Short chain fatty acids in human large intestine, portal, hepatic and venous blood
Open accessAbstract
Evidence for the occurrence of microbial breakdown of carbohydrate in the human colon has been sought by measuring short chain fatty acid (SCFA) concentrations in the contents of all regions of the large intestine and in portal, hepatic and peripheral venous blood obtained at autopsy of sudden death victims within four hours of death. Total SCFA concentration (mmol/kg) was low in the terminal ileum at 13 +/- 6 but high in all regions of the colon ranging from 131 +/- 9 in the caecum to 80 +/- 11 in the descending colon. The presence of branched chain fatty acids was also noted. A significant trend from high to low concentrations was found on passing distally from caecum to descending colon. pH also changed with region from 5.6 +/- 0.2 in the caecum to 6.6 +/- 0.1 in the descending colon. pH and SCFA concentrations were inversely related. Total SCFA (mumol/l) in blood was, portal 375 +/- 70, hepatic 148 +/- 42 and peripheral 79 +/- 22. In all samples acetate was the principal anion but molar ratios of the three principal SCFA changed on going from colonic contents to portal blood to hepatic vein indicating greater uptake of butyrate by the colonic epithelium and propionate by the liver. These data indicate that substantial carbohydrate, and possibly protein, fermentation is occurring in the human large intestine, principally in the caecum and ascending colon and that the large bowel may have a greater role to play in digestion than has previously been ascribed to it.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The remainder of butyrate and the majority of propionate are metabolized by hepatocytes, resulting in 1-15 μmol/L concentrations of propionate and butyrate in circulation, whereas acetate is found at 100-200 μmol/L.
“The remainder of butyrate, as well as the majority of propionate, is subsequently metabolized by hepatocytes, resulting in 1-to 15-µmol/L concentrations of propionate and butyrate in circulation, whereas acetate is found within a range of 100-200 µmol/L (Bloemen et al., 2009;Cummings et al., 1987;Peters et al.,”
From The Microbiota-Gut-Brain Axis (2019) · cites this paper as Cummings et al., 1987
Table 3 reports that propionate and butyrate fall substantially between portal and hepatic blood, and the Discussion attributes significant SCFA uptake to the liver. Peripheral propionate and butyrate averages are about 5 and 4 µmol/L, within the claimed range. However, peripheral acetate averages about 70 µmol/L, not 100–200 µmol/L; the paper reports an arterial acetate value of 126 µmol/L from a previous study. It also demonstrates hepatic uptake rather than directly measuring metabolism by hepatocytes. (LLM, conf=0.86)
Experimental — accuracy not yet measuredOnly a minor fraction of colon-derived acetate, propionate, and butyrate reaches the systemic circulation and other tissues.
“only a minor fraction of colon-derived acetate, propionate, and butyrate reaches the systemic circulation and other tissues (65).”
From The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication (2020) · cites this paper as [65]
Total colonic contents range from 83 to 421 g in a small study of sudden-death victims.
“with total colonic contents ranging from 83 to 421 g in a small study of sudden-death victims 12 .”
From Human microbiome myths and misconceptions (2023) · cites this paper as [12]
The total weight of the human microbiota is much more likely to be less than 500 g, and perhaps even considerably lower in some cases.
“the total weight of the human microbiota is much more likely to be less than 500 g, and perhaps even considerably lower than this in some cases.”
From Human microbiome myths and misconceptions (2023) · cites this paper as [12]
The Results and Discussion report short-chain fatty acid concentrations and fermentation in the colon, not the total weight of the human microbiota. Searches for microbial biomass, 500 g, and the weight of colonic contents found no passage supporting the claimed estimate. (LLM, conf=0.76)
Experimental — accuracy not yet measuredThe claim that the human microbiota weighs 1 to 2 kg is unlikely to be true in most cases.
“Nonetheless, it is unlikely to be true in most cases.”
From Human microbiome myths and misconceptions (2023) · cites this paper as [12]
The Discussion addresses microbial fermentation and short-chain fatty acids in the colon, but does not assess the microbiota’s weight. Searches for bacterial mass and 1–2 kg found no passage supporting or contradicting the claim. (LLM, conf=0.74)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Hungate, R. E. (2013) · Elsevier eBooks · doi:10.1016/c2013-0-12555-x · Cited by 3,060 · see citing works
Role of anaerobic bacteria in the metabolic welfare of the colonic mucosa in man.
Roediger, W. E. (1980) · Gut · doi:10.1136/gut.21.9.793 · Cited by 1,310 · see citing works
Schiff, L., & Schiff, E. R. (1975) · Andalas University Repository (Andalas University) · Cited by 1,141 · see citing works
Short chain fatty acids in the human colon.
