Cited by 134Pancreatitis Pathology and TreatmentGastrointestinal motility and disordersGallbladder and Bile Duct Disorders

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Interdigestive small bowel motility and duodenal bacterial overgrowth in experimental acute pancreatitis

Van felius, I. D., Akkermans, L. M. A., Bosscha, K., Verheem, A., Harmsen, W., Visser, M. R., Gooszen, H. G.·2003·Neurogastroenterology & Motility

DOI 10.1046/j.1365-2982.2003.00410.x

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Abstract

Abstract The objective of this study is to investigate the effects of an acute necrotizing pancreatitis (ANP), without biliary obstruction, on the migrating motor complex (MMC), small bowel bacterial overgrowth (SBBO), bacterial translocation (BT) and infection of the pancreas simultaneously. Rats were divided into four groups: mild pancreatitis, control, ANP and sham operated control. Jejunal myoelectrodes were used to measure MMCs. Blood, peritoneal fluid, bile, and abdominal organs were harvested for microbial culturing 72 h after induction of pancreatitis. The splenic portion of the pancreas was taken for histology. During ANP the MMC cycle length was significantly increased from 14.1 ± 0.2 to 22.4 ± 1.9 min (P < 0.05). The duodenum of ANP rats was in contrast with the other groups characterized by Enterobacteriacae (> 3 log 10 CFU g −1 in seven of 12 rats, P < 0.05). A positive correlation (r = 0.78, P < 0.01) existed between duodenal Gram‐negative and anaerobic flora and the MMC cycle. Correlation between MMC cycle length and BT to the pancreas was positive as well (r = 0.70, P < 0.01). A positive correlation (r = 0.85, P < 0.01) was found between the severity of pancreatitis and duodenal bacterial overgrowth. During ANP without biliary obstruction, the jejunal MMC is disturbed and consequently SBBO occurs. The correlation between the severity of pancreatitis, the disturbance of the MMC and SBBO suggests an important pathophysiological role of the proximal small bowel in the infection of pancreatic necrosis.

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A Better Model of Acute Pancreatitis for Evaluating Therapy
Schmidt, J., Rattner, D. W., Lewandrowski, K. B., Compton, C. C., Mandavilli, U., Knoefel, W. T., & Warshaw, A. L. (1992) · Annals of Surgery · doi:10.1097/00000658-199201000-00007 · Cited by 873
A migrating electric complex of canine small intestine
Szurszewski, J. (1969) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1969.217.6.1757 · Cited by 848
The interdigestive motor complex of normal subjects and patients with bacterial overgrowth of the small intestine
Vantrappen, G., Janssens, J., Hellemans, J., & Ghoos, Y. (1977) · Journal of Clinical Investigation · doi:10.1172/jci108740 · Cited by 815
Compared with parenteral nutrition, enteral feeding attenuates the acute phase response and improves disease severity in acute pancreatitis
Windsor, A. C. J., Kanwar, S. S., Li, A. G. K., Barnes, E. J., Guthrie, J. A., Spark, J. I., Welsh, F. K. S., Guillou, P. J., & Reynolds, J. V. (1998) · Gut · doi:10.1136/gut.42.3.431 · Cited by 680
Enteral nutrition is superior to parenteral nutrition in severe acute pancreatitis: Results of a randomized prospective trial
Kalfarentzos, F. E., Kehagias, J., Mead, N., Kokkinis, K., & Gogos, C. A. (1997) · British journal of surgery · doi:10.1046/j.1365-2168.1997.02851.x · Cited by 627
Human interdigestive motility: variations in patterns from esophagus to colon.
Kellow, J., Borody, T., Phillips, S., Tucker, R., & Haddad, A. (1986) · Gastroenterology · doi:10.1016/0016-5085(86)90573-1 · Cited by 397
Influence of microbial species on small intestinal myoelectric activity and transit in germ-free rats
Husebye, E., Hellström, P. M., Sundler, F., Chen, J., & Midtvedt, T. (2001) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.2001.280.3.g368 · Cited by 319
Electrical Spiking Activity and Propulsion in Small Intestine in Fed and Fasted Rats
Ruckebusch, M., & Fioramonti, J. (1975) · Gastroenterology · doi:10.1016/s0016-5085(75)80138-7 · Cited by 273
The role of infection in acute pancreatitis
Schmid, S. W., Uhl, W., Frieß, H., Malfertheiner, P., & Büchler, M. W. (1999) · Gut · doi:10.1136/gut.45.2.311 · Cited by 226
The role of the gut in the development of sepsis in acute pancreatitis
Runkel, N. S. F., Moody, F. G., Smith, G. S., Rodriguez, L. F., LaRocco, M., & Miller, T. A. (1991) · Journal of Surgical Research · doi:10.1016/0022-4804(91)90064-s · Cited by 220

