Role of colonic short-chain fatty acid transport in diarrhea

Short chain fatty acids in human large intestine, portal, hepatic and venous blood

Cummings, J. H., Pomare, E. W., Branch, W. J., Naylor, C. P., & Macfarlane, G. T. (1987) · Gut · doi:10.1136/gut.28.10.1221 · Cited by 3,119 · see citing works

Short-Chain Fatty Acids and Human Colonic Function: Roles of Resistant Starch and Nonstarch Polysaccharides

Topping, D. L., & Clifton, P. M. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.3.1031 · Cited by 3,091 · 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

Regulation of short-chain fatty acid production

Macfarlane, S., & Macfarlane, G. T. (2003) · Proceedings of the Nutrition Society · doi:10.1079/pns2002207 · Cited by 1,939 · see citing works

Clostridium difficile--more difficult than ever.

Kelly, C. P., & Lamont, J. (2008) · New England Journal of Medicine · doi:10.1056/nejmra0707500 · Cited by 1,386 · see citing works

Antibiotic-Associated Diarrhea

Bartlett, J. G. (2002) · New England Journal of Medicine · doi:10.1056/nejmcp011603 · Cited by 1,206 · see citing works

Utilization of Nutrients by Isolated Epithelial Cells of the Rat Colon

Roediger, W. E. W. (1982) · Gastroenterology · doi:10.1016/s0016-5085(82)80339-9 · Cited by 1,201 · see citing works

The magnitude of the global problem of diarrhoeal disease: a ten-year update.

Bern, C., Martines, J., Zoysa, I. D., & Glass, R. I. (1992) · Europe PMC (PubMed Central) · Cited by 773 · see citing works

Treatment of Diversion Colitis with Short-Chain-Fatty Acid Irrigation

Harig, J. M., Soergel, K. H., KOMOROWSKI, R. A., & Wood, C. M. (1989) · New England Journal of Medicine · doi:10.1056/nejm198901053200105 · Cited by 748 · see citing works

Absorption 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

Short Bowel Syndrome and Intestinal Failure: Consensus Definitions and Overview

O’Keefe, S. J., Buchman, A. L., Fishbein, T., Jeejeebhoy, K. N., Jeppesen, P. B., & Shaffer, J. (2006) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2005.10.002 · Cited by 519 · see citing works

Occurrence, absorption and metabolism of short chain fatty acids in the digestive tract of mammals

Bugaut, M. (1987) · Comparative Biochemistry and Physiology Part B Comparative Biochemistry · doi:10.1016/0305-0491(87)90433-0 · Cited by 366 · see citing works

MOLECULAR PHYSIOLOGY OF INTESTINAL N ⁺ /H ⁺ EXCHANGE

Zachos, N. C., Tse, M., & Donowitz, M. (2005) · Annual Review of Physiology · doi:10.1146/annurev.physiol.67.031103.153004 · Cited by 365 · see citing works

Mechanisms and Management of Antibiotic‐Associated Diarrhea

Hogenauer, C., Hammer, H. F., Krejs, G. J., & Reisinger, E. C. (1998) · Clinical Infectious Diseases · doi:10.1086/514958 · Cited by 348 · see citing works

Colon as a digestive organ in patients with short bowel

Nordgaard, I., Hansen, B. S., & Mortensen, P. B. (1994) · The Lancet · doi:10.1016/s0140-6736(94)91220-3 · Cited by 343 · see citing works

Proctitis and colitis following diversion of the fecal stream

Glotzer, D. J., Glick, M., & Goldman, H. (1981) · Gastroenterology · doi:10.1016/0016-5085(81)90003-2 · Cited by 306 · see citing works

Short-chain fatty acids stimulate active sodium and chloride absorption in vitro in the rat distal colon

Binder, H. J., & Mehta, P. (1989) · Gastroenterology · doi:10.1016/0016-5085(89)91614-4 · Cited by 303 · see citing works

Functional Identification of SLC5A8, a Tumor Suppressor Down-regulated in Colon Cancer, as a Na+-coupled Transporter for Short-chain Fatty Acids

Miyauchi, S., Gopal, E., Fei, Y.-J., & Ganapathy, V. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.c400059200 · Cited by 277 · see citing works

Amylase-Resistant Starch plus Oral Rehydration Solution for Cholera

Ramakrishna, B., Venkataraman, S., Srinivasan, P., Dash, P., Young, G. P., & Binder, H. J. (2000) · New England Journal of Medicine · doi:10.1056/nejm200002033420502 · Cited by 249 · see citing works

The Lactulose Hydrogen Breath Test as a Diagnostic Test for Small-Bowel Bacterial Overgrowth

Rhodes, J. M., Middleton, P., & Jewell, D. P. (1979) · Scandinavian Journal of Gastroenterology · doi:10.3109/00365527909179892 · Cited by 211 · see citing works

Studies of osmotic diarrhea induced in normal subjects by ingestion of polyethylene glycol and lactulose.

Hammer, H. F., Ana, C. A. S., Schiller, L. R., & Fordtran, J. S. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114267 · Cited by 209 · see citing works

Impact of rice based oral rehydration solution on stool output and duration of diarrhoea: meta-analysis of 13 clinical trials.

Gore, S. M., Fontaine, O., & Pierce, N. F. (1992) · BMJ · doi:10.1136/bmj.304.6822.287 · Cited by 203 · see citing works

Mammalian Na+/H+ exchanger gene family: structure and function studies

Yun, C., Tse, C., Nath, S., Levine, S. A., Brant, S. R., & Donowitz, M. (1995) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1995.269.1.g1 · Cited by 193 · see citing works

Mechanism(s) of butyrate transport in Caco-2 cells: role of monocarboxylate transporter 1

Hadjiagapiou, C., Schmidt, L. N., Dudeja, P. K., Layden, T. J., & Ramaswamy, K. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.4.g775 · Cited by 182 · see citing works

Clinical studies in persistent diarrhea: Dietary management with green banana or pectin in Bangladeshi children

Rabbani, G. H., Teka, T., Zaman, B., Majid, N., Khatun, M., & Fuchs, G. J. (2001) · Gastroenterology · doi:10.1053/gast.2001.27178 · Cited by 175 · see citing works

Colonic fermentation to short-chain fatty acids is decreased in antibiotic-associated diarrhea

Clausen, M. R., Bonnén, H., Tvede, M., & Mortensen, P. B. (1991) · Gastroenterology · doi:10.1016/0016-5085(91)90384-w · Cited by 173 · see citing works

Reduced osmolarity oral rehydration solution for treating dehydration due to diarrhoea in children: systematic review

Hahn, S., Kim, Y., & Garner, P. (2001) · BMJ · doi:10.1136/bmj.323.7304.81 · Cited by 168 · see citing works

Revised immunolocalization of the Na⁺-<scp>d</scp>-glucose cotransporter SGLT1 in rat organs with an improved antibody

Balen, D., Ljubojević, M., Breljak, D., Brzica, H., Z̆lender, V., Koepsell, H., & Sabolić, I. (2008) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00180.2008 · Cited by 166 · see citing works

Cellular expression of monocarboxylate transporters (MCT) in the digestive tract of the mouse, rat, and humans, with special reference to slc5a8.

