H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats
Hydrogen sulfide (H 2 S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful...
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Veröffentlicht in: | Inflammopharmacology 2018-04, Vol.26 (2), p.479-489 |
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creator | Kupai, Krisztina Almási, Nikoletta Kósa, Magdolna Nemcsók, János Murlasits, Zsolt Török, Szilvia Al-awar, Amin Baráth, Zoltán Pósa, Anikó Varga, Csaba |
description | Hydrogen sulfide (H
2
S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful stimuli, were found to regulate intestinal inflammation in experimental animal models of colitis. We aimed to investigate the protective effects of H
2
S against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats, and whether HO enzyme system is involved in the H
2
S-induced colonic cytoprotection. Male Wistar rats were treated with TNBS to induce colitis, and H
2
S donor (Lawesson’s reagent) was prepared two times/day at different concentrations, and delivered per os (from day 1 to day 3). Our results suggest that daily treatment (2 times/day) with H
2
S donor, could significantly decrease the extent of colonic inflammation compared to vehicle treatment, and the most effective daily dose of H
2
S donor against inflammation was 18.75 µM/kg/day. Per os administration of H
2
S donor increased the colonic HO enzyme activity; on the contrary, the protective effect of H
2
S was abolished by the co-treatment with HO inhibitor. Our findings suggest that H
2
S confers colonoprotection, probably by modulation of anti-inflammatory parameters and HO enzyme activity. |
doi_str_mv | 10.1007/s10787-017-0382-8 |
format | Article |
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2
S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful stimuli, were found to regulate intestinal inflammation in experimental animal models of colitis. We aimed to investigate the protective effects of H
2
S against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats, and whether HO enzyme system is involved in the H
2
S-induced colonic cytoprotection. Male Wistar rats were treated with TNBS to induce colitis, and H
2
S donor (Lawesson’s reagent) was prepared two times/day at different concentrations, and delivered per os (from day 1 to day 3). Our results suggest that daily treatment (2 times/day) with H
2
S donor, could significantly decrease the extent of colonic inflammation compared to vehicle treatment, and the most effective daily dose of H
2
S donor against inflammation was 18.75 µM/kg/day. Per os administration of H
2
S donor increased the colonic HO enzyme activity; on the contrary, the protective effect of H
2
S was abolished by the co-treatment with HO inhibitor. Our findings suggest that H
2
S confers colonoprotection, probably by modulation of anti-inflammatory parameters and HO enzyme activity.</description><identifier>ISSN: 0925-4692</identifier><identifier>EISSN: 1568-5608</identifier><identifier>DOI: 10.1007/s10787-017-0382-8</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Allergology ; Biomedical and Life Sciences ; Biomedicine ; Dermatology ; Gastroenterology ; Immunology ; Original Article ; Pharmacology/Toxicology ; Rheumatology</subject><ispartof>Inflammopharmacology, 2018-04, Vol.26 (2), p.479-489</ispartof><rights>Springer International Publishing AG 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-8a7531699c478eef605573c1dcbb243ea0fa877c471e9c758aa233d7a6267f8a3</citedby><cites>FETCH-LOGICAL-c387t-8a7531699c478eef605573c1dcbb243ea0fa877c471e9c758aa233d7a6267f8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10787-017-0382-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10787-017-0382-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Kupai, Krisztina</creatorcontrib><creatorcontrib>Almási, Nikoletta</creatorcontrib><creatorcontrib>Kósa, Magdolna</creatorcontrib><creatorcontrib>Nemcsók, János</creatorcontrib><creatorcontrib>Murlasits, Zsolt</creatorcontrib><creatorcontrib>Török, Szilvia</creatorcontrib><creatorcontrib>Al-awar, Amin</creatorcontrib><creatorcontrib>Baráth, Zoltán</creatorcontrib><creatorcontrib>Pósa, Anikó</creatorcontrib><creatorcontrib>Varga, Csaba</creatorcontrib><title>H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats</title><title>Inflammopharmacology</title><addtitle>Inflammopharmacol</addtitle><description>Hydrogen sulfide (H
2
S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful stimuli, were found to regulate intestinal inflammation in experimental animal models of colitis. We aimed to investigate the protective effects of H
2
S against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats, and whether HO enzyme system is involved in the H
2
S-induced colonic cytoprotection. Male Wistar rats were treated with TNBS to induce colitis, and H
2
S donor (Lawesson’s reagent) was prepared two times/day at different concentrations, and delivered per os (from day 1 to day 3). Our results suggest that daily treatment (2 times/day) with H
2
S donor, could significantly decrease the extent of colonic inflammation compared to vehicle treatment, and the most effective daily dose of H
2
