Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat
ABSTRACT Oxidative stress has been suggested as a potential mechanism in the pathogenesis of lung inflammation. The pharmacological profile of n‐acetylcysteine (NAC), a free radical scavenger, was evaluated in an experimental model of lung injury (carrageenan‐induced pleurisy). Injection of carragee...
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creator | CUZZOCREA, SALVATORE MAZZON, EMANUELA DUGO, LAURA SERRAINO, IVANA CICCOLO, ANTONIO CENTORRINO, TOMMASO SARRO, ANGELA CAPUTI, ACHILLE P. |
description | ABSTRACT
Oxidative stress has been suggested as a potential mechanism in the pathogenesis of lung inflammation. The pharmacological profile of n‐acetylcysteine (NAC), a free radical scavenger, was evaluated in an experimental model of lung injury (carrageenan‐induced pleurisy). Injection of carrageenan into the pleural cavity of rats elicited an acute inflammatory response characterized by fluid accumulation in the pleural cavitythat contained manyneutrophils (PMNs), an infiltration of PMNs in lung tissues and subsequent lipid peroxidation, and increased production of nitrite/nitrate, tumor necrosis factor α, and interleukin 1β. All parameters of inflammation were attenuated by NAC treatment. Furthermore, carrageenan induced an up‐regulation of the adhesion molecules ICAM‐1 and P‐selectin, as well as nitrotyrosine and poly (ADP‐ribose) synthetase (PARS), as determined by immuno‐histochemical analysis of lung tissues. The degree of staining for the ICAM‐1, P‐selectin, nitrotyrosine, and PARS was reduced by NAC. In vivo NAC treatment significantly reduced peroxynitrite formation as measured by the oxidation of the fluorescent dihydrorho‐damine‐123, prevented the appearance of DNA damage, an decrease in mitochondrial respiration, and partially restored the cellular level of NAD+ in ex vivo macrophages harvested from the pleural cavity of rats subjected to carrageenan‐induced pleurisy. A significant alteration in the morphology of red blood cells was observed 24 h after carrageenan administration. NAC treatment has the ability to significantly diminish the red blood cell alteration. Our results clearly demonstrate that NAC treatment exerts a protective effect and clearly indicate that NAC offers a novel therapeutic approach for the management of lung injury where radicals have been postulated to play a role.—Cuzzocrea, S., Mazzon, E., Dugo, L., Serraino, I., Ciccolo, A., Centorrino, T., De Sarro, A., Caputi, A. P. Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat. FASEB J. 15, 1187–1200 (2001) |
doi_str_mv | 10.1096/fj.00-0526hyp |
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Oxidative stress has been suggested as a potential mechanism in the pathogenesis of lung inflammation. The pharmacological profile of n‐acetylcysteine (NAC), a free radical scavenger, was evaluated in an experimental model of lung injury (carrageenan‐induced pleurisy). Injection of carrageenan into the pleural cavity of rats elicited an acute inflammatory response characterized by fluid accumulation in the pleural cavitythat contained manyneutrophils (PMNs), an infiltration of PMNs in lung tissues and subsequent lipid peroxidation, and increased production of nitrite/nitrate, tumor necrosis factor α, and interleukin 1β. All parameters of inflammation were attenuated by NAC treatment. Furthermore, carrageenan induced an up‐regulation of the adhesion molecules ICAM‐1 and P‐selectin, as well as nitrotyrosine and poly (ADP‐ribose) synthetase (PARS), as determined by immuno‐histochemical analysis of lung tissues. The degree of staining for the ICAM‐1, P‐selectin, nitrotyrosine, and PARS was reduced by NAC. In vivo NAC treatment significantly reduced peroxynitrite formation as measured by the oxidation of the fluorescent dihydrorho‐damine‐123, prevented the appearance of DNA damage, an decrease in mitochondrial respiration, and partially restored the cellular level of NAD+ in ex vivo macrophages harvested from the pleural cavity of rats subjected to carrageenan‐induced pleurisy. A significant alteration in the morphology of red blood cells was observed 24 h after carrageenan administration. NAC treatment has the ability to significantly diminish the red blood cell alteration. Our results clearly demonstrate that NAC treatment exerts a protective effect and clearly indicate that NAC offers a novel therapeutic approach for the management of lung injury where radicals have been postulated to play a role.