Cummings, J. H. (1981) · Gut · doi:10.1136/gut.22.9.763 · Cited by 1,050 · see citing works
Self-citationAbsorption of Short-Chain Fatty Acids by the Colon
Ruppin, H., Bar-Meir, S., Soergel, K. H., Wood, C. M., & Schmitt, M. G. (1980) · Gastroenterology · doi:10.1016/s0016-5085(19)30508-6 · Cited by 736 · see citing works
Digestion of the polysaccharides of some cereal foods in the human small intestine
Englyst, H. N., & Cummings, J. H. (1985) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/42.5.778 · Cited by 543 · see citing works
Self-citationSouthgate, D. A. T., & Durnin, J. V. G. A. (1970) · British Journal Of Nutrition · doi:10.1079/bjn19700050 · Cited by 465 · see citing works
Short chain fatty acid absorption by the human large intestine.
McNeil, N. I., Cummings, J. H., & James, W. P. T. (1978) · Gut · doi:10.1136/gut.19.9.819 · Cited by 462 · see citing works
Self-citationProtein Degradation by Human Intestinal Bacteria
Macfarlane, G. T., Cummings, J. H., & Allison, C. (1986) · Microbiology · doi:10.1099/00221287-132-6-1647 · Cited by 455 · see citing works
Self-citationDigestion of polysaccharides of potato in the small intestine of man
Englyst, H. N., & Cummings, J. H. (1987) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/45.2.423 · Cited by 389 · see citing works
Self-citationIncomplete Absorption of the Carbohydrate in All-Purpose Wheat Flour
Anderson, I. H., Levine, A. S., & Levitt, M. D. (1981) · New England Journal of Medicine · doi:10.1056/nejm198104093041507 · Cited by 378 · see citing works
Cummings, J. H., Hill, M. J., Bone, E., Branch, W. J., & Jenkins, D. J. A. (1979) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/32.10.2094 · Cited by 358 · see citing works
Self-citationPomare, E. W., Branch, W. J., & Cummings, J. H. (1985) · Journal of Clinical Investigation · doi:10.1172/jci111847 · Cited by 356 · see citing works
Self-citationPassage of carbohydrate into the colon. Direct measurements in humans.
Stephen, A. M., Haddad, A. C., & Phillips, S. F. (1983) · PubMed · Cited by 303 · see citing works
Digestion of the carbohydrates of banana (Musa paradisiaca sapientum) in the human small intestine
Englyst, H. N., & Cummings, J. H. (1986) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/44.1.42 · Cited by 288 · see citing works
Self-citationDirect Measurement of Hepatic Blood Flow in Surgical Patients
Schenk, W. G., McDonald, J. C., McDonald, K. E., & Drapanas, T. (1962) · Annals of Surgery · doi:10.1097/00000658-196209000-00013 · Cited by 271 · see citing works
Sites of organic acid production and absorption in gastrointestinal tract of the pig
Argenzio, R., & Southworth, M. (1975) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1975.228.2.454 · Cited by 269 · see citing works
Starch utilization by the human large intestinal microflora
Macfarlane, G. T., & Englyst, H. N. (1986) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1986.tb01073.x · Cited by 265 · see citing works
Self-citationSome current concepts in intestinal bacteriology
Moore, W., Cato, E., & Holdeman, L. V. (1978) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/31.10.s33 · Cited by 256 · see citing works
Bown, R. L., Gibson, J., Sladen, G. E., Hicks, B. D., & Dawson, A. M. (1974) · Gut · doi:10.1136/gut.15.12.999 · Cited by 232 · see citing works
Short-Chain Fatty Acids in the Normal Human Feces
Høverstad, T., FAUSA, O., BJØRNEKLETT, A., & Bøhmer, T. (1984) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365521.1984.12005738 · Cited by 200 · see citing works
Spiller, G. A., Chernoff, M. C., Hill, R. A., et al. (1980) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/33.4.754 · Cited by 187 · see citing works
VFA Production in the Pig Large Intestine
Imoto, S., & NAMIOKA, S. (1978) · Journal of Animal Science · doi:10.2527/jas1978.472467x · Cited by 145 · see citing works
Carbohydrate Metabolism in the Human Colon
Salyers, A. A., & Leedle, J. A. Z. (1983) · Elsevier eBooks · doi:10.1016/b978-0-12-341280-5.50012-4 · Cited by 124 · see citing works
Cummings, J. H. (1981) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a071678 · Cited by 120 · see citing works
Self-citationHYDROGEN AND METHANE PRODUCTION IN MAN*
Levitt, M. D., & Ingelfinger, F. J. (1968) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1968.tb19033.x · Cited by 118 · see citing works
In vivo dialysis of faeces as a method of stool analysis. IV. The organic anion component.