Iwanaga, T., Takebe, K., Kato, I., Karaki, S.-I., & Kuwahara, A. (2006) · Biomedical research · doi:10.2220/biomedres.27.243 · Cited by 161 · see citing works

Mechanism of short-chain fatty acid uptake by apical membrane vesicles of rat distal colon

Mascolo, N., Rajendran, V. M., & Binder, H. J. (1991) · Gastroenterology · doi:10.1016/0016-5085(91)90008-9 · Cited by 155 · see citing works

Intestinal NaCl transport in NHE2 and NHE3 knockout mice

Gawenis, L. R., Stien, X., Shull, G. E., Schultheis, P. J., Woo, A. L., Walker, N. M., & Clarke, L. L. (2002) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00297.2001 · Cited by 153 · see citing works

S3226, a novel inhibitor of Na + /H + exchanger subtype 3 in various cell types

Schwark, J.-R., Jansen, H. W., Lang, H., Krick, W., Burckhardt, G., & Hropot, M. (1998) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240050704 · Cited by 152 · see citing works

AGA technical review: Impact of dietary fiber on colon cancer occurrence

Kim, Y. (2000) · Gastroenterology · doi:10.1016/s0016-5085(00)70377-5 · Cited by 147 · see citing works

SCFA increase intestinal Na absorption by induction of NHE3 in rat colon and human intestinal C2/bbe cells

Musch, M. W., Bookstein, C., Xie, Y., Sellin, J. H., & Chang, E. B. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.4.g687 · Cited by 144 · see citing works

Treatment of diversion colitis by short-chain fatty acids

Guillemot, F., Colombel, J., Neut, C., Verplanck, N., Lecomte, M., Romond, C., Paris, J., & Cortot, A. (1991) · Diseases of the Colon & Rectum · doi:10.1007/bf02049697 · Cited by 138 · see citing works

Effect of volatile fatty acids on water and ion absorption from the goat colon

Argenzio, R., Miller, N. J., & Engelhardt, W. V. (1975) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1975.229.4.997 · Cited by 136 · see citing works

Alteration of Large Intestinal Electrolyte Transport by Vasoactive Intestinal Polypeptide in the Rat

Racusen, L. C., & Binder, H. J. (1977) · Gastroenterology · doi:10.1016/s0016-5085(19)31786-x · Cited by 125 · see citing works

Effect of organic acid absorption on bicarbonate transport in rat colon

Umesaki, Y., Yajima, T., Yokokura, T., & Mutai, M. (1979) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00622903 · Cited by 123 · see citing works

The antifungal antibiotic, clotrimazole, inhibits chloride secretion by human intestinal T84 cells via blockade of distinct basolateral K+ conductances. Demonstration of efficacy in intact rabbit colon and in an in vivo mouse model of cholera.

Rufo, P. A., Merlin, D., Riegler, M. F., Ferguson-Maltzman, M., Dickinson, B. L., Brugnara, C., Alper, S. L., & Lencer, W. I. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119866 · Cited by 116 · see citing works

Interrelationship of Na, HCO3, and volatile fatty acid transport by equine large intestine.

Argenzio, R. A., Southworth, M., Lowe, J. E., & Ce, S. (1977) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1977.233.6.e469 · Cited by 111 · see citing works

Partially Hydrolyzed Guar Gum–Supplemented Oral Rehydration Solution in the Treatment of Acute Diarrhea in Children

Alam, N. H., Meier, R. F., Schneider, H., Sarker, S. A., Bardhan, P. K., Mahalanabis, D., Fuchs, G. J., & Gyr, N. E. (2000) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200011000-00010 · Cited by 108 · see citing works

Impaired colonic fermentation of carbohydrate after ampicillin

Rao, S. S. C., Edwards, C. A., Austen, C. J., Bruce, C., & Read, N. W. (1988) · Gastroenterology · doi:10.1016/0016-5085(88)90549-5 · Cited by 104 · see citing works

Regulation of Cl− and K+ Channels in Airway Epithelium

McCann, J. D., & Welsh, M. J. (1990) · Annual Review of Physiology · doi:10.1146/annurev.ph.52.030190.000555 · Cited by 104 · see citing works

Absorption of short-chain fatty acids from the human ileum

Schmitt, M. G., Soergel, K. H., Wood, C. M., & Steff, J. J. (1977) · Digestive Diseases and Sciences · doi:10.1007/bf01072192 · Cited by 102 · see citing works

Nonionic diffusion of short-chain fatty acids across rat colon

Charney, A. N., Micic, L., & Egnor, R. W. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.3.g518 · Cited by 96 · see citing works

Absorption of Short Chain Fatty Acids From the Human Jejunum

Schmitt, M. G., Soergel, K. H., & Wood, C. M. (1976) · Gastroenterology · doi:10.1016/s0016-5085(76)80011-x · Cited by 93 · see citing works

Colonic Digestion and Absorption of Energy From Carbohydrates and Medium‐Chain Fat in Small Bowel Failure

Jeppesen, P. B., & Mortensen, P. B. (1999) · Journal of Parenteral and Enteral Nutrition · doi:10.1177/014860719902300525 · Cited by 87 · see citing works

Amylase‐Resistant Starch as Adjunct to Oral Rehydration Therapy in Children with Diarrhea

Raghupathy, P., Ramakrishna, B., Oommen, S. P., Ahmed, M. S., Priyaa, G., Dziura, J., Young, G. P., & Binder, H. J. (2006) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/01.mpg.0000214163.83316.41 · Cited by 87 · see citing works

Colonic dysfunction in acute diarrhoea: the role of luminal short chain fatty acids.

Ramakrishna, B., & Mathan, V. I. (1993) · Gut · doi:10.1136/gut.34.9.1215 · Cited by 86 · see citing works

Enhancing clinical efficacy of oral rehydration therapy: Is low osmolality the key?

Thillainayagam, A. V., Hunt, J. B., & Farthing, M. J. G. (1998) · Gastroenterology · doi:10.1016/s0016-5085(98)70647-x · Cited by 86 · see citing works

Transport of n-butyrate into human colonic luminal membrane vesicles

Harig, J. M., Ng, E. K., Dudeja, P. K., Brasitus, T. A., & Ramaswamy, K. (1996) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1996.271.3.g415 · Cited by 78 · see citing works

Green Banana and Pectin Improve Small Intestinal Permeability and Reduce Fluid Loss in Bangladeshi Children with Persistent Diarrhea

Rabbani, G. H., Teka, T., Saha, S. K., Zaman, B., Majid, N., Khatun, M., Wahed, M., & Fuchs, G. J. (2004) · Digestive Diseases and Sciences · doi:10.1023/b:ddas.0000020507.25910.cf · Cited by 78 · see citing works

Loss of the NHE2 Na+/H+exchanger has no apparent effect on diarrheal state of NHE3-deficient mice

Ledoussal, C., Woo, A. L., Miller, M. L., & Shull, G. E. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.281.6.g1385 · Cited by 77 · see citing works

Bile Acids, Diarrhea, and Antibiotics: Data, Speculation, and a Unifying Hypothesis

Hofmann, A. F. (1977) · The Journal of Infectious Diseases · doi:10.1093/infdis/135.supplement.s126 · Cited by 74 · see citing works

Oral Rehydration Solution Containing a Mixture of Non-Digestible Carbohydrates in the Treatment of Acute Diarrhea: A Multicenter Randomized Placebo Controlled Study on Behalf of the ESPGHAN Working Group on Intestinal Infections

Hoekstra, J. H., Szajewska, H., Zikri, M. A., Micetic‐Turk, D., Weizman, Z., Papadopoulou, A., Guarino, A., Dias, J. A., & Oostvogels, B. (2004) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/00005176-200409000-00003 · Cited by 72 · see citing works

Amino acid transport in the small intestine.