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Experimental pancreatitis disturbs gastrointestinal and colonic motility in mice: effect of the prokinetic agent tegaserod
Seerden, T. C. J., Man, J. G. D., Holzer, P. D., den Bossche, R. M. V., Herman, A. G., Pelckmans, P. A., & Winter, B. Y. D. (2007) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2007.00968.x · Cited by 21
Damage of the interstitial cells of Cajal and myenteric neurons causing ileus in acute necrotizing pancreatitis rats
Zhou, H., Liu, L., Bai, Y., Wu, W., Li, G., Li, J., Zou, D., Gao, J., & Li, Z. (2010) · Surgery · doi:10.1016/j.surg.2010.04.023 · Cited by 22
Current status of diagnosis and Mesenchymal stem cells therapy for acute pancreatitis
Munir, F., Jamshed, M. B., Shahid, N., Muhammad, S. A., Ghanem, N. B., & Qiyu, Z. (2019) · Physiological Reports · doi:10.14814/phy2.14170 · Cited by 18
Association between acute pancreatitis and small intestinal bacterial overgrowth assessed by hydrogen breath test
Zhang, M., Zhu, H., He, F., Li, B.-Y., & Li, X. (2017) · World Journal of Gastroenterology · doi:10.3748/wjg.v23.i48.8591 · Cited by 18
Impact of Global Fxr Deficiency on Experimental Acute Pancreatitis and Genetic Variation in the FXR Locus in Human Acute Pancreatitis
Nijmeijer, R. M., Schaap, F. G., Smits, A. J. J., Kremer, A. E., Akkermans, L. M. A., Kroese, A. B. A., Rijkers, G. T., Schipper, M. E. I., Verheem, A., Wijmenga, C., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114393 · Cited by 17
Self-citation
Infected pancreatic necrosis—Current trends in management
Shah, J., Viesca, M. F. Y., Jagodzinski, R., & Arvanitakis, M. (2024) · Indian Journal of Gastroenterology · doi:10.1007/s12664-023-01506-w · Cited by 16
Octreotide Ameliorates Intestinal Dysmotility by Interstitial Cells of Cajal Protection in a Rat Acute Necrotizing Pancreatitis Model
Zhou, H., Gao, J., Wu, W., Liu, L., Wei, L., Zou, D., & Li, Z. (2011) · Pancreas · doi:10.1097/mpa.0b013e318220afab · Cited by 16
Small intestinal motility
Smout, A. J. P. M. (2004) · Current Opinion in Gastroenterology · doi:10.1097/00001574-200403000-00005 · Cited by 16
Migrating motor complex in biological sciences: characterization, animal models and disturbances.
Romański, K. W. (2009) · PubMed · Cited by 15
Gut Microbiome and Autism: Recent Advances and Future Perspectives
Liu, J., Zhang, M., & Kong, X. (2016) · North American Journal of Medicine and Science · Cited by 14
Altered intestinal microflora and barrier injury in severe acute pancreatitis can be changed by zinc
Su, S., & Tang, Q. (2021) · International Journal of Medical Sciences · doi:10.7150/ijms.45980 · Cited by 14
Effects of probiotic supplementation on markers of acute pancreatitis in rats
Horst, N. L., Marques, R. G., Diestel, C. F., Matzke, B. D., Caetano, C. E. R., Simões, F. C., Andrade, A. F. B., Lobão, W. I., Vaz, L. C. A., Portela, M. C., et al. (2009) · Current Therapeutic Research · doi:10.1016/j.curtheres.2009.04.004 · Cited by 14
Intracoronary versus intravenous abciximab in ST-segment elevation myocardial infarction: rationale and design of the CICERO trial in patients undergoing primary percutaneous coronary intervention with thrombus aspiration
Gu, Y. L., Fokkema, M. L., Kampinga, M. A., de Smet, B. J. G. L., Tan, E. S., van den Heuvel, A. F. M., & Zijlstra, F. (2009) · Trials · doi:10.1186/1745-6215-10-90 · Cited by 14
Effects of Subtotal Colectomy on Bacterial Translocation During Experimental Acute Pancreatitis
van Minnen, L. P., Nieuwenhuijs, V. B., de Bruijn, M. T., Verheem, A., Visser, M. R., van Dijk, J. E., Akkermans, L. M. A., & Gooszen, H. G. (2005) · Pancreas · doi:10.1097/01.mpa.0000191650.24796.89 · Cited by 14
Self-citation
Missing link identified: GpBAR1 is a neuronal bile acid receptor
Keely, S. J. (2010) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2010.01528.x · Cited by 14
The impacts of acid suppression on duodenal microbiota during the early phase of severe acute pancreatitis
