Dietary Nitrogen and Its Role in the Gut Microbiome and Inflammatory Bowel Disease: A Narrative Review
Open accessAbstract
In recent years, gut microbiota has emerged as a critical regulator of gastrointestinal health and disease, with its role in inflammatory bowel disease (IBD)—including Crohn’s disease and ulcerative colitis—being particularly significant. Among the many factors influencing the gut microbiota, dietary components such as fibers, fats, and polyphenols have received substantial attention. However, nitrogen-containing compounds, such as amino acids, nitrates, urea, and even nucleic acids, such as purines, remain underexplored despite their integral role in shaping microbial ecology, host metabolism, and immune responses. Some of these compounds are metabolized by gut bacteria into bioactive molecules such as short-chain fatty acids, ammonia, and nitric oxide, which exert diverse effects on mucosal integrity and inflammation. IBD pathophysiology is characterized by chronic inflammation, microbial dysbiosis, and compromised epithelial barriers. Nitrogen metabolism contributes significantly to these processes by influencing microbial composition, metabolite production, and host immune pathways. The breakdown of various nitrogen-containing compounds in the body leads to the production of byproducts, such as ammonia and hydrogen sulfide, which have been implicated in mucosal damage and immune dysregulation. At the same time, nitrogen-derived molecules, such as short-chain fatty acids and nitric oxide, exhibit protective effects, underscoring the dual role of dietary nitrogen in health and disease. This narrative review highlights the complex interactions between dietary nitrogen sources, gut microbiota, and IBD pathogenesis. We summarize the mechanisms by which nitrogen compounds influence microbial dynamics, identify their contributions to inflammation and barrier dysfunction, and explore their therapeutic potential. Multidisciplinary approaches integrating clinical, metabolomic, and microbiome research are essential to unravel the full scope of nitrogen’s role in gut health and identify novel therapeutic targets.
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?
Conditions such as gastritis, inflammatory bowel disease, coeliac disease and chronic dysbiosis can disrupt the enterosalivary nitrate cycle by decreasing the effectiveness of nitrate reduction to nitrite and subsequent NO formation.
“Conditions such as gastritis, inflammatory bowel disease, coeliac disease and chronic dysbiosis can disrupt the enterosalivary nitrate cycle by decreasing the effectiveness of nitrate reduction to nitrite and the subsequent formation of NO [294].”
From Dietary Nitrate-Rich Vegetables as Natural Modulators of Health: Mechanisms and Benefits in Ageing Populations (2026) · cites this paper as [294]
Section 4 describes nitrate reduction to nitrite by oral and gut bacteria, followed by conversion to NO, and discusses altered nitrate metabolism in the inflamed gut. It does not say that gastritis, IBD, coeliac disease, or chronic dysbiosis reduce the effectiveness of that conversion or disrupt the enterosalivary nitrate cycle. Section 2.2 instead notes increased NO levels in IBD, without addressing whether the enterosalivary pathway is impaired. (LLM, conf=0.82)
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
Gut microbiota-derived metabolites as key actors in inflammatory bowel disease
Lavelle, A., & Sokol, H. (2020) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-019-0258-z · Cited by 2,015 · cited 1× · see citing works
“Modulating nitrogen intake by reducing protein consumption or shifting to plant-based protein sources can help lower the production of these metabolites, potentially alleviating IBD symptoms [131].”
De Filippis, F., Pellegrini, N., Vannini, L., Jeffery, I. B., La Storia, A., Laghi, L., Serrazanetti, D. I., Di Cagno, R., Ferrocino, I., Lazzi, C., et al. (2016) · Gut · doi:10.1136/gutjnl-2015-309957 · Cited by 1,638 · see citing works
Glutamine: Metabolism and Immune Function, Supplementation and Clinical Translation
Cruzat, V., Macedo Rogero, M., Noel Keane, K., Curi, R., & Newsholme, P. (2018) · Nutrients · doi:10.3390/nu10111564 · Cited by 1,261 · see citing works
Food sources of nitrates and nitrites: The physiologic context for potential health benefits
Hord, N. G., Tang, Y., & Bryan, N. S. (2009) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.2008.27131 · Cited by 1,069 · see citing works
Effect of Diet on the Gut Microbiota: Rethinking Intervention Duration
Leeming, E. R., Johnson, A. J., Spector, T. D., & Le Roy, C. I. (2019) · Nutrients · doi:10.3390/nu11122862 · Cited by 817 · see citing works
Dietary carbohydrate intake and mortality: a prospective cohort study and meta-analysis