Munck, L. K., & Munck, B. G. (1994) · PubMed · Cited by 69 · see citing works

Short-chain fatty acid absorption in rabbit colon in vitro

Sellin, J. H., & DeSoignie, R. C. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)90954-y · Cited by 67 · see citing works

SCFA Transport in the Forestomach of Ruminants

Gäbel, G., & Sehested, J. (1997) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/s0300-9629(96)00321-0 · Cited by 66 · see citing works

Apical membrane Cl-butyrate exchange: Mechanism of short chain fatty acid stimulation of active chloride absorption in rat distal colon

Rajendran, V., & Binder, H. J. (1994) · The Journal of Membrane Biology · doi:10.1007/bf00232873 · Cited by 64 · see citing works

Bicarbonate-stimulated [14C]butyrate uptake in basolateral membrane vesicles of rat distal colon

Reynolds, D. A., Rajendran, V. M., & Binder, H. J. (1993) · Gastroenterology · doi:10.1016/0016-5085(93)90889-k · Cited by 63 · see citing works

Role of short-chain fatty acids in colonic HCO₃secretion

Vidyasagar, S., Barmeyer, C., Geibel, J., Binder, H. J., & Rajendran, V. M. (2005) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00415.2004 · Cited by 63 · see citing works

Differential regulation of NHE isoforms by sodium depletion in proximal and distal segments of rat colon

Ikuma, M., Kashgarian, M. J., Binder, H. J., & Rajendran, V. M. (1999) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.2.g539 · Cited by 63 · see citing works

Absorption and metabolism of short‐chain fatty acids in ruminants

Kristensen, N. B., Danfær, A., & Agergaard, N. (1998) · Archiv für Tierernaehrung · doi:10.1080/17450399809381916 · Cited by 61 · see citing works

Apical NHE isoforms differentially regulate butyrate-stimulated Na absorption in rat distal colon

Krishnan, S., Rajendran, V. M., & Binder, H. J. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00598.2002 · Cited by 61 · see citing works

Short-chain fatty acids inhibit cAMP-mediated chloride secretion in rat colon

Dagher, P. C., Egnor, R. W., Taglietta-Kohlbrecher, A., & Charney, A. N. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.6.c1853 · Cited by 61 · see citing works

Effects of amiloride and ouabain on short‐chain fatty acid transport in guinea‐pig large intestine.

Engelhardt, W. V., Burmester, M., Hansen, K., Becker, G., & Rechkemmer, G. (1993) · The Journal of Physiology · doi:10.1113/jphysiol.1993.sp019481 · Cited by 59 · see citing works

Differential regulation of cholera toxin-inhibited Na-H exchange isoforms by butyrate in rat ileum

Subramanya, S. B., Rajendran, V. M., Pugazhendhi, S., Kumar, N. S. N., Ramakrishna, B., & Binder, H. J. (2007) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00462.2006 · Cited by 59 · see citing works

Structure and function of the Na+/glucose cotransporter.

Wright, E. M., Loo, D. D. F., Panayotova‐Heiermann, M., Hirayama, B. A., Turk, E., Eskandari, S., & Lam, J. T. (1998) · PubMed · Cited by 57 · see citing works

Stimulation of Sodium Chloride Absorption from Secreting Rat Colon by Short-Chain Fatty Acids

Krishnan, S., Ramakrishna, B., & Binder, H. J. (1999) · Digestive Diseases and Sciences · doi:10.1023/a:1018871412748 · Cited by 57 · see citing works

A Randomized Controlled Trial of Glucose versus Amylase Resistant Starch Hypo-Osmolar Oral Rehydration Solution for Adult Acute Dehydrating Diarrhea

Ramakrishna, B., Subramanian, V., Mohan, V., Sebastian, B. K., Young, G. P., Farthing, M. J. G., & Binder, H. J. (2008) · PLoS ONE · doi:10.1371/journal.pone.0001587 · Cited by 57 · see citing works

Diversion procto-colitis: Response to treatment with short-chain fatty acids

Kiely, E. M., Ade‐Ajayi, N., Wheeler, R. A., & Malone, M. (2001) · Journal of Pediatric Surgery · doi:10.1053/jpsu.2001.27034 · Cited by 55 · see citing works

Aldosterone induction of electrogenic sodium transport in the apical membrane vesicles of rat distal colon

Rajendran, V., Kashgarian, M. J., & Binder, H. J. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)51514-3 · Cited by 53 · see citing works

Safety of Rapid Intravenous Rehydration and Comparative Efficacy of 3 Oral Rehydration Solutions in the Treatment of Severely Malnourished Children With Dehydrating Cholera

Alam, N. H., Islam, S., Sattar, S., Monira, S., & Desjeux, J. F. (2009) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e318180af27 · Cited by 52 · see citing works

Characterization of butyrate-dependent electroneutral Na-Cl absorption in the rat distal colon

Binder, H. J., & Mehta, P. (1990) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00370654 · Cited by 50 · see citing works

The Treatment of Cholera: Clinical Science at the Bedside

Carpenter, C. C. J. (1992) · The Journal of Infectious Diseases · doi:10.1093/infdis/166.1.2 · Cited by 50 · see citing works

The Effects of Enterotoxins and Short-Chain Fatty Acids on Water and Electrolyte Fluxes in Heal and Colonic Loops in vivo in the Rat

Ramakrishna, B., Nance, S., Roberts-Thomson, I. C., & Roediger, W. E. W. (2009) · Digestion · doi:10.1159/000200229 · Cited by 49 · see citing works

Colonic Compensation in Transmissible Gastroenteritis of Swine

Argenzio, R. A., Moon, H. W., Kemeny, L. J., & Whipp, S. C. (1984) · Gastroenterology · doi:10.1016/s0016-5085(84)80165-1 · Cited by 49 · see citing works

Oral rehydration solution in the year 2000: pathophysiology, efficacy and effectiveness

Desjeux, J. F., Briend, A., & Butzner, J. D. (1997) · Baillière s Clinical Gastroenterology · doi:10.1016/s0950-3528(97)90029-4 · Cited by 48 · see citing works

Effects of butyrate on active sodium and chloride transport in rat and rabbit distal colon

Vidyasagar, S., & Ramakrishna, B. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013056 · Cited by 47 · see citing works

Oral Rehydration Therapy: New Explanations for an Old Remedy

Rao, M. C. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.032902.134726 · Cited by 45 · see citing works

