Дисбіоз кишечника, ожиріння і метаболічний синдром: як вибратися із підступного трикутника?

Автор(и)

  • N. B. Gubergrits Донецький національний медичний університет, Лиман, Ukraine
  • N. V. Byelyayeva Донецький національний медичний університет, Лиман, Ukraine
  • O. V. Tsys Запорізький державний медичний університет, Ukraine
  • V. S. Rachmetova Медичний університет Астана, Республіка Казахстан, Ukraine

DOI:

https://doi.org/10.30978/MG-2019-4-45

Ключові слова:

мікробіота, дисбіоз кишечника, сидром надлишкового бактеріального росту, ожиріння, метаболічний синдром, патогенез, лікування

Анотація

Проаналізовано дані світової літератури та результати доказових експериментальних і клінічних досліджень про взаємозв’язок особливостей харчування і мікробіоти кишечника. Особливу увагу приділено участі дис­біо­зу кишечника та синдрому надлишкового бактеріального росту в тонкій кишці в патогенезі ожиріння і метаболічного синдрому. Наведено аргументи на користь двох основних гіпотез: метаболічної ендотоксемії та «зберігання». Перша розглядає механізми впливу ліпополісахариду грамнегативної кишкової флори, підвищення проникності кишкової стінки, ендоканабіноїдної системи і кишкової лужної фосфатази. Гіпотеза «зберігання» враховує особливості ферментації харчових полісахаридів, абсорбцію моносахаридів і роль кишкової мікробіоти та метаболітів її життєдіяльності (зокрема коротколанцюгових жирних кислот) у регуляції ліпідного обміну. Особливу увагу приділено лікуванню: зміні харчового раціону, використанню про- і пребіотиків, фекальній трансплантації. Проаналізовано вплив компонентів їжі на кишкову мікробіоту, зокрема харчових волокон, таких як резистентний крохмаль та інулін, а також жиру і білків. Показано, що склад кишкової мікробіоти відображує харчові звички та склад раціону. Дієта з високим вмістом жирів різко збільшує кишкову проникність завдяки механізму, пов’язаному зі зниженою експресією білків епітеліального щільного з’єднання, зокрема зонуліну та оклюдину. Обґрунтовано гіпотезу про те, що кишковий мікробіом, пов’язаний з ожирінням, має підвищену здатність до отримання енергії з раціону («ефект накопичення»). Проаналізовано переваги антибіотика з низькою кишковою абсорбцією — рифаксиміну. Наведено результати досліджень, які доводять еубіотичні властивості рифаксиміну та його ефективність при дисбіозі кишечника.

Біографії авторів

N. B. Gubergrits, Донецький національний медичний університет, Лиман

Губергріц Наталя Борисівна, д. мед. н., проф., проф. кафедри внутрішньої медицини №2

N. V. Byelyayeva, Донецький національний медичний університет, Лиман

Н. В. Бєляєва

O. V. Tsys, Запорізький державний медичний університет

О. В. Цис

V. S. Rachmetova, Медичний університет Астана, Республіка Казахстан

В. С. Рахметова

Посилання

Metabolicheskiy sindrom [Metabolic Syndrome] (Russian). / Pod red. GY Roytberga. Moscow: MED-press-inform; 2007:224.

Plotnikova EY. Intestinal microbial landscape and metabolic syndrome - what is common? (Russian). Vestnik kluba pankreatologov [Herald of Pancreatic Club] (Russian). 2016. 2:63-72.

Plotnikova EY, Borsch MV, Krasnova MV, Baranova EN. Some aspects of the diagnosis and treatment of excessive bacterial contamination of the small intestine in clinical practice (Russian). Lechashchiy vrach [Attending doctor] (Russian). 2013. 2:52-56.

Tkach SM, Puchkov KS, Sizenko AK. Kishechnaya mikrobiota v norme i pri patologii. Sovremennyye podkhody k diagnostike i korrektsii kishechnogo disbioza [Intestinal microbiota in normal and pathological state. Modern approaches to the diagnosis and correction of intestinal dysbiosis] (Russian). Kyiv; 2014:149.

