Stress impairs murine intestinal barrier function: improvement by glucagon-like peptide-2

Increased rectal mucosal enteroendocrine cells, T lymphocytes, and increased gut permeability following acute <i>Campylobacter</i> enteritis and in post-dysenteric irritable bowel syndrome

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

Induction of intestinal epithelial proliferation by glucagon-like peptide 2.

Drucker, D. J., Erlich, P., Asa, S. L., & Brubaker, P. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.15.7911 · Cited by 880 · see citing works

The neurobiology of stress and gastrointestinal disease

MAYER, E. A. (2000) · Gut · doi:10.1136/gut.47.6.861 · Cited by 666 · 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

Biological actions and therapeutic potential of the glucagon-like peptides

Drucker, D. J. (2002) · Gastroenterology · doi:10.1053/gast.2002.31068 · Cited by 500 · see citing works

Stress and the gastrointestinal tract

Bhatia, V., & Tandon, R. (2005) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.2004.03508.x · Cited by 486 · 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

Chronic stress induces mast cell-dependent bacterial adherence and initiates mucosal inflammation in rat intestine

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

Enteroendocrine localization of GLP-2 receptor expression in humans and rodents

Yusta, B., Huang, L., Munroe, D. G., Wolff, G., Fantaske, R. P., Sharma, S., Demchyshyn, L. L., Asa, S. L., & Drucker, D. J. (2000) · Gastroenterology · doi:10.1053/gast.2000.16489 · Cited by 339 · see citing works

Modulation of specific intestinal epithelial progenitors by enteric neurons

Bjerknes, M., & Cheng, H. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211278098 · Cited by 325 · see citing works

Intestinal growth-promoting properties of glucagon-like peptide-2 in mice

Tsai, C. H., Hill, M., Asa, S. L., Brubaker, P. L., & Drucker, D. J. (1997) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1997.273.1.e77 · Cited by 319 · see citing works

Mitochondrial damage: a possible mechanism of the “topical” phase of NSAID induced injury to the rat intestine

Somasundaram, S. G., Rafi, S., Hayllar, J. S., Sigthorsson, G., Jacob, M., Price, A. B., Macpherson, A. J., Mahmod, T., Scott, D. L., Wrigglesworth, J. M., et al. (1997) · Gut · doi:10.1136/gut.41.3.344 · Cited by 314 · 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

Glucagon-like peptide-2 enhances intestinal epithelial barrier function of both transcellular and paracellular pathways in the mouse

Benjamin, M. A., McKay, D. M., Yang, P.-C., Cameron, H. L., & Perdue, M. H. (2000) · Gut · doi:10.1136/gut.47.1.112 · Cited by 277 · see citing works

IV. Modulation of intestinal inflammation by stress: basic mechanisms and clinical relevance

Collins, S. M. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.3.g315 · Cited by 224 · 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

Chronic stress impairs rat growth and jejunal epithelial barrier function: role of mast cells

Santos, J., Benjamin, M. A., Yang, P., Prior, T., & Perdue, M. H. (2000) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2000.278.6.g847 · Cited by 205 · see citing works

Epithelial permeability to proteins in the noninflamed ileum of Crohn's disease?

Söderholm, J. D., Peterson, K. H., Olaison, G., Franzén, L., Weström, B. R., Magnusson, K., & Sjödahl, R. I. (1999) · Gastroenterology · doi:10.1016/s0016-5085(99)70551-2 · Cited by 201 · see citing works

Physical and Psychological Stress in Rats Enhances Colonic Epithelial Permeability via Peripheral CRH

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

Glucagon-like peptide 2 decreases mortality and reduces the severity of indomethacin-induced murine enteritis

Boushey, R. P., Yusta, B., & Drucker, D. J. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.277.5.e937 · Cited by 179 · see citing works

Effects of temperature on slow and fast inactivation of rat skeletal muscle Na⁺channels

Ruff, R. L. (1999) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1999.277.5.c937 · Cited by 128 · 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

Treatment of inflammatory bowel disease in a rodent model with the intestinal growth factor glucagon-like peptide-2