RUBINSTEIN, L. M. R. D., Howard, A. V., & Wrong, O. M. (1969) · PubMed · Cited by 106 · see citing works
Dankert, J., Zijlstra, J. B., & Wolthers, B. G. (1981) · Clinica Chimica Acta · doi:10.1016/0009-8981(81)90359-4 · Cited by 104 · see citing works
Respiratory Hydrogen and Methane as Affected by Consumption of Gas-Forming Foods
Calloway, D. H. (1966) · Gastroenterology · doi:10.1016/s0016-5085(19)34395-1 · Cited by 88 · see citing works
PARAMETERS IN 7α‐DEHYDROXYLATION OF BILE ACIDS BY ANAEROBIC LACTOBACILLI
Midtvedt, T., & Norman, A. (1968) · Acta Pathologica Microbiologica Scandinavica · doi:10.1111/j.1699-0463.1968.tb01345.x · Cited by 82 · see citing works
Utilisation of protein by human gut bacteria
Macfarlane, G. T., & Allison, C. (1986) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.1986.tb01934.x · Cited by 73 · see citing works
Self-citationInfluence of Dietary Fiber on Fecal Excretion of Volatile Fatty Acids by Human Adults
Fleming, S. E., & Rodriguez, M. A. (1983) · Journal of Nutrition · doi:10.1093/jn/113.8.1613 · Cited by 55 · see citing works
Partition and absorption of valatile fatty acids in the alimentary canal of the rat.
Rémésy, C., & Demigné, C. (1976) · PubMed · Cited by 45 · see citing works
Imoto, S., & NAMIOKA, S. (1978) · Journal of Animal Science · doi:10.2527/jas1978.472479x · Cited by 42 · see citing works
PARTITION AND ABSORPTION OF VOLATILE FATTY ACIDS IN THE ALIMENTARY CANAL OF THE RAT
Rémésy, C., & Demigné, C. (1976) · HAL (Le Centre pour la Communication Scientifique Directe) · Cited by 37 · see citing works
Effects of dietary oat bran and diabetes on plasma and caecal volatile fatty acids in the rat
Storer, G. B., Trimble, R. P., Illman, R. J., et al. (1983) · Nutrition Research · doi:10.1016/s0271-5317(83)80013-x · Cited by 35 · see citing works
Effects of Wheat Bran and Porridge Oats on Hepatic Portal Venous Volatile Fatty Acids in the Pig
Topping, D. L., Illman, R. J., Taylor, M. N., et al. (1985) · Annals of Nutrition and Metabolism · doi:10.1159/000176989 · Cited by 33 · see citing works
Vernay, M., Marty, J., & Moatti, J.-P. (1984) · British Journal Of Nutrition · doi:10.1079/bjn19840107 · Cited by 28 · see citing works
Composition of Fecal Water Comparison of “In Vitro” Dialysis With Ultrafiltration
Vernia, P., Breuer, R. I., Gnaedinger, A., et al. (1984) · Gastroenterology · doi:10.1016/s0016-5085(84)80171-7 · Cited by 18 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- [1]1. I Anderson IH, Levine AS, Levitt MD. incomplctc absorption of the carbohydrate in all-purposc whcat flour. N Engl J Med 1981; 304: 891-2.
- [42]42. Wirthensohn, K. Der Stoffwechsel kurzkettiger Fettsauren im Colonepithel des Meerschweinchens und seine Bedeutung fur die Natriumresoption. Thesis: University of Hohenheim, 1981.
Cited by
Sorted by citations
From Dietary Fiber to Host Physiology: Short-Chain Fatty Acids as Key Bacterial Metabolites
Koh, A., De Vadder, F., Kovatcheva-Datchary, P., & Bäckhed, F. (2016) · Cell · doi:10.1016/j.cell.2016.05.041 · Cited by 7,070 · see citing works
De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579 · see citing works
Smith, P. M., Howitt, M. R., Panikov, N., Michaud, M., Gallini, C. A., Bohlooly-Y, M., Glickman, J. N., & Garrett, W. S. (2013) · Science · doi:10.1126/science.1241165 · Cited by 5,413 · see citing works
Role of the microbiota in immunity and inflammation.
Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385 · see citing works
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
den Besten, G., van Eunen, K., Groen, A. K., Venema, K., Reijngoud, D.-J., & Bakker, B. M. (2013) · Journal of Lipid Research · doi:10.1194/jlr.r036012 · Cited by 5,048 · see citing works
Parada Venegas, D., De la Fuente, M. K., Landskron, G., González, M. J., Quera, R., Dijkstra, G., Harmsen, H. J. M., Faber, K. N., & Hermoso, M. A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00277 · Cited by 3,820 · see citing works
The role of short-chain fatty acids in microbiota–gut–brain communication
Dalile, B., Van Oudenhove, L., Vervliet, B., & Verbeke, K. (2019) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0157-3 · Cited by 3,357 · see citing works
Gut microbiota, metabolites and host immunity
Rooks, M. G., & Garrett, W. S. (2016) · Nature reviews. Immunology · doi:10.1038/nri.2016.42 · Cited by 3,409 · see citing works
The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication
Silva, Y. P., Bernardi, A., & Frozza, R. L. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.00025 · Cited by 3,043 · see citing works
“Comprised mostly of acetate (C2), propionate (C3), and butyrate (C4) (63, 64) in an approximate molar rate of 60:20:20, respectively (65), approximately 500–600 mmol of SCFAs are produced in the gut per day depending on the fiber content in the diet, microbiota composition, and gut transit time (66, 67).”
