Practice of Pediatric Infectious Diseases; 6th Edition. Part III. 244 – Elsevier / W.J. Steinbach // Aspergillus Species. – 2012. – Р. 1203–1209.
Oxalobacter formigenes and its role in oxalate metabolism in the human gut / C.S. Stewart, S.H. Duncan, D.R. Cave // FEMS Microbiol Lett. – 2004. – Vol.230. – Р.1–7.
Low-methoxyl lemon pectin attenuates inflammatory responses and improves intestinal barrier integrity in caerulein-induced experimental acute pancreatitis / Y. Sun, Y. He, F. Wang [et al.] // Mol Nutr Food Res. – 2017 Apr. – Vol.61(4). – Epub 2017 Jan 30.
Microbiota metabolite short chain fatty acids, GPCR, and inflammatory bowel diseases / M. Sun, W. Wu, Z. Liu, Y. Cong // J. Gastroenterol. – 2017 Jan. – Vol.52(1). – Р.1–8.
The role of short-chain fatty acids in health and disease / J. Tan, C. McKenzie, M. Potamitis [et al.] // Adv Immunol. – 2014. – Vol.121. – Р.91–119.
A prospective randomized, double-blind, placebo-controlled, dose-response relationship study to investigate efficacy of fructo-oligosaccharides (FOS) on human gut microflora / D. Tandon, M.M. Haque, M. Gote [et al.] // Sci. Rep. – 2019. – Vol.9. – Article 5473.
Biochemical analysis and hypoglycemic activity of a polysaccharide isolated from the fruit of Lycium barbarum L / H.L. Tang, Ch. Chen, Sh.-K. Wang, G.-J. Sun // International Journal of Biological Macromolecules. – 2015. – Vol.77. – P.235–242.
Taper, H.S. Inhibitory effect of dietary inulin or oligofructose on the development of cancer metastases / H.S. Taper, M.B. Roberfroid // Anticancer Res. – 2000. – Vol. 20(6B). – Р.4291–4294.
Dietary fructooligosaccharides increase intestinal permeability in rats / S.J. Ten Bruggencate, I.M. Bovee-Oudenhoven, M.L. Lettink-Wissink, R. Van der Meer // J. Nutr. – 2005. – Vol.135. – Р.837–842.
Analysis of the sugar speсifiсity and moleсular loсation of the beta-gluсan-binding leсtin site of сomplement reсeptor type 3 (CD11b/CD18) / B.P. Thornton, V. V?tvicka, M. Pitman [et al.] // J. Immunol. – 1996. – Vol.156(3). – Р.1235–1246.
Torres, D.P. Galacto-oligosaccharides: production, properties, applications, and significance as prebiotics / D.P. Torres // Compr. Rev. Food Sci. Food Saf. – 2010. – Vol.9, №5. – P.438–454.
Gut microbiota metabolism of dietary fiber influences allergic airway disease and hematopoiesis / A. Trompette, E.S. Gollwitzer, K. Yadava [et al.] // Nat. Med. – 2014. – Vol.20. – Р.159–166.
A case of a 7-year-old girl with anaphylaxis caused by pectin in Albedo of Citrus Unshiu but not by the fruit itself / H. Uno, H. Sekimoto, T. Kitamura // Arerugi. – 2017. – Vol.66. – Р.1244–1247.
Prebiotic inulin-type fructans induce specific changes in the human gut microbiota / D. Vandeputte, G. Falony, S. Vieira-Silva [et al.] // Gut. – 2017. – Vol.66. – Р.1968–1974.
Tzortzis G., Gibson G.R. Modulation of the fecal microflora profile and immune function by a novel trans-galactooligosaccharide mixture (b-gos) in healthy elderly volunteers / J. Vulevic, A. Drakoularakou, P. Yaqoob [et al.] // Am. J. Clin. Nutr. – 2008. – Vol.88. – Р.1438–1446.
A mixture of trans-galactooligosaccharides reduces markers of metabolic syndrome and modulates the fecal microbiota and immune function of overweight adults / J. Vulevic, A. Juric, G. Tzortzis, G.R. Gibson // J. Nutr. – 2013. – Vol.143. – Р.324–331.
Influence of galacto-oligosaccharide mixture (b-gos) on gut microbiota, immune parameters and metabonomics in elderly persons / J. Vulevic, A. Juric, G.E. Walton [et al.] // Br. J. Nutr. – 2015. – Vol.114. – Р.586–595.
