The role of poly(ADP-ribose) polymerase-1 inhibitor in carrageenan-induced lung inflammation in mice
The role of poly(ADP-ribose) polymerase-1 (PARP-1) treatment in carrageenan-induced pleurisy in mice. •Studies the effect of PARP-1 inhibitor on carrageenan induced pleurisy.•PARP-1 inhibitor alleviated Cg-induced pleurisy.•Studied the change in T cell subsets, IL-17 and T regulatory cells.•Signific...
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Veröffentlicht in: | Molecular immunology 2015-02, Vol.63 (2), p.394-405 |
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creator | Ahmad, Sheikh Fayaz Zoheir, Khairy M.A. Ansari, Mushtaq Ahmad Korashy, Hesham M. Bakheet, Saleh A. Ashour, Abdelkader E. Al-Shabanah, Othman A. Al-harbi, Mohammed M. Attia, Sabry M. |
description | The role of poly(ADP-ribose) polymerase-1 (PARP-1) treatment in carrageenan-induced pleurisy in mice.
•Studies the effect of PARP-1 inhibitor on carrageenan induced pleurisy.•PARP-1 inhibitor alleviated Cg-induced pleurisy.•Studied the change in T cell subsets, IL-17 and T regulatory cells.•Significant change in pro-inflammatory mediators and adhesion molecules.•Significant change in COX-2, STAT-3, NF-kB, PARP-1, IkB-α, IL-4 protein expression.
Increasing indication is unveiling a role for poly(ADP-ribose) polymerase (PARP)-1 in the regulation of inflammatory/immune responses. The aim of the present study was to determine the potential anti-inflammatory effects of PARP-1 inhibitor 5-aminoisoquinolinone (5-AIQ) to explore the role of PARP-1 inhibitor in a mouse model of carrageenan-induced lung inflammation. A single dose of 5-AIQ (1.5mg/kg) was administered intraperitoneally (i.p.) 1h before λ-carrageenan (Cg) administration. We assessed the effects of 5-AIQ treatment on CD25+, GITR+, CD25+GITR+, IL-17+ and Foxp3+ cells which were investigated using flowcytometry in pleural exudates and heparinized blood. We also evaluated mRNA expressions of IL-6, TNF-α, IL-1β, IL-10, CD11a, l-selectin (CD62L), ICAM-1, MCP-1, iNOS and COX-2 in the lung tissue. We further examined the effects of 5-AIQ on the key mediators of inflammation, namely COX-2, STAT-3, NF-kB p65, PARP-1, IkB-α and IL-4 protein expression in the lung tissue using western blotting. The results illustrated that the numbers of T cell subsets, IL-17+ cytokine levels were markedly increased and Foxp3+ production decreased in the Cg group. Furthermore, Cg-induced up-regulation of adhesion molecules, pro-inflammatory mediators and chemokine expressions. Western blot analysis revealed an increased protein expressions of COX-2, STAT-3 NF-kB p65 and PARP-1 and decreased IkB-α and IL-4 in the Cg group. PARP-1 inhibitor via 5-AIQ treatment reverses the action significantly of all the previously mentioned effects. Moreover, histological examinations revealed anti-inflammatory effects of 5-AIQ, whereas Cg-group aggravated Cg-induced inflammation. Present findings demonstrate the potent anti-inflammatory action of the PARP-1 inhibitor in acute lung injury induced by carrageenan. |
doi_str_mv | 10.1016/j.molimm.2014.09.009 |
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•Studies the effect of PARP-1 inhibitor on carrageenan induced pleurisy.•PARP-1 inhibitor alleviated Cg-induced pleurisy.•Studied the change in T cell subsets, IL-17 and T regulatory cells.•Significant change in pro-inflammatory mediators and adhesion molecules.•Significant change in COX-2, STAT-3, NF-kB, PARP-1, IkB-α, IL-4 protein expression.
