Loading…
Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats
Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with n...
Saved in:
Published in: | Cellular immunology 1998-06, Vol.186 (2), p.121-132 |
---|---|
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-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13 |
---|---|
cites | cdi_FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13 |
container_end_page | 132 |
container_issue | 2 |
container_start_page | 121 |
container_title | Cellular immunology |
container_volume | 186 |
creator | Masson, Isabelle Mathieu, Jacques Nolland, Xavier-Bernard De Sousa, Martine Chanaud, Brigitte Strzalko, Suzanne Chancerelle, Yves Kergonou, Jean-François Giroud, Jean-Paul Florentin, Irene |
description | Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with nitric oxide (NO) production. In all burned rats, the proliferative response was depressed by more than 80% and NO production corresponded to a nitrite concentration above 20 μM. Proliferative responses in burned rats were fully restored in the presence of 250 μMNG-monomethyl-l-arginine (NMMA). A time course study of NO production in response to Con A, LPS, anti-CD3, and IFN-γ showed that splenic macrophages from burned rats responded to direct and indirect stimuli more rapidly and more intensively than normal macrophages. In the second part of this work, the effect of the overproduction of NO on the synthesis of immunoregulatory and proinflammatory cytokines was investigated. Although it was inhibited, IFN-γ production by splenocytes from burned rats remained sufficient for NO synthase induction and was restored by NMMA. Concomitantly, IL-2 concentration was enhanced but returned to normal in the presence of NMMA. TNF production was halved after burn injury and NMMA partially restored it. In contrast, IL-6 production was enhanced and increased further in the presence of NMMA. Therefore, cytokines were differently affected by burn injury and variously regulated by NO. |
doi_str_mv | 10.1006/cimm.1998.1296 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_80005816</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0008874998912965</els_id><sourcerecordid>16481568</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13</originalsourceid><addsrcrecordid>eNqFkc9vFCEYhonR1LV69WbCydusMD-AOTar1SYbazb1TBj4xlIZGIGp7s0_XSa78WY8EfI9vOR7H4ReU7KlhLB32k7Tlva92NK6Z0_QhpKeVDVlzVO0IYSISvC2f45epPRACKVtTy7QRc9Yx7t2g34fggMcRvzZ5mg1vv1lDWDr8XuYI6QEBu-P03wf5hicHSGqbB8BHyDNwSdIWHmDr1yGWMjdMYfv1gP-EoNZdLbB4-vgXPhp_Td8dw9xUg7f-IclHtc_Diqnl-jZqFyCV-fzEn29_nC3-1Ttbz_e7K72lW44yVWntWZqbNlQNxRq0SgyQgO6ZoSDAc7VUO6UD7ozBWm5Hmir1dD2IwdiaHOJ3p5yyyI_FkhZTjZpcE55CEuSonTViVLb_0DKWkE7Jgq4PYE6hpQijHKOdlLxKCmRqxu5upGrG7m6KQ_enJOXYQLzFz_LKHNxmkPp4dFClElb8BqMjaCzNMH-K_oPCgmg-Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16481568</pqid></control><display><type>article</type><title>Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats</title><source>ScienceDirect Freedom Collection</source><creator>Masson, Isabelle ; Mathieu, Jacques ; Nolland, Xavier-Bernard ; De Sousa, Martine ; Chanaud, Brigitte ; Strzalko, Suzanne ; Chancerelle, Yves ; Kergonou, Jean-François ; Giroud, Jean-Paul ; Florentin, Irene</creator><creatorcontrib>Masson, Isabelle ; Mathieu, Jacques ; Nolland, Xavier-Bernard ; De Sousa, Martine ; Chanaud, Brigitte ; Strzalko, Suzanne ; Chancerelle, Yves ; Kergonou, Jean-François ; Giroud, Jean-Paul ; Florentin, Irene</creatorcontrib><description>Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with nitric oxide (NO) production. In all burned rats, the proliferative response was depressed by more than 80% and NO production corresponded to a nitrite concentration above 20 μM. Proliferative responses in burned rats were fully restored in the presence