Alavi, K., Schwartz, M. Z., Palazzo, J., & Prasad, R. (2000) · Journal of Pediatric Surgery · doi:10.1053/jpsu.2000.6861 · Cited by 110 · see citing works

Colonic mucin release in response to immobilization stress is mast cell dependent

Castagliuolo, I., Wershil, B. K., Karalis, K. P., Pasha, A., Nikulásson, S. Þ., & Pothoulakis, C. (1998) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.1998.274.6.g1094 · Cited by 102 · see citing works

Role of Bacterial Adherence and the Mucus Barrier on Bacterial Translocation

Katayama, M., Xu, D.-Z., Specian, R. D., & Deitch, E. A. (1997) · Annals of Surgery · doi:10.1097/00000658-199703000-00012 · Cited by 102 · see citing works

An alternate pathway of cAMP-stimulated Cl− secretion across the NKCC1-null murine duodenum

Walker, N. M., Flagella, M., Gawenis, L. R., Shull, G. E., & Clarke, L. L. (2002) · Gastroenterology · doi:10.1053/gast.2002.34757 · Cited by 100 · see citing works

Effect of stress on the paracellular barrier in the rat ileum

Mazzon, E., Sturniolo, G. C., Puzzolo, D., Frisina, N., & Fries, W. (2002) · Gut · doi:10.1136/gut.51.4.507 · Cited by 86 · see citing works

Glucagon-like peptide-2-enhanced barrier function reduces pathophysiology in a model of food allergy

Cameron, H. L., Yang, P., & Perdue, M. H. (2003) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00231.2002 · Cited by 74 · see citing works

The effect of glucagon-like peptide 2 on intestinal permeability and bacterial translocation in acute necrotizing pancreatitis

Kouris, G. J., Liu, Q., Rossi, H., et al. (2001) · The American Journal of Surgery · doi:10.1016/s0002-9610(01)00635-3 · Cited by 70 · see citing works

Inhibition of polyamine synthesis influences contractility of intestinal smooth muscle in culture

Swärd, K., Nilsson, B., & Hellstrand, P. (1997) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1997.273.1.c77 · Cited by 65 · see citing works

Psychosocial Aspects of Crohn's Disease

Ringel, Y., & Drossman, D. A. (2001) · Surgical Clinics of North America · doi:10.1016/s0039-6109(05)70283-8 · Cited by 61 · see citing works

Review: Abnormal Intestinal Permeability in Crohn's Disease: A Possible Pathogenic Factor

Olaison, G., Sjödahl, R. I., & Tagesson, C. (1990) · Scandinavian Journal of Gastroenterology · doi:10.3109/00365529009095493 · Cited by 52 · see citing works

Intestinal permeability in patients with Crohn's disease.

Meddings, J. B., Sutherland, L. R., & May, G. R. (1994) · Gut · doi:10.1136/gut.35.11.1675-b · Cited by 23 · see citing works

Cancer risk in patients treated surgically for duodenal ulcer.

CAYGILL, C. P. J., & Hill, M. J. (1994) · Gut · doi:10.1136/gut.35.11.1675 · Cited by 6 · see citing works

Changes in gut microbiota control inflammation in obese mice through a mechanism involving GLP-2-driven improvement of gut permeability

Cani, P. D., Possemiers, S., Van de Wiele, T., Guiot, Y., Everard, A., Rottier, O., Geurts, L., Naslain, D., Neyrinck, A., Lambert, D. M., et al. (2009) · Gut · doi:10.1136/gut.2008.165886 · Cited by 2,518 · see citing works

Bacterial infection causes stress-induced memory dysfunction in mice

Gareau, M. G., Wine, E., Rodrigues, D. M., Cho, J. H., Whary, M. T., Philpott, D. J., MacQueen, G., & Sherman, P. M. (2011) · Gut · doi:10.1136/gut.2009.202515 · Cited by 909 · see citing works

Stress-induced gastrointestinal barrier dysfunction and its inflammatory effects1