Increasing indication is unveiling a role for poly(ADP-ribose) polymerase (PARP)-1 in the regulation of inflammatory/immune responses. The aim of the present study was to determine the potential anti-inflammatory effects of PARP-1 inhibitor 5-aminoisoquinolinone (5-AIQ) to explore the role of PARP-1 inhibitor in a mouse model of carrageenan-induced lung inflammation. A single dose of 5-AIQ (1.5mg/kg) was administered intraperitoneally (i.p.) 1h before λ-carrageenan (Cg) administration. We assessed the effects of 5-AIQ treatment on CD25+, GITR+, CD25+GITR+, IL-17+ and Foxp3+ cells which were investigated using flowcytometry in pleural exudates and heparinized blood. We also evaluated mRNA expressions of IL-6, TNF-α, IL-1β, IL-10, CD11a, l-selectin (CD62L), ICAM-1, MCP-1, iNOS and COX-2 in the lung tissue. We further examined the effects of 5-AIQ on the key mediators of inflammation, namely COX-2, STAT-3, NF-kB p65, PARP-1, IkB-α and IL-4 protein expression in the lung tissue using western blotting. The results illustrated that the numbers of T cell subsets, IL-17+ cytokine levels were markedly increased and Foxp3+ production decreased in the Cg group. Furthermore, Cg-induced up-regulation of adhesion molecules, pro-inflammatory mediators and chemokine expressions. Western blot analysis revealed an increased protein expressions of COX-2, STAT-3 NF-kB p65 and PARP-1 and decreased IkB-α and IL-4 in the Cg group. PARP-1 inhibitor via 5-AIQ treatment reverses the action significantly of all the previously mentioned effects. Moreover, histological examinations revealed anti-inflammatory effects of 5-AIQ, whereas Cg-group aggravated Cg-induced inflammation. Present findings demonstrate the potent anti-inflammatory action of the PARP-1 inhibitor in acute lung injury induced by carrageenan.</description><identifier>ISSN: 0161-5890</identifier><identifier>EISSN: 1872-9142</identifier><identifier>DOI: 10.1016/j.molimm.2014.09.009</identifier><identifier>PMID: 25304310</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Carrageenan ; Cell Adhesion Molecules - genetics ; Cell Adhesion Molecules - metabolism ; Cyclooxygenase 2 - genetics ; Cyclooxygenase 2 - metabolism ; Cytokines - genetics ; Cytokines - metabolism ; Enzyme Inhibitors - pharmacology ; Enzyme Inhibitors - therapeutic use ; Female ; Forkhead Transcription Factors - metabolism ; Gene Expression Regulation - drug effects ; Glucocorticoid-Induced TNFR-Related Protein - metabolism ; Inflammation Mediators - metabolism ; Inflammatory mediators ; Interleukin-17 - biosynthesis ; Interleukin-2 Receptor alpha Subunit - metabolism ; Isoquinolines - pharmacology ; Isoquinolines - therapeutic use ; Lipid Peroxidation - drug effects ; Lipid Peroxidation - genetics ; Lung tissue ; Mice, Inbred BALB C ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - metabolism ; PARP-1 inhibitor ; Pleural exudate ; Pneumonia - drug therapy ; Pneumonia - enzymology ; Pneumonia - pathology ; Poly(ADP-ribose) Polymerase Inhibitors ; Poly(ADP-ribose) Polymerases - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; T-Lymphocytes, Regulatory - drug effects ; T-Lymphocytes, Regulatory - metabolism</subject><ispartof>Molecular immunology, 2015-02, Vol.63 (2), p.394-405</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-31940881d01ec5cbdf43d88d67e9c7c8091d42da14aed82bff5fb15158c835123</citedby><cites>FETCH-LOGICAL-c441t-31940881d01ec5cbdf43d88d67e9c7c8091d42da14aed82bff5fb15158c835123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0161589014002545$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25304310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ahmad, Sheikh Fayaz</creatorcontrib><creatorcontrib>Zoheir, Khairy M.A.</creatorcontrib><creatorcontrib>Ansari, Mushtaq Ahmad</creatorcontrib><creatorcontrib>Korashy, Hesham M.</creatorcontrib><creatorcontrib>Bakheet, Saleh A.</creatorcontrib><creatorcontrib>Ashour, Abdelkader E.</creatorcontrib><creatorcontrib>Al-Shabanah, Othman A.</creatorcontrib><creatorcontrib>Al-harbi, Mohammed M.</creatorcontrib><creatorcontrib>Attia, Sabry M.</creatorcontrib><title>The role of poly(ADP-ribose) polymerase-1 inhibitor in carrageenan-induced lung inflammation in mice</title><title>Molecular immunology</title><addtitle>Mol Immunol</addtitle><description>The role of poly(ADP-ribose) polymerase-1 (PARP-1) treatment in carrageenan-induced pleurisy in mice.
