Phenotypic changes in colonocytes following acute stress or activation of mast cells in mice: implications for delayed epithelial barrier dysfunction
Open accessAbstract
BACKGROUND AND AIMS: Stressful life events are known to modulate the development or relapse of disease in both inflammatory bowel disease and irritable bowel disease patients but underlying mechanisms remain unclear. Stress is known to effect mast cells, interferon gamma (IFN-gamma), and myosin light chain phosphorylation to trigger colonic epithelial barrier dysfunction. The aim of this study was to investigate whether acute stress induced or chemical mast cell activation impaired expression and function of epithelial tight junctions, and altered colonocyte differentiation in mice. METHODS: Colonic paracellular permeability was assessed as the in vivo lumen to blood ratio of 51Cr-EDTA in different groups of mice (controls, stressed, mast cell degranulator BrX-537A treated), pretreated or not with the mast cell stabiliser doxantrazole. Involvement of mast cells and IFN-gamma was evaluated in wild-type and IFN-gamma deficient mice. Tight junction alteration was assessed by histology, transmission electron microscopy, and real time reverse transcription-polymerase chain reaction. Colonocyte differentiation was determined by protein kinase C zeta (PKCzeta) immunofluorescence and western blotting, and alkaline phosphatase activity assay. RESULTS: Acute stress induced a three day delayed increase in colonic paracellular permeability which involved mast cell degranulation and overproduction of IFN-gamma. The colonic epithelial barrier was morphologically altered and expression of mRNA encoding tight junction proteins ZO-2 and occludin was decreased. Moreover, three days after acute stress, colonocyte differentiation was reduced, as shown by decreased expression of both PKCzeta isotype and alkaline phosphatase. CONCLUSION: These data highlight new mechanisms whereby an acute stress acts on the gastrointestinal tract by inducing alterations in colonocyte differentiation and decreased expression of mRNA encoding tight junction proteins. Thus phenotypic changes in colonocytes could pave the way for stress related intestinal disorders.
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?
Inflammatory intestinal leukocytes, including IL17+ T cells and mast cells, may contribute to breakdown of the intestinal epithelial barrier and downregulation of CLDN5, OCLN, and ZO-2.
“Mechanistically, inflammatory intestinal leukocytes, including IL17+ T cells as well as mast cells, may contribute to the breakdown of the intestinal epithelial barrier and the accompanying downregulation of tight junction proteins CLDN5, occludin (OCLN) and tight junction protein 2 (ZO-2)106,107.”
From Central regulation of stress-evoked peripheral immune responses (2023) · cites this paper as [107]
The Results and ‘Role of mast cells and IFN-c’ sections report increased colonic permeability after stress or mast-cell activation in mice, alongside decreased occludin and ZO-2 mRNA. They do not establish downregulation of CLDN5 or implicate IL17+ T cells; the measured decreases are in mRNA, not protein abundance. Page numbers are unavailable in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredStress-induced changes in permeability involve activation of glial and mast cells in the gut, overproduction of interferon-γ and changes in the morphology of the colonic epithelium via reduced expression of tight junction protein 2 and by occlusion of important components of the intestinal tight junction.
“Stress-induced changes in permeability involve activation of glial and mast cells in the gut, overproduction of interferon-γ and changes in the morphology of the colonic epithelium via reduced expression of tight junction protein 2 (zona occludens 2) and by occlusion of important components of the intestinal tight junction.28”
From Principles and clinical implications of the brain-gut-enteric microbiota axis (2009) · cites this paper as [28]
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
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860 · see citing works
Mutation of the mouse klotho gene leads to a syndrome resembling ageing
Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works
Multiple Defects of Immune Cell Function in Mice with Disrupted Interferon-γ Genes
Dalton, D. K., Pitts-Meek, S., Keshav, S., Figari, I. S., Bradley, A., & Stewart, T. A. (1993) · Science · doi:10.1126/science.8456300 · Cited by 1,733 · see citing works
Metcalfe, D. D., Baram, D., & Mekori, Y. A. (1997) · Physiological Reviews · doi:10.1152/physrev.1997.77.4.1033 · Cited by 1,723 · see citing works
Barbara, G., Stanghellini, V., De Giorgio, R., Cremon, C., Cottrell, G. S., Santini, D., Pasquinelli, G., Morselli-Labate, A. M., Grady, E. F., Bunnett, N. W., et al. (2004) · Gastroenterology · doi:10.1053/j.gastro.2003.11.055 · Cited by 1,475 · see citing works
Antibodies to interleukin 12 abrogate established experimental colitis in mice.