Seidelmann, S. B., Claggett, B., Cheng, S., Henglin, M., Shah, A., Steffen, L. M., Folsom, A. R., Rimm, E. B., Willett, W. C., & Solomon, S. D. (2018) · The Lancet Public Health · doi:10.1016/s2468-2667(18)30135-x · Cited by 776 · see citing works
Health Benefits of the Mediterranean Diet: Metabolic and Molecular Mechanisms
Tosti, V., Bertozzi, B., & Fontana, L. (2018) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glx227 · Cited by 762 · see citing works
Dietary protein and gut microbiota composition and function
Zhao, J., Zhang, X., Liu, H., Brown, M. A., & Qiao, S. (2018) · Current Protein & Peptide Science · doi:10.2174/1389203719666180514145437 · Cited by 363 · see citing works
Nitrates/Nitrites in Food—Risk for Nitrosative Stress and Benefits
Karwowska, M., & Kononiuk, A. (2020) · Antioxidants · doi:10.3390/antiox9030241 · Cited by 360 · see citing works
Beaumont, M., Portune, K. J., Steuer, N., Lan, A., Cerrudo, V., Audebert, M., Dumont, F., Mancano, G., Khodorova, N., Andriamihaja, M., et al. (2017) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.117.158816 · Cited by 250 · see citing works
Diet-Microbiome Interactions in Health Are Controlled by Intestinal Nitrogen Source Constraints
Holmes, A. J., Chew, Y. V., Colakoglu, F., Cliff, J. B., Klaassens, E., Read, M. N., Solon-Biet, S. M., McMahon, A. C., Cogger, V. C., Ruohonen, K., et al. (2017) · Cell Metabolism · doi:10.1016/j.cmet.2016.10.021 · Cited by 183 · see citing works
Abdallah, A., Elemba, E., Zhong, Q., & Sun, Z. (2020) · Current Protein & Peptide Science · doi:10.2174/1389203721666200212095503 · Cited by 59 · see citing works
Role of Oral and Gut Microbiota in Dietary Nitrate Metabolism and Its Impact on Sports Performance
González-Soltero, R., Bailén, M., de Lucas, B., Ramírez-Goercke, M. I., Pareja-Galeano, H., & Larrosa, M. (2020) · Nutrients · doi:10.3390/nu12123611 · Cited by 54 · see citing works
Flagged first, then by citations
Research works printed but not linked: 125
- [1]Qiu P. Ishimoto T. Fu L. Zhang J. Zhang Z. Liu Y. The Gut Microbiota in Inflammatory Bowel Disease Front. Cell. Infect. Microbiol. 2022 12 733992 10.3389/fcimb.2022.733992 35273921 PMC8902753 · DOI
- [2]Zheng J. Sun Q. Zhang J. Ng S.C. The role of gut microbiome in inflammatory bowel disease diagnosis and prognosis United Eur. Gastroenterol. J. 2022 10 1091 1102 10.1002/ueg2.12338 36461896 PMC9752296 · DOI
- [3]Khan I. Ullah N. Zha L. Bai Y. Khan A. Zhao T. Che T. Zhang C. Alteration of Gut Microbiota in Inflammatory Bowel Disease (IBD): Cause or Consequence? IBD Treatment Targeting the Gut Microbiome Pathogens 2019 8 126 10.3390/pathogens8030126 31412603 PMC6789542 · DOI · Paper page
- [4]Lloyd-Price J. Arze C. Ananthakrishnan A.N. Schirmer M. Avila-Pacheco J. Poon T.W. Andrews E. Ajami N.J. Bonham K.S. Brislawn C.J. Multi-omics of the gut microbial ecosystem in inflammatory bowel diseases Nature 2019 569 655 662 10.1038/s41586-019-1237-9 31142855 PMC6650278 · DOI · Paper page
- [5]Gyriki D. Nikolaidis C. Stavropoulou E. Bezirtzoglou I. Tsigalou C. Vradelis S. Bezirtzoglou E. Exploring the Gut Microbiome’s Role in Inflammatory Bowel Disease: Insights and Interventions J. Pers. Med. 2024 14 507 10.3390/jpm14050507 38793089 PMC11122163 · DOI
- [6]Kasahara K. Kerby R.L. Zhang Q. Pradhan M. Mehrabian M. Lusis A.J. Bergstrom G. Backhed F. Rey F.E. Gut bacterial metabolism contributes to host global purine homeostasis Cell Host Microbe 2023 31 1038 1053.e1010 10.1016/j.chom.2023.05.011 37279756 PMC10311284 · DOI
- [7]Choden T. Cohen N.A. The gut microbiome and the immune system Explor. Med. 2022 3 219 233 10.37349/emed.2022.00087 · DOI
- [8]Wiertsema S.P. van Bergenhenegouwen J. Garssen J. Knippels L.M.J. The Interplay between the Gut Microbiome and the Immune System in the Context of Infectious Diseases throughout Life and the Role of Nutrition in Optimizing Treatment Strategies Nutrients 2021 13 886 10.3390/nu13030886 33803407 PMC8001875 · DOI
- [9]Wu H.J. Wu E. The role of gut microbiota in immune homeostasis and autoimmunity Gut Microbes 2012 3 4 14 10.4161/gmic.19320 22356853 PMC3337124 · DOI · Paper page
- [10]Blaak E.E. Canfora E.E. Theis S. Frost G. Groen A.K. Mithieux G. Nauta A. Scott K. Stahl B. van Harsselaar J. Short chain fatty acids in human gut and metabolic health Benef. Microbes 2020 11 411 455 10.3920/BM2020.0057 32865024 · DOI · Paper page
- [11]Yang Q. Liang Q. Balakrishnan B. Belobrajdic D.P. Feng Q.J. Zhang W. Role of Dietary Nutrients in the Modulation of Gut Microbiota: A Narrative Review Nutrients 2020 12 381 10.3390/nu12020381 32023943 PMC7071260 · DOI
- [12]Igai K. Itakura M. Nishijima S. Tsurumaru H. Suda W. Tsutaya T. Tomitsuka E. Tadokoro K. Baba J. Odani S. Nitrogen fixation and nifH diversity in human gut microbiota Sci. Rep. 2016 6 31942 10.1038/srep31942 27554344 PMC4995403 · DOI