of 250 μMNG-monomethyl-l-arginine (NMMA). A time course study of NO production in response to Con A, LPS, anti-CD3, and IFN-γ showed that splenic macrophages from burned rats responded to direct and indirect stimuli more rapidly and more intensively than normal macrophages. In the second part of this work, the effect of the overproduction of NO on the synthesis of immunoregulatory and proinflammatory cytokines was investigated. Although it was inhibited, IFN-γ production by splenocytes from burned rats remained sufficient for NO synthase induction and was restored by NMMA. Concomitantly, IL-2 concentration was enhanced but returned to normal in the presence of NMMA. TNF production was halved after burn injury and NMMA partially restored it. In contrast, IL-6 production was enhanced and increased further in the presence of NMMA. Therefore, cytokines were differently affected by burn injury and variously regulated by NO.</description><identifier>ISSN: 0008-8749</identifier><identifier>EISSN: 1090-2163</identifier><identifier>DOI: 10.1006/cimm.1998.1296</identifier><identifier>PMID: 9665754</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Animals ; Burns - immunology ; Cell Division ; Cells, Cultured ; Concanavalin A - pharmacology ; Cytokines - biosynthesis ; Dexamethasone - pharmacology ; Dinoprostone - biosynthesis ; Glucocorticoids - pharmacology ; Immune Tolerance - immunology ; Interferon-gamma - biosynthesis ; Interferon-gamma - pharmacology ; Interleukin-2 - biosynthesis ; Interleukin-6 - biosynthesis ; Lipopolysaccharides - pharmacology ; Macrophages - immunology ; Male ; Nitric Oxide - metabolism ; Nitric Oxide - physiology ; Rats ; Rats, Wistar ; Spleen - cytology ; Time Factors ; Tumor Necrosis Factor-alpha - biosynthesis</subject><ispartof>Cellular immunology, 1998-06, Vol.186 (2), p.121-132</ispartof><rights>1998 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13</citedby><cites>FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9665754$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masson, Isabelle</creatorcontrib><creatorcontrib>Mathieu, Jacques</creatorcontrib><creatorcontrib>Nolland, Xavier-Bernard</creatorcontrib><creatorcontrib>De Sousa, Martine</creatorcontrib><creatorcontrib>Chanaud, Brigitte</creatorcontrib><creatorcontrib>Strzalko, Suzanne</creatorcontrib><creatorcontrib>Chancerelle, Yves</creatorcontrib><creatorcontrib>Kergonou, Jean-François</creatorcontrib><creatorcontrib>Giroud, Jean-Paul</creatorcontrib><creatorcontrib>Florentin, Irene</creatorcontrib><title>Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats</title><title>Cellular immunology</title><addtitle>Cell Immunol</addtitle><description>Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with nitric oxide (NO) production. In all burned rats, the proliferative response was depressed by more than 80% and NO production corresponded to a nitrite concentration above 20 μM. Proliferative responses in burned rats were fully restored in the presence of 250 μMNG-monomethyl-l-arginine (NMMA). A time course study of NO production in response to Con A, LPS, anti-CD3, and IFN-γ showed that splenic macrophages from burned rats responded to direct and indirect stimuli more rapidly and more intensively than normal macrophages. In the second part of this work, the effect of the overproduction of NO on the synthesis of immunoregulatory and proinflammatory cytokines was investigated. Although it was inhibited, IFN-γ production by splenocytes from burned rats remained sufficient for NO synthase induction and was restored by NMMA. Concomitantly, IL-2 concentration was enhanced but returned to normal in the presence of NMMA. TNF production was halved after burn injury and NMMA partially restored it. In contrast, IL-6 production was enhanced and increased further in the presence of NMMA. Therefore, cytokines were differently affected by burn injury and variously regulated by NO.