Neurath, M., Fuss, I. J., Kelsall, B. L., Stuber, E. R., & Strober, W. (1995) · The Journal of Experimental Medicine · doi:10.1084/jem.182.5.1281 · Cited by 1,334 · see citing works
Spiller, R. C., Jenkins, D., Thornley, J. P., Hebden, J. M., Wright, T., Skinner, M., & Neal, K. R. (2000) · Gut · doi:10.1136/gut.47.6.804 · Cited by 1,155 · see citing works
Proinflammatory Cytokines Disrupt Epithelial Barrier Function by Apoptosis-Independent Mechanisms
Bruewer, M., Luegering, A., Kucharzik, T. F., Parkos, C. A., Madara, J., Hopkins, A. M., & Nusrat, A. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.11.6164 · Cited by 897 · see citing works
Intestinal permeability and the prediction of relapse in Crohn's disease
Wyatt, J., Vogelsang, H., Hübl, W., Waldhoer, T., & Lochs, H. (1993) · The Lancet · doi:10.1016/0140-6736(93)90882-h · Cited by 626 · see citing works
Mittermaier, C., Dejaco, C., Waldhoer, T., Oefferlbauer-Ernst, A., Miehsler, W., Beier, M., Tillinger, W., Gangl, A., & Moser, G. (2004) · Psychosomatic Medicine · doi:10.1097/01.psy.0000106907.24881.f2 · Cited by 532 · see citing works
IV. Regulation of tight junctions by extracellular stimuli: nutrients, cytokines, and immune cells
Nusrat, A., Turner, J. R., & Madara, J. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.279.5.g851 · Cited by 499 · see citing works
Stress and Exacerbation in Ulcerative Colitis: A Prospective Study of Patients Enrolled in Remission
Levenstein, S., Prantera, C., Varvo, V., Scribano, M. L., Andreoli, A., Luzi, C., Arcà, M., Berto, E., Milite, G., & Marcheggiano, A. (2000) · American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2000.02012.x · Cited by 451 · see citing works
Induction of intestinal inflammation in mouse by activation of proteinase-activated receptor-2.
Cénac, N., Coelho, A., Nguyen, C., Compton, S., Andrade-Gordon, P., MacNaughton, W., Wallace, J., Hollenberg, M., Bunnett, N., Garcia-Villar, R., et al. (2002) · American Journal of Pathology · doi:10.1016/s0002-9440(10)64466-5 · Cited by 386 · see citing works
Zolotarevsky, Y., Hecht, G. A., Koutsouris, A., Gonzalez, D. E., Quan, C., Tom, J., Mrsny, R. J., & Turner, J. R. (2002) · Gastroenterology · doi:10.1053/gast.2002.34235 · Cited by 385 · see citing works
Inflammatory bowel disease is associated with changes of enterocytic junctions
Gaßler, N., Rohr, C. M., Schneider, A., Kartenbeck, J., Bach, A., Obermüller, N., Otto, H. F., & Autschbach, F. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.281.1.g216 · Cited by 363 · see citing works
Söderholm, J. D., Yang, P., Ceponis, P., Vohra, A., Riddell, R., Sherman, P. M., & Perdue, M. H. (2002) · Gastroenterology · doi:10.1053/gast.2002.36019 · Cited by 362 · see citing works
Youakim, A., & Ahdieh, M. (1999) · American Journal of Physiology - Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1999.276.5.g1279 · Cited by 340 · see citing works
Is small intestinal permeability really increased in relatives of patients with Crohn's disease?
May, G. R., Sutherland, L. R., & Meddings, J. B. (1993) · Gastroenterology · doi:10.1016/0016-5085(93)90638-s · Cited by 316 · see citing works
Role of mast cells in chronic stress induced colonic epithelial barrier dysfunction in the rat
Santos, J., Yang, P.-C., Söderholm, J. D., Benjamin, M., & Perdue, M. H. (2001) · Gut · doi:10.1136/gut.48.5.630 · Cited by 313 · see citing works
Marshall, J. K., Thabane, M., Garg, A. X., Clark, W., Meddings, J., Collins, S. M., & for the WEL Investigators (2004) · Alimentary Pharmacology & Therapeutics · doi:10.1111/j.1365-2036.2004.02284.x · Cited by 292 · see citing works
Söderholm, J. D., Olaison, G., Peterson, K. H., Franzén, L. E., Lindmark, T., Wirén, M., Tagesson, C., & Sjödahl, R. (2002) · Gut · doi:10.1136/gut.50.3.307 · Cited by 290 · see citing works
Expression from the human occludin promoter is affected by tumor necrosis factor α and interferon γ
Mankertz, J., Tavalali, S., Schmitz, H., Mankertz, A., Riecken, E. O., Fromm, M., & Schulzke, J. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.11.2085 · Cited by 287 · see citing works
Meddings, J. B., & Swain, M. G. (2000) · Gastroenterology · doi:10.1053/gast.2000.18152 · Cited by 269 · see citing works
Qiu, B., Vallance, B. A., Blennerhassett, P. A., & Collins, S. M. (1999) · Nature Medicine · doi:10.1038/13503 · Cited by 252 · see citing works
Pearce, F. L., Befus, A. D., Gauldie, J., & Bienenstock, J. (1982) · The Journal of Immunology · doi:10.4049/jimmunol.128.6.2481 · Cited by 247 · see citing works
Pearce, F. L., Befus, A. D., & Bienenstock, J. (1984) · Journal of Allergy and Clinical Immunology · doi:10.1016/0091-6749(84)90453-6 · Cited by 234 · see citing works