—Cuzzocrea, S., Mazzon, E., Dugo, L., Serraino, I., Ciccolo, A., Centorrino, T., De Sarro, A., Caputi, A. P. Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat. FASEB J. 15, 1187–1200 (2001)</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.00-0526hyp</identifier><identifier>PMID: 11344087</identifier><language>eng</language><publisher>United States: Federation of American Societies for Experimental Biology</publisher><subject>Acetylcysteine - pharmacology ; Animals ; Blotting, Western ; Carrageenan - toxicity ; Disease Models, Animal ; DNA Damage - drug effects ; DNA-Binding Proteins - metabolism ; Erythrocytes - drug effects ; Erythrocytes - ultrastructure ; Free Radical Scavengers - pharmacology ; I-kappa B Proteins ; Immunohistochemistry ; inflammation ; Intercellular Adhesion Molecule-1 - metabolism ; Lung - pathology ; Lung - physiopathology ; Macrophages - drug effects ; Macrophages - physiology ; Male ; Malondialdehyde - metabolism ; n-acetylcysteine ; Neutrophils - physiology ; NF-KappaB Inhibitor alpha ; Nitrates - metabolism ; nitric oxide ; Nitric Oxide - metabolism ; P-Selectin - metabolism ; Peroxidase - metabolism ; peroxynitrite ; Pleurisy - chemically induced ; Pleurisy - drug therapy ; Pleurisy - pathology ; Pleurisy - physiopathology ; Poly(ADP-ribose) Polymerases - metabolism ; Rats ; Rats, Sprague-Dawley ; superoxide ; Tyrosine - analogs & derivatives ; Tyrosine - metabolism</subject><ispartof>The FASEB journal, 2001-05, Vol.15 (7), p.1187-1200</ispartof><rights>FASEB</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371P-5656a85b545f603bfd9722b7f71463decf4331c6855b23aec3d7c6923d90849a3</citedby><cites>FETCH-LOGICAL-c371P-5656a85b545f603bfd9722b7f71463decf4331c6855b23aec3d7c6923d90849a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.00-0526hyp$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.00-0526hyp$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11344087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CUZZOCREA, SALVATORE</creatorcontrib><creatorcontrib>MAZZON, EMANUELA</creatorcontrib><creatorcontrib>DUGO, LAURA</creatorcontrib><creatorcontrib>SERRAINO, IVANA</creatorcontrib><creatorcontrib>CICCOLO, ANTONIO</creatorcontrib><creatorcontrib>CENTORRINO, TOMMASO</creatorcontrib><creatorcontrib>SARRO, ANGELA</creatorcontrib><creatorcontrib>CAPUTI, ACHILLE P.</creatorcontrib><title>Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><description>ABSTRACT
Oxidative stress has been suggested as a potential mechanism in the pathogenesis of lung inflammation. The pharmacological profile of n‐acetylcysteine (NAC), a free radical scavenger, was evaluated in an experimental model of lung injury (carrageenan‐induced pleurisy). Injection of carrageenan into the pleural cavity of rats elicited an acute inflammatory response characterized by fluid accumulation in the pleural cavitythat contained manyneutrophils (PMNs), an infiltration of PMNs in lung tissues and subsequent lipid peroxidation, and increased production of nitrite/nitrate, tumor necrosis factor α, and interleukin 1β. All parameters of inflammation were attenuated by NAC treatment. Furthermore, carrageenan induced an up‐regulation of the adhesion molecules ICAM‐1 and P‐selectin, as well as nitrotyrosine and poly (ADP‐ribose) synthetase (PARS), as determined by immuno‐histochemical analysis of lung tissues. The degree of staining for the ICAM‐1, P‐selectin, nitrotyrosine, and PARS was reduced by NAC. In vivo NAC treatment significantly reduced peroxynitrite formation as measured by the oxidation of the fluorescent dihydrorho‐damine‐123, prevented the appearance of DNA damage, an decrease in mitochondrial respiration, and partially restored the cellular level of NAD+ in ex vivo macrophages harvested from the pleural cavity of rats subjected to carrageenan‐induced pleurisy. A significant alteration in the morphology of red blood cells was observed 24 h after carrageenan administration. NAC treatment has the ability to significantly diminish the red blood cell alteration. Our results clearly demonstrate that NAC treatment exerts a protective effect and clearly indicate that NAC offers a novel therapeutic approach for the management of lung injury where radicals have been postulated to play a role.