Reduced osmolarity oral rehydration solution for treating cholera

Murphy, C. K., Hahn, S., & Volmink, J. A. (2004) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd003754.pub2 · Cited by 43 · see citing works

Segmental differences of short‐chain fatty acid transport across guinea‐pig large intestine

Engelhardt, W. V., & Rechkemmer, G. (1992) · Experimental Physiology · doi:10.1113/expphysiol.1992.sp003609 · Cited by 42 · see citing works

Kinetic analysis of butyrate transport in human colon adenocarcinoma cells reveals two different carrier-mediated mechanisms

Lecona, E., Olmo, N., Turnay, J., Santiago-Gómez, A., de Silanes, I. L., Gorospe, M., & Lizarbe, M. A. (2007) · Biochemical Journal · doi:10.1042/bj20070374 · Cited by 42 · see citing works

Pathogenesis and Clinical Manifestations of Clostridium difficile Diarrhea and Colitis

Farrell, R. J., & LaMont, J. T. (2000) · Current topics in microbiology and immunology · doi:10.1007/978-3-662-06272-2_6 · Cited by 41 · see citing works

Segmental differences in short-chain fatty acid transport in rabbit colon: Effect of pH and Na

Sellin, J. H., DeSoignie, R. C., & Burlingame, S. M. (1993) · The Journal of Membrane Biology · doi:10.1007/bf02505759 · Cited by 40 · see citing works

Amino acid absorption in the mammalian colon

Binder, H. J. (1970) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(70)90233-6 · Cited by 35 · see citing works

Regulation of butyrate uptake in Caco-2 cells by phorbol 12-myristate 13-acetate

Alrefai, W. A., Tyagi, S., Gill, R. K., Saksena, S., Hadjiagapiou, C., Mansour, F., Ramaswamy, K., & Dudeja, P. K. (2004) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00144.2003 · Cited by 32 · see citing works

Absorption of Short-Chain Fatty Acids from the In-Situ-Perfused Caecum and Colon of the Guinea Pig

Oltmer, S., & Engelhardt, W. V. (1994) · Scandinavian Journal of Gastroenterology · doi:10.3109/00365529409094878 · Cited by 29 · see citing works

Effects of short chain fatty acids on colonic Na+ absorption and enzyme activity

Zaharia, V., Varzescu, M., Djavadi, I., Newman, E., Egnor, R. W., Alexander-Chacko, J. T., & Charney, A. N. (2001) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(00)00318-4 · Cited by 29 · see citing works

Evaluation of the pathogenesis of flatulence and abdominal cramps in patients with lactose malabsorption.

Hammer, H., Petritsch, W., Pristautz, H., & Krejs, G. J. (1996) · PubMed · Cited by 27 · see citing works

Short-chain fatty acids in bowel contents after intestinal surgery

Mortensen, P. B., Hegnhøj, J., Rannem, T., Rasmussen, H. S., & Holtug, K. (1989) · Gastroenterology · doi:10.1016/0016-5085(89)91676-4 · Cited by 23 · see citing works

Effect of short-chain fatty acids on cyclic 3′,5′-guanosine monophosphate-mediated colonic secretion

Charney, A. N., Giannella, R. A., & Egnor, R. W. (1999) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/s1095-6433(99)00107-5 · Cited by 22 · see citing works

Alanine‐ and glucose‐based hypo‐osmolar oral rehydration solution in infants with persistent diarrhoea: a controlled trial

Sarker, S., Majid, N., & Mahalanabis, D. (1995) · Acta Paediatrica · doi:10.1111/j.1651-2227.1995.tb13755.x · Cited by 18 · see citing works

Unidirectional fluxes of short-chain fatty acids across segments of the large intestine in pig, sheep and pony compared with guinea pig

Engelhardt, W. V., Burmester, M., Hansen, K., & Becker, G. (1995) · Journal of Comparative Physiology B · doi:10.1007/bf00264683 · Cited by 14 · see citing works

Transport of Propionate across the Distal Colonic Epithelium of Guinea Pig in the Presence and Absence of Bicarbonate and of Chloride

Engelhardt, W. V., Busche, R., Burmester, M., Hansen, K., & Becker, G. (1997) · Zentralblatt für Veterinärmedizin Reihe A · doi:10.1111/j.1439-0442.1997.tb01088.x · Cited by 11 · see citing works

Transport of SCFA across the large intestinal epithelium of guinea pig.

von Engelhardt, W., Luciano, L., Reale, E., Gros, G., & Rechkemmer, G. (1989) · PubMed · Cited by 8 · see citing works

The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism

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

The impact of diet and lifestyle on gut microbiota and human health

Conlon, M., & Bird, A. (2014) · Nutrients · doi:10.3390/nu7010017 · Cited by 1,567 · see citing works

Potential beneficial effects of butyrate in intestinal and extraintestinal diseases

Canani, R. B. (2011) · World Journal of Gastroenterology · doi:10.3748/wjg.v17.i12.1519 · Cited by 1,381 · see citing works

Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTOR–S6K pathway

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

Free Fatty Acid Receptors in Health and Disease

Kimura, I., Ichimura, A., Ohue‐Kitano, R., & Igarashi, M. (2019) · Physiological Reviews · doi:10.1152/physrev.00041.2018 · Cited by 1,032 · 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

Short chain fatty acids prevent high-fat-diet-induced obesity in mice by regulating g protein-coupled receptors and gut microbiota

Lu, Y., Fan, C., Li, P., Lu, Y., Chang, X., & Qi, K. (2016) · Scientific Reports · doi:10.1038/srep37589 · Cited by 638 · see citing works

Gut-derived short-chain fatty acids are vividly assimilated into host carbohydrates and lipids

den Besten, G., Lange, K., Havinga, R., van Dijk, T. H., Gerding, A., van Eunen, K., Müller, M. M., Groen, A. K., Hooiveld, G. J. E. J., Bakker, B. M., et al. (2013) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00265.2013 · Cited by 606 · see citing works

Fermentable carbohydrate restriction reduces luminal bifidobacteria and gastrointestinal symptoms in patients with irritable bowel syndrome

Staudacher, H. M., Lomer, M. C. E., Anderson, J. L., Barrett, J. S., Muir, J. G., Irving, P. M., & Whelan, K. (2012) · The Journal of Nutrition · doi:10.3945/jn.112.159285 · Cited by 590 · see citing works

Higher Fecal Short-Chain Fatty Acid Levels Are Associated with Gut Microbiome Dysbiosis, Obesity, Hypertension and Cardiometabolic Disease Risk Factors

De la Cuesta-Zuluaga, J., Mueller, N., Álvarez-Quintero, R., Velásquez-Mejía, E., Sierra, J., Corrales-Agudelo, V., Carmona, J., Abad, J., & Escobar, J. (2018) · Nutrients · doi:10.3390/nu11010051 · Cited by 533 · see citing works

An isotope-labeled chemical derivatization method for the quantitation of short-chain fatty acids in human feces by liquid chromatography–tandem mass spectrometry

Han, J., Lin, K., Sequeira, C., & Borchers, C. H. (2014) · Analytica Chimica Acta · doi:10.1016/j.aca.2014.11.015 · Cited by 516 · see citing works

Microbial butyrate and its role for barrier function in the gastrointestinal tract