Psychosocial determinants of relapse in ulcerative colitis: A longitudinal study
Bitton, A., Sewitch, M. J., Peppercorn, M. A., de B Edwardes, M. D., Shah, S., Ransil, B., & Locke, S. E. (2003) · American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2003.07717.x · Cited by 226 · see citing works
Stress stimulates transepithelial macromolecular uptake in rat jejunum
Kiliaan, A. J., Saunders, P. R., Bijlsma, P. B., Berin, M. C., Taminiau, J. A., Groot, J. A., & Perdue, M. H. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.275.5.g1037 · Cited by 223 · see citing works
Acute stressors stimulate ion secretion and increase epithelial permeability in rat intestine
Saunders, P. R., Kosecka, U., McKay, D. M., & Perdue, M. H. (1994) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1994.267.5.g794 · Cited by 215 · see citing works
Irritable bowel syndrome patients show enhanced modulation of visceral perception by auditory stress
Dickhaus, B., Mayer, E. A., Firooz, N., Stains, J., Conde, F. A., Olivas, T. I., Fass, R., Chang, L., Mayer, M., & Naliboff, B. D. (2003) · The American Journal of Gastroenterology · doi:10.1111/j.1572-0241.2003.07156.x · Cited by 204 · see citing works
Saunders, P. R., Santos, J., Hanssen, N. P. M., Yates, D. A., Groot, J. A., & Perdue, M. H. (2002) · Digestive Diseases and Sciences · doi:10.1023/a:1013204612762 · Cited by 198 · see citing works
Ferrier, L., Mazelin, L., Cénac, N., Desreumaux, P., Janin, A., Émilie, D., Colombel, J., Villar, R. G., Fioramonti, J., & Bueno, L. P. (2003) · Gastroenterology · doi:10.1016/s0016-5085(03)01057-6 · Cited by 197 · see citing works
Gamet, L., Daviaud, D., Denis, C., Rémésy, C., & Murat, J. (1992) · International Journal of Cancer · doi:10.1002/ijc.2910520222 · Cited by 195 · see citing works
Ait-Belgnaoui, A., Bradesi, S., Fioramonti, J., Theodorou, V., & Bueno, L. (2005) · Pain · doi:10.1016/j.pain.2004.10.002 · Cited by 171 · see citing works
Barreau, F., Cartier, C., Ferrier, L., Fioramonti, J., & Bueno, L. P. (2004) · Gastroenterology · doi:10.1053/j.gastro.2004.05.019 · Cited by 171 · see citing works
Cholinergic nerves mediate stress-induced intestinal transport abnormalities in Wistar-Kyoto rats
Saunders, P. R., Hanssen, N. P. M., & Perdue, M. H. (1997) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1997.273.2.g486 · Cited by 118 · see citing works
Butyrate-Induced Differentiation of Colon Cancer Cells Is PKC and JNK Dependent
Orchel, A., Dzierżewicz, Z., Parfiniewicz, B., Weglarz, L., & Wilczok, T. (2005) · Digestive Diseases and Sciences · doi:10.1007/s10620-005-2463-6 · Cited by 95 · cited 1× · see citing works
“These two markers are validated to describe proliferation/differentiation process in colonocyte.[26, 38] This 3-day delay between the stimulus and observed alterations in colonocyte differentiation is fully in agreement with all published data showing that it corresponds to the time for epithelial cell”
Result51CrEDTA colonic permeability and therapy response in patients with ulcerative colitis
Arslan, G., Atasever, T., Cindoruk, M., & Yıldırım, İ. (2001) · Nuclear Medicine Communications · doi:10.1097/00006231-200109000-00009 · Cited by 64 · see citing works
Verstovsek, G., Byrd, A. E., Frey, M. R., Petrelli, N. J., & Black, J. D. (1998) · Gastroenterology · doi:10.1016/s0016-5085(98)70367-1 · Cited by 64 · see citing works
Tavalali, S., Schmitz, H., Fromm, M., Schulzke, J.-D., & Mankertz, J. (2000) · Gastroenterology · doi:10.1016/s0016-5085(00)84547-3 · Cited by 58 · see citing works
Francoeur, C., Escaffit, F., Vachon, P. H., & Beaulieu, J. (2004) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00535.2003 · Cited by 53 · see citing works
Fargeas, M. J., Theodourou, V., Fioramonti, J., & Bueno, L. P. (1992) · Gastroenterology · doi:10.1016/0016-5085(92)91795-6 · Cited by 51 · see citing works
Changes in intestinal permeability and epithelial differentiation during inflammation in the rat.
Ramage, J. K., Hunt, R. H., & Perdue, M. H. (1988) · Gut · doi:10.1136/gut.29.1.57 · Cited by 43 · see citing works
Fonti, R., Latella, G., Bises, G., Magliocca, F. M., Nobili, F., Caprilli, R., & Sambuy, Y. (1994) · International Journal of Colorectal Disease · doi:10.1007/bf00304294 · Cited by 35 · see citing works
de Pater-Huijsen, F. L., de Riemer, M. J., Reijneke, R. M. R., Pompen, M., Lutter, R., Jansen, H. M., & Out, T. A. (2002) · Immunology · doi:10.1046/j.1365-2567.2002.01411.x · Cited by 10 · see citing works
Flagged first, then by citations
2 of the 47 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- [29]29. Metcalfe DD, Baram D, Mekori YA. Mast cells. Physiol Rev 1997;77:1033-79.