Tkach SM., Yuzvenko TY., Cheverda TL. Modern pharmacotherapy of non-alcoholic fatty liver disease (Russian). Zdorov’ya Ukrayiny [Health of Ukraine] (Ukrainian). 2017. 18:68-71.

Alhamoruni A, Wright KL, Larvin M, O’Sullivan SE. Cannabinoids mediate opposing effects on inflammation-induced intestinal permeability. Br J Pharmacol. 2012;165:2598-2610. DOI: 10.1111/j.1476-5381.2011.01589.x.

al-Waiz M, Mikov M, Mitchell SC, Smith RL. The exogenous origin of trimethylamine in the mouse. Metabolism. 1992;41:135-136. DOI: 10.1016/0026-0495 (92)90140-6.

Amar J, Serino M, Lange C et al. Involvement of tissue bacteria in the onset of diabetes in humans: evidence for a concept. Diabetologia. 2011;54:3055-3061. DOI: 10.1007/s00125-011-2329-8.

Arpaia N, Campbell C, Fan X et al. Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation. Nature. 2013;504 (7480):451-455. DOI: 10.1038/nature12726.

Arumugam M, Raes J, Pelletier E et al. Enterotypes of the human gut microbiome. Nature. 2011;473 (7346):174-180. DOI: 10.1038/nature09944.

Backhed F, Ding H, Wang T et al. The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci USA. 2004;101 (44):15718-15723. DOI: 10.1073/pnas.0407076101.

Backhed F, Manchester JK, Semenkovich CF, Gordon JI. Mechanisms underlying the resistance to diet-induced obesity in germ-free mice. Proc Natl Acad Sci USA. 2007;104:979-984. DOI: 10.1073/pnas.0605374104.

Bajaj JS, Barbara G, DuPont HL et al. New concepts on intestinal microbiota and the role of the non-absorbable antibiotics with special reference to rifaximin in digestive diseases. Dig Liver Dis. 2018;50(8):741-749. DOI: 10.1016/j.dld.2018.04.020.

Barcenilla A, Pryde SE, Martin JC et al. Phylogenetic relationships of butyrate-producing bacteria from the human gut. Appl Environ Microbiol. 2000;66:1654-1661. DOI: 10.1128/aem.66.4.1654-1661.2000.

Bates JM, Akerlund J, Mittge E, Guillemin K. Intestinal alkaline phosphatase detoxifies lipopolysaccharide and prevents inflammation in zebrafish in response to the gut microbiota. Cell Host Microbe. 2004;N 2:371-382. DOI: 10.1016/j.chom.2007.10.010.

Belkaid Y, Hand TW. Role of the microbiota in immunity and inflammation. Cell. 2014;157(1):121-141. DOI: 10.1016/j.cell.2014.03.011.

Bezkorovainy A. Probiotics: determinants of survival and growth in the gut. Am J Clin Nutr. 2001;73, N2:399S-405S. DOI: 10.1093/ajcn/73.2.399s.

Bhatti JS, Bhatti GK, Reddy PH. Mitochondrial dysfunction and oxidative stress in metabolic disorders - A step towards mitochondria based therapeutic strategies. Biochim Biophys Acta. 2017;N 1863:1066-1077. DOI: 10.1016/j.bbadis.2016.11.010.

Bjursell M, Admyre T, Goransson M et al. Improved glucose control and reduced body fat mass in free fatty acid receptor 2-deficient mice fed a high-fat diet. Am J Physiol Endocrinol Metab. 2011;N 300:E211-220. DOI: 10.1152/ajpendo.00229.2010.

Bluher M, Engeli S, Kloting N et al. Dysregulation of the peripheral and adipose tissue endocannabinoid system in human abdominal obesity. Diabetes. 2006;55:3053-3060. DOI: 10.2337/db06-0812.

Caesar R, Reigstad CS, Backhed HK et al. Gut-derived lipopolysaccharide augments adipose macrophage accumulation but is not essential for impaired glucose or insulin tolerance in mice. Gut. 2012;61 (12):1701-1707. DOI: 10.1136/gutjnl-2011-301689.