Ma, X., Huang, L., Huang, Z., Jiang, J., Zhao, C., Tong, H., Feng, Z., Gao, J., Liu, R., Zhang, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-77245-1 · Cited by 12
Characterization of Duodenal Microbiota in Patients with Acute Pancreatitis and Healthy Controls
Zhao, M.-Q., Cui, M.-Y., Jiang, Q.-L., Wang, J., Fan, M.-Y., & Lu, Y.-Y. (2023) · Digestive Diseases and Sciences · doi:10.1007/s10620-023-07948-8 · Cited by 11
Influence of Gut Microbiota on Behavior and Its Disturbances
Ignatova, V. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.85317 · Cited by 13
Effect of Octreotide on Enteric Motor Neurons in Experimental Acute Necrotizing Pancreatitis
Zhou, H. J., Gao, J., Zou, D., Wu, W., & Li, Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052163 · Cited by 11
Exploring the gut microbiota’s crucial role in acute pancreatitis and the novel therapeutic potential of derived extracellular vesicles
Li, Y., Li, J., Li, S., Zhou, S., Yang, J., Xu, K., & Chen, Y. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1437894 · Cited by 10
The Effects of Total Colectomy on Bacterial Translocation in a Model of Acute Pancreatitis
Şenocak, R., Yiğit, T., Kılbaş, Z., Coskun, A. K., Harlak, A., Mentes, M., Kılıç, A., Günal, A., & Kozak, O. (2013) · Indian Journal of Surgery · doi:10.1007/s12262-013-0855-y · Cited by 10
The Chinese herbal preparation Qing Yi Tang (QYT) improves intestinal myoelectrical activity and Increases intestinal transit during acute pancreatitis in Rodents
Li, Y., Sibaev, A., Zhou, M., Zhu, G., Yüce, B., & Storr, M. (2007) · Phytotherapy Research · doi:10.1002/ptr.2071 · Cited by 9
Cholesterol Crystals Enhance and Phospholipids Protect Against Pancreatitis Induced by Hydrophobic Bile Salts
van Minnen, L. P., Venneman, N. G., van Dijk, J. E., Verheem, A., Gooszen, H. G., Akkermans, L. M. A., & van Erpecum, K. J. (2006) · Pancreas · doi:10.1097/01.mpa.0000220861.78248.1f · Cited by 9
Self-citation
Enteric glial cells contribute to chronic stress-induced alterations in the intestinal microbiota and barrier in rats
Lu, T., Huang, C., Weng, R., Wang, Z., Sun, H., & Ma, X. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24899 · Cited by 9
A prospective observational study of the effect of critical illness on ultrastructural and microscopic morphology of duodenal mucosa
Liew, V. Y., Chapman, M. J., Nguyen, N. Q., Cousins, C. E., Plummer, M. P., Chapple, L. S., Abdelhamid, Y. A., Manton, N. D., Swalling, A., Sutton‐Smith, P., et al. (2016) · Critical Care and Resuscitation · doi:10.1016/s1441-2772(23)00999-7 · Cited by 8
Association between increased breath hydrogen methane concentration and prevalence of glucose intolerance in acute pancreatitis
Kim, D. B., Paik, C. N., Lee, J. M., & Kim, Y. (2019) · Journal of Breath Research · doi:10.1088/1752-7163/ab5460 · Cited by 8
Integrating metagenomics with metabolomics for gut microbiota and metabolites profiling in acute pancreatitis
Jia, Y. J., Shi, Y., Wang, J., Liu, H., Huang, Y., Wang, H., Liu, Y., & Peng, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-72057-z · Cited by 9
The intricate interplay between acute pancreatitis and small intestinal bacterial overgrowth: Unraveling the unknown
Cui, X., Guo, H., Liu, Z., Lei, Y., Wei, Y., Sun, G., Zhang, D., Hao, J., Zhang, D., & Liu, X. (2025) · Clinical Nutrition · doi:10.1016/j.clnu.2025.06.008 · Cited by 5
Involvement of interstitial cells of Cajal in experimental severe acute pancreatitis in rats
Shi, L. (2013) · World Journal of Gastroenterology · doi:10.3748/wjg.v19.i14.2179 · Cited by 5
[Potential role for probiotics in the prevention of infectious complications during acute pancreatitis].
van Santvoort, H. C., Besselink, M. G., van Minnen, L. P., Timmerman, H. M., Akkermans, L. M. A., & Gooszen, H. G. (2006) · PubMed · Cited by 5
Self-citation
Protective effect of exogenous IGF-I on the intestinal mucosal barrier in rats with severe acute pancreatitis
Wang, Y., Wang, S., Zhang, Y., & Sun, Z.-J. (2012) · World Journal of Emergency Medicine · doi:10.5847/wjem.j.issn.1920-8642.2012.03.010 · Cited by 4

