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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Veröffentlicht in:The FASEB journal 2001-05, Vol.15 (7), p.1187-1200
Hauptverfasser: CUZZOCREA, SALVATORE, MAZZON, EMANUELA, DUGO, LAURA, SERRAINO, IVANA, CICCOLO, ANTONIO, CENTORRINO, TOMMASO, SARRO, ANGELA, CAPUTI, ACHILLE P.
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container_issue 7
container_start_page 1187
container_title The FASEB journal
container_volume 15
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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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. 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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 &amp; 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 &amp; 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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