- [14]Schimmel P. Stahl B. Knol J. Belzer C. The infant gut microbiota: In pursuit of non-protein nitrogen Gut Microbes 2023 15 2211917 10.1080/19490976.2023.2211917 37226420 PMC10215027 · DOI
- [15]Jian X. Zhu Y. Ouyang J. Wang Y. Lei Q. Xia J. Guan Y. Zhang J. Guo J. He Y. Alterations of gut microbiome accelerate multiple myeloma progression by increasing the relative abundances of nitrogen-recycling bacteria Microbiome 2020 8 74 10.1186/s40168-020-00854-5 32466801 PMC7257554 · DOI
- [17]Diether N.E. Willing B.P. Microbial Fermentation of Dietary Protein: An Important Factor in Diet(-)Microbe(-)Host Interaction Microorganisms 2019 7 19 10.3390/microorganisms7010019 30642098 PMC6352118 · DOI
- [18]Ni J. Shen T.-C.D. Chen E.Z. Bittinger K. Bailey A. Roggiani M. Sirota-Madi A. Friedman E.S. Chau L. Lin A. A role for bacterial urease in gut dysbiosis and Crohn’s disease Sci. Transl. Med. 2017 9 eaah6888 10.1126/scitranslmed.aah6888 29141885 PMC5808452 · DOI
- [19]Andriamihaja M. Lan A. Beaumont M. Audebert M. Wong X. Yamada K. Yin Y. Tome D. Carrasco-Pozo C. Gotteland M. The deleterious metabolic and genotoxic effects of the bacterial metabolite p-cresol on colonic epithelial cells Free Radic. Biol. Med. 2015 85 219 227 10.1016/j.freeradbiomed.2015.04.004 25881551 · DOI
- [20]Calvez J. Azzout-Marniche D. Tome D. Protein quality, nutrition and health Front. Nutr. 2024 11 1406618 10.3389/fnut.2024.1406618 38863590 PMC11165183 · DOI
- [21]Silk D.B. Fairclough P.D. Clark M.L. Hegarty J.E. Marrs T.C. Addison J.M. Burston D. Clegg K.M. Matthews D.M. Use of a peptide rather than free amino acid nitrogen source in chemically defined “elemental” diets JPEN J. Parenter. Enter. Nutr. 1980 4 548 553 10.1177/0148607180004006548 6780707 · DOI
- [22]Bartlett A. Kleiner M. Dietary protein and the intestinal microbiota: An understudied relationship iScience 2022 25 105313 10.1016/j.isci.2022.105313 36339270 PMC9626677 · DOI
- [23]Carlstrom M. Moretti C.H. Weitzberg E. Lundberg J.O. Microbiota, diet and the generation of reactive nitrogen compounds Free Radic. Biol. Med. 2020 161 321 325 10.1016/j.freeradbiomed.2020.10.025 33131695 · DOI
- [24]Wu S. Bhat Z.F. Gounder R.S. Mohamed Ahmed I.A. Al-Juhaimi F.Y. Ding Y. Bekhit A.E.A. Effect of Dietary Protein and Processing on Gut Microbiota-A Systematic Review Nutrients 2022 14 453 10.3390/nu14030453 35276812 PMC8840478 · DOI
- [25]Duncan S.H. Iyer A. Russell W.R. Impact of protein on the composition and metabolism of the human gut microbiota and health Proc. Nutr. Soc. 2021 80 173 185 10.1017/S0029665120008022 33349284 · DOI
- [28]Chalvon-Demersay T. Luise D. Le Floc’h N. Tesseraud S. Lambert W. Bosi P. Trevisi P. Beaumont M. Corrent E. Functional Amino Acids in Pigs and Chickens: Implication for Gut Health Front. Vet. Sci. 2021 8 663727 10.3389/fvets.2021.663727 34113671 PMC8185281 · DOI
- [29]Broer S. Intestinal Amino Acid Transport and Metabolic Health Annu. Rev. Nutr. 2023 43 73 99 10.1146/annurev-nutr-061121-094344 37285555 · DOI
- [30]Kumar M. Tomar M. Punia S. Dhakane-Lad J. Dhumal S. Changan S. Senapathy M. Berwal M.K. Sampathrajan V. Sayed A.A.S. Plant-based proteins and their multifaceted industrial applications LWT 2022 154 112620 10.1016/j.lwt.2021.112620 · DOI
- [31]Hertzler S.R. Lieblein-Boff J.C. Weiler M. Allgeier C. Plant Proteins: Assessing Their Nutritional Quality and Effects on Health and Physical Function Nutrients 2020 12 3704 10.3390/nu12123704 33266120 PMC7760812 · DOI · Paper page
- [32]Nimni M.E. Han B. Cordoba F. Are we getting enough sulfur in our diet? Nutr. Metab. 2007 4 24 10.1186/1743-7075-4-24 17986345 PMC2198910 · DOI
- [35]Keller R.M. Beaver L. Prater M.C. Hord N.G. Dietary Nitrate and Nitrite Concentrations in Food Patterns and Dietary Supplements Nutr. Today 2020 55 218 226 10.1097/NT.0000000000000253 · DOI
- [36]Schlagenhauf U. On the Role of Dietary Nitrate in the Maintenance of Systemic and Oral Health Dent. J. 2022 10 84 10.3390/dj10050084 35621537 PMC9139378 · DOI
- [37]Kamalian A. Sohrabi Asl M. Dolatshahi M. Afshari K. Shamshiri S. Momeni Roudsari N. Momtaz S. Rahimi R. Abdollahi M. Abdolghaffari A.H. Interventions of natural and synthetic agents in inflammatory bowel disease, modulation of nitric oxide pathways World J. Gastroenterol. 2020 26 3365 3400 10.3748/wjg.v26.i24.3365 32655263 PMC7327787 · DOI
- [38]Jakhar D. Sarin S.K. Kaur S. Gut microbiota and dynamics of ammonia metabolism in liver disease npj Gut Liver 2024 1 11 10.1038/s44355-024-00011-x · DOI
- [39]Barmore W. Azad F. Stone W.L. Physiology, Urea Cycle Available online: https://www.ncbi.nlm.nih.gov/books/NBK513323/ (accessed on 1 March 2025)
- [40]Lapierre H. Lobley G.E. Nitrogen Recycling in the Ruminant: A Review J. Dairy Sci. 2001 84 E223 E236 10.3168/jds.S0022-0302(01)70222-6 · DOI
