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Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo

Ischaemia and reperfusion (I/R) play an important role in human pathophysiology as they occur in many clinical conditions and are associated with high morbidity and mortality. Interruption of blood supply rapidly damages metabolically active tissues. Restoration of blood flow after a period of ischa...

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Autores principales: Nosál'ová, Viera, Sotníková, Ružena, Drábiková, Katarína, Fialová, Silvia, Košťálová, Daniela, Banášová, Silvia, Navarová, Jana
Formato: Texto
Lenguaje:English
Publicado: Slovak Toxicology Society SETOX 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984138/
https://www.ncbi.nlm.nih.gov/pubmed/21217883
http://dx.doi.org/10.2478/v10102-010-0021-3
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author Nosál'ová, Viera
Sotníková, Ružena
Drábiková, Katarína
Fialová, Silvia
Košťálová, Daniela
Banášová, Silvia
Navarová, Jana
author_facet Nosál'ová, Viera
Sotníková, Ružena
Drábiková, Katarína
Fialová, Silvia
Košťálová, Daniela
Banášová, Silvia
Navarová, Jana
author_sort Nosál'ová, Viera
collection PubMed
description Ischaemia and reperfusion (I/R) play an important role in human pathophysiology as they occur in many clinical conditions and are associated with high morbidity and mortality. Interruption of blood supply rapidly damages metabolically active tissues. Restoration of blood flow after a period of ischaemia may further worsen cell injury due to an increased formation of free radicals. The aim of our work was to assess macroscopically the extent of intestinal pathological changes caused by mesenteric I/R, and to study free radical production by luminol enhanced chemiluminescence (CL) of ileal samples. In further experiments, the antioxidative activity of the drugs tested was evaluated spectrophotometrically by the use of the DPPH radical. We studied the potential protective ex vivo effect of the plant origin compound arbutin as well as of the pyridoindole stobadine and its derivative SMe1EC2. I/R induced pronounced haemorrhagic intestinal injury accompanied by increase of myeloperoxidase (MPO) and N-acetyl-β-D-glucosaminidase (NAGA) activity. Compared to sham operated (control) rats, there was only a slight increase of CL response after I/R, probably in association with neutrophil increase, indicated by enhanced MPO activity. All compounds significantly reduced the peak values of CL responses of the ileal samples ex vivo, thus reducing the I/R induced increase of free radical production. The antioxidants studied showed a similar inhibitory effect on the CL response influenced by mesenteric I/R. If proved in vivo, these compounds would represent potentially useful therapeutic antioxidants.
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spelling pubmed-29841382011-01-07 Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo Nosál'ová, Viera Sotníková, Ružena Drábiková, Katarína Fialová, Silvia Košťálová, Daniela Banášová, Silvia Navarová, Jana Interdiscip Toxicol Original Article Ischaemia and reperfusion (I/R) play an important role in human pathophysiology as they occur in many clinical conditions and are associated with high morbidity and mortality. Interruption of blood supply rapidly damages metabolically active tissues. Restoration of blood flow after a period of ischaemia may further worsen cell injury due to an increased formation of free radicals. The aim of our work was to assess macroscopically the extent of intestinal pathological changes caused by mesenteric I/R, and to study free radical production by luminol enhanced chemiluminescence (CL) of ileal samples. In further experiments, the antioxidative activity of the drugs tested was evaluated spectrophotometrically by the use of the DPPH radical. We studied the potential protective ex vivo effect of the plant origin compound arbutin as well as of the pyridoindole stobadine and its derivative SMe1EC2. I/R induced pronounced haemorrhagic intestinal injury accompanied by increase of myeloperoxidase (MPO) and N-acetyl-β-D-glucosaminidase (NAGA) activity. Compared to sham operated (control) rats, there was only a slight increase of CL response after I/R, probably in association with neutrophil increase, indicated by enhanced MPO activity. All compounds significantly reduced the peak values of CL responses of the ileal samples ex vivo, thus reducing the I/R induced increase of free radical production. The antioxidants studied showed a similar inhibitory effect on the CL response influenced by mesenteric I/R. If proved in vivo, these compounds would represent potentially useful therapeutic antioxidants. Slovak Toxicology Society SETOX 2010-09 2010-09 /pmc/articles/PMC2984138/ /pubmed/21217883 http://dx.doi.org/10.2478/v10102-010-0021-3 Text en Copyright © 2010 Slovak Toxicology Society SETOX http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Nosál'ová, Viera
Sotníková, Ružena
Drábiková, Katarína
Fialová, Silvia
Košťálová, Daniela
Banášová, Silvia
Navarová, Jana
Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title_full Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title_fullStr Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title_full_unstemmed Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title_short Chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
title_sort chemiluminescence response induced by mesenteric ischaemia/reperfusion: effect of antioxidative compounds ex vivo
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984138/
https://www.ncbi.nlm.nih.gov/pubmed/21217883
http://dx.doi.org/10.2478/v10102-010-0021-3
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