BackgroundGut Microbiota Metabolism of Dietary Fiber Influences Allergic Airway Disease and Hematopoiesis
Trompette, A., Gollwitzer, E. S., Yadava, K., Sichelstiel, A. K., Sprenger, N., Ngom-Bru, C., Blanchard, C., Junt, T., Nicod, L. P., Harris, N. L., et al. (2014) · Nature Medicine · doi:10.1038/nm.3444 · Cited by 2,862 · see citing works
Review article: the role of butyrate on colonic function
HAMER, H. M., JONKERS, D., VENEMA, K., VANHOUTVIN, S., TROOST, F. J., & BRUMMER, R. ‐. (2008) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2007.03562.x · Cited by 2,721 · see citing works
Short-chain fatty acids in control of body weight and insulin sensitivity
Canfora, E. E., Jocken, J. W., & Blaak, E. E. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.128 · Cited by 2,298 · see citing works
Microbiota-Generated Metabolites Promote Metabolic Benefits via Gut-Brain Neural Circuits
De Vadder, F., Kovatcheva-Datchary, P., Goncalves, D., Vinera, J., Zitoun, C., Duchampt, A., Bäckhed, F., & Mithieux, G. (2014) · Cell · doi:10.1016/j.cell.2013.12.016 · Cited by 2,200 · see citing works
Dietary fiber and prebiotics and the gastrointestinal microbiota
Holscher, H. D. (2017) · Gut Microbes · doi:10.1080/19490976.2017.1290756 · Cited by 1,808 · see citing works
Regulation of inflammation by short chain fatty acids
Vinolo, M. A. R., Rodrigues, H. G., Nachbar, R. T., & Curi, R. (2011) · Nutrients · doi:10.3390/nu3100858 · Cited by 1,724 · see citing works
Gut microbial metabolites in obesity, NAFLD and T2DM
Canfora, E. E., Meex, R. C. R., Venema, K., & Blaak, E. E. (2019) · Nature Reviews Endocrinology · doi:10.1038/s41574-019-0156-z · Cited by 1,493 · see citing works
The control and consequences of bacterial fermentation in the human colon
Cummings, J. H., & Macfarlane, G. T. (1991) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1991.tb02739.x · Cited by 1,499 · see citing works
Self-citationGut/brain axis and the microbiota
Mayer, E. A., Tillisch, K., & Gupta, A. (2015) · Journal of Clinical Investigation · doi:10.1172/jci76304 · Cited by 1,503 · see citing works
Chambers, E. S., Viardot, A., Psichas, A., Morrison, D. J., Murphy, K. G., Zac-Varghese, S. E. K., MacDougall, K., Preston, T., Tedford, C., Finlayson, G. S., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-307913 · Cited by 1,424 · see citing works
Park, J., Kim, M., Kang, S. G., Jannasch, A. H., Cooper, B., Patterson, J., & Kim, C. H. (2015) · Mucosal Immunology · doi:10.1038/mi.2014.44 · Cited by 1,307 · see citing works
Homeostatic Immunity and the Microbiota
Belkaid, Y., & Harrison, O. J. (2017) · Immunity · doi:10.1016/j.immuni.2017.04.008 · Cited by 1,261 · see citing works
Pluznick, J. L., Protzko, R. J., Gevorgyan, H., Peterlin, Z., Sipos, A., Han, J., Brunet, I., Wan, L.-X., Rey, F., Wang, T., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1215927110 · Cited by 1,191 · see citing works
Dietary lipids, gut microbiota and lipid metabolism
Schoeler, M., & Caesar, R. (2019) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-019-09512-0 · Cited by 1,163 · see citing works
Short chain fatty acids in human gut and metabolic health
Blaak, E. E., Canfora, E. E., Theis, S., Frost, G., Groen, A. K., Mithieux, G., Nauta, A., Scott, K., Stahl, B., van Harsselaar, J., et al. (2020) · Beneficial Microbes · doi:10.3920/bm2020.0057 · Cited by 1,103 · see citing works
Donohoe, D. R., Collins, L. B., Wali, A., Bigler, R., Sun, W., & Bultman, S. J. (2012) · Molecular Cell · doi:10.1016/j.molcel.2012.08.033 · Cited by 993 · see citing works
Bacteria, Colonic Fermentation, and Gastrointestinal Health
Macfarlane, G. T., & Macfarlane, S. (2012) · Journal of AOAC INTERNATIONAL · doi:10.5740/jaoacint.sge_macfarlane · Cited by 970 · see citing works
Self-citationCommensal bacteria at the interface of host metabolism and the immune system
Brestoff, J. R., & Artis, D. (2013) · Nature Immunology · doi:10.1038/ni.2640 · Cited by 945 · see citing works
Dietary fatty acids directly impact central nervous system autoimmunity via the small intestine
Haghikia, A., Jörg, S., Duscha, A., Berg, J., Manzel, A., Waschbisch, A., Hammer, A., Lee, D.-H., May, C., Wilck, N., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.09.007 · Cited by 927 · see citing works
Gut Microbial Metabolites Fuel Host Antibody Responses
Kim, M., Qie, Y., Park, J., & Kim, C. H. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.07.001 · Cited by 893 · see citing works
“The total luminal SCFA concentration in humans reaches ~130 mmol/Kg in the colon and ~15 mmol/Kg in the small intestine (SI) (Cummings et al., 1987).”