Calder PC. Fatty acids and inflammation: the cutting edge between food and pharma. Eur J Pharmacol. 2011;668:50-58. DOI: 10.1016/j.ejphar.2011.05.085.

Cani PD, Amar J, Iglesias MA et al. Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes. 2014;56:1761-1772. DOI: 10.2337/db06-1491.

Cani PD, Bibiloni R, Knauf C et al. Changes in gut microbiota control metabolic endotoxemia-induced inflammation in high-fat diet-induced obesity and diabetes in mice. Diabetes. 2008;57:1470-1481. DOI: 10.2337/db07-1403.

Cani PD, Everard A. Talking microbes: when gut bacteria interact with diet and host organs. Mol Nutr Food Res. 2016;60(1):58-66. DOI: 10.1002/mnfr.201500406.

Cani PD, Neyrinck AM, Fava F et al. Selective increases of bifidobacteria in gut microflora improve high-fat-diet-induced diabetes in mice through a mechanism associated with endotoxaemia. Diabetologia. 2007;50:2374-2383. DOI: 10.1007/s00125-007-0791-0.

Cani PD, Possemiers S, Van De Wiele T et al. Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability. Gut. 2009;58:1091-1103. DOI: 10.1136/gut.2008.165886.

Chakraborti CK. Role of adiponectin and some other factors linking type 2 diabetes mellitus and obesity. World J Diabetes. 2015;N 6 (15):1296-1308. DOI: 10.4239/wjd.v6.i15.1296.

Chalasani N, Younossi Z, Lavine JE et al. The diagnosis and management of nonalcoholic fatty liver disease: practice guideline by the American Gastroenterological Association, American Association for the Study of Liver Diseases, and American College of Gastroenterology. Gastroenterology. 2012;142, N7:1592-1609. DOI: 10.1016/j.cgh.2016.10.023.

Conterno L, Fava F, Viola R, Tuohy KM. Obesity and the gut microbiota: does up-regulating colonic fermentation protect against obesity and metabolic disease?. Genes Nutr. 2011;N 6 (3):241-260. DOI: 10.1007/s12263-011-0230-1.

Cote M, Matias I, Lemieux I et al. Circulating endocannabinoid levels, abdominal adiposity and related cardiometabolic risk factors in obese men. Int J Obes. 2007;31:692-699. DOI: 10.1038/sj.ijo.0803539.

Dao MC, Everard A, Aron-Wisnewsky J et al. Akkermansia muciniphila and improved metabolic health during a dietary intervention in obesity: relationship with gut microbiome richness and ecology. Gut. 2016;65(3):426-436. DOI: 10.1136/gutjnl-2014-308778.

David LA, Maurice CF, Carmody RN et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature. 2014;505 (7484):559-563. DOI: 10.1038/nature12820.

De Filippo C, Cavalieri D, Di Paola M et al. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc Natl Acad Sci USA. 2010;107:14691-14696. DOI: 10.1073/pnas.1005963107.

De La Serre CB, Ellis CL, Lee J et al. Propensity to high-fat diet-induced obesity in rats is associated with changes in the gut microbiota and gut inflammation. Am J Physiol. 2010;299:G440-448. DOI: 10.1152/ajpgi.00098.2010.

den Besten G, van Eunen K, Groen AK et al. The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism. J Lipid Res. 2013;54(9):2325-2340. DOI: 10.1194/jlr.R036012.

Ding H, Wang T, Hooper LV et al. The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci USA. 2004;101:15718-15712. DOI: 10.1073/pnas.0407076101.

Ding S, Chi MM, Scull BP et al. High-fatdiet: bacteria interactions promote intestinal inflammation which precedes and correlates with obesity and insulin resistance in mouse. PLoS One. 2010;N 5. e12191. DOI: 10.1371/journal.pone.0012191.

Duranti S, Ferrario C, van Sinderen D et al. Obesity and microbiota: an example of an intricate relationship. Genes Nutr. 2017;N 12:18. DOI: 10.1186/s12263-017-0566-2.