</description><subject>Animals</subject><subject>Burns - immunology</subject><subject>Cell Division</subject><subject>Cells, Cultured</subject><subject>Concanavalin A - pharmacology</subject><subject>Cytokines - biosynthesis</subject><subject>Dexamethasone - pharmacology</subject><subject>Dinoprostone - biosynthesis</subject><subject>Glucocorticoids - pharmacology</subject><subject>Immune Tolerance - immunology</subject><subject>Interferon-gamma - biosynthesis</subject><subject>Interferon-gamma - pharmacology</subject><subject>Interleukin-2 - biosynthesis</subject><subject>Interleukin-6 - biosynthesis</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Spleen - cytology</subject><subject>Time Factors</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><issn>0008-8749</issn><issn>1090-2163</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkc9vFCEYhonR1LV69WbCydusMD-AOTar1SYbazb1TBj4xlIZGIGp7s0_XSa78WY8EfI9vOR7H4ReU7KlhLB32k7Tlva92NK6Z0_QhpKeVDVlzVO0IYSISvC2f45epPRACKVtTy7QRc9Yx7t2g34fggMcRvzZ5mg1vv1lDWDr8XuYI6QEBu-P03wf5hicHSGqbB8BHyDNwSdIWHmDr1yGWMjdMYfv1gP-EoNZdLbB4-vgXPhp_Td8dw9xUg7f-IclHtc_Diqnl-jZqFyCV-fzEn29_nC3-1Ttbz_e7K72lW44yVWntWZqbNlQNxRq0SgyQgO6ZoSDAc7VUO6UD7ozBWm5Hmir1dD2IwdiaHOJ3p5yyyI_FkhZTjZpcE55CEuSonTViVLb_0DKWkE7Jgq4PYE6hpQijHKOdlLxKCmRqxu5upGrG7m6KQ_enJOXYQLzFz_LKHNxmkPp4dFClElb8BqMjaCzNMH-K_oPCgmg-Q</recordid><startdate>19980615</startdate><enddate>19980615</enddate><creator>Masson, Isabelle</creator><creator>Mathieu, Jacques</creator><creator>Nolland, Xavier-Bernard</creator><creator>De Sousa, Martine</creator><creator>Chanaud, Brigitte</creator><creator>Strzalko, Suzanne</creator><creator>Chancerelle, Yves</creator><creator>Kergonou, Jean-François</creator><creator>Giroud, Jean-Paul</creator><creator>Florentin, Irene</creator><general>Elsevier Inc</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><scope>7X8</scope></search><sort><creationdate>19980615</creationdate><title>Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats</title><author>Masson, Isabelle ; Mathieu, Jacques ; Nolland, Xavier-Bernard ; De Sousa, Martine ; Chanaud, Brigitte ; Strzalko, Suzanne ; Chancerelle, Yves ; Kergonou, Jean-François ; Giroud, Jean-Paul ; Florentin, Irene</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Burns - immunology</topic><topic>Cell Division</topic><topic>Cells, Cultured</topic><topic>Concanavalin A - pharmacology</topic><topic>Cytokines - biosynthesis</topic><topic>Dexamethasone - pharmacology</topic><topic>Dinoprostone - biosynthesis</topic><topic>Glucocorticoids - pharmacology</topic><topic>Immune Tolerance - immunology</topic><topic>Interferon-gamma - biosynthesis</topic><topic>Interferon-gamma - pharmacology</topic><topic>Interleukin-2 - biosynthesis</topic><topic>Interleukin-6 - biosynthesis</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Spleen - cytology</topic><topic>Time Factors</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masson, Isabelle</creatorcontrib><creatorcontrib>Mathieu, Jacques</creatorcontrib><creatorcontrib>Nolland, Xavier-Bernard</creatorcontrib><creatorcontrib>De Sousa, Martine</creatorcontrib><creatorcontrib>Chanaud, Brigitte</creatorcontrib><creatorcontrib>Strzalko, Suzanne</creatorcontrib><creatorcontrib>Chancerelle, Yves</creatorcontrib><creatorcontrib>Kergonou, Jean-François</creatorcontrib><creatorcontrib>Giroud, Jean-Paul</creatorcontrib><creatorcontrib>Florentin, Irene</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><collection>MEDLINE - Academic</collection><jtitle>Cellular immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masson, Isabelle</au><au>Mathieu, Jacques</au><au>Nolland, Xavier-Bernard</au><au>De