BackgroundInfluentialNogal, A., Valdes, A. M., & Menni, C. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1897212 · Cited by 917 · see citing works
Dietary gut microbial metabolites, short-chain fatty acids, and host metabolic regulation
Kasubuchi, M., Hasegawa, S., Hiramatsu, T., Ichimura, A., & Kimura, I. (2015) · Nutrients · doi:10.3390/nu7042839 · Cited by 904 · see citing works
Postler, T. S., & Ghosh, S. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2017.05.008 · Cited by 876 · see citing works
“Acetate (C2), propionate (C3), and butyrate (C4) are by far the most abundant of the intestinal SCFAs (Cummings et al., 1987; Morrison and Preston, 2016).”
BackgroundThe neuropharmacology of butyrate: the bread and butter of the microbiota-gut-brain axis
Stilling, R. M., van de Wouw, M., Clarke, G., Stanton, C., Dinan, T. G., & Cryan, J. F. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.011 · Cited by 891 · see citing works
Mechanisms and consequences of intestinal dysbiosis
Weiss, G. A., & Hennet, T. (2017) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-017-2509-x · Cited by 775 · see citing works
The role of short chain fatty acids in appetite regulation and energy homeostasis
Byrne, C. S., Chambers, E. S., Morrison, D. J., & Frost, G. (2015) · International Journal of Obesity · doi:10.1038/ijo.2015.84 · Cited by 707 · see citing works
Regulatory effects of bifidobacteria on the growth of other colonic bacteria
Gibson, G. R., & Wang, X. (1994) · Journal of Applied Bacteriology · doi:10.1111/j.1365-2672.1994.tb03443.x · Cited by 682 · see citing works
Honeybee gut microbiota promotes host weight gain via bacterial metabolism and hormonal signaling
Zheng, H., Powell, J. E., Steele, M. I., Dietrich, C., & Moran, N. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701819114 · Cited by 664 · see citing works
Al-Lahham, S. H., Peppelenbosch, M. P., Roelofsen, H., Vonk, R. J., & Venema, K. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2010.07.007 · Cited by 614 · see citing works
Microbiome–host systems interactions: protective effects of propionate upon the blood–brain barrier
Hoyles, L., Snelling, T., Umlai, U.-K., Nicholson, J. K., Carding, S. R., Glen, R. C., & McArthur, S. (2018) · Microbiome · doi:10.1186/s40168-018-0439-y · Cited by 591 · see citing works
Butt, M. S., Tahir-Nadeem, M., Khan, M. K. I., Shabir, R., & Butt, M. S. (2008) · European Journal of Nutrition · doi:10.1007/s00394-008-0698-7 · Cited by 559 · see citing works
Impact of Diet-Modulated Butyrate Production on Intestinal Barrier Function and Inflammation
Bach Knudsen, K. E., Lærke, H. N., Hedemann, M. S., Nielsen, T. S., Ingerslev, A. K., Gundelund Nielsen, D. S., Theil, P. K., Purup, S., Hald, S., Schioldan, A. G., et al. (2018) · Nutrients · doi:10.3390/nu10101499 · Cited by 572 · see citing works
Gut Microbiota and Colonization Resistance against Bacterial Enteric Infection
Ducarmon, Q. R., Zwittink, R. D., Hornung, B. V. H., van Schaik, W., Young, V. B., & Kuijper, E. J. (2019) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00007-19 · Cited by 566 · see citing works
Macfarlane, G. T., Macfarlane, S., & Gibson, G. R. (1998) · Microbial Ecology · doi:10.1007/s002489900072 · Cited by 539 · see citing works
Self-citationShort-Chain Fatty Acids Regulate the Enteric Neurons and Control Gastrointestinal Motility in Rats
Soret, R., Chevalier, J., De Coppet, P., Poupeau, G., Derkinderen, P., Segain, J. P., & Neunlist, M. (2010) · Gastroenterology · doi:10.1053/j.gastro.2010.01.053 · Cited by 530 · see citing works
Brain gut microbiome interactions and functional bowel disorders
Mayer, E. A., Savidge, T., & Shulman, R. J. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.02.037 · Cited by 496 · see citing works
Fermentation in the human large intestine and the available substrates
Cummings, J. H., & Englyst, H. N. (1987) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/45.5.1243 · Cited by 490 · see citing works
Self-citationMicrobiota-gut-brain axis: Modulator of host metabolism and appetite
van de Wouw, M., Schellekens, H., Dinan, T. G., & Cryan, J. F. (2017) · The Journal of Nutrition · doi:10.3945/jn.116.240481 · Cited by 461 · see citing works
Zeng, H., Umar, S., Rust, B., Lazarova, D., & Bordonaro, M. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20051214 · Cited by 480 · see citing works
Short-chain fatty acids stimulate colonic transit via intraluminal 5-HT release in rats
Fukumoto, S., Tatewaki, M., Yamada, T., Fujimiya, M., Mantyh, C., Voss, M., Eubanks, S., Harris, M., Pappas, T. N., & Takahashi, T. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00442.2002 · Cited by 465 · see citing works
Butyrate and other short-chain fatty acids as modulators of immunity: What relevance for health?