•Studies the effect of PARP-1 inhibitor on carrageenan induced pleurisy.•PARP-1 inhibitor alleviated Cg-induced pleurisy.•Studied the change in T cell subsets, IL-17 and T regulatory cells.•Significant change in pro-inflammatory mediators and adhesion molecules.•Significant change in COX-2, STAT-3, NF-kB, PARP-1, IkB-α, IL-4 protein expression.
Increasing indication is unveiling a role for poly(ADP-ribose) polymerase (PARP)-1 in the regulation of inflammatory/immune responses. The aim of the present study was to determine the potential anti-inflammatory effects of PARP-1 inhibitor 5-aminoisoquinolinone (5-AIQ) to explore the role of PARP-1 inhibitor in a mouse model of carrageenan-induced lung inflammation. A single dose of 5-AIQ (1.5mg/kg) was administered intraperitoneally (i.p.) 1h before λ-carrageenan (Cg) administration. We assessed the effects of 5-AIQ treatment on CD25+, GITR+, CD25+GITR+, IL-17+ and Foxp3+ cells which were investigated using flowcytometry in pleural exudates and heparinized blood. We also evaluated mRNA expressions of IL-6, TNF-α, IL-1β, IL-10, CD11a, l-selectin (CD62L), ICAM-1, MCP-1, iNOS and COX-2 in the lung tissue. We further examined the effects of 5-AIQ on the key mediators of inflammation, namely COX-2, STAT-3, NF-kB p65, PARP-1, IkB-α and IL-4 protein expression in the lung tissue using western blotting. The results illustrated that the numbers of T cell subsets, IL-17+ cytokine levels were markedly increased and Foxp3+ production decreased in the Cg group. Furthermore, Cg-induced up-regulation of adhesion molecules, pro-inflammatory mediators and chemokine expressions. Western blot analysis revealed an increased protein expressions of COX-2, STAT-3 NF-kB p65 and PARP-1 and decreased IkB-α and IL-4 in the Cg group. PARP-1 inhibitor via 5-AIQ treatment reverses the action significantly of all the previously mentioned effects. Moreover, histological examinations revealed anti-inflammatory effects of 5-AIQ, whereas Cg-group aggravated Cg-induced inflammation. Present findings demonstrate the potent anti-inflammatory action of the PARP-1 inhibitor in acute lung injury induced by carrageenan.</description><subject>Animals</subject><subject>Carrageenan</subject><subject>Cell Adhesion Molecules - genetics</subject><subject>Cell Adhesion Molecules - metabolism</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Cytokines - genetics</subject><subject>Cytokines - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Enzyme Inhibitors - therapeutic use</subject><subject>Female</subject><subject>Forkhead Transcription Factors - metabolism</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glucocorticoid-Induced TNFR-Related Protein - metabolism</subject><subject>Inflammation Mediators - metabolism</subject><subject>Inflammatory mediators</subject><subject>Interleukin-17 - biosynthesis</subject><subject>Interleukin-2 Receptor alpha Subunit - metabolism</subject><subject>Isoquinolines - pharmacology</subject><subject>Isoquinolines - therapeutic use</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipid Peroxidation - genetics</subject><subject>Lung tissue</subject><subject>Mice, Inbred BALB C</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>PARP-1 inhibitor</subject><subject>Pleural exudate</subject><subject>Pneumonia - drug therapy</subject><subject>Pneumonia - enzymology</subject><subject>Pneumonia - pathology</subject><subject>Poly(ADP-ribose) Polymerase Inhibitors</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>T-Lymphocytes, Regulatory - drug effects</subject><subject>T-Lymphocytes, Regulatory - metabolism</subject><issn>0161-5890</issn><issn>1872-9142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kDtPxDAMgCMEguPxDxDqCEOL3aa9dEFCvCUkGGCO0sSFnJrmSFqk-_f0OGBksmV_tuWPsWOEDAGr80XmfGedy3JAnkGdAdRbbIZinqc18nybzSYM01LUsMf2Y1wAQAVVucv28rIAXiDMmHl5pyT4jhLfJkvfrU4vr5_TYBsf6ey74CioSCkmtn-3jR18mLJEqxDUG1Gv-tT2ZtRkkm7s36Ze2ynn1GB9vwad1XTIdlrVRTr6iQfs9fbm5eo-fXy6e7i6fEw15zikBdYchEADSLrUjWl5YYQw1ZxqPdcCajQ8Nwq5IiPypm3LtsESS6FFUWJeHLDTzd5l8B8jxUE6GzV1nerJj1FiVQGHCsUa5RtUBx9joFYug3UqrCSCXPuVC7nxK9d-JdRy8juNnfxcGBtH5m_oV-gEXGwAmv78tBRk1Jb6SY8NpAdpvP3_whecE43k</recordid><startdate>201502</startdate><enddate>201502</enddate><creator>Ahmad, Sheikh Fayaz</creator><creator>Zoheir, Khairy M.A.