Estall JL, Drucker DJ. Glucagon-like Peptide-2. Annu Rev Nutr. 2006;26:391-411. DOI: 10.1146/annurev.nutr.26.061505.111223.

Fandriks L. Roles of the metabolic syndrome: an overview. J Intern Med. 2017;281(4):319-336. DOI: 10.1111/joim.12584.

Fasano A. Zonulin and its regulation of intestinal barrier function: the biological door to inflammation, autoimmunity, and cancer. Physiol Rev. 2011;91:151-175. DOI: 10.1152/physrev.00003.2008.

Federico A, Dallio M, Godos J et al. Targeting gut-liver axis for the treatment of nonalcoholic steatohepatitis: translational and clinical evidence. Transl Res. 2016;167:116-124. DOI: 10.1016/j.trsl.2015.08.002.

Furet J, Kong L, Tap J et al. Differential Adaptation of Human Gut Microbiota to bariatric surgery-induced weight loss: links with metabolic and low-grade inflammation markers. Diabetes. 2010;59:3049-3057. DOI: 10.2337/db10-0253.

Gatta L, Scarpignato C. Systematic review with meta-analysis: rifaximin is effective and safe for the treatment of small intestine bacterial overgrowth. Aliment Pharmacol Ther. 2017;45(5):604-616. DOI: 10.1111/apt.13928.

Ghoshal S, Witta J, Zhong J et al. Chylomicrons promote intestinal absorption of lipopolysaccharides. J Lipid Res. 2009;50:90-97. DOI: 10.1194/jlr.M800156-JLR200.

Goodrich JK, Waters JL, Poole AC et al. Human genetics shape the gut microbiome. Cell. 2014;159(4):789-799. DOI: 10.1016/j.cell.2014.09.053.

Groschwitz KR, Hogan SP. Intestinal barrier function: molecular regulation and disease pathogenesis. J Allergy Clin Immunol. 2009;124:3-22. DOI: 10.1016/j.jaci.2009.05.038.

Haro C, Rangel-Zúñiga OA, Alcalá-Díaz JF et al. Intestinal microbiota is influenced by gender and body mass index. PLoS One. 2016;11(5). e0154090. DOI: 10.1371/journal.pone.0154090.

Huang S, Rutkowsky JM, Snodgrass RG et al. Saturated fatty acids activate TLR-mediated proinflammatory signaling pathways. J Lipid Res. 2012;53:2002-2013. DOI: 10.1194/jlr.D029546.

Ignacio A, Fernandes MR, Rodrigues VA et al. Correlation between body mass index and faecal microbiota from children. Clin Microbiol Infect. 2016;N 22 (3):e1-8. DOI: 10.1016/j.cmi.2015.10.031.

Isacco L, Roche J, Quinart S et al. Cardiometabolic risk is associated with the severity of sleep-disordered breathing in children with obesity. Physiol Behav. 2016;170:62-67. DOI: 10.1016/j.physbeh.2016.12.018.

Islam KB.M. S., Fukiya S, Hagio M et al. Bile acid is a host factor that regulates the composition of the cecal microbiota in rats. Gastroenterology. 2011;141(5):1773-1781. DOI: 10.1053/j.gastro.2011.07.046.

Kadooka Y, Sato M, Imaizumi K et al. Regulation of abdominal adiposity by probiotics (Lactobacillus gasseri SBT 2055) in adults with obesetendencies in a randomized controlled trial. Eur J Clin Nutr. 2010;64:636-643. DOI: 10.1038/ejcn.2010.19.

Karlsson FH, Tremaroli V, Nookaew I et al. Gut metagenome in European women with normal, impaired and diabetic glucose control. Nature. 2013;498:99-103. DOI: 10.1038/nature12198.

Klaus DA, Motal MC, Burger-Klepp U et al. Increased plasma zonulin in patients with sepsis. Biochem Medica. 2013;23:107-111. PMID: 23457771.