Plöger, S., Stumpff, F., Penner, G. B., Schulzke, J., Gäbel, G., Märtens, H., Shen, Z., Günzel, D., & Aschenbach, J. R. (2012) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2012.06553.x · Cited by 445 · see citing works

Short-chain fatty acids in control of energy metabolism

Hu, J., Lin, S., Zheng, B., & Cheung, P. C. K. (2016) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2016.1245650 · Cited by 441 · see citing works

Gut Microbiota Profiling: Metabolomics Based Approach to Unravel Compounds Affecting Human Health

Vernocchi, P., Del Chierico, F., & Putignani, L. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01144 · Cited by 426 · see citing works

Update on lactose malabsorption and intolerance: pathogenesis, diagnosis and clinical management

Misselwitz, B., Butter, M., Verbeke, K., & Fox, M. R. (2019) · Gut · doi:10.1136/gutjnl-2019-318404 · Cited by 390 · see citing works

Variable responses of human microbiomes to dietary supplementation with resistant starch

Venkataraman, A., Sieber, J. R., Schmidt, A. W., Waldron, C., Theis, K. R., & Schmidt, T. M. (2016) · Microbiome · doi:10.1186/s40168-016-0178-x · Cited by 384 · see citing works

Comparative Digestive Physiology

Karasov, W. H., & Douglas, A. E. (2013) · Comprehensive physiology · doi:10.1002/cphy.c110054 · Cited by 366 · see citing works

Human-origin probiotic cocktail increases short-chain fatty acid production via modulation of mice and human gut microbiome

Nagpal, R., Wang, S., Ahmadi, S., Hayes, J., Gagliano, J., Subashchandrabose, S., Kitzman, D. W., Becton, T., Read, R., & Yadav, H. (2018) · Scientific Reports · doi:10.1038/s41598-018-30114-4 · Cited by 355 · see citing works

A Microbiota-Derived Bacteriocin Targets the Host to Confer Diarrhea Resistance in Early-Weaned Piglets

Hu, J., Ma, L., Nie, Y., Chen, J., Zheng, W., Wang, X., Xie, C., Zheng, Z., Wang, Z., Yang, T., et al. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.11.006 · Cited by 334 · see citing works

Short‐Chain Fatty Acid Transporters: Role in Colonic Homeostasis

Sivaprakasam, S., Bhutia, Y. D., Yang, S., & Ganapathy, V. (2017) · Comprehensive physiology · doi:10.1002/cphy.c170014 · Cited by 321 · see citing works

Health effects of resistant starch

Lockyer, S., & Nugent, A. P. (2017) · Nutrition Bulletin · doi:10.1111/nbu.12244 · Cited by 319 · see citing works

Interindividual variability in gut microbiota and host response to dietary interventions

Healey, G. R., Murphy, R., Brough, L., Butts, C. A., & Coad, J. (2017) · Nutrition Reviews · doi:10.1093/nutrit/nux062 · Cited by 296 · see citing works

Alternative method for gas chromatography-mass spectrometry analysis of short-chain fatty acids in faecal samples

Garcı́a-Villalba, R., Giménez‐Bastida, J. A., García‐Conesa, M., Tomás-Barberán, F. A., Espı́n, J. C., & Larrosa, M. (2012) · Journal of Separation Science · doi:10.1002/jssc.201101121 · Cited by 291 · see citing works

Peripheral Mechanisms in Irritable Bowel Syndrome

Kassam, Z., Collins, S. M., & Moayyedi, P. (2013) · New England Journal of Medicine · doi:10.1056/nejmc1214185 · Cited by 285 · see citing works

Slimy partners: the mucus barrier and gut microbiome in ulcerative colitis

Fang, J. C., Wang, H., Zhou, Y., Zhang, H., Zhou, H., & Zhang, X. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00617-8 · Cited by 242 · see citing works

Molecular mechanisms of probiotic prevention of antibiotic-associated diarrhea

Mekonnen, S. A., Merenstein, D. J., Fraser, C. M., & Marco, M. L. (2020) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2020.01.005 · Cited by 198 · see citing works

Fecal short-chain fatty acid concentrations and dysbiosis in dogs with chronic enteropathy

Minamoto, Y., Minamoto, T. B., Isaiah, A., Sattasathuchana, P., Buono, A., Rangachari, V. R., McNeely, I. H., Lidbury, J. A., Steiner, J. M., & Suchodolski, J. S. (2019) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.15520 · Cited by 183 · see citing works

Probiotics in the prevention of antibiotic-associated diarrhoea and Clostridium difficile infection

Hickson, M. (2011) · Therapeutic Advances in Gastroenterology · doi:10.1177/1756283x11399115 · Cited by 169 · see citing works

The metabolic activity of gut microbiota in obese children is increased compared with normal-weight children and exhibits more exhaustive substrate utilization

Payne, A. N., Chassard, C., Zimmermann, M. B., Müller, P., Stinca, S., & Lacroix, C. (2011) · Nutrition and Diabetes · doi:10.1038/nutd.2011.8 · Cited by 165 · see citing works

From microbe to man: the role of microbial short chain fatty acid metabolites in host cell biology

Natarajan, N., & Pluznick, J. L. (2014) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00228.2014 · Cited by 163 · see citing works

The short chain fatty acids, butyrate and propionate, have differential effects on the motility of the guinea pig colon

Hurst, N. R., Kendig, D. M., Murthy, K. S., & Grider, J. R. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12425 · Cited by 140 · see citing works

A look at the smelly side of physiology: transport of short chain fatty acids

Stumpff, F. (2018) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-2105-9 · Cited by 140 · see citing works

Glucose sensing and signalling; regulation of intestinal glucose transport

Shirazi-Beechey, S. P., Moran, A. W., Batchelor, D. J., Daly, K., & Al-Rammahi, M. (2011) · Proceedings of the Nutrition Society · doi:10.1017/s0029665111000103 · Cited by 139 · see citing works

Postbiotics in human health: Possible new functional ingredients?

Hernández-Granados, M. J., & Franco‐Robles, E. (2020) · Food Research International · doi:10.1016/j.foodres.2020.109660 · Cited by 122 · see citing works

Proton pump inhibitor-induced gut dysbiosis and immunomodulation: current knowledge and potential restoration by probiotics

Kiecka, A., & Szczepanik, M. (2023) · Pharmacological Reports · doi:10.1007/s43440-023-00489-x · Cited by 117 · see citing works

Impact of Antibiotics on Necrotizing Enterocolitis and Antibiotic-Associated Diarrhea

Silverman, M. A., Konnikova, L., & Gerber, J. S. (2017) · Gastroenterology Clinics of North America · doi:10.1016/j.gtc.2016.09.010 · Cited by 113 · see citing works

Tributyrin Supplementation Protects Mice from Acute Ethanol-Induced Gut Injury

Cresci, G., Bush, K., & Nagy, L. E. (2014) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12428 · Cited by 111 · see citing works

Gut commensals and their metabolites in health and disease

Krishnamurthy, H. K., Pereira, M., Bosco, J., George, J., Jayaraman, V., Krishna, K., Wang, T., Bei, K., & Rajasekaran, J. J. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1244293 · Cited by 111 · see citing works