Meijer, K., de Vos, P., & Priebe, M. G. (2010) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e32833eebe5 · Cited by 443 · see citing works
Activation of HIF-1α and LL-37 by commensal bacteria inhibits Candida albicans colonization
Fan, D., Coughlin, L. A., Neubauer, M. M., Kim, J., Kim, M. S., Zhan, X., Simms-Waldrip, T. R., Xie, Y., Hooper, L. V., & Koh, A. Y. (2015) · Nature Medicine · doi:10.1038/nm.3871 · Cited by 426 · see citing works
Aho, V. T. E., Houser, M. C., Pereira, P. A. B., Chang, J., Rudi, K., Paulin, L., Hertzberg, V., Auvinen, P., Tansey, M. G., & Scheperjans, F. (2021) · Molecular Neurodegeneration · doi:10.1186/s13024-021-00427-6 · Cited by 435 · see citing works
The effect of short-chain fatty acids on human monocyte-derived dendritic cells
Nastasi, C., Candela, M., Bonefeld, C. M., Geisler, C., Hansen, M., Krejsgaard, T., Biagi, E., Andersen, M. H., Brigidi, P., Ødum, N., et al. (2015) · Scientific Reports · doi:10.1038/srep16148 · Cited by 414 · see citing works
The gut-bone axis: How bacterial metabolites bridge the distance
Zaiss, M. M., Jones, R. M., Schett, G., & Pacifici, R. (2019) · Journal of Clinical Investigation · doi:10.1172/jci128521 · Cited by 403 · see citing works
Macfarlane, G. T., & Macfarlane, S. (2011) · Journal of Clinical Gastroenterology · doi:10.1097/mcg.0b013e31822fecfe · Cited by 406 · see citing works
Self-citationControl of lymphocyte functions by gut microbiota-derived short-chain fatty acids
Kim, C. H. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-00625-0 · Cited by 404 · see citing works
Espey, M. G. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.10.554 · Cited by 396 · see citing works
Nomura, M., Nagatomo, R., Doi, K., Shimizu, J., Baba, K., Saito, T., Matsumoto, S., Inoue, K., & Muto, M. (2020) · JAMA Network Open · doi:10.1001/jamanetworkopen.2020.2895 · Cited by 396 · see citing works
Ho, L., Ono, K., Tsuji, M., Mazzola, P., Singh, R., & Pasinetti, G. M. (2018) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2018.1400909 · Cited by 376 · see citing works
Le Gall, G., Noor, S. O., Ridgway, K., Scovell, L., Jamieson, C., Johnson, I. T., Colquhoun, I. J., Kemsley, E. K., & Narbad, A. (2011) · Journal of Proteome Research · doi:10.1021/pr2003598 · Cited by 348 · see citing works
Emergent Sources of Prebiotics: Seaweeds and Microalgae
De Jesus Raposo, M., De Morais, A., & De Morais, R. (2016) · Marine Drugs · doi:10.3390/md14020027 · Cited by 331 · see citing works
Metabolite-Sensing Receptor Ffar2 Regulates Colonic Group 3 Innate Lymphoid Cells and Gut Immunity
Chun, E., Lavoie, S., Fonseca-Pereira, D., Bae, S., Michaud, M., Hoveyda, H. R., Fraser, G. L., Gallini Comeau, C. A., Glickman, J. N., Fuller, M. H., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.09.014 · Cited by 336 · see citing works
The metabolic fate of acetate in cancer
Schug, Z. T., Vande Voorde, J., & Gottlieb, E. (2016) · Nature reviews. Cancer · doi:10.1038/nrc.2016.87 · Cited by 331 · see citing works
Connecting the immune system, systemic chronic inflammation and the gut microbiome: the role of sex
Rizzetto, L., Fava, F., Tuohy, K. M., & Selmi, C. (2018) · Journal of Autoimmunity · doi:10.1016/j.jaut.2018.05.008 · Cited by 331 · see citing works
Microbial metabolite butyrate facilitates M2 macrophage polarization and function
Ji, J., Shu, D., Zheng, M., Wang, J., Luo, C., Wang, Y., Guo, F., Zou, X., Lv, X., Li, Y., et al. (2016) · Scientific Reports · doi:10.1038/srep24838 · Cited by 334 · see citing works
Interactions Between Commensal Bacteria and Gut Sensorimotor Function in Health and Disease
Barbara, G., Stanghellini, V., Brandi, G., Cremon, C., Nardo, G. D., De Giorgio, R., & Corinaldesi, R. (2005) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2005.00230.x · Cited by 325 · see citing works
Intestinal microbiota influence the early postnatal development of the enteric nervous system
Collins, J., Borojevic, R., Verdu, E. F., Huizinga, J. D., & Ratcliffe, E. M. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12236 · Cited by 318 · see citing works
