The gut origin of bacterial pancreatic infection during acute experimental pancreatitis in rats. 2002

Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
Department of Surgery, University Hospital Mannheim, Germany. stephan.samel@chir.ma.uni-heidelberg.de

BACKGROUND Infections are frequent complications and determine clinical course and outcome in severe pancreatitis. A novel animal model was used to assess minimal transit time of bacterial translocation (BT) across the gut mucosa in vivo using green fluorescent protein-transfected Escherichia coli and intravital video microscopy. METHODS Three hours after induction of acute pancreatitis by i.p. injection of 40 microg/kg cerulein, 0.5 ml of a suspension of green fluorescent protein-transfected E. coli were injected into the lumen of a small bowel reservoir formed by ligature in anesthetized Wistar rats. Translocation of E. coli was assessed by intravital microscopy. Animals were sacrificed 5 h after induction of pancreatitis. RESULTS BT across the mucosa and into the muscularis propria took a mean +/- SD of 36.4 +/- 8 min and 80.9 +/- 9.5 min, respectively, in sham animals. Pancreatitis resulted in a significantly shorter minimal transit time across the mucosa (16.4 +/- 4.9 min, p = 0.007) and into the muscularis propria (47.7 +/- 2.5 min, p = 0.001). E. coli were detected on frozen cross-sections and on bacteriological examination of pancreatic tissue in animals with acute pancreatitis but not in controls. CONCLUSIONS Intravital microscopy of fluorescent bacteria is a new approach towards studying BT in vivo. Minimal transit time of BT serves as a novel functional aspect of mucosal barrier function during acute pancreatitis. The observation of fluorescent bacteria translocating from the small bowel lumen into the pancreas provides substantial experimental proof for the gut-origin-hypothesis of infectious complications in pancreatitis.

UI MeSH Term Description Entries
D007082 Ileum The distal and narrowest portion of the SMALL INTESTINE, between the JEJUNUM and the ILEOCECAL VALVE of the LARGE INTESTINE.
D007413 Intestinal Mucosa Lining of the INTESTINES, consisting of an inner EPITHELIUM, a middle LAMINA PROPRIA, and an outer MUSCULARIS MUCOSAE. In the SMALL INTESTINE, the mucosa is characterized by a series of folds and abundance of absorptive cells (ENTEROCYTES) with MICROVILLI. Intestinal Epithelium,Intestinal Glands,Epithelium, Intestinal,Gland, Intestinal,Glands, Intestinal,Intestinal Gland,Mucosa, Intestinal
D008297 Male Males
D009130 Muscle, Smooth Unstriated and unstriped muscle, one of the muscles of the internal organs, blood vessels, hair follicles, etc. Contractile elements are elongated, usually spindle-shaped cells with centrally located nuclei. Smooth muscle fibers are bound together into sheets or bundles by reticular fibers and frequently elastic nets are also abundant. (From Stedman, 25th ed) Muscle, Involuntary,Smooth Muscle,Involuntary Muscle,Involuntary Muscles,Muscles, Involuntary,Muscles, Smooth,Smooth Muscles
D009336 Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply.
D010195 Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. Acute Edematous Pancreatitis,Acute Pancreatitis,Pancreatic Parenchyma with Edema,Pancreatic Parenchymal Edema,Pancreatitis, Acute,Pancreatitis, Acute Edematous,Peripancreatic Fat Necrosis,Acute Edematous Pancreatitides,Acute Pancreatitides,Edema, Pancreatic Parenchymal,Edematous Pancreatitides, Acute,Edematous Pancreatitis, Acute,Fat Necrosis, Peripancreatic,Necrosis, Peripancreatic Fat,Pancreatic Parenchymal Edemas,Pancreatitides, Acute,Pancreatitides, Acute Edematous,Parenchymal Edema, Pancreatic,Peripancreatic Fat Necroses
D002108 Ceruletide A specific decapeptide obtained from the skin of Hila caerulea, an Australian amphibian. Caerulein is similar in action and composition to CHOLECYSTOKININ. It stimulates gastric, biliary, and pancreatic secretion; and certain smooth muscle. It is used in paralytic ileus and as diagnostic aid in pancreatic malfunction. Caerulein,Cerulein,Ceruletid,FI-6934,Takus,FI 6934,FI6934
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D004926 Escherichia coli A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc. Alkalescens-Dispar Group,Bacillus coli,Bacterium coli,Bacterium coli commune,Diffusely Adherent Escherichia coli,E coli,EAggEC,Enteroaggregative Escherichia coli,Enterococcus coli,Diffusely Adherent E. coli,Enteroaggregative E. coli,Enteroinvasive E. coli,Enteroinvasive Escherichia coli
D000208 Acute Disease Disease having a short and relatively severe course. Acute Diseases,Disease, Acute,Diseases, Acute

Related Publications

Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
April 2000, Surgery,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
February 1993, The European journal of surgery = Acta chirurgica,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
October 2002, World journal of gastroenterology,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
January 1996, Revista do Hospital das Clinicas,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
January 1988, Revista do Hospital das Clinicas,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
January 2001, Digestive surgery,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
April 2002, Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
January 1999, Annals of the Academy of Medicine, Singapore,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
January 1990, Tsitologiia,
Stephan Samel, and Sybille Lanig, and Alexander Lux, and Michael Keese, and Norbert Gretz, and Thomas Nichterlein, and Jörg Sturm, and Matthias Löhr, and Stefan Post
February 1993, The British journal of surgery,
Copied contents to your clipboard!