Infection Strategies of Intestinal Parasite Pathogens and Host Cell Responses

Genova, B. M. D., & Tonelli, R. R. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00256 · Cited by 109 · see citing works

Heat-Labile Enterotoxin: Beyond G M1 Binding

Mudrak, B., & Kuehn, M. J. (2010) · Toxins · doi:10.3390/toxins2061445 · Cited by 107 · see citing works

Butyrate esterified to starch is released in the human gastrointestinal tract

Clarke, J. M., Topping, D. L., Christophersen, C. T., Bird, A. R., Lange, K. M., Saunders, I. W., & Cobiac, L. (2011) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.111.017228 · Cited by 104 · see citing works

High-protein diet modifies colonic microbiota and luminal environment but not colonocyte metabolism in the rat model: The increased luminal bulk connection

Liu, X., Blouin, J.-M., Santacruz, A., Lan, A., Andriamihaja, M., Wilkanowicz, S., Benetti, P.-H., Tomé, D., Sanz, Y., Blachier, F., et al. (2014) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00400.2013 · Cited by 103 · see citing works

Development of a fast and cost-effective gas chromatography–mass spectrometry method for the quantification of short-chain and medium-chain fatty acids in human biofluids

Lotti, C., Rubert, J., Fava, F., Tuohy, K. M., Mattivi, F., & Vrhovšek, U. (2017) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-017-0493-5 · Cited by 103 · see citing works

The effect of 2′-fucosyllactose on simulated infant gut microbiome and metabolites; a pilot study in comparison to GOS and lactose

Salli, K. M., Anglenius, H., Hirvonen, J., Hibberd, A. A., Ahonen, I., Saarinen, M., Tiihonen, K., Maukonen, J., & Ouwehand, A. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-49497-z · Cited by 100 · see citing works

The Importance of Lactose in the Human Diet: Outcomes of a Mexican Consensus Meeting

Romero‐Velarde, E., Delgado‐Franco, D., García-Gutiérrez, M., Gurrola‐Díaz, C. M., Larrosa‐Haro, A., Montijo-Barrios, É., Muskiet, F. A. J., Vargas‐Guerrero, B., & Geurts, J. M. W. (2019) · Nutrients · doi:10.3390/nu11112737 · Cited by 100 · see citing works

Online breath analysis using metal oxide semiconductor sensors (electronic nose) for diagnosis of lung cancer

Kononov, A. S., Korotetski, B., Jahatspanian, I. E., Gubal, A. R., Vasiliev, A. A., Arsenjev, A., Nefedov, A., Барчук, А. А., Gorbunov, I., Kozyrev, K., et al. (2019) · Journal of Breath Research · doi:10.1088/1752-7163/ab433d · Cited by 97 · see citing works

Resistant Starch Regulates Gut Microbiota: Structure, Biochemistry and Cell Signalling

Yang, X., Darko, K. O., Huang, Y., He, C., Yang, H., He, S., Li, J., Li, J., Hocher, B., & Yin, Y. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000477386 · Cited by 95 · see citing works

Structural Changes of Starch–Lipid Complexes during Postprocessing and Their Effect on In Vitro Enzymatic Digestibility

Qin, R., Yu, J., Li, Y., Copeland, L., Wang, S., & Wang, S. (2019) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b06371 · Cited by 94 · see citing works

The Therapeutic Effect of SCFA-Mediated Regulation of the Intestinal Environment on Obesity

You, H., Tan, Y., Yu, D., Qiu, S., Bai, Y., He, J., Cao, H., Che, Q., Guo, J., & Su, Z. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.886902 · Cited by 93 · see citing works

Chinese yam (Dioscorea opposita Thunb.) alleviates antibiotic-associated diarrhea, modifies intestinal microbiota, and increases the level of short-chain fatty acids in mice

Zhang, N., Liang, T., Jin, Q., Shen, C., Zhang, Y., & Jing, P. (2019) · Food Research International · doi:10.1016/j.foodres.2019.04.016 · Cited by 88 · see citing works

Nutrient sensing and signalling by the gut

Rasoamanana, R., Darcel, N., Fromentin, G., & Tomé, D. (2012) · Proceedings of The Nutrition Society · doi:10.1017/s0029665112000110 · Cited by 88 · see citing works

A novel LCMSMS method for quantitative measurement of short-chain fatty acids in human stool derivatized with 12 C- and 13 C-labelled aniline

Chan, J. C. Y., Kioh, D. Y. Q., Yap, G. C., Lee, B. W., & Chan, E. C. Y. (2017) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/j.jpba.2017.01.044 · Cited by 85 · see citing works

The emerging role of microbiota-derived short-chain fatty acids in immunometabolism

Jasim, S. A., Opulencia, M. J. C., Ramírez‐Coronel, A. A., Abdelbasset, W. K., Abed, M. H., Markov, A. A., Al‐Awsi, G. R. L., Shamsiev, J. A., Hammid, A. T., Shalaby, M. N., et al. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.108983 · Cited by 84 · see citing works

Precision medicine in alcoholic and nonalcoholic fatty liver disease via modulating the gut microbiota

Bluemel, S., Williams, B., Knight, R. D., & Schnabl, B. (2016) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00245.2016 · Cited by 83 · see citing works

Diarrhoea in the critically ill

Blaser, A. R., Deane, A. M., & Fruhwald, S. M. (2015) · Current Opinion in Critical Care · doi:10.1097/mcc.0000000000000188 · Cited by 83 · see citing works

The probiotic Lactobacillus plantarum counteracts TNF-α-induced downregulation of SMCT1 expression and function

Borthakur, A., Anbazhagan, A. N., Kumar, A., Raheja, G., Singh, V., Ramaswamy, K., & Dudeja, P. K. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00279.2010 · Cited by 81 · see citing works

Regulation of virulence: the rise and fall of gastrointestinal pathogens

Kitamoto, S., Nagao‐Kitamoto, H., Kuffa, P., & Kamada, N. (2015) · Journal of Gastroenterology · doi:10.1007/s00535-015-1141-5 · Cited by 81 · see citing works

Branched Short-Chain Fatty Acid Isovaleric Acid Causes Colonic Smooth Muscle Relaxation via cAMP/PKA Pathway

Blakeney, B. A., Crowe, M. S., Mahavadi, S., Murthy, K. S., & Grider, J. R. (2018) · Digestive Diseases and Sciences · doi:10.1007/s10620-018-5417-5 · Cited by 80 · see citing works

The Extracellular Calcium-Sensing Receptor in the Intestine: Evidence for Regulation of Colonic Absorption, Secretion, Motility, and Immunity

Tang, L., Cheng, C. Y., Sun, X., Pedicone, A. J., Mahamadzadeh, M., & Cheng, S. X. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00245 · Cited by 79 · see citing works

Berberine treatment-emergent mild diarrhea associated with gut microbiota dysbiosis

Yue, S., Liu, J., Wang, W., Wang, A.-T., Yang, X., Guan, H., Wang, C., & Yan, D. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.109002 · Cited by 79 · see citing works

Cell-Surface and Nuclear Receptors in the Colon as Targets for Bacterial Metabolites and Its Relevance to Colon Health

