Loading…
Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase
Objective Na-H exchanger-1 (NHE-1) is induced in experimental colitis. It has not yet been established whether its inhibition ameliorates colitis. The effects of amiloride, an inhibitor of NHE-1, on colitis were examined in this study. Levels of mitogen-activated protein (MAP) kinases ERK, p38 and i...
Saved in:
Published in: | Scandinavian journal of gastroenterology 2005-05, Vol.40 (5), p.578-585 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3 |
container_end_page | 585 |
container_issue | 5 |
container_start_page | 578 |
container_title | Scandinavian journal of gastroenterology |
container_volume | 40 |
creator | Khan, Islam Oriowo, Mabayoje A. Anim, Jehoram T. |
description | Objective
Na-H exchanger-1 (NHE-1) is induced in experimental colitis. It has not yet been established whether its inhibition ameliorates colitis. The effects of amiloride, an inhibitor of NHE-1, on colitis were examined in this study. Levels of mitogen-activated protein (MAP) kinases ERK, p38 and interleukin 1β which participate in intestinal inflammation were also examined in the colonic smooth muscle of rats with colitis.
Material and methods
Colitis was induced in Sprague-Dawley male rats by intrarectal administration of trinitrobenzenesulphonic acid (TNBS) and treated daily with amiloride (3, 5, and 10 mg/kg b.w. (body-weight), orally) starting 1 h before induction of colitis. The animals were sacrificed on day 5 post-TNBS. Controls received phosphate buffered saline in a similar manner.
Results
The highest dose of amiloride (10 mg/kg) was lethal. The lowest dose (3 mg/kg) was tolerated and was used in this study. Amiloride significantly reversed the colitis-reduced contractility and induction of MPO activity, NHE-1, IL-1β and ERK, but not of p38 in inflamed colonic smooth muscle. Splenomegaly, increased colonic mass and decreased sodium pump activity were significantly reversed by amiloride treatment. There was no recovery of b.w. loss in the treated colitic animals. Urine output was increased, whereas food and water intake remained unchanged following amiloride treatment.
Conclusions
These findings suggest that the beneficial effects of NHE-1 inhibition in experimental colitis are mediated through IL-1β and ERK MAP kinase. |
doi_str_mv | 10.1080/00365520510012352 |
format | article |
fullrecord | <record><control><sourceid>informahealthcare_infor</sourceid><recordid>TN_cdi_informaworld_taylorfrancis_310_1080_00365520510012352</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_00365520510012352</sourcerecordid><originalsourceid>FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3</originalsourceid><addsrcrecordid>eNp9kMFu1DAQhi1EJZbCA3DzhaPp2Ik3ieBSVaWtWIFUwTmaOOPGJbFXtmnZZ-EteJA-U10WhBBST3OY__tn9DH2SsIbCS0cAVRrrRVoCSBVpdUTtpIalGgaaJ-y1cNelIB8xp6ndA0Auqm7FftxvNDsQsTsgufBcvq-pegW8hlnbsLsskt82PGPKM7L0kzorygKyZ2f3OByiBwXN4foRuIliikF4zDTyG9dnnikG4qpdJXui42Qdz85-pGfXn7gS6GvyAs02d38IrYxZHKef3UeE71gBxbnRC9_z0P25f3p55Nzsfl0dnFyvBFGdToLqZsOWmVMAzUhyU7bGqvRtNRSPSqrumbQQzcMqltTR0DWGo2oVTtaqFqsDpnc95oYUopk-20xgHHXS-gf7Pb_2S3M6z2zxWRwthG9cekvuG70uq50yb3b55y3IS54G-I89hl3xdgfqHrszNt_8IlwzpPBSP11-BZ90fLIk_cP36KF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase</title><source>Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)</source><creator>Khan, Islam ; Oriowo, Mabayoje A. ; Anim, Jehoram T.</creator><creatorcontrib>Khan, Islam ; Oriowo, Mabayoje A. ; Anim, Jehoram T.</creatorcontrib><description>Objective
Na-H exchanger-1 (NHE-1) is induced in experimental colitis. It has not yet been established whether its inhibition ameliorates colitis. The effects of amiloride, an inhibitor of NHE-1, on colitis were examined in this study. Levels of mitogen-activated protein (MAP) kinases ERK, p38 and interleukin 1β which participate in intestinal inflammation were also examined in the colonic smooth muscle of rats with colitis.
Material and methods
Colitis was induced in Sprague-Dawley male rats by intrarectal administration of trinitrobenzenesulphonic acid (TNBS) and treated daily with amiloride (3, 5, and 10 mg/kg b.w. (body-weight), orally) starting 1 h before induction of colitis. The animals were sacrificed on day 5 post-TNBS. Controls received phosphate buffered saline in a similar manner.