Suppression of intestinal absorption of radioactive strontium by naturally occurring non-absorbable polyelectrolytes / D. Waldron-Edward, T.M. Paul, S.C. Skoryna // Nature. – 1965. – Vol.205. – Р.1117–1118.
Polysaccharide from tuberous roots of Ophiopogon japonicus regulates gut microbiota and its metabolites during alleviation of high-fat diet-induced type-2 diabetes in mice / H.-Y. Wang, L.-X. Guo, W.-H. Hu [et al.] // J. Func. Foods. – 2019. – Vol. 63. – Article 103593.
Hypoglycemic property of acidic polysaccharide extracted from Saccharina japonica and its potential mechanism / J. Wang, W. Jin, W. Zhang, [et al.] // Carbohydr. Polym. – 2013. – Vol.95. – Р.143–147.
Hypoglycemic and hypolipidemic effects of a polysaccharide from Fructus Corni in streptozotocin-induced diabetic rats / D. Wang, C. Li, W. Fan [et al.] // Int. J. Biol. Macromol. – 2019. –Vol.133. – Р.420–427.
Alginate oligosaccharide improves lipid metabolism and inflammation by modulating gut microbiota in high-fat diet fed mice / Y. Wang, L. Li, C. Ye [et al.] // Appl Microbiol Biotechnol. – 2020. – Vol.104 – Р.3541–3554.
Retracted: Polysaccharide from Angelica sinensis ameliorates high-fat diet and STZ-induced hepatic oxidative stress and inflammation in diabetic mice by activating the Sirt1–AMPK pathway / K. Wang, Zh.Tang, J. Wang [et al.] // J. of Nutr. Biochem. – 2017. – Vol.43. – P.88–97.
Williams, D.L. Overview of (1–>3)-beta-D-glucan immunobiology / D.L. Williams // Mediators Inflamm. – 1997. – Vol.6(4). – Р.247–250.
«Dietary fibre»: Moving beyond the «soluble/insoluble» classification for monogastric nutrition, with an emphasis on humans and pigs / B.A. Williams, D. Mikkelsen, B.M. Flanagan, M.J. Gidley // J. Anim. Sci. Biotechnol. – 2019. – Vol.10. – Article 45.
Wilson, B. Prebiotic inulin-type fructans and galacto-oligosaccharides: Definition, specificity, function, and application in gastrointestinal disorders / B. Wilson, K. Whelan // J. Gastroenterol. Hepatol. – 2017. – Vol.32. – Р.64–68. doi: 10.1111/jgh.13700. [PubMed] [CrossRef] [Google Scholar]
Wood, P.J. Cereal ?-glucans in diet and health / P.J. Wood // J. Cereal Sci. – 2007. – Vol.46. – P.230–238.
Probiotics with anti-type 2 diabetes mellitus properties: targets of polysaccharides from traditional Chinese medicine / L. Wu, Y. Gao, Y. Su [et al.] // Chin. J. Nat Med. – 2022 Sep. – Vol.20(9). – Р.641–655.
Comparison of hypoglycemic effects of polysaccharides from four legume species / G.-J. Wu, D. Liu, Y.-J. Wan [et al.] // Food Hydrocolloids. – 2019 – Vol.90. – P.299–304.
Modulation of gut microbiota by low methoxyl pectin attenuates type 1 diabetes in non-obese diabetic mice / C. Wu, L.-L. Pan, Niu W, [et al.] // Front Immunol. – 2019. – Vol.10. – Article 1733.
Mechanisms underlying the effect of polysaccharides in the treatment of type 2 diabetes: A review / J. Wu, S. Shi, H. Wang, Sh. Wang // Carbohydrate Polymers. – 2016. – Vol.144. – P.474–494.
Physicochemical characterization, antioxidant and hypoglycemic activities of selenized polysaccharides from Sargassum pallidum / H. Xiao, C. Chen, C. Li [et al.] // Int. J. Biol. Macromol. – 2019. – Vol.132. – Р.308–315.
Effect of inulin-type fructans in patients undergoing cancer treatments: A systematic review. Structural characterization and anti-tumor effects of an inulin-type fructan from Atractylodes chinensis / J. Xu, D. Chen, C. Liu [et al.] // Int. J. Biol. Macromol. – 2016. – Vol.82. – Р.765–771.