Koeth RA, Wang Z, Levison BS et al. Intestinal microbiota metabolism of L-carnitine, a nutrient in red meat, promotes atherosclerosis. Nat Med. 2013;19:576-585. DOI: 10.1038/nm.3145.

Korner J, Leibe RI. To eat or not to eat - how the gut talks to the brain. N Engl J Med. 2003;349:926-928. DOI: 10.1056/NEJMp038114.

Koyama I, Matsunaga T, Harada T et al. Alkaline phosphatases reduce toxicity of lipopolysaccharides in vivo and in vitro through dephosphorylation. Clin Biochem. 2002;35:455-461. PMID: 12413606.

Krishnadath IS, Toelsie JR, Hofman A, Jaddoe VW. Ethnic disparities in the prevalence of metabolic syndrome and its risk factors in the Suriname Health Study: a cross-sectional population study. BMJ- - Open. 2016;N 6. e013183. DOI: 10.1136/bmjopen-2016-013183.

Lalles J.-P. Intestinal alkaline phosphatase: multiple biological roles in maintenance of intestinal homeostasis and modulation by diet. Nutr Rev. 2010;68:323-332. DOI: 10.1111/j.1753-4887.2010.00292.x.

Lamprecht M, Bogner S, Schippinger G et al. Probiotic supplementation affects markers of intestinal barrier, oxidation, andinflammation in trained men; arandomized, double-blinded, placebo-controlled trial. J Int Soc Sports Nutr. 2012;N 9:45. DOI: 10.1186/1550-2783-9-45.

Lang DH, Yeung CK, Peter RM et al. Isoform specificity of trimethylamine N-oxygenation by human flavin-containing monooxygenase (FMO) and P450 enzymes: selective catalysis by FM03. Biochem Pharmacol. 1998;56:1005-1012. DOI: 10.1016/s0006-2952 (98)00218-4.

Larsen N, Vogensen FK, van den Berg FW.J. et al. Gut microbiota in human adults with type 2 diabetes differs from non-diabetic adults. PLoS One. 2010;N 5. e9085. DOI: 10.1371/journal.pone.0009085.

Lau E, Carvalho D, Pina-Vaz C et al. Beyond gut microbiota: understanding obesity and type 2 diabetes. Hormones (Athens). 2015;14(3):358-369. DOI: 10.14310/horm.2002.1571.

Laugerette F, Vors C, Geloen A et al. Emulsified lipids increase endotoxemia: possible role in early postprandial low-grade inflammation. J Nutr Biochem. 2011;22:53-59. DOI: 10.1016/j.jnutbio.2009.11.011.

Le Chatelier E, Nielsen T, Qin J et al. Richness of human gut microbiome correlates with metabolic markers. Nature. 2013;500:541-546. DOI: 10.1038/nature12506.

Le Poul E, Loison C, Struyf S et al. Functional characterization of human receptors for short chain fatty acids and their role in polymorphonuclear cell activation. J Biol Chem. 2003;278:25481-25489. DOI: 10.1074/jbc.M301403200.

Lee HY, Park JH, Seok SH et al. Human originated bacteria, Lactobacillus rhamnosus PL60, produce conjugated linoleic acid and show anti-obesity effects indiet-induced obese mice. Biochim Biophys Acta. 2006;1761:736-744. DOI: 10.1016/j.bbalip.2006.05.007.

Lee JY, Sohn KH, Rhee SH, Hwang D. Saturated fatty acids, but not unsaturated fatty acids, induce the expression of cyclooxygenase-2 mediated through Toll-like receptor 4. J Biol Chem. 2001;276:16683-16689. DOI: 10.1074/jbc.M011695200.

Ley RE, Backhed F, Turnbaugh P et al. Obesity alters gut microbial ecology. Proc Natl Acad Sci USA. 2005;102 (31):11070-11075. DOI: 10.1073/pnas.0504978102.

Ley RE, Turnbaugh PJ, Klein S, Gordon JI. Microbial ecology: human gut microbes associated with obesity. Nature. 2006;444 (7122):1022-1023. DOI: 10.1038/4441022a.

