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Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease

BACKGROUND: Increased delivery of taurine‐conjugated bile acids to the distal bowel can lead to dysbiosis resulting in colitis in mouse models of inflammatory bowel disease. A similar situation also could occur in cats with intestinal disease and might therefore result in decreased whole‐body taurin...

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Autores principales: Kathrani, A., Fascetti, A.J., Larsen, J.A., Maunder, C., Hall, E.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508316/
https://www.ncbi.nlm.nih.gov/pubmed/28626960
http://dx.doi.org/10.1111/jvim.14773
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author Kathrani, A.
Fascetti, A.J.
Larsen, J.A.
Maunder, C.
Hall, E.J.
author_facet Kathrani, A.
Fascetti, A.J.
Larsen, J.A.
Maunder, C.
Hall, E.J.
author_sort Kathrani, A.
collection PubMed
description BACKGROUND: Increased delivery of taurine‐conjugated bile acids to the distal bowel can lead to dysbiosis resulting in colitis in mouse models of inflammatory bowel disease. A similar situation also could occur in cats with intestinal disease and might therefore result in decreased whole‐body taurine concentration. HYPOTHESIS/OBJECTIVES: To determine whether whole‐blood taurine concentrations are decreased at the time of diagnosis in cats with intestinal disease and to correlate concentrations with clinical and laboratory variables. ANIMALS: Twenty‐one cats with chronic inflammatory enteropathy and 7 cats with intestinal neoplasia from the University of Bristol. METHODS: Cats that had undergone a thorough investigation consisting of a CBC, serum biochemistry, serum cobalamin and folate concentrations, transabdominal ultrasound examination and histopathology of intestinal biopsy specimens, as well as additional testing if indicated, were included. Whole‐blood from these cats collected at the time of histologic diagnosis and stored in ethylenediaminetetraacetic acid was retrospectively analyzed for taurine with an automated high‐performance liquid chromatography amino acid analyzer. RESULTS: Although whole‐blood taurine concentrations remained within the reference range, those cats with predominantly large intestinal clinical signs had significantly lower concentrations than did cats with small intestinal and mixed bowel clinical signs (P = 0.033) and this difference also was significant when assessed only in cats with chronic inflammatory enteropathy (P = 0.019). CONCLUSIONS AND CLINICAL IMPORTANCE: Additional studies are needed to determine whether large intestinal signs in cats with chronic inflammatory enteropathy are caused by alterations in the microbiota arising as a consequence of increased delivery of taurine‐conjugated bile acids.
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spelling pubmed-55083162017-07-14 Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease Kathrani, A. Fascetti, A.J. Larsen, J.A. Maunder, C. Hall, E.J. J Vet Intern Med SMALL ANIMAL BACKGROUND: Increased delivery of taurine‐conjugated bile acids to the distal bowel can lead to dysbiosis resulting in colitis in mouse models of inflammatory bowel disease. A similar situation also could occur in cats with intestinal disease and might therefore result in decreased whole‐body taurine concentration. HYPOTHESIS/OBJECTIVES: To determine whether whole‐blood taurine concentrations are decreased at the time of diagnosis in cats with intestinal disease and to correlate concentrations with clinical and laboratory variables. ANIMALS: Twenty‐one cats with chronic inflammatory enteropathy and 7 cats with intestinal neoplasia from the University of Bristol. METHODS: Cats that had undergone a thorough investigation consisting of a CBC, serum biochemistry, serum cobalamin and folate concentrations, transabdominal ultrasound examination and histopathology of intestinal biopsy specimens, as well as additional testing if indicated, were included. Whole‐blood from these cats collected at the time of histologic diagnosis and stored in ethylenediaminetetraacetic acid was retrospectively analyzed for taurine with an automated high‐performance liquid chromatography amino acid analyzer. RESULTS: Although whole‐blood taurine concentrations remained within the reference range, those cats with predominantly large intestinal clinical signs had significantly lower concentrations than did cats with small intestinal and mixed bowel clinical signs (P = 0.033) and this difference also was significant when assessed only in cats with chronic inflammatory enteropathy (P = 0.019). CONCLUSIONS AND CLINICAL IMPORTANCE: Additional studies are needed to determine whether large intestinal signs in cats with chronic inflammatory enteropathy are caused by alterations in the microbiota arising as a consequence of increased delivery of taurine‐conjugated bile acids. John Wiley and Sons Inc. 2017-06-19 2017 /pmc/articles/PMC5508316/ /pubmed/28626960 http://dx.doi.org/10.1111/jvim.14773 Text en Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
Kathrani, A.
Fascetti, A.J.
Larsen, J.A.
Maunder, C.
Hall, E.J.
Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title_full Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title_fullStr Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title_full_unstemmed Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title_short Whole‐Blood Taurine Concentrations in Cats With Intestinal Disease
title_sort whole‐blood taurine concentrations in cats with intestinal disease
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5508316/
https://www.ncbi.nlm.nih.gov/pubmed/28626960
http://dx.doi.org/10.1111/jvim.14773
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