Uribe-Herranz, M., Rafail, S., Beghi, S., Gil-de-Gómez, L., Verginadis, I., Bittinger, K., Pustylnikov, S., Pierini, S., Perales-Linares, R., Blair, I. A., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124332 · Cited by 316 · see citing works
Role of colonic short-chain fatty acid transport in diarrhea
Binder, H. J. (2010) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021909-135817 · Cited by 315 · see citing works
The gut microbiota promotes hepatic fatty acid desaturation and elongation in mice
Kindt, A., Liebisch, G., Clavel, T., Haller, D., Hörmannsperger, G., Yoon, H., Kolmeder, D., Sigruener, A., Krautbauer, S., Seeliger, C., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-05767-4 · Cited by 311 · see citing works
Chen, Y.-M., Wei, L., Chiu, Y.-S., Hsu, Y.-J., Tsai, T.-Y., Wang, M.-F., & Huang, C.-C. (2016) · Nutrients · doi:10.3390/nu8040205 · Cited by 297 · see citing works
Fusobacterium nucleatum in colorectal carcinoma tissue according to tumor location
Mima, K., Cao, Y., Chan, A. T., Qian, Z. R., Nowak, J. A., Masugi, Y., Shi, Y., Song, M., da Silva, A., Gu, M., et al. (2016) · Clinical and Translational Gastroenterology · doi:10.1038/ctg.2016.53 · Cited by 284 · see citing works
Cultivable bacterial diversity from the human colon
Duncan, S. H., Louis, P., & Flint, H. J. (2007) · Letters in Applied Microbiology · doi:10.1111/j.1472-765x.2007.02129.x · Cited by 279 · see citing works
Freeland, K. R., & Wolever, T. M. S. (2010) · British Journal of Nutrition · doi:10.1017/s0007114509991863 · Cited by 275 · see citing works
Compartmentalised acyl-CoA metabolism and roles in chromatin regulation
Trefely, S., Lovell, C. D., Snyder, N. W., & Wellen, K. E. (2020) · Molecular Metabolism · doi:10.1016/j.molmet.2020.01.005 · Cited by 272 · see citing works
Is butyrate the link between diet, intestinal microbiota and obesity-related metabolic diseases?
Brahe, L. K., Astrup, A., & Larsen, L. H. (2013) · Obesity Reviews · doi:10.1111/obr.12068 · Cited by 264 · see citing works
Chen, S.-J., Chen, C.-C., Liao, H.-Y., Lin, Y.-T., Wu, Y.-W., Liou, J.-M., Wu, M.-S., Kuo, C.-H., & Lin, C.-H. (2022) · Neurology · doi:10.1212/wnl.0000000000013225 · Cited by 269 · see citing works
Microbes, immunity, and behavior: psychoneuroimmunology meets the microbiome
Dinan, T. G., & Cryan, J. F. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2016.103 · Cited by 246 · see citing works
Machate, D. J., Figueiredo, P. S., Marcelino, G., Guimarães, R. D. C. A., Hiane, P. A., Bogo, D., Pinheiro, V. A. Z., Oliveira, L. C. S. D., & Pott, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21114093 · Cited by 243 · see citing works
Weak Organic Acids: A Panoply of Effects on Bacteria
Hirshfield, I. N., Terzulli, S., & O'Byrne, C. (2003) · Science Progress · doi:10.3184/003685003783238626 · Cited by 245 · see citing works
Impacts of microbiome metabolites on immune regulation and autoimmunity
Haase, S., Haghikia, A., Wilck, N., Müller, D. N., & Linker, R. A. (2018) · Immunology · doi:10.1111/imm.12933 · Cited by 239 · see citing works
Microbiome, inflammation, epigenetic alterations, and mental diseases
Alam, R., Abdolmaleky, H. M., & Zhou, J. (2017) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32567 · Cited by 240 · see citing works
McOrist, A. L., Miller, R. B., Bird, A. R., Keogh, J. B., Noakes, M., Topping, D. L., & Conlon, M. A. (2011) · The Journal of Nutrition · doi:10.3945/jn.110.128504 · Cited by 231 · see citing works
Butyrate enhances mitochondrial function during oxidative stress in cell lines from boys with autism
Rose, S., Bennuri, S. C., Davis, J. E., Wynne, R., Slattery, J. C., Tippett, M., Delhey, L., Melnyk, S., Kahler, S. G., MacFabe, D. F., et al. (2018) · Translational Psychiatry · doi:10.1038/s41398-017-0089-z · Cited by 226 · see citing works
Gut microbiota and energy balance: role in obesity
Blaut, M. (2015) · Proceedings of The Nutrition Society · doi:10.1017/s0029665114001700 · Cited by 232 · see citing works
van der Beek, C. M., Canfora, E. E., Lenaerts, K., Troost, F. J., Olde Damink, S. W. M., Holst, J. J., Masclee, A. A. M., Dejong, C. H. C., & Blaak, E. E. (2016) · Clinical Science · doi:10.1042/cs20160263 · Cited by 230 · see citing works