Lizana PA, Paula CV, Araya L et al. Obesity, Body fat distribution, and physical activity in school-age children: an urban and rural comparison in Valparaíso, Chile. Biomed Environ Sci. 2016;29:834-839. DOI: 10.3967/bes2016.112.

Loguericio C. Gut microbiota and gastrointestinal tract, liver and pancreas: from phisiology to pathology. Torino: Edizioni Minerva Medica, 2018:123.

Loomba R, Sanyal AJ. The global NAFLD epidemic. Nat Rev Gastroenterol Hepatol. 2013;10, N11:686-690. DOI: 10.1038/nrgastro.2013.171.

Lopetuso LR, Petito V, Scaldaferri F, Gasbarrini A. Gut microbiota modulation and mucosal immunity: focus on rifaximin. Mini Rev Med Chem. 2015;16(3):179-185. PMID: 26643042.

Louis P, Flint HJ, Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine. FEMS Microbiol Lett. 2009;294:1-8. DOI: 10.1111/j.1574-6968.2009.01514.x.

Louis P, Hold GL, Flint HJ. The gut microbiota, bacterial metabolites and colorectal cancer. Nat Rev Microbiol. 2014;12 (10):661-672. DOI: 10.1038/nrmicro3344.

Louis P, Scott KP, Duncan SH, Flint HJ. Understanding the effects of diet on bacterial metabolism in the large intestine. J Appl Microbiol. 2007;102:1197-1208. DOI: 10.1111/j.1365-2672.2007.03322.x.

Lu Y, Fan C, Liang A et al. Effects of SCFA on the DNA methylation pattern of adiponectin and resistin in high-fat-diet-induced obese male mice. Br J Nutr. 2018;120(4):385-392. DOI: 10.1017/S0007114518001526.

Madsen KI. The use of probiotics in gastrointestinal disease. Can J Gastroenterol. 2001;15, N12:817-822. DOI: 10.1017/S0007114518001526.

Mar Rodríguez M, Pérez D, Javier Chaves F et al. Obesity changes the human gut mycobiome. Sci Rep. 2015;N 5:14600. DOI: 10.1038/srep14600.

Membrez M, Blancher F, Jaquet M et al. Gut microbiota modulation with norfloxacin and ampicillin enhances glucose tolerance in mice. FASEB. 2008;22:2416-2426. DOI: 10.1096/fj.07-102723.

Million M, Angelakis E, Maraninchi M et al. Correlation between body mass index and gut concentrations of Lactobacillus reuteri, Bifidobacterium animalis, Methanobrevibacter smithii and Escherichia coli. Int J Obes (Lond). 2013;37 (11):1460-1466. DOI: 10.1038/ijo.2013.20.

Muccioli GG, Naslain D, Backhed F et al. The endocannabinoid system links gut microbiota to adipogenesis. Mol Syst Biol. 2010;N 6:392. DOI: 10.1038/msb.2010.46.

Neumark-Sztainer D, Wall M, Guo J et al. Obesity, disordered eating, and eating disorders in a longitudinal study of adolescents: how do dieters fare 5 years later?. J Am Diet Assoc. 2006;106(4):559-568. DOI: 10.1038/msb.2010.46.

Ng M, Fleming T, Robinson M et al. Global, regional, and national prevalence of overweight and obesity in children and adults during 1980-2013 : a systematic analysis for the Global Burden of Disease Study 2013. Lancet- - 2014;384, N9945:766-781. DOI: 10.1016/S0140-6736 (14)60460-8.

Nilsson AC, Ostman EM, Holst JJ, Björck IM. Including indigestible carbohydrates in the evening meal of healthy subjects improves glucose tolerance, lowers inflammatory markers, and increases satiety after a subsequent standardized breakfast. J Nutr. 2008;138:732-739. DOI: 10.1093/jn/138.4.732.

Parnell JA, Reimer RA. Weight loss during oligofructose supplementation is associated with decreased ghrelin and increased peptide YY in overweight and obese adults. Am J Clin Nutr. 2009;89:1751-1759. DOI: 10.3945/ajcn.2009.27465.