—Cuzzocrea, S., Mazzon, E., Dugo, L., Serraino, I., Ciccolo, A., Centorrino, T., De Sarro, A., Caputi, A. P. Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat. FASEB J. 15, 1187–1200 (2001)</description><subject>Acetylcysteine - pharmacology</subject><subject>Animals</subject><subject>Blotting, Western</subject><subject>Carrageenan - toxicity</subject><subject>Disease Models, Animal</subject><subject>DNA Damage - drug effects</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Erythrocytes - drug effects</subject><subject>Erythrocytes - ultrastructure</subject><subject>Free Radical Scavengers - pharmacology</subject><subject>I-kappa B Proteins</subject><subject>Immunohistochemistry</subject><subject>inflammation</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>Lung - pathology</subject><subject>Lung - physiopathology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - physiology</subject><subject>Male</subject><subject>Malondialdehyde - metabolism</subject><subject>n-acetylcysteine</subject><subject>Neutrophils - physiology</subject><subject>NF-KappaB Inhibitor alpha</subject><subject>Nitrates - metabolism</subject><subject>nitric oxide</subject><subject>Nitric Oxide - metabolism</subject><subject>P-Selectin - metabolism</subject><subject>Peroxidase - metabolism</subject><subject>peroxynitrite</subject><subject>Pleurisy - chemically induced</subject><subject>Pleurisy - drug therapy</subject><subject>Pleurisy - pathology</subject><subject>Pleurisy - physiopathology</subject><subject>Poly(ADP-ribose) Polymerases - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>superoxide</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - metabolism</subject><issn>0892-6638</issn><issn>1530-6860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLFOwzAQhi0EoqUwsiK_QMo5jp2EDSpKQZWoBAxMkWOfW1dpUjkJKBuPwDPyJKRqJTamu_vv0z98hFwyGDNI5bVdjwECEKFcddsjMmSCQyATCcdkCEkaBlLyZEDO6noNAAyYPCUDxngUQRIPSbfwVYO6cR9I0dp-q2llafnz9a00Nl2hu7pBVyKtSlq05ZK6ct36jqrSUI-G5kVVGaqxKOimMs46rRrXs640rd79O6qV92qJWKpdTJsVUq-ac3JiVVHjxWGOyNv0_nUyC-bPD4-T23mgecwWgZBCqkTkIhJWAs-tSeMwzGMbs0hyg9pGnDMtEyHykCvU3MRapiE3KSRRqviIBPte7au69mizrXcb5buMQbZTmNl1BpAdFPb81Z7ftvkGzR99cNYDN3vg0xXY_d-WTV_uwulTb76_Z-8L_gtDT4IT</recordid><startdate>200105</startdate><enddate>200105</enddate><creator>CUZZOCREA, SALVATORE</creator><creator>MAZZON, EMANUELA</creator><creator>DUGO, LAURA</creator><creator>SERRAINO, IVANA</creator><creator>CICCOLO, ANTONIO</creator><creator>CENTORRINO, TOMMASO</creator><creator>SARRO, ANGELA</creator><creator>CAPUTI, ACHILLE P.</creator><general>Federation of American Societies for Experimental Biology</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></search><sort><creationdate>200105</creationdate><title>Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat</title><author>CUZZOCREA, SALVATORE ; MAZZON, EMANUELA ; DUGO, LAURA ; SERRAINO, IVANA ; CICCOLO, ANTONIO ; CENTORRINO, TOMMASO ; SARRO, ANGELA ; CAPUTI, ACHILLE P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371P-5656a85b545f603bfd9722b7f71463decf4331c6855b23aec3d7c6923d90849a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Acetylcysteine - pharmacology</topic><topic>Animals</topic><topic>Blotting, Western</topic><topic>Carrageenan - toxicity</topic><topic>Disease Models, Animal</topic><topic>DNA Damage - drug effects</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Erythrocytes - drug effects</topic><topic>Erythrocytes - ultrastructure</topic><topic>Free Radical Scavengers - pharmacology</topic><topic>I-kappa B Proteins</topic><topic>Immunohistochemistry</topic><topic>inflammation</topic><topic>Intercellular Adhesion Molecule-1 - metabolism</topic><topic>Lung - pathology</topic><topic>Lung - physiopathology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - physiology</topic><topic>Male</topic><topic>Malondialdehyde - metabolism</topic><topic>n-acetylcysteine</topic><topic>Neutrophils - physiology</topic><topic>NF-KappaB Inhibitor alpha</topic><topic>Nitrates - metabolism</topic><topic>nitric oxide</topic><topic>Nitric Oxide - metabolism</topic><topic>P-Selectin - metabolism</topic><topic>Peroxidase - metabolism</topic><topic>peroxynitrite</topic><topic>Pleurisy - chemically induced</topic><topic>Pleurisy - drug therapy</topic><topic>Pleurisy - pathology</topic><topic>Pleurisy - physiopathology</topic><topic>Poly(ADP-ribose) Polymerases - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>superoxide</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CUZZOCREA, SALVATORE</creatorcontrib><creatorcontrib>MAZZON, EMANUELA</creatorcontrib><creatorcontrib>DUGO, LAURA</creatorcontrib><creatorcontrib>SERRAINO, IVANA</creatorcontrib><creatorcontrib>CICCOLO, ANTONIO</creatorcontrib><creatorcontrib>CENTORRINO, TOMMASO</creatorcontrib><creatorcontrib>SARRO, ANGELA</creatorcontrib><creatorcontrib>CAPUTI, ACHILLE P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The FASEB journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CUZZOCREA, SALVATORE</au><au>MAZZON, EMANUELA</au><au>DUGO, LAURA</au><au>SERRAINO, IVANA</au><au>CICCOLO, ANTONIO</au><au>CENTORRINO, TOMMASO</au><au>SARRO, ANGELA</au><au>CAPUTI, ACHILLE P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat</atitle><jtitle>The FASEB journal</jtitle><addtitle>FASEB J</addtitle><date>2001-05</date><risdate>2001</risdate><volume>15</volume><issue>7</issue><spage>1187</spage><epage>1200</epage><pages>1187-1200</pages><issn>0892-6638</issn><eissn>1530-6860</eissn><abstract>ABSTRACT
Oxidative stress has been suggested as a potential mechanism in the pathogenesis of lung inflammation. The pharmacological profile of n‐acetylcysteine (NAC), a free radical scavenger, was evaluated in an experimental model of lung injury (carrageenan‐induced pleurisy). Injection of carrageenan into the pleural cavity of rats elicited an acute inflammatory response characterized by fluid accumulation in the pleural cavitythat contained manyneutrophils (PMNs), an infiltration of PMNs in lung tissues and subsequent lipid peroxidation, and increased production of nitrite/nitrate, tumor necrosis factor α, and interleukin 1β. All parameters of inflammation were attenuated by NAC treatment. Furthermore, carrageenan induced an up‐regulation of the adhesion molecules ICAM‐1 and P‐selectin, as well as nitrotyrosine and poly (ADP‐ribose) synthetase (PARS), as determined by immuno‐histochemical analysis of lung tissues. The degree of staining for the ICAM‐1, P‐selectin, nitrotyrosine, and PARS was reduced by NAC. In vivo NAC treatment significantly reduced peroxynitrite formation as measured by the oxidation of the fluorescent dihydrorho‐damine‐123, prevented the appearance of DNA damage, an decrease in mitochondrial respiration, and partially restored the cellular level of NAD+ in ex vivo macrophages harvested from the pleural cavity of rats subjected to carrageenan‐induced pleurisy. A significant alteration in the morphology of red blood cells was observed 24 h after carrageenan administration. NAC treatment has the ability to significantly diminish the red blood cell alteration. Our results clearly demonstrate that NAC treatment exerts a protective effect and clearly indicate that NAC offers a novel therapeutic approach for the management of lung injury where radicals have been postulated to play a role.—Cuzzocrea, S., Mazzon, E., Dugo, L., Serraino, I., Ciccolo, A., Centorrino, T., De Sarro, A., Caputi, A. P. Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat. FASEB J. 15, 1187–1200 (2001)</abstract><cop>United States</cop><pub>Federation of American Societies for Experimental Biology</pub><pmid>11344087</pmid><doi>10.1096/fj.00-0526hyp</doi><tpages>14</tpages></addata></record> |
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subjects | Acetylcysteine - pharmacology Animals Blotting, Western Carrageenan - toxicity Disease Models, Animal DNA Damage - drug effects DNA-Binding Proteins - metabolism Erythrocytes - drug effects Erythrocytes - ultrastructure Free Radical Scavengers - pharmacology I-kappa B Proteins Immunohistochemistry inflammation Intercellular Adhesion Molecule-1 - metabolism Lung - pathology Lung - physiopathology Macrophages - drug effects Macrophages - physiology Male Malondialdehyde - metabolism n-acetylcysteine Neutrophils - physiology NF-KappaB Inhibitor alpha Nitrates - metabolism nitric oxide Nitric Oxide - metabolism P-Selectin - metabolism Peroxidase - metabolism peroxynitrite Pleurisy - chemically induced Pleurisy - drug therapy Pleurisy - pathology Pleurisy - physiopathology Poly(ADP-ribose) Polymerases - metabolism Rats Rats, Sprague-Dawley superoxide Tyrosine - analogs & derivatives Tyrosine - metabolism |
title | Protective effects of n‐acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat |
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