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Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats

Dysregulation of the protease–antiprotease balance in the gastrointestinal tract has been suggested as a mechanism underlying visceral hypersensitivity in conditions such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). We aimed to study the potential therapeutic role of an in...

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Autores principales: Hanning, Nikita, De bruyn, Michelle, Ceuleers, Hannah, Boogaerts, Tim, Berg, Maya, Smet, Annemieke, De Schepper, Heiko U., Joossens, Jurgen, van Nuijs, Alexander L. N., De Man, Joris G., Augustyns, Koen, De Meester, Ingrid, De Winter, Benedicte Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229129/
https://www.ncbi.nlm.nih.gov/pubmed/34072320
http://dx.doi.org/10.3390/pharmaceutics13060811
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author Hanning, Nikita
De bruyn, Michelle
Ceuleers, Hannah
Boogaerts, Tim
Berg, Maya
Smet, Annemieke
De Schepper, Heiko U.
Joossens, Jurgen
van Nuijs, Alexander L. N.
De Man, Joris G.
Augustyns, Koen
De Meester, Ingrid
De Winter, Benedicte Y.
author_facet Hanning, Nikita
De bruyn, Michelle
Ceuleers, Hannah
Boogaerts, Tim
Berg, Maya
Smet, Annemieke
De Schepper, Heiko U.
Joossens, Jurgen
van Nuijs, Alexander L. N.
De Man, Joris G.
Augustyns, Koen
De Meester, Ingrid
De Winter, Benedicte Y.
author_sort Hanning, Nikita
collection PubMed
description Dysregulation of the protease–antiprotease balance in the gastrointestinal tract has been suggested as a mechanism underlying visceral hypersensitivity in conditions such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). We aimed to study the potential therapeutic role of an intracolonically administered serine protease inhibitor for the treatment of abdominal pain in a post-inflammatory rat model for IBS. An enema containing 2,4,6-trinitrobenzene sulfonic acid (TNBS) was used to induce colitis in male Sprague–Dawley rats, whereas controls received a saline solution. Colonoscopies were performed to confirm colitis and follow-up mucosal healing. In the post-inflammatory phase, the serine protease inhibitor UAMC-00050 (0.1–5 mg/kg) or its vehicle alone (5% DMSO in H(2)O) was administered in the colon. Thirty minutes later, visceral mechanosensitivity to colorectal distensions was quantified by visceromotor responses (VMRs) and local effects on colonic compliance and inflammatory parameters were assessed. Specific proteolytic activities in fecal and colonic samples were measured using fluorogenic substrates. Pharmacokinetic parameters were evaluated using bioanalytical measurements with liquid chromatography–tandem mass spectrometry. Post-inflammatory rats had increased trypsin-like activity in colonic tissue and elevated elastase-like activity in fecal samples compared to controls. Treatment with UAMC-00050 decreased trypsin-like activity in colonic tissue of post-colitis animals. Pharmacokinetic experiments revealed that UAMC-00050 acted locally, being taken up in the bloodstream only minimally after administration. Local administration of UAMC-00050 normalized visceral hypersensitivity. These results support the role of serine proteases in the pathophysiology of visceral pain and the potential of locally administered serine protease inhibitors as clinically relevant therapeutics for the treatment of IBS patients with abdominal pain.
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spelling pubmed-82291292021-06-26 Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats Hanning, Nikita De bruyn, Michelle Ceuleers, Hannah Boogaerts, Tim Berg, Maya Smet, Annemieke De Schepper, Heiko U. Joossens, Jurgen van Nuijs, Alexander L. N. De Man, Joris G. Augustyns, Koen De Meester, Ingrid De Winter, Benedicte Y. Pharmaceutics Article Dysregulation of the protease–antiprotease balance in the gastrointestinal tract has been suggested as a mechanism underlying visceral hypersensitivity in conditions such as inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS). We aimed to study the potential therapeutic role of an intracolonically administered serine protease inhibitor for the treatment of abdominal pain in a post-inflammatory rat model for IBS. An enema containing 2,4,6-trinitrobenzene sulfonic acid (TNBS) was used to induce colitis in male Sprague–Dawley rats, whereas controls received a saline solution. Colonoscopies were performed to confirm colitis and follow-up mucosal healing. In the post-inflammatory phase, the serine protease inhibitor UAMC-00050 (0.1–5 mg/kg) or its vehicle alone (5% DMSO in H(2)O) was administered in the colon. Thirty minutes later, visceral mechanosensitivity to colorectal distensions was quantified by visceromotor responses (VMRs) and local effects on colonic compliance and inflammatory parameters were assessed. Specific proteolytic activities in fecal and colonic samples were measured using fluorogenic substrates. Pharmacokinetic parameters were evaluated using bioanalytical measurements with liquid chromatography–tandem mass spectrometry. Post-inflammatory rats had increased trypsin-like activity in colonic tissue and elevated elastase-like activity in fecal samples compared to controls. Treatment with UAMC-00050 decreased trypsin-like activity in colonic tissue of post-colitis animals. Pharmacokinetic experiments revealed that UAMC-00050 acted locally, being taken up in the bloodstream only minimally after administration. Local administration of UAMC-00050 normalized visceral hypersensitivity. These results support the role of serine proteases in the pathophysiology of visceral pain and the potential of locally administered serine protease inhibitors as clinically relevant therapeutics for the treatment of IBS patients with abdominal pain. MDPI 2021-05-29 /pmc/articles/PMC8229129/ /pubmed/34072320 http://dx.doi.org/10.3390/pharmaceutics13060811 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hanning, Nikita
De bruyn, Michelle
Ceuleers, Hannah
Boogaerts, Tim
Berg, Maya
Smet, Annemieke
De Schepper, Heiko U.
Joossens, Jurgen
van Nuijs, Alexander L. N.
De Man, Joris G.
Augustyns, Koen
De Meester, Ingrid
De Winter, Benedicte Y.
Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title_full Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title_fullStr Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title_full_unstemmed Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title_short Local Colonic Administration of a Serine Protease Inhibitor Improves Post-Inflammatory Visceral Hypersensitivity in Rats
title_sort local colonic administration of a serine protease inhibitor improves post-inflammatory visceral hypersensitivity in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8229129/
https://www.ncbi.nlm.nih.gov/pubmed/34072320
http://dx.doi.org/10.3390/pharmaceutics13060811
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