Korcz, E., Kerényi, Z., & Varga, L. (2018) · Food & Function · doi:10.1039/c8fo00118a · Cited by 222 · see citing works
The function of gut microbiota in immune-related neurological disorders: a review
Sittipo, P., Choi, J., Lee, S., & Lee, Y. K. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02510-1 · Cited by 221 · see citing works
Zhu, X., Li, K., Liu, G., Wu, R., Zhang, Y., Wang, S., Xu, M., Lu, L., & Li, P. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2249143 · Cited by 220 · see citing works
Butyrate, a metabolite of intestinal bacteria, enhances sleep
Szentirmai, É., Millican, N. S., Massie, A. R., & Kapás, L. (2019) · Scientific Reports · doi:10.1038/s41598-019-43502-1 · Cited by 216 · see citing works
Microbiome potentiates endurance exercise through intestinal acetate production
Okamoto, T., Morino, K., Ugi, S., Nakagawa, F., Lemecha, M., Ida, S., Ohashi, N., Sato, D., Fujita, Y., & Maegawa, H. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00510.2018 · Cited by 210 · see citing works
Byrne, C. S., Chambers, E. S., Alhabeeb, H., Chhina, N., Morrison, D. J., Preston, T., Tedford, C., Fitzpatrick, J., Irani, C., Busza, A., et al. (2016) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.126706 · Cited by 201 · see citing works
Dalile, B., Vervliet, B., Bergonzelli, G., Verbeke, K., & Van Oudenhove, L. (2020) · Neuropsychopharmacology · doi:10.1038/s41386-020-0732-x · Cited by 201 · see citing works
The "Gut Feeling": Breaking Down the Role of Gut Microbiome in Multiple Sclerosis
Freedman, S. N., Shahi, S. K., & Mangalam, A. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-017-0588-x · Cited by 168 · see citing works
Targeting fatty acid metabolism to improve glucose metabolism
Stinkens, R., Goossens, G. H., Jocken, J. W. E., & Blaak, E. E. (2015) · Obesity Reviews · doi:10.1111/obr.12298 · Cited by 183 · see citing works
Short-Chain Fatty Acid Receptor and Its Contribution to Glucagon-Like Peptide-1 Release
Kaji, I., Karaki, S.-I., & Kuwahara, A. (2014) · Digestion · doi:10.1159/000356211 · Cited by 177 · see citing works
Mcbain, A. J., & Macfarlane, G. T. (1998) · Journal of Medical Microbiology · doi:10.1099/00222615-47-5-407 · Cited by 179 · see citing works
Self-citationTrapecar, M., Wogram, E., Svoboda, D., Communal, C., Omer, A., Lungjangwa, T., Sphabmixay, P., Velazquez, J., Schneider, K., Wright, C. W., et al. (2021) · Science Advances · doi:10.1126/sciadv.abd1707 · Cited by 176 · see citing works
Carbohydrate fermentation decreases hepatic glucose output in healthy subjects
Thorburn, A., Muir, J., & Proietto, J. (1993) · Metabolism · doi:10.1016/0026-0495(93)90249-n · Cited by 178 · see citing works
- Authors
- Cummings, J. H., Pomare, E. W., Branch, W. J., Naylor, C. P., & Macfarlane, G. T.
- ORCID
- Cummings, J H
- Venue
- Gut
- Publisher
- BMJ
- Published
- 1987-10
- Volume
- 28
- Issue
- 10
- Pages
- 1221-1227
- ISSN
- 0017-5749 (ISSN-L)
- 1468-3288
- PMC
- PMC1433442
- OpenAlex
- W2135232490
- Semantic Scholar
- 0b69822ab4496079e2f7a3e1df829e5fa9a9926c
- Cited by
- 3,119
- References
- 39
- Citations by year
- 2026: 171 · 2025: 194 · 2024: 240 · 2023: 237 · 2022: 277 · 2021: 270 · 2020: 216 · 2019: 180 · 2018: 142 · 2017: 99 · 2016: 113 · 2015: 66 · 2014: 59 · 2013: 66 · 2012: 58
- FWCI
- 5.92
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gut (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Otago
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Keywords
- short-chain fatty acids, colonic fermentation, cecum, large intestine, portal blood, hepatic vein, peripheral venous blood, propionate, acetate, branched-chain fatty acids, colonic pH, carbohydrate fermentation, protein fermentation, colonic epithelium, human colon
- MeSH terms
- Acetates, Animals, Butyrates, Fatty Acids, Female, Fermentation, Gastrointestinal Contents, Hepatic Veins, Humans, Hydrogen-Ion Concentration, Intestine, Large, Male, Portal Vein, Propionates, Swine, Acetic Acid, Butyric Acid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review