Cited by
Sorted by citations
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
The gut-brain axis: interactions between enteric microbiota, central and enteric nervous systems.
(2015) · PubMed Central · Cited by 2,540 · see citing works
Inflammatory bowel disease: cause and immunobiology
Baumgart, D. C., & Carding, S. R. (2007) · The Lancet · doi:10.1016/s0140-6736(07)60750-8 · Cited by 2,147 · see citing works
Interactions between the microbiota, immune and nervous systems in health and disease
Fung, T. C., Olson, C. A., & Hsiao, E. Y. (2017) · Nature Neuroscience · doi:10.1038/nn.4476 · Cited by 1,900 · see citing works
Principles and clinical implications of the brain-gut-enteric microbiota axis
Rhee, S. H., Pothoulakis, C., & Mayer, E. A. (2009) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2009.35 · Cited by 1,342 · see citing works
Martin, C. R., Osadchiy, V., Kalani, A., & Mayer, E. A. (2018) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2018.04.003 · Cited by 1,284 · see citing works
Brain-gut-microbe communication in health and disease
Grenham, S., Clarke, G., Cryan, J. F., & Dinan, T. G. (2011) · Frontiers in Physiology · doi:10.3389/fphys.2011.00094 · Cited by 952 · see citing works
Intestinal barrier function in health and gastrointestinal disease
Camilleri, M., Madsen, K., Spiller, R., Van Meerveld, B. G., & Verne, G. N. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01921.x · Cited by 908 · see citing works
Mechanism of cytokine modulation of epithelial tight junction barrier
Al–Sadi, R. (2009) · Frontiers in bioscience · doi:10.2741/3413 · Cited by 649 · see citing works
Ait-Belgnaoui, A., Durand, H., Cartier, C., Chaumaz, G., Eutamene, H., Ferrier, L., Houdeau, E., Fioramonti, J., Bueno, L., & Theodorou, V. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.024 · Cited by 612 · see citing works
Regulation of the stress response by the gut microbiota: implications for psychoneuroendocrinology
Dinan, T. G., & Cryan, J. F. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.007 · Cited by 577 · see citing works
Camilleri, M., Lasch, K. L., & Zhou, W. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00155.2012 · Cited by 397 · see citing works
The Gut-Brain Axis: Influence of Microbiota on Mood and Mental Health.
Appleton, J. (2018) · Europe PMC (PubMed Central) · Cited by 337 · see citing works
Stress signaling pathways activated by weaning mediate intestinal dysfunction in the pig
Moeser, A. J., Klok, C. V., Ryan, K. A., Wooten, J. G., Little, D., Cook, V. L., & Blikslager, A. T. (2006) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00197.2006 · Cited by 320 · see citing works
Keita, Å. V., & Söderholm, J. D. (2010) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2010.01498.x · Cited by 286 · see citing works
Martínez, C., Lobo, B., Pigrau, M., Ramos, L., González-Castro, A. M., Alonso, C., Guilarte, M., Guilá, M., de Torres, I., Azpiroz, F., et al. (2013) · Gut · doi:10.1136/gutjnl-2012-302093 · Cited by 283 · see citing works
Irritable bowel syndrome: A clinical review
Soares, R. L. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i34.12144 · Cited by 266 · see citing works
Moeser, A. J., Ryan, K. A., Nighot, P. K., & Blikslager, A. T. (2007) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00304.2006 · Cited by 247 · see citing works
Physiological and pathophysiological functions of intestinal mast cells
Bischoff, S. C. (2009) · Seminars in Immunopathology · doi:10.1007/s00281-009-0165-4 · Cited by 225 · see citing works
Gender-related differences in irritable bowel syndrome: Potential mechanisms of sex hormones
Méleine, M. (2014) · World Journal of Gastroenterology · doi:10.3748/wjg.v20.i22.6725 · Cited by 220 · see citing works
Winston, J. H., Shenoy, M. M., Medley, D., Naniwadekar, A. S., & Pasricha, P. J. (2006) · Gastroenterology · doi:10.1053/j.gastro.2006.11.014 · Cited by 219 · see citing works
Stress and visceral pain: From animal models to clinical therapies
Larauche, M. H., Mulak, A., & Taché, Y. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.04.020 · Cited by 212 · see citing works
Central regulation of stress-evoked peripheral immune responses
Chan, K. L., Poller, W. C., Swirski, F. K., & Russo, S. J. (2023) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00729-2 · Cited by 207 · see citing works
Development of the Pediatric Gut Microbiome: Impact on Health and Disease
Ihekweazu, F. D., & Versalovic, J. A. (2018) · The American Journal of the Medical Sciences · doi:10.1016/j.amjms.2018.08.005 · Cited by 201 · see citing works