</creator><creator>Ansari, Mushtaq Ahmad</creator><creator>Korashy, Hesham M.</creator><creator>Bakheet, Saleh A.</creator><creator>Ashour, Abdelkader E.</creator><creator>Al-Shabanah, Othman A.</creator><creator>Al-harbi, Mohammed M.</creator><creator>Attia, Sabry M.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>201502</creationdate><title>The role of poly(ADP-ribose) polymerase-1 inhibitor in carrageenan-induced lung inflammation in mice</title><author>Ahmad, Sheikh Fayaz ; Zoheir, Khairy M.A. ; Ansari, Mushtaq Ahmad ; Korashy, Hesham M. ; Bakheet, Saleh A. ; Ashour, Abdelkader E. ; Al-Shabanah, Othman A. ; Al-harbi, Mohammed M. ; Attia, Sabry M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-31940881d01ec5cbdf43d88d67e9c7c8091d42da14aed82bff5fb15158c835123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Carrageenan</topic><topic>Cell Adhesion Molecules - genetics</topic><topic>Cell Adhesion Molecules - metabolism</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Cytokines - genetics</topic><topic>Cytokines - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Enzyme Inhibitors - therapeutic use</topic><topic>Female</topic><topic>Forkhead Transcription Factors - metabolism</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Glucocorticoid-Induced TNFR-Related Protein - metabolism</topic><topic>Inflammation Mediators - metabolism</topic><topic>Inflammatory mediators</topic><topic>Interleukin-17 - biosynthesis</topic><topic>Interleukin-2 Receptor alpha Subunit - metabolism</topic><topic>Isoquinolines - pharmacology</topic><topic>Isoquinolines - therapeutic use</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipid Peroxidation - genetics</topic><topic>Lung tissue</topic><topic>Mice, Inbred BALB C</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>PARP-1 inhibitor</topic><topic>Pleural exudate</topic><topic>Pneumonia - drug therapy</topic><topic>Pneumonia - enzymology</topic><topic>Pneumonia - pathology</topic><topic>Poly(ADP-ribose) Polymerase Inhibitors</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>T-Lymphocytes, Regulatory - drug effects</topic><topic>T-Lymphocytes, Regulatory - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmad, Sheikh Fayaz</creatorcontrib><creatorcontrib>Zoheir, Khairy M.A.</creatorcontrib><creatorcontrib>Ansari, Mushtaq Ahmad</creatorcontrib><creatorcontrib>Korashy, Hesham M.</creatorcontrib><creatorcontrib>Bakheet, Saleh A.</creatorcontrib><creatorcontrib>Ashour, Abdelkader E.</creatorcontrib><creatorcontrib>Al-Shabanah, Othman A.</creatorcontrib><creatorcontrib>Al-harbi, Mohammed M.</creatorcontrib><creatorcontrib>Attia, Sabry M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Molecular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmad, Sheikh Fayaz</au><au>Zoheir, Khairy M.A.</au><au>Ansari, Mushtaq Ahmad</au><au>Korashy, Hesham M.</au><au>Bakheet, Saleh A.</au><au>Ashour, Abdelkader E.</au><au>Al-Shabanah, Othman A.</au><au>Al-harbi, Mohammed M.</au><au>Attia, Sabry M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of poly(ADP-ribose) polymerase-1 inhibitor in carrageenan-induced lung inflammation in mice</atitle><jtitle>Molecular immunology</jtitle><addtitle>Mol Immunol</addtitle><date>2015-02</date><risdate>2015</risdate><volume>63</volume><issue>2</issue><spage>394</spage><epage>405</epage><pages>394-405</pages><issn>0161-5890</issn><eissn>1872-9142</eissn><abstract>The role of poly(ADP-ribose) polymerase-1 (PARP-1) treatment in carrageenan-induced pleurisy in mice.