Pendyala S, Walker JM, Holt PR. A high-fat diet is associated with endotoxemia that originates from the gut. Gastroenterology. 2012;142:1100-1101. DOI: 10.1053/j.gastro.2012.01.034.

Poggi M, Bastelica D, Gual P et al. C3H/HeJ mice carrying a toll-like receptor 4 mutation are protected against the development of insulin resistance in white adipose tissue in response to a high-fat diet. Diabetologia. 2007;50:1267-1276. DOI: 10.1007/s00125-007-0654-8.

Qin J, Li Y, Cai Z et al. A metagenome-wide associati on study of gut microbiota in type 2 diabetes. Nature. 2012;490:55-60. DOI: 10.1038/nature11450.

Rashmi HM, Namita R et al. Management of metabolic syndrome through probiotic and prebiotic interventions. Indian J Endocrinol Metab. 2012;16, N1:20-27. DOI: 10.4103/2230-8210.91178.

Rastmaneh R. High polyphenol, low probiotic diet for weightloss because of intestinal microbiota interaction. Chem Biol Interact. 2011;189:1-8. DOI: 10.1016/j.cbi.2010.10.002.

Rinella ME. Nonalcoholic fatty liver disease: a systematic review. JAMA- - 2015;313:2263-2273. DOI: 10.1001/jama.2015.5370.

Rodriguez JM, Murphy K, Stanton C et al. The composition of the gut microbiota throughout life, with an emphasis on early life. Microb Ecol Health Dis. 2015;26. 26050. DOI: 10.3402/mehd.v26.26050.

Russell WR, Gratz SW, Duncan SH et al. High-protein, reduced-carbohydrate weight-loss diets promote metabolite profiles likely to be detrimental to colonic health. Am J Clin Nutr. 2011;93(5):1062-1072. DOI: 10.3945/ajcn.110.002188.

Saarni SE, Rissanen A, Sarna S et al. Weight cycling of athletes and subsequent weight gain in middleage. Int J Obes (Lond). 2006;30 (11):1639-1644. DOI: 10.1038/sj.ijo.0803325.

Saavedra JM. Clinical applications of probiotic agents. Am J Clin Nutr. 2001;73, N6:1147S-1151S. DOI: 10.1093/ajcn/73.6.1147S.

Samuel BS, Shaito A, Motoike T et al. Effects of the gut microbiota on host adiposity are modulated by the short-chain fatty-acid binding G protein-coupled receptor, Gpr41. Proc Natl Acad Sci USA. 2008;105:16767-16772. DOI: 10.1073/pnas.0808567105.

Scarpellini E, Gabrielli M, Lauritano CE et al. High dosage rifaximin for the treatment of small intestinal bacterial overgrowth. Aliment Pharmacol Ther. 2007;25, N7:781-786. DOI: 10.1111/j.1365-2036.2007.03259.x.

Scarpignato C, Pelosini I. Rifaximin, a poorly absorbed antibiotic: pharmacology and clinicalpotential. Chemotherapy. 2005;51, suppl. 1:36-66. DOI: 10.1159/000081990.

Schwiertz A, Taras D, Schafer K et al. Microbiota and SCFA in lean and overweight healthy subjects. Obesity. 2010;18(1):190-195. DOI: 10.1038/oby.2009.167.

Silvestri C, Di Marzo V. The endocannabinoid system in energy homeostasis and the etiopathology of metabolic disorders. Cell Metab. 2013;17:475-490. DOI: 10.1016/j.cmet.2013.03.001.

Solga SF, Buckley G, Clark JM et al. The effect of a probiotic on hepatic steatosis. J Clin Gastroenterol. 2008;42:1117-1119. DOI: 10.1097/MCG.0b013e31816d920c.

Sonier B, Patrick C, Ajjikuttira P, Scott FW. Intestinal immune regulation as a potential diet-modifiable feature of gut inflammation and autoimmunity. Int Rev Immunol. 2009;28:414-445. DOI: 10.3109/08830180903208329.