Authors: Van felius, I. D., Akkermans, L. M. A., Bosscha, K., Verheem, A., Harmsen, W., Visser, M. R., & Gooszen, H. G.
Affiliations: University Medical Center Utrecht (NL)
Corresponding author: Akkermans, L. M. A.
ORCID: Bosscha, K.
Verheem, A.
Visser, M. R.
Gooszen, H. G.
Venue: Neurogastroenterology & Motility
Publisher: Wiley
Published: 2003-06
Volume: 15
Issue: 3
Pages: 267-276
ISSN: 1350-1925 (ISSN-L)
1365-2982
DOI: 10.1046/j.1365-2982.2003.00410.x
OpenAlex: W2019343717
Cited by: 134
References: 30
Citations by year: 2026: 6 · 2025: 2 · 2024: 7 · 2023: 3 · 2022: 4 · 2021: 9 · 2020: 7 · 2019: 12 · 2018: 9 · 2017: 8 · 2016: 5 · 2015: 3 · 2014: 5 · 2013: 3 · 2012: 3
FWCI: 4.47
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 3 d)
Locations: Neurogastroenterology & Motility (publishedVersion)
PubMed (publishedVersion)
Topics: Health Sciences › Medicine › Surgery › Pancreatitis Pathology and Treatment
Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Health Sciences › Medicine › Gastroenterology › Gallbladder and Bile Duct Disorders
Keywords: acute necrotizing pancreatitis, migrating motor complex, small intestinal bacterial overgrowth, bacterial translocation, jejunal motility, Enterobacteriaceae, pancreatitis severity
MeSH terms: Animals, Ascitic Fluid, Bile, Blood, Gastrointestinal Motility, Intestine, Small, Male, Pancreas, Myoelectric Complex, Migrating, Bacterial Translocation, Pancreatitis, Acute Necrotizing, Models, Animal, Rats

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Interdigestive small bowel motility and duodenal bacterial overgrowth in experimental acute pancreatitis

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