Results
The highest dose of amiloride (10 mg/kg) was lethal. The lowest dose (3 mg/kg) was tolerated and was used in this study. Amiloride significantly reversed the colitis-reduced contractility and induction of MPO activity, NHE-1, IL-1β and ERK, but not of p38 in inflamed colonic smooth muscle. Splenomegaly, increased colonic mass and decreased sodium pump activity were significantly reversed by amiloride treatment. There was no recovery of b.w. loss in the treated colitic animals. Urine output was increased, whereas food and water intake remained unchanged following amiloride treatment.
Conclusions
These findings suggest that the beneficial effects of NHE-1 inhibition in experimental colitis are mediated through IL-1β and ERK MAP kinase.</description><identifier>ISSN: 0036-5521</identifier><identifier>EISSN: 1502-7708</identifier><identifier>DOI: 10.1080/00365520510012352</identifier><identifier>CODEN: SJGRA4</identifier><language>eng</language><publisher>Copenhagen: Informa UK Ltd</publisher><subject>Biological and medical sciences ; Crohn's colitis ; Gastroenterology. Liver. Pancreas. Abdomen ; IL-β ; MAP kinase ; Medical sciences ; Na-H exchanger ; Other diseases. Semiology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; ulcerative colitis</subject><ispartof>Scandinavian journal of gastroenterology, 2005-05, Vol.40 (5), p.578-585</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3</citedby><cites>FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16756435$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, Islam</creatorcontrib><creatorcontrib>Oriowo, Mabayoje A.</creatorcontrib><creatorcontrib>Anim, Jehoram T.</creatorcontrib><title>Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase</title><title>Scandinavian journal of gastroenterology</title><description>Objective
Na-H exchanger-1 (NHE-1) is induced in experimental colitis. It has not yet been established whether its inhibition ameliorates colitis. The effects of amiloride, an inhibitor of NHE-1, on colitis were examined in this study. Levels of mitogen-activated protein (MAP) kinases ERK, p38 and interleukin 1β which participate in intestinal inflammation were also examined in the colonic smooth muscle of rats with colitis.
Material and methods
Colitis was induced in Sprague-Dawley male rats by intrarectal administration of trinitrobenzenesulphonic acid (TNBS) and treated daily with amiloride (3, 5, and 10 mg/kg b.w. (body-weight), orally) starting 1 h before induction of colitis. The animals were sacrificed on day 5 post-TNBS. Controls received phosphate buffered saline in a similar manner.
Results
The highest dose of amiloride (10 mg/kg) was lethal. The lowest dose (3 mg/kg) was tolerated and was used in this study. Amiloride significantly reversed the colitis-reduced contractility and induction of MPO activity, NHE-1, IL-1β and ERK, but not of p38 in inflamed colonic smooth muscle. Splenomegaly, increased colonic mass and decreased sodium pump activity were significantly reversed by amiloride treatment. There was no recovery of b.w. loss in the treated colitic animals. Urine output was increased, whereas food and water intake remained unchanged following amiloride treatment.
Conclusions
These findings suggest that the beneficial effects of NHE-1 inhibition in experimental colitis are mediated through IL-1β and ERK MAP kinase.</description><subject>Biological and medical sciences</subject><subject>Crohn's colitis</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>IL-β</subject><subject>MAP kinase</subject><subject>Medical sciences</subject><subject>Na-H exchanger</subject><subject>Other diseases. Semiology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>ulcerative colitis</subject><issn>0036-5521</issn><issn>1502-7708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kMFu1DAQhi1EJZbCA3DzhaPp2Ik3ieBSVaWtWIFUwTmaOOPGJbFXtmnZZ-EteJA-U10WhBBST3OY__tn9DH2SsIbCS0cAVRrrRVoCSBVpdUTtpIalGgaaJ-y1cNelIB8xp6ndA0Auqm7FftxvNDsQsTsgufBcvq-pegW8hlnbsLsskt82PGPKM7L0kzorygKyZ2f3OByiBwXN4foRuIliikF4zDTyG9dnnikG4qpdJXui42Qdz85-pGfXn7gS6GvyAs02d38IrYxZHKef3UeE71gBxbnRC9_z0P25f3p55Nzsfl0dnFyvBFGdToLqZsOWmVMAzUhyU7bGqvRtNRSPSqrumbQQzcMqltTR0DWGo2oVTtaqFqsDpnc95oYUopk-20xgHHXS-gf7Pb_2S3M6z2zxWRwthG9cekvuG70uq50yb3b55y3IS54G-I89hl3xdgfqHrszNt_8IlwzpPBSP11-BZ90fLIk_cP36KF</recordid><startdate>200505</startdate><enddate>200505</enddate><creator>Khan, Islam</creator><creator>Oriowo, Mabayoje A.</creator><creator>Anim, Jehoram T.