Leigh, S., Uhlig, F., Wilmes, L., Sánchez-Díaz, P., Gheorghe, C. E., Goodson, M. S., Kelley‐Loughnane, N., Hyland, N. P., Cryan, J. F., & Clarke, G. A. (2023) · The Journal of Physiology · doi:10.1113/jp281951 · Cited by 193 · see citing works
Xu, Y., Shrestha, N., Véronique Préat, A., & Beloqui, A. (2021) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2021.05.005 · Cited by 183 · see citing works
Human mast cells, bacteria, and intestinal immunity
Bischoff, S. C., & Krämer, S. (2007) · Immunological Reviews · doi:10.1111/j.1600-065x.2007.00523.x · Cited by 164 · see citing works
Effect of Lactobacilli on Paracellular Permeability in the Gut
Ahrné, S., & Hagslätt, M.-L. J. (2011) · Nutrients · doi:10.3390/nu3010104 · Cited by 157 · see citing works
Microbes and the mind: emerging hallmarks of the gut microbiota-brain axis
Bauer, K. C., Huus, K. E., & Finlay, B. B. (2016) · Cellular Microbiology · doi:10.1111/cmi.12585 · Cited by 151 · see citing works
Murray, E., Sharma, R., Smith, K. B., Mar, K. D., Barve, R., Lukasik, M., Pirwani, A. F., Malette-Guyon, E., Lamba, S., Thomas, B. J., et al. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.06.016 · Cited by 150 · see citing works
The Microbiome-Gut-Brain Axis and Resilience to Developing Anxiety or Depression under Stress
Bear, T., Dalziel, J. E., Coad, J., Roy, N. C., Butts, C. A., & Gopal, P. K. (2021) · Microorganisms · doi:10.3390/microorganisms9040723 · Cited by 132 · see citing works
Zheng, P.-Y., Feng, B.-S., Oluwole, C., Struiksma, S., Chen, X., Li, P., Tang, S.-G., & Yang, P.-C. (2009) · Gut · doi:10.1136/gut.2009.181701 · Cited by 129 · see citing works
Kiank, C., Zeden, J.-P., Drude, S., Domańska, G., Fusch, G., Otten, W., & Schuett, C. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011825 · Cited by 123 · see citing works
Role of Corticotropin-releasing Factor in Gastrointestinal Permeability
Rodiño‐Janeiro, B. K., Alonso, C., Pigrau, M., Lobo, B., Vicario, M., & Santos, J. (2014) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm14084 · Cited by 119 · see citing works
Lee, H., Park, J. H., Park, D. I., Kim, H. J., Cho, Y. K., Sohn, C. I., Jeon, W. K., Kim, B. I., & Chae, S. W. (2013) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm.2013.19.2.244 · Cited by 119 · see citing works
Gut microbial communities modulating brain development and function
Al‐Asmakh, M., Anuar, F., Zadjali, F., Rafter, J. J., & Pettersson, S. (2012) · Gut Microbes · doi:10.4161/gmic.21287 · Cited by 117 · see citing works
The Role of Psychological Stress in Inflammatory Bowel Disease
Mawdsley, J. E. D., & Rampton, D. S. (2006) · NeuroImmunoModulation · doi:10.1159/000104861 · Cited by 116 · see citing works
Wang, H. (2012) · World Journal of Gastroenterology · doi:10.3748/wjg.v18.i18.2180 · Cited by 111 · see citing works
Ponferrada, Á., Caso, J. R., Alou, L., Rodríguez, A. C., Sevillano, D., Moro, M. Á., Lizasoaín, I., Menchén, P. L., Gómez-Lus, M. L., Lorenzo, P. L., et al. (2007) · Gastroenterology · doi:10.1053/j.gastro.2007.02.032 · Cited by 111 · see citing works
Mujagic, Z., Ludidi, S., Keszthelyi, D., Hesselink, M., Kruimel, J. W., Lenaerts, K., Hanssen, N. M. J., Conchillo, J. M., Jonkers, D. M. A. E., & Masclee, A. (2014) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.12829 · Cited by 108 · see citing works
Role of Gut Microbiota in Neurological Disorders and Its Therapeutic Significance
Tiwari, P., Dwivedi, R., Bansal, M., Tripathi, M., & Dada, R. (2023) · Journal of Clinical Medicine · doi:10.3390/jcm12041650 · Cited by 106 · see citing works
Montagnani, M., Bottalico, L., Potenza, M. A., Charitos, I. A., Topi, S., Colella, M., & Santacroce, L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210322 · Cited by 106 · see citing works
Mucosal pathogenesis in gastro‐esophageal reflux disease
Ustaoglu, A., Nguyen, A. D., Spechler, S. J., Sifrim, D. A., Souza, R. F., & Woodland, P. J. (2020) · Neurogastroenterology & Motility · doi:10.1111/nmo.14022 · Cited by 105 · see citing works
Mast cell mediation of visceral sensation and permeability in irritable bowel syndrome
Hasler, W. L., Grabauskas, G., Singh, P., & Owyang, C. (2022) · Neurogastroenterology & Motility · doi:10.1111/nmo.14339 · Cited by 105 · see citing works
Interferon-γ Regulation of Intestinal Epithelial Permeability
Beaurepaire, C., Smyth, D. R., & McKay, D. M. (2009) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2008.0057 · Cited by 102 · see citing works