Lambert, G. P. (2009) · Journal of Animal Science · doi:10.2527/jas.2008-1339 · Cited by 529 · see citing works

Signalling cognition: The gut microbiota and hypothalamic-pituitary-adrenal axis

Rusch, J. A., Layden, B. T., & Dugas, L. R. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1130689 · Cited by 415 · see citing works

Microbiota-gut-brain axis and cognitive function

Gareau, M. G. (2014) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4939-0897-4_16 · Cited by 189 · see citing works

Synergy between Lactobacillus paracasei and its bacterial products to counteract stress-induced gut permeability and sensitivity increase in rats

Eutamene, H., Lamine, F., Chabo, C., Theodorou, V., Rochat, F., Bergonzelli, G. E., Corthésy-Theulaz, I., Fioramonti, J., & Bueno, L. (2007) · The Journal of Nutrition · doi:10.1093/jn/137.8.1901 · Cited by 169 · see citing works

Stress-induced corticotropin-releasing hormone-mediated NLRP6 inflammasome inhibition and transmissible enteritis in mice

Sun, Y., Zhang, M., Chen, C., Gillilland, M., Sun, X., El–Zaatari, M., Huffnagle, G. B., Young, V. B., Zhang, J., Hong, S., et al. (2013) · Gastroenterology · doi:10.1053/j.gastro.2013.02.038 · Cited by 157 · see citing works

Chronic peripheral administration of corticotropin-releasing factor causes colonic barrier dysfunction similar to psychological stress

Teitelbaum, A. A., Gareau, M. G., Jury, J., Yang, P. C., & Perdue, M. H. (2008) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.90210.2008 · Cited by 116 · see citing works

The contributing role of the intestinal microbiota in stressor-induced increases in susceptibility to enteric infection and systemic immunomodulation

Bailey, M. T. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.02.006 · Cited by 69 · see citing works

Glucagon-like peptide-2 modulates neurally evoked mucosal chloride secretion in guinea pig small intestine in vitro

Baldassano, S., Liu, S., Qu, M.-H., Mulè, F., & Wood, J. D. (2009) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00170.2009 · Cited by 56 · see citing works

Bile acid mediated effects on gut integrity and performance of early weaned piglets

de Diego-Cabero, N., Mereu, A., Menoyo, D., Holst, J. J., & Ipharraguerre, I. R. (2015) · BMC Veterinary Research · doi:10.1186/s12917-015-0425-6 · Cited by 35 · see citing works

136 Intestinal Barrier Function: Physiological Regulation, Injury, and Repair in Horses and Swine

Blikslager, A. T. (2022) · Journal of Animal Science · doi:10.1093/jas/skac247.125 · Cited by 1 · see citing works

Interleukin‐18 disrupts tight junctions in gastric and intestinal epithelial monolayers

Lapointe, T. K., Hirota, C. L., Ménard, D., et al. (2010) · The FASEB Journal · doi:10.1096/fasebj.24.1_supplement.348.6 · Cited by 1 · see citing works

Lactobacillus plantarum MB452 enhances the function of the intestinal barrier by increasing the expression levels of genes involved in tight junction formation

Anderson, R. C., Cookson, A. L., McNabb, W. C., Park, Z., McCann, M. J., Kelly, W. J., & Roy, N. C. (2010) · BMC Microbiology · doi:10.1186/1471-2180-10-316 · Cited by 510 · see citing works

Claudin-1 decrease impacts epidermal barrier function in atopic dermatitis lesions dose-dependently

Bergmann, S., von Buenau, B., Vidal‐y‐Sy, S., Haftek, M., Wladykowski, E., Houdek, P., Lezius, S., Duplan, H., Bäsler, K., Dähnhardt‐Pfeiffer, S., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-58718-9 · Cited by 137 · see citing works

MiR-34c and PlncRNA1 mediated the function of intestinal epithelial barrier by regulating tight junction proteins in inflammatory bowel disease

Chen, T., Xue, H., Lin, R., et al. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.01.115 · Cited by 62 · see citing works