- [41]Wu G. Wu Z. Dai Z. Yang Y. Wang W. Liu C. Wang B. Wang J. Yin Y. Dietary requirements of “nutritionally non-essential amino acids” by animals and humans Amino Acids 2013 44 1107 1113 10.1007/s00726-012-1444-2 23247926 · DOI
- [42]Ren W. Wang K. Yin J. Chen S. Liu G. Tan B. Wu G. Bazer F.W. Peng Y. Yin Y. Glutamine-Induced Secretion of Intestinal Secretory Immunoglobulin A: A Mechanistic Perspective Front. Immunol. 2016 7 503 10.3389/fimmu.2016.00503 27933057 PMC5121228 · DOI
- [43]Perna S. Alalwan T.A. Alaali Z. Alnashaba T. Gasparri C. Infantino V. Hammad L. Riva A. Petrangolini G. Allegrini P. The Role of Glutamine in the Complex Interaction between Gut Microbiota and Health: A Narrative Review Int. J. Mol. Sci. 2019 20 5232 10.3390/ijms20205232 31652531 PMC6834172 · DOI
- [44]Wang W.W. Qiao S.Y. Li D.F. Amino acids and gut function Amino Acids 2009 37 105 110 10.1007/s00726-008-0152-4 18670730 · DOI
- [45]Fotiadis C. Adamis S. Misiakos E.P. Genetzakis M. Antonakis P.T. Tsekouras D.K. Gorgoulis V.G. Zografos G.C. Papalois A. Fotinou M. The prophylactic effect of L-arginine in acute ischaemic colitis in a rat model of ischaemia/reperfusion injury Acta Chir. Belg. 2007 107 192 200 10.1080/00015458.2007.11680039 17515270 · DOI
- [46]Coburn L.A. Gong X. Singh K. Asim M. Scull B.P. Allaman M.M. Williams C.S. Rosen M.J. Washington M.K. Barry D.P. L-arginine supplementation improves responses to injury and inflammation in dextran sulfate sodium colitis PLoS ONE 2012 7 e33546 10.1371/journal.pone.0033546 22428068 PMC3299802 · DOI
- [47]Beaumont M. Blachier F. Amino Acids in Intestinal Physiology and Health Adv. Exp. Med. Biol. 2020 1265 1 20 10.1007/978-3-030-45328-2_1 32761567 · DOI
- [48]Kucharzik T. Stoll R. Lugering N. Domschke W. Circulating antiinflammatory cytokine IL-10 in patients with inflammatory bowel disease (IBD) Clin. Exp. Immunol. 1995 100 452 456 10.1111/j.1365-2249.1995.tb03721.x 7774055 PMC1534463 · DOI
- [49]Ikeda Y. Matsuda S. Gut Protective Effect from D-Methionine or Butyric Acid against DSS and Carrageenan-Induced Ulcerative Colitis Molecules 2023 28 4392 10.3390/molecules28114392 37298868 PMC10254188 · DOI
- [50]Hara T. Meng S. Motooka D. Sato H. Arao Y. Tsuji Y. Yabumoto T. Doki Y. Eguchi H. Uchida S. Fat and proteolysis due to methionine, tryptophan, and niacin deficiency leads to alterations in gut microbiota and immune modulation in inflammatory bowel disease Cancer Sci. 2024 115 2473 2485 10.1111/cas.16153 38679799 PMC11247612 · DOI
- [51]Liu G. Yu L. Fang J. Andy Hu C.-A. Yin J. Ni H. Ren W. Duraipandiyan V. Chen S. Abdullah Al-Dhabi N. Methionine restriction on oxidative stress and immune response in dss-induced colitis mice Oncotarget 2017 8 44511 44520 10.18632/oncotarget.17812 28562346 PMC5546498 · DOI
- [52]Liu Y. Wang X. Hu C.A. Therapeutic Potential of Amino Acids in Inflammatory Bowel Disease Nutrients 2017 9 920 10.3390/nu9090920 28832517 PMC5622680 · DOI
- [54]Muro P. Zhang L. Li S. Zhao Z. Jin T. Mao F. Mao Z. The emerging role of oxidative stress in inflammatory bowel disease Front. Endocrinol. 2024 15 1390351 10.3389/fendo.2024.1390351 39076514 PMC11284038 · DOI
- [55]Levine J.J. Pettei M.J. Valderrama E. Gold D.M. Kessler B.H. Trachtman H. Nitric oxide and inflammatory bowel disease: Evidence for local intestinal production in children with active colonic disease J. Pediatr. Gastroenterol. Nutr. 1998 26 34 38 10.1097/00005176-199801000-00006 9443117 · DOI
- [56]Cross R.K. Wilson K.T. Nitric oxide in inflammatory bowel disease Inflamm. Bowel Dis. 2003 9 179 189 10.1097/00054725-200305000-00006 12792224 · DOI
- [57]Baldelli V. Scaldaferri F. Putignani L. Del Chierico F. The Role of Enterobacteriaceae in Gut Microbiota Dysbiosis in Inflammatory Bowel Diseases Microorganisms 2021 9 697 10.3390/microorganisms9040697 33801755 PMC8066304 · DOI
- [58]Kostic A.D. Xavier R.J. Gevers D. The microbiome in inflammatory bowel disease: Current status and the future ahead Gastroenterology 2014 146 1489 1499 10.1053/j.gastro.2014.02.009 24560869 PMC4034132 · DOI · Paper page
- [60]Konozy E.H.E. Osman M.E.M. From inflammation to immune regulation: The dual nature of dietary lectins in health and disease Heliyon 2024 10 e39471 10.1016/j.heliyon.2024.e39471 39502251 PMC11535980 · DOI
- [61]Banwell J.G. Howard R. Kabir I. Costerton J.W. Bacterial overgrowth by indigenous microflora in the phytohemagglutinin-fed rat Can. J. Microbiol. 1988 34 1009 1013 10.1139/m88-177 3061624 · DOI
- [62]Greer F. Pusztai A. Toxicity of kidney bean (Phaseolus vulgaris) in rats: Changes in intestinal permeability Digestion 1985 32 42 46 10.1159/000199215 4018443 · DOI
- [63]Cohen L.J. Han S.M. Lau P. Guisado D. Liang Y. Nakashige T.G. Ali T. Chiang D. Rahman A. Brady S.F. Unraveling function and diversity of bacterial lectins in the human microbiome Nat. Commun. 2022 13 3101 10.1038/s41467-022-29949-3 35661736 PMC9166713 · DOI