Sivaprakasam, S., Bhutia, Y. D., Ramachandran, S., & Ganapathy, V. (2017) · Nutrients · doi:10.3390/nu9080856 · Cited by 78 · see citing works

Gut-microbiota derived bioactive metabolites and their functions in host physiology

Debnath, N., Kumar, R., Kumar, A., Mehta, P. K., & Yadav, A. K. (2021) · Biotechnology and Genetic Engineering Reviews · doi:10.1080/02648725.2021.1989847 · Cited by 77 · see citing works

The changing microbial landscape of Western society: Diet, dwellings and discordance

Broussard, J. L., & Devkota, S. (2016) · Molecular Metabolism · doi:10.1016/j.molmet.2016.07.007 · Cited by 74 · see citing works

Efficiency of Resistant Starch and Dextrins as Prebiotics: A Review of the Existing Evidence and Clinical Trials

Włodarczyk, M., & Śliżewska, K. (2021) · Nutrients · doi:10.3390/nu13113808 · Cited by 73 · see citing works

The gut microbiome and antibiotic resistome of chronic diarrhea rhesus macaques (Macaca mulatta) and its similarity to the human gut microbiome

Yang, S., Liu, Y., Yang, N., Lan, Y., Lan, W., Feng, J., Yue, B., He, M., Zhang, L., Zhang, A., et al. (2022) · Microbiome · doi:10.1186/s40168-021-01218-3 · Cited by 73 · see citing works

The multiple facets of acetyl-CoA metabolism: Energetics, biosynthesis, regulation, acylation and inborn errors

Wang, Y., Yang, H., Geerts, C., Fürtös, A., Waters, P. J., Cyr, D., Wang, S., & Mitchell, G. A. (2022) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2022.106966 · Cited by 73 · see citing works

Prevention and treatment of antibiotics-associated adverse effects through the use of probiotics: A review

Yang, S., Qiao, J., Zhang, M., Kwok, L., Matijašić, B. B., Zhang, H., & Zhang, W. (2024) · Journal of Advanced Research · doi:10.1016/j.jare.2024.06.006 · Cited by 72 · see citing works

Lactobacillus acidophilus counteracts enteropathogenic E. coli-induced inhibition of butyrate uptake in intestinal epithelial cells

Kumar, A., Alrefai, W. A., Borthakur, A., & Dudeja, P. K. (2015) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00186.2015 · Cited by 72 · see citing works

Gut microbiota: a potential manipulator for host adipose tissue and energy metabolism

Rong, B., Tianyu, X., Tiantian, Z., Feng, R., Huang, H., Wu, Q., & Sun, C. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.10.020 · Cited by 72 · see citing works

Kaempferol alleviates acute alcoholic liver injury in mice by regulating intestinal tight junction proteins and butyrate receptors and transporters

Chen, J., Xuan, Y.-H., Luo, M.-X., Ni, X.-G., Ling, L.-Q., Hu, S.-J., Chen, J.-Q., Xu, J., Jiang, L., Si, W.-Z., et al. (2019) · Toxicology · doi:10.1016/j.tox.2019.152338 · Cited by 71 · see citing works

Associations of gut microbiota, dietary intake, and serum short-chain fatty acids with fecal short-chain fatty acids

Yamamura, R., Nakamura, K., Kitada, N., Aizawa, T., Shimizu, Y., Nakamura, K., Ayabe, T., Kimura, T., & Tamakoshi, A. (2019) · Bioscience of Microbiota Food and Health · doi:10.12938/bmfh.19-010 · Cited by 71 · see citing works

Bifidobacterium animalis subsp. lactis XLTG11 improves antibiotic-related diarrhea by alleviating inflammation, enhancing intestinal barrier function and regulating intestinal flora

Xu, B., Liang, S., Zhao, J., Li, X., Guo, J., Xin, B., Li, B., Huo, G., & Ma, W. (2022) · Food & Function · doi:10.1039/d1fo04305f · Cited by 67 · see citing works

Mechanistic basis and preliminary practice of butyric acid and butyrate sodium to mitigate gut inflammatory diseases: a comprehensive review

Zhang, M., Wang, Y., Zhao, X., Liu, C., Wang, B., & Zhou, J. (2021) · Nutrition Research · doi:10.1016/j.nutres.2021.08.007 · Cited by 66 · see citing works

Epigenetic Metabolite Acetate Inhibits Class I/II Histone Deacetylases, Promotes Histone Acetylation, and Increases HIV-1 Integration in CD4+T Cells

Bolduc, J.-F., Hany, L., Barat, C., Ouellet, M., & Tremblay, M. J. (2017) · Journal of Virology · doi:10.1128/jvi.01943-16 · Cited by 65 · see citing works

Identification of the key physiological characteristics of Lactobacillus plantarum strains for ulcerative colitis alleviation

Yang, L., Sheng, Y., Pan, Q., Xue, Y., Yu, L., Tian, F., Zhao, J., Zhang, H., Zhai, Q., & Chen, W. (2020) · Food & Function · doi:10.1039/c9fo02935d · Cited by 64 · see citing works

SLC9 Gene Family: Function, Expression, and Regulation

Xu, H. J., Ghishan, F. K., & Kiela, P. R. (2018) · Comprehensive physiology · doi:10.1002/cphy.c170027 · Cited by 63 · see citing works

Bifidobacterium animalis subsp. lactis BB-12 Protects against Antibiotic-Induced Functional and Compositional Changes in Human Fecal Microbiome

Merenstein, D. J., Fraser, C. M., Roberts, R., Liu, T., Grant-Beurmann, S., Tan, T., Smith, K. H., Cronin, T., Martin, O. A., Sanders, M. E., et al. (2021) · Nutrients · doi:10.3390/nu13082814 · Cited by 62 · see citing works

Megasphaera in the Stool Microbiota Is Negatively Associated With Diarrheal Cryptosporidiosis

Carey, M. A., Medlock, G. L., Alam, M., Kabir, M., Uddin, M. J., Nayak, U., Papin, J. A., Faruque, A. S. G., Haque, R., Petri, W. A., et al. (2021) · Clinical Infectious Diseases · doi:10.1093/cid/ciab207 · Cited by 61 · see citing works

Pectin mediates the mechanism of host blood glucose regulation through intestinal flora

Guo, Q., Hou, X., Cui, Q., Li, S., Shen, G., Luo, Q., Wu, H., Chen, H., Liu, Y., Chen, A., et al. (2023) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2023.2173719 · Cited by 60 · see citing works

Carbohydrate Maldigestion and Intolerance

Fernández‐Bañares, F. (2022) · Nutrients · doi:10.3390/nu14091923 · Cited by 59 · see citing works

Undernourished Children and Milk Lactose

Grenov, B., Briend, A., Sangild, P. T., Thymann, T., Rytter, M. J. H., Hother, A.-L., Mølgaard, C., & Michaelsen, K. F. (2016) · Food and Nutrition Bulletin · doi:10.1177/0379572116629024 · Cited by 59 · see citing works

The beneficial effects of purple yam ( Dioscorea alata L.) resistant starch on hyperlipidemia in high-fat-fed hamsters