Hypoglycemic effects of MDG-1, a polysaccharide derived from Ophiopogon japonicas, in the ob/ob mouse model of type 2 diabetes mellitus / J. Xu, Y. Wang, D.-Sh. Xu [et al.] // Internat. J. Biol. Macromol. – 2011. – Vol.49. – Issue 4. – P.657–662.
Anti-diabetic effects of polysaccharides from Talinum triangulare in streptozotocin (STZ)-induced type 2 diabetic male mice / W. Xu, Q. Zhou, J.-J. Yin [et al.] // Int. J. Biol. Macromol. – 2015. – Vol.2. – Р. 575–579.
Mannan biotechnology: From biofuels to health / M. Yamabhai, S. Sak-Ubol, W. Srila, D. Haltrich // Crit Rev Biotechnol. – 2016. – Vol.36 (1). – Р.32–42.
Effects of prebiotic galacto-oligosaccharide on postoperative cognitive dysfunction and neuroinflammation through targeting of the gut-brain axis / X.D. Yang, L.K. Wang, H.Y. Wu, L. Jiao // BMC Anesthesiol. – 2018. – Vol.18. – Articlt 177.
Purification, characterization and hypoglycemic activity of extracellular polysaccharides from Lachnum calyculiforme / M. Ye, T. Qiu, W. Peng [et al.] // Carbohydr. Polym. – 2011. – Vol.86. – Р. 285–290.
Modification and Application of Dietary Fi-ber in Foods / Y. Yueyue, M. Sen, W. Xiao-xi [et al.] // Journal of Chemistry. – 2017. – Vol.10. – P.1–8.
Ruminococcus bromii is a keystone species for the degradation of resistant starch in the human colon / X. Ze, S.H. Duncan, P. Louis, H.J. Flint // ISME J. – 2012. – Vol.6. – Р.1535–1543.
A novel pectin from Polygala tenuifolia blocks A?42 aggregation and production by enhancing insulin-degradation enzyme and neprilysin / H. Zeng, P. Li, L. Zhou, K. Ding // Int J Biol Macromol. – 2020. – Vol.161. – Р.35–43.
Effect of fractionated lotus seed resistant starch on proliferation of Bifidobacterium longum and Lactobacillus delbrueckii subsp. bulgaricus and its structural changes following fermentation / H. Zeng, Y. Zheng, Y. Lin [et al.] // Food Chem. – 2018. – Vol.268. – Р.134–142.
Purification, characterization and anti-diabetic activity of a polysaccharide from mulberry leaf / Y. Zhang, C. Ren, G. Lu [et al.] // Regulatory Toxicology and Pharmacology. – 2014. – Vol. 70. – Issue 3. – P.687–695.
Dietary fiber intake regulates intestinal microflora and inhibits ovalbumin-induced allergic airway inflammation in a mouse mode / Z. Zhang, L. Shi, W. Pang [et al.] // PLoS ONE. – 2016. – Vol.11. – e0147778.
Interactions between gut microbiota, host genetics and diet relevant to development of metabolic syndromes in mice / C. Zhang, M. Zhang, S. Wang [et al.] // ISME J. – 2010. – Vol.4. – Р.232–241.
Lycium barbarum polysaccharides ameliorates renal injury and inflammatory reaction in alloxan-induced diabetic nephropathy rabbits / Q. Zhao, J. Li, J. Yan [et al.] // Life Sciences. – 2016. – Vol.157. – P.82–90.
Anti-diabetic effects of polysaccharides from ethanol-insoluble residue of Schisandra chinensis (Turcz.) Baill on alloxan-induced diabetic mice / T. Zhao, G.-H. Mao, M. Zhang [et al.] // Chem. Res. Chin. Univ. – 2012. – Vol.29. – Р.99–102.
Polysaccharides from Chinese herbal medicine for anti-diabetes recent advances / Y. Zheng, L. Bai, Y. Zhou [et al.] // International Journal of Biological Macromolecules. – 2019. – Vol.121. – P.1240–1253.
Characterization and hypoglycemic effect of a polysaccharide extracted from the fruit of Lycium barbarum L. / J. Zhu, W. Liu, J. Yu [et al.] // Carbohydrate Polymers. – 2013. – Vol.98. – Issue 1. – P.8–16.
Downloads
Published
How to Cite
Issue
Section
License
Reproduction of any materials without the written permission of the publisher is prohibited.
The responsibility for the accuracy of the information contained in articles and advertisements are the authors and advertisers.