- [64]Lee J.S. Wang R.X. Goldberg M.S. Clifford G.P. Kao D.J. Colgan S.P. Microbiota-Sourced Purines Support Wound Healing and Mucous Barrier Function iScience 2020 23 101226 10.1016/j.isci.2020.101226 32554188 PMC7303675 · DOI
- [65]Chen T. Tao Y. Wang Q. Pei Y. Zhao Z. Yang W. Lu Y. Utilizing an integrated bioinformatics and machine learning approach to uncover biomarkers linking ulcerative colitis to purine metabolism-related genes Heliyon 2024 10 e38403 10.1016/j.heliyon.2024.e38403 39524758 PMC11550743 · DOI
- [66]Worledge C.S. Kostelecky R.E. Zhou L. Bhagavatula G. Colgan S.P. Lee J.S. Allopurinol Disrupts Purine Metabolism to Increase Damage in Experimental Colitis Cells 2024 13 373 10.3390/cells13050373 38474337 PMC10930830 · DOI
- [67]Swidsinski A. Loening-Baucke V. Theissig F. Engelhardt H. Bengmark S. Koch S. Lochs H. Dorffel Y. Comparative study of the intestinal mucus barrier in normal and inflamed colon Gut 2007 56 343 350 10.1136/gut.2006.098160 16908512 PMC1856798 · DOI
- [68]Wang Z. Li Y. Liao W. Huang J. Liu Y. Li Z. Tang J. Gut microbiota remodeling: A promising therapeutic strategy to confront hyperuricemia and gout Front. Cell. Infect. Microbiol. 2022 12 935723 10.3389/fcimb.2022.935723 36034697 PMC9399429 · DOI
- [69]Hamid O. Alsabbagh Alchirazi K. Eltelbany A. Nanah R. Regueiro M. Increased prevalence of gout in patients with inflammatory bowel disease: A population-based study JGH Open 2023 7 640 644 10.1002/jgh3.12963 37744707 PMC10517438 · DOI
- [70]Li N. Lewis P. Samuelson D. Liboni K. Neu J. Glutamine regulates Caco-2 cell tight junction proteins Am. J. Physiol. Gastrointest. Liver Physiol. 2004 287 G726 G733 10.1152/ajpgi.00012.2004 15130874 · DOI
- [71]Li N. Neu J. Glutamine deprivation alters intestinal tight junctions via a PI3-K/Akt mediated pathway in Caco-2 cells J. Nutr. 2009 139 710 714 10.3945/jn.108.101485 19211824 PMC2666365 · DOI
- [72]De-Souza D.A. Greene L.J. Intestinal permeability and systemic infections in critically ill patients: Effect of glutamine Crit. Care Med. 2005 33 1125 1135 10.1097/01.CCM.0000162680.52397.97 15891348 · DOI
- [73]Li J.Y. Guo Y.C. Zhou H.F. Yue T.T. Wang F.X. Sun F. Wang W.Z. Arginine metabolism regulates the pathogenesis of inflammatory bowel disease Nutr. Rev. 2023 81 578 586 10.1093/nutrit/nuac070 36040377 PMC10086623 · DOI
- [74]Singh K. Coburn L.A. Barry D.P. Asim M. Scull B.P. Allaman M.M. Lewis N.D. Washington M.K. Rosen M.J. Williams C.S. Deletion of cationic amino acid transporter 2 exacerbates dextran sulfate sodium colitis and leads to an IL-17-predominant T cell response Am. J. Physiol. Gastrointest. Liver Physiol. 2013 305 G225 G240 10.1152/ajpgi.00091.2013 23703655 PMC3742860 · DOI
- [75]Hong S.K. Maltz B.E. Coburn L.A. Slaughter J.C. Chaturvedi R. Schwartz D.A. Wilson K.T. Increased serum levels of L-arginine in ulcerative colitis and correlation with disease severity Inflamm. Bowel Dis. 2010 16 105 111 10.1002/ibd.21035 19637336 PMC2795785 · DOI
- [76]Coburn L.A. Horst S.N. Allaman M.M. Brown C.T. Williams C.S. Hodges M.E. Druce J.P. Beaulieu D.B. Schwartz D.A. Wilson K.T. L-Arginine Availability and Metabolism Is Altered in Ulcerative Colitis Inflamm. Bowel Dis. 2016 22 1847 1858 10.1097/MIB.0000000000000790 27104830 PMC4956554 · DOI
- [77]Andrade M.E.R. Barros P.A.V.d. Menta P.L.d.R. Costa G.M.F. Miranda S.E.M. Leocádio P.C.L. Almeida-Leite C.M.d. Generoso S.d.V. Leite J.I.A. Cardoso V.N. Arginine supplementation reduces colonic injury, inflammation and oxidative stress of DSS-induced colitis in mice J. Funct. Foods 2019 52 360 369 10.1016/j.jff.2018.11.019 · DOI
- [78]Kruidenier L. Kuiper I. Lamers C.B. Verspaget H.W. Intestinal oxidative damage in inflammatory bowel disease: Semi-quantification, localization, and association with mucosal antioxidants J. Pathol. 2003 201 28 36 10.1002/path.1409 12950014 · DOI
- [79]Dudzinska E. Gryzinska M. Ognik K. Gil-Kulik P. Kocki J. Oxidative Stress and Effect of Treatment on the Oxidation Product Decomposition Processes in IBD Oxid. Med. Cell Longev. 2018 2018 7918261 10.1155/2018/7918261 30057685 PMC6051053 · DOI
- [80]Jahanian R. Immunological responses as affected by dietary protein and arginine concentrations in starting broiler chicks Poult. Sci. 2009 88 1818 1824 10.3382/ps.2008-00386 19687265 · DOI
- [81]Fernandez-Tome S. Ortega Moreno L. Chaparro M. Gisbert J.P. Gut Microbiota and Dietary Factors as Modulators of the Mucus Layer in Inflammatory Bowel Disease Int. J. Mol. Sci. 2021 22 10224 10.3390/ijms221910224 34638564 PMC8508624 · DOI
- [82]Blander J.M. Longman R.S. Iliev I.D. Sonnenberg G.F. Artis D. Regulation of inflammation by microbiota interactions with the host Nat. Immunol. 2017 18 851 860 10.1038/ni.3780 28722709 PMC5800875 · DOI