Epigenetics in depression and gut-brain axis: A molecular crosstalk
Begum, N., Mandhare, A., Tryphena, K. P., Srivastava, S., Shaikh, M. F., Singh, S. B., & Khatri, D. K. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1048333 · Cited by 99 · see citing works
Langhorst, J., Mueller, T., Luedtke, R., Franken, U., Paul, A., Michalsen, A., Schedlowski, M., Dobos, G. J., & Elsenbruch, S. (2007) · Scandinavian Journal of Gastroenterology · doi:10.1080/00365520601101682 · Cited by 94 · see citing works
Intestinal barrier dysfunction in severe burn injury
He, W., Wang, Y., Wang, P., & Wang, F. (2019) · Burns & Trauma · doi:10.1186/s41038-019-0162-3 · Cited by 93 · see citing works
Stress-Related Alterations of Visceral Sensation: Animal Models for Irritable Bowel Syndrome Study
Larauche, M. H., Mulak, A., & Taché, Y. (2011) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm.2011.17.3.213 · Cited by 92 · see citing works
Elevated circulating miR-150 and miR-342-3p in patients with irritable bowel syndrome
Fourie, N. H., Peace, R. M., Abey, S. K., Sherwin, L. B., Rahim-Williams, B., Smyser, P. A., Wiley, J. W., & Henderson, W. A. (2014) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2014.04.009 · Cited by 91 · see citing works
Mast cells in gastrointestinal disorders
Bischoff, S. C. (2016) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2016.02.018 · Cited by 84 · see citing works
Pigrau, M., Rodiño‐Janeiro, B. K., Casado‐Bedmar, M., Lobo, B., Vicario, M., Santos, J., & Alonso, C. (2015) · Neurogastroenterology & Motility · doi:10.1111/nmo.12717 · Cited by 79 · see citing works
Sato, H., Zhang, L. S., Martinez, K., Chang, E. B., Yang, Q., Wang, F., Howles, P. N., Hokari, R., Miura, S., & Tso, P. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.07.009 · Cited by 75 · see citing works
Alonso, C., Guilarte, M., Vicario, M., Ramos, L., Rezzi, S., Martínez, C., Lobo, B., Martin, F., Pigrau, M., González-Castro, A. M., et al. (2012) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2012.01928.x · Cited by 72 · see citing works
Role of probiotics in correcting abnormalities of colonic flora induced by stress: Figure 1
Eutamène, H., & Bueno, L. P. (2007) · Gut · doi:10.1136/gut.2007.124040 · Cited by 72 · see citing works
Chronic Stress, Inflammation, and Colon Cancer: A CRH System-Driven Molecular Crosstalk
Baritaki, S., de Bree, E., Chatzaki, Ε., & Pothoulakis, C. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8101669 · Cited by 67 · see citing works
Management of stress in inflammatory bowel disease: a therapeutic option?
Goodhand, J., Wahed, M., & Rampton, D. S. (2009) · Expert Review of Gastroenterology & Hepatology · doi:10.1586/egh.09.55 · Cited by 56 · see citing works
Gut Microbiome and Modulation of <scp>CNS</scp> Function
Osadchiy, V., Martin, C. R., & Mayer, E. A. (2019) · Comprehensive Physiology · doi:10.1002/cphy.c180031 · Cited by 53 · see citing works
Clerici, L., Bottari, D., & Bottari, B. (2025) · Current Nutrition Reports · doi:10.1007/s13668-025-00619-2 · Cited by 53 · see citing works
Söderholm, J. D. (2009) · Digestive Diseases · doi:10.1159/000268133 · Cited by 52 · see citing works
Zoppi, S., Madrigal, J. L. M., Perez‐Nievas, B. G., Marín‐Jiménez, I., Caso, J. R., Alou, L., García‐Bueno, B., Colón, A., Manzanares, J., Gómez-Lus, M. L., et al. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00158.2011 · Cited by 52 · see citing works
Psychological stress reactivates dextran sulfate sodium-induced chronic colitis in mice
Melgar, S., Engström, K., Jägervall, Å., & Martı́nez, V. (2008) · Stress · doi:10.1080/10253890701820166 · Cited by 49 · see citing works
Yan, R., Ho, C., & Zhang, X. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000187 · Cited by 49 · see citing works
Present and Future Therapeutic Approaches to Barrier Dysfunction
Fortea, M., Albert-Bayo, M., Abril-Gil, M., Mall, J. G., Serra-Ruiz, X., Henao-Paez, A., Expósito, E., González-Castro, A. M., Guagnozzi, D., Lobo, B., et al. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.718093 · Cited by 48 · see citing works
Subacute stress and chronic stress interact to decrease intestinal barrier function in rats
Lauffer, A., Vanuytsel, T., Vanormelingen, C., Vanheel, H., Rasoel, S. S., Tóth, J. G., Tack, J. F., Fornari, F., & Farré, R. (2016) · Stress · doi:10.3109/10253890.2016.1154527 · Cited by 47 · see citing works
Stress and Chronic Pelvic Pain
Pierce, A. N., & Christianson, J. A. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2014.11.009 · Cited by 47 · see citing works