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Scandinavian University Press</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200505</creationdate><title>Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase</title><author>Khan, Islam ; Oriowo, Mabayoje A. ; Anim, Jehoram T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>Crohn's colitis</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>IL-β</topic><topic>MAP kinase</topic><topic>Medical sciences</topic><topic>Na-H exchanger</topic><topic>Other diseases. Semiology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khan, Islam</creatorcontrib><creatorcontrib>Oriowo, Mabayoje A.</creatorcontrib><creatorcontrib>Anim, Jehoram T.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Scandinavian journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khan, Islam</au><au>Oriowo, Mabayoje A.</au><au>Anim, Jehoram T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase</atitle><jtitle>Scandinavian journal of gastroenterology</jtitle><date>2005-05</date><risdate>2005</risdate><volume>40</volume><issue>5</issue><spage>578</spage><epage>585</epage><pages>578-585</pages><issn>0036-5521</issn><eissn>1502-7708</eissn><coden>SJGRA4</coden><abstract>Objective
Na-H exchanger-1 (NHE-1) is induced in experimental colitis. It has not yet been established whether its inhibition ameliorates colitis. The effects of amiloride, an inhibitor of NHE-1, on colitis were examined in this study. Levels of mitogen-activated protein (MAP) kinases ERK, p38 and interleukin 1β which participate in intestinal inflammation were also examined in the colonic smooth muscle of rats with colitis.
Material and methods
Colitis was induced in Sprague-Dawley male rats by intrarectal administration of trinitrobenzenesulphonic acid (TNBS) and treated daily with amiloride (3, 5, and 10 mg/kg b.w. (body-weight), orally) starting 1 h before induction of colitis. The animals were sacrificed on day 5 post-TNBS. Controls received phosphate buffered saline in a similar manner.
Results
The highest dose of amiloride (10 mg/kg) was lethal. The lowest dose (3 mg/kg) was tolerated and was used in this study. Amiloride significantly reversed the colitis-reduced contractility and induction of MPO activity, NHE-1, IL-1β and ERK, but not of p38 in inflamed colonic smooth muscle. Splenomegaly, increased colonic mass and decreased sodium pump activity were significantly reversed by amiloride treatment. There was no recovery of b.w. loss in the treated colitic animals. Urine output was increased, whereas food and water intake remained unchanged following amiloride treatment.
Conclusions
These findings suggest that the beneficial effects of NHE-1 inhibition in experimental colitis are mediated through IL-1β and ERK MAP kinase.</abstract><cop>Copenhagen</cop><cop>Oslo</cop><cop>Stockholm</cop><pub>Informa UK Ltd</pub><doi>10.1080/00365520510012352</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0036-5521 |
ispartof | Scandinavian journal of gastroenterology, 2005-05, Vol.40 (5), p.578-585 |
issn | 0036-5521 1502-7708 |
language | eng |
recordid | cdi_informaworld_taylorfrancis_310_1080_00365520510012352 |
source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Biological and medical sciences Crohn's colitis Gastroenterology. Liver. Pancreas. Abdomen IL-β MAP kinase Medical sciences Na-H exchanger Other diseases. Semiology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ulcerative colitis |
title | Amelioration of experimental colitis by Na-H exchanger-1 inhibitor amiloride is associated with reversal of IL-1β and ERK mitogen-activated protein kinase |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T11%3A13%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-informahealthcare_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Amelioration%20of%20experimental%20colitis%20by%20Na-H%20exchanger-1%20inhibitor%20amiloride%20is%20associated%20with%20reversal%20of%20IL-1%CE%B2%20and%20ERK%20mitogen-activated%20protein%20kinase&rft.jtitle=Scandinavian%20journal%20of%20gastroenterology&rft.au=Khan,%20Islam&rft.date=2005-05&rft.volume=40&rft.issue=5&rft.spage=578&rft.epage=585&rft.pages=578-585&rft.issn=0036-5521&rft.eissn=1502-7708&rft.coden=SJGRA4&rft_id=info:doi/10.1080/00365520510012352&rft_dat=%3Cinformahealthcare_infor%3E10_1080_00365520510012352%3C/informahealthcare_infor%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c295t-1579082cc704eae195f4a3dc8e8e4d2f297b5b9bb296e9e0effc5aa528df038a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |