Cargando…
An objective in vivo diagnostic method for inflammatory bowel disease
Inflammatory damage to the bowel, as occurs in inflammatory bowel disease (IBD), is debilitating to patients. In both patients and animal experimental models, histological analyses of biopsies and endoscopic examinations are used to evaluate the disease state. However, such measurements often have d...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882753/ https://www.ncbi.nlm.nih.gov/pubmed/29657828 http://dx.doi.org/10.1098/rsos.180107 |
_version_ | 1783311513711280128 |
---|---|
author | Payne, Sophie C. Shepherd, Robert K. Sedo, Alicia Fallon, James B. Furness, John B. |
author_facet | Payne, Sophie C. Shepherd, Robert K. Sedo, Alicia Fallon, James B. Furness, John B. |
author_sort | Payne, Sophie C. |
collection | PubMed |
description | Inflammatory damage to the bowel, as occurs in inflammatory bowel disease (IBD), is debilitating to patients. In both patients and animal experimental models, histological analyses of biopsies and endoscopic examinations are used to evaluate the disease state. However, such measurements often have delays and are invasive, while endoscopy is not quantitatively objective. Therefore, a real-time quantitative method to assess compromised mucosal barrier function is advantageous. We investigated the correlation of in vivo changes in electrical transmural impedance with histological measures of inflammation. Four platinum (Pt) ball electrodes were placed in the lumen of the rat small intestine, with a return electrode under the skin. Electrodes placed within the non-inflamed intestine generated stable impedances during the 3 h testing period. Following an intraluminal injection of 2,4,6-trinitrobenzene sulfonic acid (TNBS), an established animal model of IBD, impedances in the inflamed region significantly decreased relative to a region not exposed to TNBS (p < 0.05). Changes in intestinal transmural impedance were correlated (p < 0.05) with histologically assessed damage to the mucosa and increases in neutrophil, eosinophil and T-cell populations at 3 h compared with tissue from control regions. This quantitative, real-time assay may have application in the diagnosis and clinical management of IBD. |
format | Online Article Text |
id | pubmed-5882753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58827532018-04-13 An objective in vivo diagnostic method for inflammatory bowel disease Payne, Sophie C. Shepherd, Robert K. Sedo, Alicia Fallon, James B. Furness, John B. R Soc Open Sci Biology (Whole Organism) Inflammatory damage to the bowel, as occurs in inflammatory bowel disease (IBD), is debilitating to patients. In both patients and animal experimental models, histological analyses of biopsies and endoscopic examinations are used to evaluate the disease state. However, such measurements often have delays and are invasive, while endoscopy is not quantitatively objective. Therefore, a real-time quantitative method to assess compromised mucosal barrier function is advantageous. We investigated the correlation of in vivo changes in electrical transmural impedance with histological measures of inflammation. Four platinum (Pt) ball electrodes were placed in the lumen of the rat small intestine, with a return electrode under the skin. Electrodes placed within the non-inflamed intestine generated stable impedances during the 3 h testing period. Following an intraluminal injection of 2,4,6-trinitrobenzene sulfonic acid (TNBS), an established animal model of IBD, impedances in the inflamed region significantly decreased relative to a region not exposed to TNBS (p < 0.05). Changes in intestinal transmural impedance were correlated (p < 0.05) with histologically assessed damage to the mucosa and increases in neutrophil, eosinophil and T-cell populations at 3 h compared with tissue from control regions. This quantitative, real-time assay may have application in the diagnosis and clinical management of IBD. The Royal Society Publishing 2018-03-21 /pmc/articles/PMC5882753/ /pubmed/29657828 http://dx.doi.org/10.1098/rsos.180107 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Payne, Sophie C. Shepherd, Robert K. Sedo, Alicia Fallon, James B. Furness, John B. An objective in vivo diagnostic method for inflammatory bowel disease |
title | An objective in vivo diagnostic method for inflammatory bowel disease |
title_full | An objective in vivo diagnostic method for inflammatory bowel disease |
title_fullStr | An objective in vivo diagnostic method for inflammatory bowel disease |
title_full_unstemmed | An objective in vivo diagnostic method for inflammatory bowel disease |
title_short | An objective in vivo diagnostic method for inflammatory bowel disease |
title_sort | objective in vivo diagnostic method for inflammatory bowel disease |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5882753/ https://www.ncbi.nlm.nih.gov/pubmed/29657828 http://dx.doi.org/10.1098/rsos.180107 |
work_keys_str_mv | AT paynesophiec anobjectiveinvivodiagnosticmethodforinflammatoryboweldisease AT shepherdrobertk anobjectiveinvivodiagnosticmethodforinflammatoryboweldisease AT sedoalicia anobjectiveinvivodiagnosticmethodforinflammatoryboweldisease AT fallonjamesb anobjectiveinvivodiagnosticmethodforinflammatoryboweldisease AT furnessjohnb anobjectiveinvivodiagnosticmethodforinflammatoryboweldisease AT paynesophiec objectiveinvivodiagnosticmethodforinflammatoryboweldisease AT shepherdrobertk objectiveinvivodiagnosticmethodforinflammatoryboweldisease AT sedoalicia objectiveinvivodiagnosticmethodforinflammatoryboweldisease AT fallonjamesb objectiveinvivodiagnosticmethodforinflammatoryboweldisease AT furnessjohnb objectiveinvivodiagnosticmethodforinflammatoryboweldisease |