The Brain-Gut Axis: A Target for Treating Stress-Related Disorders
Scott, L. V., Clarke, G. A., & Dinan, T. G. (2013) · Modern trends in psychiatry · doi:10.1159/000343971 · Cited by 46 · see citing works
Evaluation of two laboratory model methods for diarrheal irritable bowel syndrome
Chen, Q., Zhang, H., Sun, C., He, Q., Zhang, R.-R., Luo, B.-F., Zhou, Z., & Chen, X. (2023) · Molecular Medicine · doi:10.1186/s10020-022-00599-x · Cited by 41 · see citing works
Wen, Z., Du, M., Tang, Z., Zhou, T.-Y., Zhang, Z., Song, H., Xiang, X., & Han, X. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20225727 · Cited by 40 · see citing works
Intestinal barrier in chronic gut and liver diseases: Pathogenesis and therapeutic targets
Zhang, Y., Liu, Y., Liang, X., Wen, Y., Zhao, J., He, Y., Xie, Q., & Xie, C. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.08.028 · Cited by 37 · see citing works
Enteric Microbiota–Gut–Brain Axis from the Perspective of Nuclear Receptors
Duszka, K., & Wahli, W. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19082210 · Cited by 37 · see citing works
Xu, L., Zhang, C., He, D., Jiang, N., Bai, Y., & Xin, Y. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.117747 · Cited by 35 · see citing works
Demaude, J., Levêque, M., Chaumaz, G., Eutamène, H., Fioramonti, J., Bueno, L. P., & Ferrier, L. (2009) · Life Sciences · doi:10.1016/j.lfs.2009.03.016 · Cited by 33 · see citing works
Self-citationA gut (microbiome) feeling about addiction: Interactions with stress and social systems
García‐Cabrerizo, R., & Cryan, J. F. (2024) · Neurobiology of Stress · doi:10.1016/j.ynstr.2024.100629 · Cited by 30 · see citing works
Psychological stress‐induced colonic barrier dysfunction: Role of immune‐mediated mechanisms
Hattay, P., Prusator, D. K., Tran, L., & Meerveld, B. G. (2017) · Neurogastroenterology & Motility · doi:10.1111/nmo.13043 · Cited by 30 · see citing works
Peripheral relays in stress-induced activation of visceral afferents in the gut
van den Wijngaard, R. M., Klooker, T. K., de Jonge, W. J., & Boeckxstaens, G. E. (2009) · Autonomic Neuroscience · doi:10.1016/j.autneu.2009.07.004 · Cited by 30 · see citing works
Guilarte, M., Vicario, M., Martínez, C., de Torres, I. M., Lobo, B., Pigrau, M., González-Castro, A. M., Rodiño‐Janeiro, B. K., Salvo‐Romero, E., Fortea, M., et al. (2020) · The American Journal of Gastroenterology · doi:10.14309/ajg.0000000000000789 · Cited by 29 · see citing works
The Role of Nutritional Factors and Intestinal Microbiota in Rheumatoid Arthritis Development
Alpizar-Rodriguez, D., Finckh, A., & Gilbert, B. T. P. (2020) · Nutrients · doi:10.3390/nu13010096 · Cited by 28 · see citing works
Role of Stress on Driving the Intestinal Paracellular Permeability
Molotla‐Torres, D. E., Guzmán‐Mejía, F., Godínez‐Victoria, M., & Drago-Serrano, M. E. (2023) · Current Issues in Molecular Biology · doi:10.3390/cimb45110581 · Cited by 26 · see citing works
Stress-related changes in oesophageal permeability: filling the gaps of GORD?: Figure 1
Söderholm, J. D. (2007) · Gut · doi:10.1136/gut.2007.120691 · Cited by 25 · see citing works
Lyte, J. M., Eckenberger, J., Keane, J., Robinson, K., Bacon, T., Assumpcao, A. L. F. V., Donoghue, A. M., Liyanage, R., Daniels, K. M., Caputi, V., et al. (2024) · Poultry Science · doi:10.1016/j.psj.2023.103393 · Cited by 25 · see citing works
Ferrier, L. (2007) · Gut · doi:10.1136/gut.2007.129841 · Cited by 25 · see citing works
Possible Roles of Cyclic Meditation in Regulation of the Gut-Brain Axis
Ningthoujam, D. S., Singh, N., & Mukherjee, S. (2021) · Frontiers in Psychology · doi:10.3389/fpsyg.2021.768031 · Cited by 24 · see citing works
Paschos, K. A., Kolios, G. C., & Chatzaki, Ε. (2009) · Drug Discovery Today · doi:10.1016/j.drudis.2009.04.002 · Cited by 24 · see citing works
Ferrier, L., Gal, C. S., Schulte, A. M., Vasina, V. I., Gaultier, E., Schroedel, S., Ursino, M. G., Chaumaz, G., Pascal, M., Ponti, F. D., et al. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00022.2010 · Cited by 23 · see citing works
Innate Immune Factors in the Development and Maintenance of Pouchitis
Landy, J., Al-Hassi, H. O., Ronde, E., English, N. R., Mann, E. R., Bernardo, D., Ciclitira, P. J., Clark, S. K., Knight, S. C., & Hart, A. L. (2014) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000182 · Cited by 23 · see citing works
Novel Mechanisms and Therapeutic Targets for Ischemic Stroke: A Focus on Gut Microbiota
