Effect of bacterial chemotactic peptides on intestinal inflammation in animal models of acute and chronic relapsed colitis

It is known that bacterial chemotactic peptides such as formyl-methionyl-leucyl-phenylalanine (fMLP) exacerbate colitis during the acute phase, but the precise role of fMLP during chronic "relapse" is unknown. In this study we examined the effect of bacterial peptides in animal models of a...

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Published inDigestive diseases and sciences Vol. 50; no. 8; pp. 1444 - 1453
Main Authors HERNANDEZ, Gerardo A, VALENTIN, Melanie R, APPLEYARD, Caroline B
Format Journal Article
LanguageEnglish
Published Heidelberg Springer 01.08.2005
Springer Nature B.V
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Abstract It is known that bacterial chemotactic peptides such as formyl-methionyl-leucyl-phenylalanine (fMLP) exacerbate colitis during the acute phase, but the precise role of fMLP during chronic "relapse" is unknown. In this study we examined the effect of bacterial peptides in animal models of acute and chronic "relapsed" colitis. Different parameters were evaluated, such as tissue damage, myeloperoxidase activity, and mucosal function. In acute trinitrobenezene sulfonic acid colitis, fMLP had significant adverse effects on mucosal function and worsened several parameters. In contrast, in chronic "relapsed" colitis the ability of fMLP to exacerbate the inflammation was dependent on whether it was confined to the lumen of the colon. Bacterial peptides such as fMLP appear to play a different role in the acute phase of inflammation compared with the chronic phase, depending on the integrity of the mucosal barrier.
AbstractList It is known that bacterial chemotactic peptides such as formyl-methionyl-leucyl-phenylalanine (fMLP) exacerbate colitis during the acute phase, but the precise role of fMLP during chronic "relapse" is unknown. In this study we examined the effect of bacterial peptides in animal models of acute and chronic "relapsed" colitis. Different parameters were evaluated, such as tissue damage, myeloperoxidase activity, and mucosal function. In acute trinitrobenezene sulfonic acid colitis, fMLP had significant adverse effects on mucosal function and worsened several parameters. In contrast, in chronic "relapsed" colitis the ability of fMLP to exacerbate the inflammation was dependent on whether it was confined to the lumen of the colon. Bacterial peptides such as fMLP appear to play a different role in the acute phase of inflammation compared with the chronic phase, depending on the integrity of the mucosal barrier.
Author APPLEYARD, Caroline B
HERNANDEZ, Gerardo A
VALENTIN, Melanie R
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CitedBy_id crossref_primary_10_1016_j_phrs_2019_01_041
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crossref_primary_10_1158_0008_5472_CAN_07_1418
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IsPeerReviewed true
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Issue 8
Keywords Animal model
Rat
Acute
Rodentia
Metabolic diseases
Inflammation
Chemotactic peptide
inflammatory bowel disease
Inflammatory disease
Crohn disease
Vertebrata
Chronic
Mammalia
Animal
bacterial peptides
Gastroenterology
Digestive diseases
Intestinal disease
trinitrobenzenesulfonic acid
Colitis
Ulcerative colitis
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Snippet It is known that bacterial chemotactic peptides such as formyl-methionyl-leucyl-phenylalanine (fMLP) exacerbate colitis during the acute phase, but the precise...
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StartPage 1444
SubjectTerms Acute Disease
Animals
Bacteria
Bacterial Proteins - pharmacology
Biological and medical sciences
Chronic Disease
Colitis - etiology
Colitis - metabolism
Colitis - physiopathology
Disease Models, Animal
Feeding. Feeding behavior
Fundamental and applied biological sciences. Psychology
Gastric Mucosa - drug effects
Gastric Mucosa - metabolism
Gastric Mucosa - physiopathology
Gastroenterology. Liver. Pancreas. Abdomen
Male
Medical sciences
N-Formylmethionine Leucyl-Phenylalanine - pharmacology
Other diseases. Semiology
Rats
Rats, Sprague-Dawley
Recurrence
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Title Effect of bacterial chemotactic peptides on intestinal inflammation in animal models of acute and chronic relapsed colitis
URI https://www.ncbi.nlm.nih.gov/pubmed/16110833
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Volume 50
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