Li, T., Teng, H., An, F., Huang, Q., Chen, L., & Song, H. (2019) · Food & Function · doi:10.1039/c8fo02502a · Cited by 55 · see citing works

Gut microbiota short-chain fatty acids and their impact on the host thyroid function and diseases

Mendoza-León, M. J., Mangalam, A. K., Regaldiz, A., González-Madrid, E., Rangel-Ramírez, M. A., Álvarez-Mardones, O., Vallejos, O. P., Méndez, C., Bueno, S. M., Melo-González, F., et al. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1192216 · Cited by 53 · see citing works

Characterization of potentially probiotic lactic acid bacteria isolated from olives: Evaluation of short chain fatty acids production and analysis of the extracellular proteome

Pessione, A., Bianco, G. L., Mangiapane, E., Cirrincione, S., & Pessione, E. (2014) · Food Research International · doi:10.1016/j.foodres.2014.11.029 · Cited by 53 · see citing works

Discovery and Development of Antisecretory Drugs for Treating Diarrheal Diseases

Thiagarajah, J. R., Ko, E., Tradtrantip, L., Donowitz, M., & Verkman, A. S. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.12.001 · Cited by 53 · see citing works

Faecalibacterium prausnitzii and a Prebiotic Protect Intestinal Health in a Mouse Model of Antibiotic and Clostridium difficile Exposure

Roychowdhury, S., Cadnum, J. L., Glueck, B., Obrenovich, M. E., Donskey, C. J., & Cresci, G. (2018) · Journal of Parenteral and Enteral Nutrition · doi:10.1002/jpen.1053 · Cited by 53 · see citing works

Galactooligosaccharide pretreatment alleviates damage of the intestinal barrier and inflammatory responses in LPS-challenged mice

Wang, G., Sun, W., Pei, X., Jin, Y., Wang, H., Tao, W., Xiao, Z., Liu, L., & Wang, M. (2021) · Food & Function · doi:10.1039/d0fo03020a · Cited by 53 · see citing works

Physiology of Electrolyte Transport in the Gut: Implications for Disease

Rao, M. C. (2019) · Comprehensive physiology · doi:10.1002/cphy.c180011 · Cited by 53 · see citing works

The propionic acid and butyric acid in serum but not in feces are increased in patients with diarrhea-predominant irritable bowel syndrome

Tian, Z., Zhuang, X., Luo, M., Yin, W. H., & Xiong, L. (2020) · BMC Gastroenterology · doi:10.1186/s12876-020-01212-3 · Cited by 52 · see citing works

Gut microbiota and its derived SCFAs regulate the HPGA to reverse obesity-induced precocious puberty in female rats

Wang, L., Xu, H., Tan, B., Yi, Q., Liu, H., Deng, H., Chen, Y., Wang, R., Tian, J., & Zhu, J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1051797 · Cited by 49 · see citing works

Vinegar Treatment Prevents the Development of Murine Experimental Colitis via Inhibition of Inflammation and Apoptosis

Shen, F., Feng, J., Wang, X., Zhi-min, Q., Shi, X., An, Y., Zhang, Q., Wang, C., Liu, M., Liu, B., et al. (2016) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b05415 · Cited by 47 · see citing works

Pectic Oligosaccharides and Other Emerging Prebiotics

Míguez, B., Gómez, B., Gullón, P., Gullón, B., & Alonsó, J. L. (2016) · InTech eBooks · doi:10.5772/62830 · Cited by 47 · see citing works

Slc26a3 (DRA) in the Gut: Expression, Function, Regulation, Role in Infectious Diarrhea and Inflammatory Bowel Disease

Yu, Q. (2020) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izaa256 · Cited by 47 · see citing works

Estimation and Interpretation of Fermentation in the Gut: Coupling Results from a 24 h Batch <i>in Vitro</i> System with Fecal Measurements from a Human Intervention Feeding Study Using Fructo-oligosaccharides, Inulin, Gum Acacia, and Pea Fiber

Koecher, K. J., Noack, J. A., Timm, D. A., Klosterbuer, A. S., Thomas, W., & Slavin, J. L. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf404688n · Cited by 47 · see citing works

The critical role of short-chain fatty acids in health and disease: A subtle focus on cardiovascular disease-NLRP3 inflammasome-angiogenesis axis

Juan, Y., Chen, Y., & Xu, M. (2022) · Clinical Immunology · doi:10.1016/j.clim.2022.109013 · Cited by 46 · see citing works

Green banana-supplemented diet in the home management of acute and prolonged diarrhoea in children: a community-based trial in rural Bangladesh

Rabbani, G. H., Larson, C. P., Islam, R., Saha, U. R., & Kabir, A. (2010) · Tropical Medicine & International Health · doi:10.1111/j.1365-3156.2010.02608.x · Cited by 46 · see citing works

Calcium-sensing receptor: A new target for therapy of diarrhea

Cheng, S. X. (2016) · World Journal of Gastroenterology · doi:10.3748/wjg.v22.i9.2711 · Cited by 46 · see citing works

Molecular mechanisms and therapeutic possibilities of short-chain fatty acids in posttraumatic stress disorder patients: a mini-review

Petakh, P., Duve, K. V., Oksenych, V., Behzadi, P., & Kamyshnyi, O. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1394953 · Cited by 45 · see citing works

Prebiotic oligosaccharides from dragon fruits alter gut motility in mice

Khuituan, P., K-da, S., Bannob, K., Hayeeawaema, F., Peerakietkhajorn, S., Tipbunjong, C., Wichienchot, S., & Charoenphandhu, N. (2019) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2019.108821 · Cited by 45 · see citing works

Regulation of Enteroendocrine Cell Networks by the Major Human Gut Symbiont Bacteroides thetaiotaomicron

Modasia, A. A., Parker, A., Jones, E. J., Stentz, R., Brion, A., Goldson, A. J., Defernez, M., Wileman, T., Blackshaw, L. A., & Carding, S. R. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.575595 · Cited by 45 · see citing works

Colonic dysfunction in acute diarrhoea: the role of luminal short chain fatty acids.

Ramakrishna, B., & Mathan, V. I. (1993) · Gut · doi:10.1136/gut.34.9.1215 · Cited by 86 · see citing works

Inhibition of short-chain fatty acid absorption and Na+ absorption during acute colitis in the rabbit

Butzner, J. D., Meddings, J. B., & Dalal, V. (1994) · Gastroenterology · doi:10.1016/0016-5085(94)90009-4 · Cited by 26 · see citing works

Short-Chain Fatty Acids Inhibit Fluid and Electrolyte Loss Induced by Cholera Toxin in Proximal Colon of Rabbit In Vivo

Rabbani, G. H., Albert, M. J., Rahman, H., & Chowdhury, A. K. (1999) · Digestive Diseases and Sciences · doi:10.1023/a:1026650624193 · Cited by 55 · see citing works

Reversal by short-chain fatty acids of colonic fluid secretion induced by enteral feeding

Bowling, T. E., Raimundo, A. H., GRIMBLE, G. K., & Silk, D. B. A. (1993) · The Lancet · doi:10.1016/0140-6736(93)92360-6 · Cited by 133 · see citing works

Absorption 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