Sousa, Martine</au><au>Chanaud, Brigitte</au><au>Strzalko, Suzanne</au><au>Chancerelle, Yves</au><au>Kergonou, Jean-François</au><au>Giroud, Jean-Paul</au><au>Florentin, Irene</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats</atitle><jtitle>Cellular immunology</jtitle><addtitle>Cell Immunol</addtitle><date>1998-06-15</date><risdate>1998</risdate><volume>186</volume><issue>2</issue><spage>121</spage><epage>132</epage><pages>121-132</pages><issn>0008-8749</issn><eissn>1090-2163</eissn><abstract>Immunodeficiency follows extensive burns. We investigated some underlying mechanisms in rats, 10 days after a full-thickness skin burn affecting 20% of total body surface area. In both normal and burned rats the splenocyte proliferative response to Con A was linearly and negatively correlated with nitric oxide (NO) production. In all burned rats, the proliferative response was depressed by more than 80% and NO production corresponded to a nitrite concentration above 20 μM. Proliferative responses in burned rats were fully restored in the presence of 250 μMNG-monomethyl-l-arginine (NMMA). A time course study of NO production in response to Con A, LPS, anti-CD3, and IFN-γ showed that splenic macrophages from burned rats responded to direct and indirect stimuli more rapidly and more intensively than normal macrophages. In the second part of this work, the effect of the overproduction of NO on the synthesis of immunoregulatory and proinflammatory cytokines was investigated. Although it was inhibited, IFN-γ production by splenocytes from burned rats remained sufficient for NO synthase induction and was restored by NMMA. Concomitantly, IL-2 concentration was enhanced but returned to normal in the presence of NMMA. TNF production was halved after burn injury and NMMA partially restored it. In contrast, IL-6 production was enhanced and increased further in the presence of NMMA. Therefore, cytokines were differently affected by burn injury and variously regulated by NO.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>9665754</pmid><doi>10.1006/cimm.1998.1296</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0008-8749 |
ispartof | Cellular immunology, 1998-06, Vol.186 (2), p.121-132 |
issn | 0008-8749 1090-2163 |
language | eng |
recordid | cdi_proquest_miscellaneous_80005816 |
source | ScienceDirect Freedom Collection |
subjects | Animals Burns - immunology Cell Division Cells, Cultured Concanavalin A - pharmacology Cytokines - biosynthesis Dexamethasone - pharmacology Dinoprostone - biosynthesis Glucocorticoids - pharmacology Immune Tolerance - immunology Interferon-gamma - biosynthesis Interferon-gamma - pharmacology Interleukin-2 - biosynthesis Interleukin-6 - biosynthesis Lipopolysaccharides - pharmacology Macrophages - immunology Male Nitric Oxide - metabolism Nitric Oxide - physiology Rats Rats, Wistar Spleen - cytology Time Factors Tumor Necrosis Factor-alpha - biosynthesis |
title | Role of Nitric Oxide in Depressed Lymphoproliferative Responses and Altered Cytokine Production Following Thermal Injury in Rats |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T02%3A19%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20Nitric%20Oxide%20in%20Depressed%20Lymphoproliferative%20Responses%20and%20Altered%20Cytokine%20Production%20Following%20Thermal%20Injury%20in%20Rats&rft.jtitle=Cellular%20immunology&rft.au=Masson,%20Isabelle&rft.date=1998-06-15&rft.volume=186&rft.issue=2&rft.spage=121&rft.epage=132&rft.pages=121-132&rft.issn=0008-8749&rft.eissn=1090-2163&rft_id=info:doi/10.1006/cimm.1998.1296&rft_dat=%3Cproquest_cross%3E16481568%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c370t-5ccc6af46b231e283a0fe3ec2607ede77abfe317bc5db2347cb14cab49f7e0d13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=16481568&rft_id=info:pmid/9665754&rfr_iscdi=true |