Bao, Z., Zhang, Z., Zhou, G., Zhang, A., Shao, A., & Zhou, F. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.871720 · Cited by 22 · see citing works
Bodo, C. R., Sălcudean, A., Nirestean, A. P., Lukács, E., Lica, M. M., Muntean, D.-L., Anculia, R. C., Popovici, R. A., Neda-Stepan, O., ENĂTESCU, V. R., et al. (2024) · Children · doi:10.3390/children11060699 · Cited by 20 · see citing works
The role and therapeutic potential of gut microbiome in severe burn
Huang, Z., Huang, Y., Chen, J., Tang, Z., Chen, Y., Liu, H., Huang, M., Qing, L., Li, L., Wang, Q. L., et al. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.974259 · Cited by 19 · see citing works
Sensory Phenotype of the Oesophageal Mucosa in Gastro-Oesophageal Reflux Disease
Ustaoglu, A., & Woodland, P. J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032502 · Cited by 18 · see citing works
Noninflammatory Gluten Peptide Analogs as Biomarkers for Celiac Sprue
Bethune, M. T., Crespo-Bosque, M., Bergseng, E., Mazumdar, K., Doyle, L. A., Sestak, K., Sollid, L. M., & Khosla, C. (2009) · Chemistry & Biology · doi:10.1016/j.chembiol.2009.07.009 · Cited by 18 · see citing works
Cotoia, A., Charitos, I. A., Corriero, A., Tamburrano, S., & Cinnella, G. (2024) · Nutrients · doi:10.3390/nu16244359 · Cited by 17 · see citing works
Yvon, S., Beaumont, M., Dayonnet, A., Eutamène, H., Lambert, W., Tondereau, V., Chalvon‐Demersay, T., Belloir, P., & Paës, C. (2024) · Scientific Reports · doi:10.1038/s41598-023-50852-4 · Cited by 15 · see citing works
Stress-induced breakdown of intestinal barrier function in the rat: Reversal by wood creosote
Kuge, T., Meerveld, B. G., & Sokabe, M. (2006) · Life Sciences · doi:10.1016/j.lfs.2006.03.002 · Cited by 15 · see citing works
Ultrastructure of intestinal mucosa in diarrhea-predominant irritable bowel syndrome
Zhao, D.-Y., Qi, Q. ‐., Long, X., Li, X., Chen, F.-X., Yu, Y.-B., & Zuo, X.-L. (2019) · Physiology International · doi:10.1556/2060.106.2019.20 · Cited by 14 · see citing works
Gut Microorganisms and Neurological Disease Perspectives
Faruqui, N. A., Prium, D. H., Mowna, S. A., Ullah, M. A., Araf, Y., Sarkar, B., Zohora, U. S., & Rahman, M. S. (2021) · Future Neurology · doi:10.2217/fnl-2020-0026 · Cited by 14 · see citing works
Occludin and hydromineral balance inXenopus laevis
Chasiotis, H., & Kelly, S. P. (2008) · Journal of Experimental Biology · doi:10.1242/jeb.022822 · Cited by 14 · see citing works
Mechanisms of the effect of gut microbes on depression through the microbiota-gut-brain axis
Zhou, X., Wang, S., Wang, X., Chen, X., Zhou, P., Ma, K., & Zhang, P. (2025) · Frontiers in Nutrition · doi:10.3389/fnut.2025.1634548 · Cited by 13 · see citing works
Karailiev, P., Hlaváčová, N., Chmelová, M., Homer, N. Z. M., & Ježová, D. (2021) · Neurogastroenterology & Motility · doi:10.1111/nmo.14084 · Cited by 13 · see citing works
Asano, T., & Takenaga, M. (2017) · Journal of Clinical Medicine · doi:10.3390/jcm6110104 · Cited by 12 · see citing works
- Authors
- Demaude, J.
- Affiliations
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
- Corresponding author
- Demaude, J
- Venue
- Gut
- Publisher
- BMJ
- Published
- 2006-05-01
- Volume
- 55
- Issue
- 5
- Pages
- 655-661
- ISSN
- 0017-5749 (ISSN-L)
- PMC
- PMC1856132
- OpenAlex
- W2119510464
- Cited by
- 167
- References
- 47
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 8 · 2023: 13 · 2022: 12 · 2021: 12 · 2020: 9 · 2019: 7 · 2018: 7 · 2017: 6 · 2016: 7 · 2015: 6 · 2014: 7 · 2013: 3 · 2012: 12
- FWCI
- 4.36
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gut (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Institut National de la Santé et de la Recherche Médicale
- Institut National de la Recherche Agronomique
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
- Keywords
- acute stress, mast cell activation, mast cell degranulation, tight junction proteins, ZO-2, occludin, interferon-gamma, doxantrazole, paracellular permeability, protein kinase C zeta, alkaline phosphatase, irritable bowel disease, inflammatory bowel disease
- MeSH terms
- Alkaline Phosphatase, Animals, Cell Differentiation, Cell Membrane Permeability, Colon, Epithelial Cells, Interferon-gamma, Intestinal Mucosa, Male, Mast Cells, Membrane Proteins, Mice, Inbred Strains, Phosphorylation, Protein Kinase C, Stress, Psychological, Time Factors, Cell Degranulation, Mice, Knockout, Myosin Light Chains, Tight Junctions, Reverse Transcriptase Polymerase Chain Reaction, Microscopy, Electron, Transmission, Mice, Occludin, Zonula Occludens-2 Protein
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