S donor against inflammation was 18.75 µM/kg/day. Per os administration of H
2
S donor increased the colonic HO enzyme activity; on the contrary, the protective effect of H
2
S was abolished by the co-treatment with HO inhibitor. Our findings suggest that H
2
S confers colonoprotection, probably by modulation of anti-inflammatory parameters and HO enzyme activity.</description><subject>Allergology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Dermatology</subject><subject>Gastroenterology</subject><subject>Immunology</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Rheumatology</subject><issn>0925-4692</issn><issn>1568-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kDtPAzEQhC0EEuHxA-hc0hj8iB9XQgQEKSJFAq3l-HyRo4sdbF-Rf4_DUVOsptiZ1c4HwB3BDwRj-ZgJlkoiTOowRZE6AxPChUJcYHUOJrihHE1FQy_BVc47jLGQopmArzldQRtD51Ku2scQDykWZ4uPAZqt8SEXuP54XiEf2sG69uTyxWe4OcL5EhE4HJLbDr35TfgAkyn5Blx0ps_u9k-vwefry3o2R4vl2_vsaYEsU7IgZSRnRDSNnUrlXCcw55JZ0trNhk6ZM7gzSsq6Ja6xkitjKGOtNIIK2SnDrsH9eLc-_T24XPTeZ-v63gQXh6xJra3qBUaqlYxWm2LOyXX6kPzepKMmWJ8Y6pGhrgz1iaFWNUPHTK7esHVJ7-KQQm30T-gH1otz9w</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Kupai, Krisztina</creator><creator>Almási, Nikoletta</creator><creator>Kósa, Magdolna</creator><creator>Nemcsók, János</creator><creator>Murlasits, Zsolt</creator><creator>Török, Szilvia</creator><creator>Al-awar, Amin</creator><creator>Baráth, Zoltán</creator><creator>Pósa, Anikó</creator><creator>Varga, Csaba</creator><general>Springer International Publishing</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20180401</creationdate><title>H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats</title><author>Kupai, Krisztina ; Almási, Nikoletta ; Kósa, Magdolna ; Nemcsók, János ; Murlasits, Zsolt ; Török, Szilvia ; Al-awar, Amin ; Baráth, Zoltán ; Pósa, Anikó ; Varga, Csaba</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-8a7531699c478eef605573c1dcbb243ea0fa877c471e9c758aa233d7a6267f8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Allergology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Dermatology</topic><topic>Gastroenterology</topic><topic>Immunology</topic><topic>Original Article</topic><topic>Pharmacology/Toxicology</topic><topic>Rheumatology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kupai, Krisztina</creatorcontrib><creatorcontrib>Almási, Nikoletta</creatorcontrib><creatorcontrib>Kósa, Magdolna</creatorcontrib><creatorcontrib>Nemcsók, János</creatorcontrib><creatorcontrib>Murlasits, Zsolt</creatorcontrib><creatorcontrib>Török, Szilvia</creatorcontrib><creatorcontrib>Al-awar, Amin</creatorcontrib><creatorcontrib>Baráth, Zoltán</creatorcontrib><creatorcontrib>Pósa, Anikó</creatorcontrib><creatorcontrib>Varga, Csaba</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inflammopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kupai, Krisztina</au><au>Almási, Nikoletta</au><au>Kósa, Magdolna</au><au>Nemcsók, János</au><au>Murlasits, Zsolt</au><au>Török, Szilvia</au><au>Al-awar, Amin</au><au>Baráth, Zoltán</au><au>Pósa, Anikó</au><au>Varga, Csaba</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats</atitle><jtitle>Inflammopharmacology</jtitle><stitle>Inflammopharmacol</stitle><date>2018-04-01</date><risdate>2018</risdate><volume>26</volume><issue>2</issue><spage>479</spage><epage>489</epage><pages>479-489</pages><issn>0925-4692</issn><eissn>1568-5608</eissn><abstract>Hydrogen sulfide (H
2
S) is an endogenous mediator that contributes to many important physiological processes including vasodilation and vascular smooth muscle relaxation; in turn, preventing tissue damage and reducing inflammation. Heme oxygenase (HO) enzymes, of which HO-1 is inducible by harmful stimuli, were found to regulate intestinal inflammation in experimental animal models of colitis. We aimed to investigate the protective effects of H
2
S against 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats, and whether HO enzyme system is involved in the H
2
S-induced colonic cytoprotection. Male Wistar rats were treated with TNBS to induce colitis, and H
2
S donor (Lawesson’s reagent) was prepared two times/day at different concentrations, and delivered per os (from day 1 to day 3). Our results suggest that daily treatment (2 times/day) with H
2
S donor, could significantly decrease the extent of colonic inflammation compared to vehicle treatment, and the most effective daily dose of H
2
S donor against inflammation was 18.75 µM/kg/day. Per os administration of H
2
S donor increased the colonic HO enzyme activity; on the contrary, the protective effect of H
2
S was abolished by the co-treatment with HO inhibitor. Our findings suggest that H
2
S confers colonoprotection, probably by modulation of anti-inflammatory parameters and HO enzyme activity.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s10787-017-0382-8</doi><tpages>11</tpages></addata></record> |
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subjects | Allergology Biomedical and Life Sciences Biomedicine Dermatology Gastroenterology Immunology Original Article Pharmacology/Toxicology Rheumatology |
title | H2S confers colonoprotection against TNBS-induced colitis by HO-1 upregulation in rats |
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