- [83]Fernandez-Tome S. Marin A.C. Ortega Moreno L. Baldan-Martin M. Mora-Gutierrez I. Lanas-Gimeno A. Moreno-Monteagudo J.A. Santander C. Sanchez B. Chaparro M. Immunomodulatory Effect of Gut Microbiota-Derived Bioactive Peptides on Human Immune System from Healthy Controls and Patients with Inflammatory Bowel Disease Nutrients 2019 11 2605 10.3390/nu11112605 31683517 PMC6893616 · DOI
- [84]Fernández-Tomé S. Hernández-Ledesma B. Chaparro M. Indiano-Romacho P. Bernardo D. Gisbert J.P. Role of food proteins and bioactive peptides in inflammatory bowel disease Trends Food Sci. Technol. 2019 88 194 206 10.1016/j.tifs.2019.03.017 · DOI
- [85]Colgan S.P. Curtis V.F. Campbell E.L. The inflammatory tissue microenvironment in IBD Inflamm. Bowel Dis. 2013 19 2238 2244 10.1097/MIB.0b013e31828dcaaf 23702808 PMC3749286 · DOI
- [86]Zhang C. Li Q. Xing J. Yang Y. Zhu M. Lin L. Yu Y. Cai X. Wang X. Tannic acid and zinc ion coordination of nanase for the treatment of inflammatory bowel disease by promoting mucosal repair and removing reactive oxygen and nitrogen species Acta Biomater. 2024 177 347 360 10.1016/j.actbio.2024.02.015 38373525 · DOI
- [87]Boughton-Smith N.K. Evans S.M. Hawkey C.J. Cole A.T. Balsitis M. Whittle B.J. Moncada S. Nitric oxide synthase activity in ulcerative colitis and Crohn’s disease Lancet 1993 342 338 340 10.1016/0140-6736(93)91476-3 7687730 · DOI
- [88]Seril D.N. Liao J. Yang G.Y. Yang C.S. Oxidative stress and ulcerative colitis-associated carcinogenesis: Studies in humans and animal models Carcinogenesis 2003 24 353 362 10.1093/carcin/24.3.353 12663492 · DOI · Paper page
- [89]Stettner N. Rosen C. Bernshtein B. Gur-Cohen S. Frug J. Silberman A. Sarver A. Carmel-Neiderman N.N. Eilam R. Biton I. Induction of Nitric-Oxide Metabolism in Enterocytes Alleviates Colitis and Inflammation-Associated Colon Cancer Cell Rep. 2018 23 1962 1976 10.1016/j.celrep.2018.04.053 29768197 PMC5976577 · DOI
- [90]Abot A. Fried S. Cani P.D. Knauf C. Reactive Oxygen Species/Reactive Nitrogen Species as Messengers in the Gut: Impact on Physiology and Metabolic Disorders Antioxid. Redox Signal. 2022 37 394 415 10.1089/ars.2021.0100 34714099 · DOI
- [91]Linares R. Frances R. Gutierrez A. Juanola O. Bacterial Translocation as Inflammatory Driver in Crohn’s Disease Front. Cell Dev. Biol. 2021 9 703310 10.3389/fcell.2021.703310 34557484 PMC8452966 · DOI
- [92]Stummer N. Feichtinger R.G. Weghuber D. Kofler B. Schneider A.M. Role of Hydrogen Sulfide in Inflammatory Bowel Disease Antioxidants 2023 12 1570 10.3390/antiox12081570 37627565 PMC10452036 · DOI
- [93]Moon J.Y. Kye B.H. Ko S.H. Yoo R.N. Sulfur Metabolism of the Gut Microbiome and Colorectal Cancer: The Threat to the Younger Generation Nutrients 2023 15 1966 10.3390/nu15081966 37111185 PMC10146533 · DOI
- [94]Beaumont M. Andriamihaja M. Lan A. Khodorova N. Audebert M. Blouin J.M. Grauso M. Lancha L. Benetti P.H. Benamouzig R. Detrimental effects for colonocytes of an increased exposure to luminal hydrogen sulfide: The adaptive response Free Radic. Biol. Med. 2016 93 155 164 10.1016/j.freeradbiomed.2016.01.028 26849947 · DOI
- [95]Blachier F. Andriamihaja M. Larraufie P. Ahn E. Lan A. Kim E. Production of hydrogen sulfide by the intestinal microbiota and epithelial cells and consequences for the colonic and rectal mucosa Am. J. Physiol. Gastrointest. Liver Physiol. 2021 320 G125 G135 10.1152/ajpgi.00261.2020 33084401 · DOI
- [96]Braccia D.J. Jiang X. Pop M. Hall A.B. The Capacity to Produce Hydrogen Sulfide (H(2)S) via Cysteine Degradation Is Ubiquitous in the Human Gut Microbiome Front. Microbiol. 2021 12 705583 10.3389/fmicb.2021.705583 34745023 PMC8564485 · DOI
- [97]Cremin J.D. Jr. Fitch M.D. Fleming S.E. Glucose alleviates ammonia-induced inhibition of short-chain fatty acid metabolism in rat colonic epithelial cells Am. J. Physiol. Gastrointest. Liver Physiol. 2003 285 G105 G114 10.1152/ajpgi.00437.2002 12637251 · DOI
- [98]Andriamihaja M. Davila A.M. Eklou-Lawson M. Petit N. Delpal S. Allek F. Blais A. Delteil C. Tome D. Blachier F. Colon luminal content and epithelial cell morphology are markedly modified in rats fed with a high-protein diet Am. J. Physiol. Gastrointest. Liver Physiol. 2010 299 G1030 G1037 10.1152/ajpgi.00149.2010 20689060 · DOI
- [99]Blachier F. Andriamihaja M. Effects of the L-tyrosine-derived bacterial metabolite p-cresol on colonic and peripheral cells Amino Acids 2022 54 325 338 10.1007/s00726-021-03064-x 34468872 · DOI
- [100]Toft P.B. Vanslette A.M. Trost K. Moritz T. Gillum M.P. Backhed F. Arora T. Microbial metabolite p-cresol inhibits gut hormone expression and regulates small intestinal transit in mice Front. Endocrinol. 2023 14 1200391 10.3389/fendo.2023.1200391 37534214 PMC10391832 · DOI
- [101]Al Hinai E.A. Kullamethee P. Rowland I.R. Swann J. Walton G.E. Commane D.M. Modelling the role of microbial p-cresol in colorectal genotoxicity Gut Microbes 2019 10 398 411 10.1080/19490976.2018.1534514 30359553 PMC6546321 · DOI
- [102]Mimoun S. Andriamihaja M. Chaumontet C. Atanasiu C. Benamouzig R. Blouin J.M. Tome D. Bouillaud F. Blachier F. Detoxification of H2S by differentiated colonic epithelial cells: Implication of the sulfide oxidizing unit and of the cell respiratory capacity Antioxid. Redox Signal. 2012 17 1 10 10.1089/ars.2011.4186 22369066 · DOI
- [103]Blachier F. Beaumont M. Andriamihaja M. Davila A.M. Lan A. Grauso M. Armand L. Benamouzig R. Tome D. Changes in the Luminal Environment of the Colonic Epithelial Cells and Physiopathological Consequences Am. J. Pathol. 2017 187 476 486 10.1016/j.ajpath.2016.11.015 28082121 · DOI
- [104]De Preter V. Arijs I. Windey K. Vanhove W. Vermeire S. Schuit F. Rutgeerts P. Verbeke K. Decreased mucosal sulfide detoxification is related to an impaired butyrate oxidation in ulcerative colitis Inflamm. Bowel Dis. 2012 18 2371 2380 10.1002/ibd.22949 22434643 · DOI · Paper page
- [105]Kou Y. Zhang S. Chen J. Shen Y. Zhang Z. Huang H. Ma Y. Xiang Y. Liao L. Zhou J. A mouse protozoan boosts antigen-specific mucosal IgA responses in a specific lipid metabolism- and signaling-dependent manner Nat. Commun. 2024 15 7914 10.1038/s41467-024-52336-z 39256385 PMC11387640 · DOI
- [106]Liu Y. Rhoads J.M. Communication between B-Cells and Microbiota for the Maintenance of Intestinal Homeostasis Antibodies 2013 2 535 553 10.3390/antib2040535 · DOI
- [107]Takeuchi T. Ohno H. IgA in human health and diseases: Potential regulator of commensal microbiota Front. Immunol. 2022 13 1024330 10.3389/fimmu.2022.1024330 36439192 PMC9685418 · DOI
- [109]Brown K.A. Back S.J. Ruchelli E.D. Markowitz J. Mascarenhas M. Verma R. Piccoli D.A. Baldassano R.N. Lamina propria and circulating interleukin-6 in newly diagnosed pediatric inflammatory bowel disease patients Am. J. Gastroenterol. 2002 97 2603 2608 10.1111/j.1572-0241.2002.06030.x 12385446 · DOI
- [110]Xue H. Sufit A.J. Wischmeyer P.E. Glutamine therapy improves outcome of in vitro and in vivo experimental colitis models JPEN J. Parenter. Enter. Nutr. 2011 35 188 197 10.1177/0148607110381407 21378248 · DOI
- [111]Katinios G. Casado-Bedmar M. Walter S.A. Vicario M. Gonzalez-Castro A.M. Bednarska O. Soderholm J.D. Hjortswang H. Keita A.V. Increased Colonic Epithelial Permeability and Mucosal Eosinophilia in Ulcerative Colitis in Remission Compared With Irritable Bowel Syndrome and Health Inflamm. Bowel Dis. 2020 26 974 984 10.1093/ibd/izz328 31944236 PMC7301402 · DOI
- [112]Sultan S. El-Mowafy M. Elgaml A. Ahmed T.A.E. Hassan H. Mottawea W. Metabolic Influences of Gut Microbiota Dysbiosis on Inflammatory Bowel Disease Front. Physiol. 2021 12 715506 10.3389/fphys.2021.715506 34646151 PMC8502967 · DOI
- [113]Michielan A. D’Inca R. Intestinal Permeability in Inflammatory Bowel Disease: Pathogenesis, Clinical Evaluation, and Therapy of Leaky Gut Mediat. Inflamm. 2015 2015 628157 10.1155/2015/628157 26582965 PMC4637104 · DOI · Paper page
- [114]Reese A.T. Pereira F.C. Schintlmeister A. Berry D. Wagner M. Hale L.P. Wu A. Jiang S. Durand H.K. Zhou X. Microbial nitrogen limitation in the mammalian large intestine Nat. Microbiol. 2018 3 1441 1450 10.1038/s41564-018-0267-7 30374168 PMC6264799 · DOI
- [116]De Angelis M. Ferrocino I. Calabrese F.M. De Filippis F. Cavallo N. Siragusa S. Rampelli S. Di Cagno R. Rantsiou K. Vannini L. Diet influences the functions of the human intestinal microbiome Sci. Rep. 2020 10 4247 10.1038/s41598-020-61192-y 32144387 PMC7060259 · DOI
- [118]Leclerc M. Bedu-Ferrari C. Etienne-Mesmin L. Mariadassou M. Lebreuilly L. Tran S.L. Brazeau L. Mayeur C. Delmas J. Rue O. Nitric Oxide Impacts Human Gut Microbiota Diversity and Functionalities mSystems 2021 6 e0055821 10.1128/msystems.00558-21 34519530 PMC8547463 · DOI
- [119]Davila A.M. Blachier F. Gotteland M. Andriamihaja M. Benetti P.H. Sanz Y. Tome D. Intestinal luminal nitrogen metabolism: Role of the gut microbiota and consequences for the host Pharmacol. Res. 2013 68 95 107 10.1016/j.phrs.2012.11.005 23183532 · DOI · Paper page
- [120]Prindiville T.P. Sheikh R.A. Cohen S.H. Tang Y.J. Cantrell M.C. Silva J. Jr. Bacteroides fragilis enterotoxin gene sequences in patients with inflammatory bowel disease Emerg. Infect. Dis. 2000 6 171 174 10.3201/eid0602.000210 10756151 PMC2640860 · DOI
- [121]Steck N. Hoffmann M. Sava I.G. Kim S.C. Hahne H. Tonkonogy S.L. Mair K. Krueger D. Pruteanu M. Shanahan F. Enterococcus faecalis Metalloprotease Compromises Epithelial Barrier and Contributes to Intestinal Inflammation Gastroenterology 2011 141 959 971 10.1053/j.gastro.2011.05.035 21699778 · DOI · Paper page
- [122]Cai J. Chen Z. Wu W. Lin Q. Liang Y. High animal protein diet and gut microbiota in human health Crit. Rev. Food Sci. Nutr. 2022 62 6225 6237 10.1080/10408398.2021.1898336 33724115 · DOI
- [123]Tiso M. Schechter A.N. Nitrate reduction to nitrite, nitric oxide and ammonia by gut bacteria under physiological conditions PLoS ONE 2015 10 e0119712 10.1371/journal.pone.0119712 25803049 PMC4372352 · DOI · Paper page
- [124]Wu L. Tang Z. Chen H. Ren Z. Ding Q. Liang K. Sun Z. Mutual interaction between gut microbiota and protein/amino acid metabolism for host mucosal immunity and health Anim. Nutr. 2021 7 11 16 10.1016/j.aninu.2020.11.003 33997326 PMC8110859 · DOI
- [125]Schanuel C. Dias E. Ferreira A. Bertges K. Bertges L. Glutamine as A Therapeutic Strategy in Inflammatory Bowel Diseases: A Systematic Review Gastroenterol. Hepatol. Dig. Disord. 2019 2 1 6 10.33425/2639-9334.1033 · DOI
- [126]Singh K. Gobert A.P. Coburn L.A. Barry D.P. Allaman M. Asim M. Luis P.B. Schneider C. Milne G.L. Boone H.H. Dietary Arginine Regulates Severity of Experimental Colitis and Affects the Colonic Microbiome Front. Cell. Infect. Microbiol. 2019 9 66 10.3389/fcimb.2019.00066 30972302 PMC6443829 · DOI
- [127]Nciri N. Cho N. Bergaoui N. Mhamdi F.E. Ammar A.B. Trabelsi N. Zekri S. Guémira F. Mansour A.B. Sassi F.H. Effect of White Kidney Beans (Phaseolus vulgaris L. var. Beldia) on Small Intestine Morphology and Function in Wistar Rats J. Med. Food 2015 18 1387 1399 10.1089/jmf.2014.0193 26488416 · DOI
- [128]Kordás K. Szalmay G. Bardocz S. Pusztai Á. Varga G. Phytohaemagglutinin inhibits gastric acid but not pepsin secretion in conscious rats J. Physiol.-Paris 2001 95 309 314 10.1016/S0928-4257(01)00043-2 11595455 · DOI
- [129]Lucius K. Dietary Lectins: Gastrointestinal and Immune Effects Altern. Complement. Ther. 2020 26 168 174 10.1089/act.2020.29286.klu · DOI
- [130]Ungaro R. Mehandru S. Allen P.B. Peyrin-Biroulet L. Colombel J.F. Ulcerative colitis Lancet 2017 389 1756 1770 10.1016/S0140-6736(16)32126-2 27914657 PMC6487890 · DOI
- [132]Wellens J. Vissers E. Matthys C. Vermeire S. Sabino J. Personalized Dietary Regimens for Inflammatory Bowel Disease: Current Knowledge and Future Perspectives Pharmgenom. Pers. Med. 2023 16 15 27 10.2147/PGPM.S359365 36660362 PMC9842524 · DOI
- [133]Biesiekierski J.R. Jalanka J. Staudacher H.M. Can Gut Microbiota Composition Predict Response to Dietary Treatments? Nutrients 2019 11 1134 10.3390/nu11051134 31121812 PMC6566829 · DOI
- [134]Olendzki B. Bucci V. Cawley C. Maserati R. McManus M. Olednzki E. Madziar C. Chiang D. Ward D.V. Pellish R. Dietary manipulation of the gut microbiome in inflammatory bowel disease patients: Pilot study Gut Microbes 2022 14 2046244 10.1080/19490976.2022.2046244 35311458 PMC8942410 · DOI
- [135]Aleksandrova K. Romero-Mosquera B. Hernandez V. Diet, Gut Microbiome and Epigenetics: Emerging Links with Inflammatory Bowel Diseases and Prospects for Management and Prevention Nutrients 2017 9 962 10.3390/nu9090962 28867793 PMC5622722 · DOI
- [138]Haskey N. Estaki M. Ye J. Shim R.K. Singh S. Dieleman L.A. Jacobson K. Gibson D.L. A Mediterranean Diet Pattern Improves Intestinal Inflammation Concomitant with Reshaping of the Bacteriome in Ulcerative Colitis: A Randomised Controlled Trial J. Crohns Colitis 2023 17 1569 1578 10.1093/ecco-jcc/jjad073 37095601 PMC10637046 · DOI
- [139]Eom T. Kim Y.S. Choi C.H. Sadowsky M.J. Unno T. Current understanding of microbiota- and dietary-therapies for treating inflammatory bowel disease J. Microbiol. 2018 56 189 198 10.1007/s12275-018-8049-8 29492876 · DOI
Cited by
Sorted by citations
Kurhaluk, N., Kołodziejska, R., Buyun, L., Kamiński, P., & Tkaczenko, H. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27083461 · Cited by 3 · see citing works
“Conditions such as gastritis, inflammatory bowel disease, coeliac disease and chronic dysbiosis can disrupt the enterosalivary nitrate cycle by decreasing the effectiveness of nitrate reduction to nitrite and the subsequent formation of NO [294].”
- Authors
- Herrera, M., & Byerley, L. O.
- Affiliations
- Louisiana State University Health Sciences Center New Orleans (US)
- Corresponding author
- Byerley, Lauri O.
- Venue
- Nutrients
- Publisher
- MDPI AG
- Published
- 2025-07-20
- Volume
- 17
- Issue
- 14
- Pages
- 2373
- ISSN
- 2072-6643 (ISSN-L)
- PMC
- PMC12299043
- OpenAlex
- W4412513302
- Cited by
- 15
- References
- 13
- Citations by year
- 2026: 14 · 2025: 1
- FWCI
- 1.33
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Nutrients (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Nutrition and Physiology
- Keywords
- dietary nitrogen, gut microbiota, inflammatory bowel disease, Crohn's disease, ulcerative colitis, nitrogen metabolism, short-chain fatty acids, nitric oxide, ammonia, hydrogen sulfide, mucosal barrier dysfunction, dysbiosis, purines, amino acids, nitrate, host-microbe interactions
- MeSH terms
- Gastrointestinal Microbiome, Animals, Diet, Humans, Nitrogen, Inflammatory Bowel Diseases, Dysbiosis
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