•Studies the effect of PARP-1 inhibitor on carrageenan induced pleurisy.•PARP-1 inhibitor alleviated Cg-induced pleurisy.•Studied the change in T cell subsets, IL-17 and T regulatory cells.•Significant change in pro-inflammatory mediators and adhesion molecules.•Significant change in COX-2, STAT-3, NF-kB, PARP-1, IkB-α, IL-4 protein expression.
Increasing indication is unveiling a role for poly(ADP-ribose) polymerase (PARP)-1 in the regulation of inflammatory/immune responses. The aim of the present study was to determine the potential anti-inflammatory effects of PARP-1 inhibitor 5-aminoisoquinolinone (5-AIQ) to explore the role of PARP-1 inhibitor in a mouse model of carrageenan-induced lung inflammation. A single dose of 5-AIQ (1.5mg/kg) was administered intraperitoneally (i.p.) 1h before λ-carrageenan (Cg) administration. We assessed the effects of 5-AIQ treatment on CD25+, GITR+, CD25+GITR+, IL-17+ and Foxp3+ cells which were investigated using flowcytometry in pleural exudates and heparinized blood. We also evaluated mRNA expressions of IL-6, TNF-α, IL-1β, IL-10, CD11a, l-selectin (CD62L), ICAM-1, MCP-1, iNOS and COX-2 in the lung tissue. We further examined the effects of 5-AIQ on the key mediators of inflammation, namely COX-2, STAT-3, NF-kB p65, PARP-1, IkB-α and IL-4 protein expression in the lung tissue using western blotting. The results illustrated that the numbers of T cell subsets, IL-17+ cytokine levels were markedly increased and Foxp3+ production decreased in the Cg group. Furthermore, Cg-induced up-regulation of adhesion molecules, pro-inflammatory mediators and chemokine expressions. Western blot analysis revealed an increased protein expressions of COX-2, STAT-3 NF-kB p65 and PARP-1 and decreased IkB-α and IL-4 in the Cg group. PARP-1 inhibitor via 5-AIQ treatment reverses the action significantly of all the previously mentioned effects. Moreover, histological examinations revealed anti-inflammatory effects of 5-AIQ, whereas Cg-group aggravated Cg-induced inflammation. Present findings demonstrate the potent anti-inflammatory action of the PARP-1 inhibitor in acute lung injury induced by carrageenan.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25304310</pmid><doi>10.1016/j.molimm.2014.09.009</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Carrageenan Cell Adhesion Molecules - genetics Cell Adhesion Molecules - metabolism Cyclooxygenase 2 - genetics Cyclooxygenase 2 - metabolism Cytokines - genetics Cytokines - metabolism Enzyme Inhibitors - pharmacology Enzyme Inhibitors - therapeutic use Female Forkhead Transcription Factors - metabolism Gene Expression Regulation - drug effects Glucocorticoid-Induced TNFR-Related Protein - metabolism Inflammation Mediators - metabolism Inflammatory mediators Interleukin-17 - biosynthesis Interleukin-2 Receptor alpha Subunit - metabolism Isoquinolines - pharmacology Isoquinolines - therapeutic use Lipid Peroxidation - drug effects Lipid Peroxidation - genetics Lung tissue Mice, Inbred BALB C Nitric Oxide Synthase Type II - genetics Nitric Oxide Synthase Type II - metabolism PARP-1 inhibitor Pleural exudate Pneumonia - drug therapy Pneumonia - enzymology Pneumonia - pathology Poly(ADP-ribose) Polymerase Inhibitors Poly(ADP-ribose) Polymerases - metabolism RNA, Messenger - genetics RNA, Messenger - metabolism T-Lymphocytes, Regulatory - drug effects T-Lymphocytes, Regulatory - metabolism |
title | The role of poly(ADP-ribose) polymerase-1 inhibitor in carrageenan-induced lung inflammation in mice |
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