Stappenbeck TS, Hooper LV, Gordon JI. Developmental regulation of intestinal angiogenesis by indigenous microbes via Paneth cells. Proc Natl Acad Sci USA. 2002;99:15451-15455. DOI: 10.1073/pnas.202604299.

Thaiss CA, Zmora N, Levy M, Elinav E. The microbiome and innate immunity. Nature. 2016;535 (7610):65-74. DOI: 10.1038/nature18847.

Tilg H, Adolph TE. Influence of the human intestinal microbiome on obesity and metabolic dysfunction. Curr Opin Pediatr. 2015;27(4):496-501. DOI: 10.1097/MOP.0000000000000234.

Tilg H, Moschen AR. Food, immunity, and the microbiome. Gastroenterology. 2015;148:1107-1119. DOI: 10.1053/j.gastro.2014.12.036.

Tims S, Derom C, Jonkers DM et al. Microbiota conservation and BMI signatures in adult monozygotic twins. Isme J. 2013;N 7 (4):707-717. DOI: 10.1038/ismej.2012.146.

Tuohy KM, Fava F, Viola R. «The way to a man’s heart is through his gut microbiota» - dietary pro- and prebiotics for the management of cardiovascular risk. Proceedings of the Nutrition Society. 2014;73:172-185. DOI: 10.1017/S0029665113003911.

Turnbaugh PJ, Hamady M, Yatsunenko T et al. A core gut microbiome in obese and lean twins. Nature. 2009;457:480-484. DOI: 10.1038/nature07540.

Turnbaugh PJ, Ley RE, Mahowald MA et al. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature. 2006;444 (7122):1027-1031. DOI: 10.1038/nature05414.

Waitzberg DL, Pereira CC.A., Logullo L et al. Microbiota benefits after inulin and partially hydrolized guar gum supplementation - a randomized clinical trial in constipated women. Nutr Hosp. 2012;27(1):123-129. DOI: 10.1590/S0212-16112012000100014.

Walker AW, Ince J, Duncan SH et al. Dominant and diet-responsive groups of bacteria within the human colonic microbiota. Isme J. 2011;N 5 (2):220-230. DOI: 10.1038/ismej.2010.118.

Walters WA, Xu Z, Knight R. Meta-analyses of human gut microbes associated with obesity and IBD. Febs Letters. 2014;588 (22):4223-4233. DOI: 10.1016/j.febslet.2014.09.039.

Weisberg SP, McCann D, Desai M et al. Obesity is associated with macrophage accumulation in a diposet issue. J Clin Invest. 2003;112:1796-1808. DOI: 10.1172/JCI19246.

Wong RJ, Aguilar M, Cheung R et al. Nonalcoholic steatohepatitis is the second leading etiology of liver disease among adults awaiting liver transplantation in the United States. Gastroenterology. 2015;148, N3:547-555. DOI: 10.1053/j.gastro.2014.11.039.

World Health Organization (WHO), Fact Sheet No 311 (updated March 2013). URL: http://www.who.int/mediacentre/factsheets/fs311/en/.

Wu GD, Chen J, Hoffmann C et al. Linking long-term dietary patterns with gut microbial enterotypes. Science. 2011;334 (6052):105-108. DOI: 10.1126/science.1208344.

Xiao S, Fei N, Pang X et al. A gut microbiota-targeted dietary intervention for amelioration of chronic inflammation underlying metabolic syndrome. FEMS Microbiol Ecol. 2014;87:357-367. DOI: 10.1111/1574-6941.12228.

Ze X, Le Mougen F, Duncan SH et al. Some are more equal than others: the role of «keystone» species in the degradation of recalcitrant substrates. Gut Microbes. 2013;N 4 (3):236-40. DOI: 10.4161/gmic.23998.

Zuo HJ, Xie ZM, Zhang WW et al. Gut bacteria alteration in obese people and its relationship with gene polymorphism. World J Gastroenterol. 2011;17(8):1076-1081. DOI: 10.3748/wjg.v17.i8.1076.

##submission.downloads##

Опубліковано

2019-09-30

Номер

Розділ

Лікарські засоби