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Bleomycin-Induced Lung Injury in the Rat: Effects of the Platelet-Activating Factor (PAF) Receptor Antagonist BN 52021 and Platelet Depletion
Bleomycin is a highly effective antitumor agent, but pulmonary toxicity, characterized by an acute inflammatory reaction and associated pulmonary edema, limits clinical use of the drug. Platelets and platelet-activating factor (PAF), a membrane-derived phospholipid, have been implicated in the mecha...
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Published in: | Environmental health perspectives 1990-04, Vol.85, p.65-69 |
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description | Bleomycin is a highly effective antitumor agent, but pulmonary toxicity, characterized by an acute inflammatory reaction and associated pulmonary edema, limits clinical use of the drug. Platelets and platelet-activating factor (PAF), a membrane-derived phospholipid, have been implicated in the mechanisms that can mediate pulmonary microvascular injury. We sought to investigate the role of PAF in bleomycin-induced lung injury in the rat, using the PAF receptor antagonist BN 52021; and the role of platelets though the use of an anti-platelet antibody. Lung injury was induced by intratracheal bleomycin (1.5 mg) and assessed by measurements of lung wet weight and total pulmonary extravascular albumin space (TPEAS). Bleomycin caused a significant increase in both indices after 48 hr, compared with control animals (p < 0.05). A single dose of BN 52021 (20 mg/kg orally) significantly reduced the bleomycin-induced increase in lung weight, but not the rise in TPEAS (p > 0.05). Increasing the dose of BN 52021 (20 mg/kg/12 hr, orally) had no additional effect. Reducing circulating platelet numbers by approximately 75% had no effect on either the increase in lung weight or TPEAS, observed 48 hr after bleomycin (p > 0.05). PAF may partially contribute to the acute inflammatory reaction seen after intratracheal bleomycin in rats. |
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Fan ; Barnes, Peter J. ; Laurent, Geoffrey J.</creator><creatorcontrib>Evans, Timothy W. ; McAnulty, Robin J. ; Rogers, Duncan F. ; Chung, K. Fan ; Barnes, Peter J. ; Laurent, Geoffrey J.</creatorcontrib><description>Bleomycin is a highly effective antitumor agent, but pulmonary toxicity, characterized by an acute inflammatory reaction and associated pulmonary edema, limits clinical use of the drug. Platelets and platelet-activating factor (PAF), a membrane-derived phospholipid, have been implicated in the mechanisms that can mediate pulmonary microvascular injury. We sought to investigate the role of PAF in bleomycin-induced lung injury in the rat, using the PAF receptor antagonist BN 52021; and the role of platelets though the use of an anti-platelet antibody. Lung injury was induced by intratracheal bleomycin (1.5 mg) and assessed by measurements of lung wet weight and total pulmonary extravascular albumin space (TPEAS). Bleomycin caused a significant increase in both indices after 48 hr, compared with control animals (p < 0.05). A single dose of BN 52021 (20 mg/kg orally) significantly reduced the bleomycin-induced increase in lung weight, but not the rise in TPEAS (p > 0.05). Increasing the dose of BN 52021 (20 mg/kg/12 hr, orally) had no additional effect. Reducing circulating platelet numbers by approximately 75% had no effect on either the increase in lung weight or TPEAS, observed 48 hr after bleomycin (p > 0.05). PAF may partially contribute to the acute inflammatory reaction seen after intratracheal bleomycin in rats.</description><identifier>ISSN: 0091-6765</identifier><identifier>EISSN: 1552-9924</identifier><identifier>DOI: 10.2307/3430666</identifier><identifier>PMID: 1696541</identifier><language>eng</language><publisher>United States: National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</publisher><subject>560300 - Chemicals Metabolism & Toxicology ; Administration, Inhalation ; Administration, Oral ; Adult respiratory distress syndrome ; Albumins ; Albumins - analysis ; Animals ; ANTI-INFECTIVE AGENTS ; ANTIBIOTICS ; ANTIMITOTIC DRUGS ; ANTINEOPLASTIC DRUGS ; ANTIPYRETICS ; BIOLOGICAL EFFECTS ; BIOLOGICAL MATERIALS ; BLEOMYCIN ; Bleomycin - administration & dosage ; Bleomycin - toxicity ; BLOOD ; BLOOD CELLS ; BLOOD COUNT ; BLOOD PLATELETS ; BODY ; BODY FLUIDS ; CENTRAL NERVOUS SYSTEM DEPRESSANTS ; Diterpenes ; Dosage ; Dose-Response Relationship, Drug ; DRUGS ; EDEMA ; ESTERS ; Extracellular Space - drug effects ; Ginkgolides ; Human resources ; INFLAMMATION ; INHIBITION ; Lactones ; LIPIDS ; Lung Diseases - blood ; Lung Diseases - chemically induced ; Lung Diseases - pathology ; Lung injury ; LUNGS ; Male ; MATERIALS ; MEMBRANE PROTEINS ; Neutrophils ; Organ Size - drug effects ; ORGANIC COMPOUNDS ; ORGANIC PHOSPHORUS COMPOUNDS ; ORGANS ; PATHOLOGICAL CHANGES ; PHOSPHOLIPIDS ; Platelet Activating Factor - antagonists & inhibitors ; Platelet Activating Factor - physiology ; Platelet Count - drug effects ; Platelets ; PROTEINS ; RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT ; Rats ; Rats, Inbred Lew ; RECEPTORS ; RESPIRATORY SYSTEM ; Symposium on Chemicals and Lung Toxicity. To Study the Agent or the Disease. July 24-25, 1988. 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Fan</creatorcontrib><creatorcontrib>Barnes, Peter J.</creatorcontrib><creatorcontrib>Laurent, Geoffrey J.</creatorcontrib><title>Bleomycin-Induced Lung Injury in the Rat: Effects of the Platelet-Activating Factor (PAF) Receptor Antagonist BN 52021 and Platelet Depletion</title><title>Environmental health perspectives</title><addtitle>Environ Health Perspect</addtitle><description>Bleomycin is a highly effective antitumor agent, but pulmonary toxicity, characterized by an acute inflammatory reaction and associated pulmonary edema, limits clinical use of the drug. Platelets and platelet-activating factor (PAF), a membrane-derived phospholipid, have been implicated in the mechanisms that can mediate pulmonary microvascular injury. We sought to investigate the role of PAF in bleomycin-induced lung injury in the rat, using the PAF receptor antagonist BN 52021; and the role of platelets though the use of an anti-platelet antibody. Lung injury was induced by intratracheal bleomycin (1.5 mg) and assessed by measurements of lung wet weight and total pulmonary extravascular albumin space (TPEAS). Bleomycin caused a significant increase in both indices after 48 hr, compared with control animals (p < 0.05). A single dose of BN 52021 (20 mg/kg orally) significantly reduced the bleomycin-induced increase in lung weight, but not the rise in TPEAS (p > 0.05). Increasing the dose of BN 52021 (20 mg/kg/12 hr, orally) had no additional effect. Reducing circulating platelet numbers by approximately 75% had no effect on either the increase in lung weight or TPEAS, observed 48 hr after bleomycin (p > 0.05). PAF may partially contribute to the acute inflammatory reaction seen after intratracheal bleomycin in rats.</description><subject>560300 - Chemicals Metabolism & Toxicology</subject><subject>Administration, Inhalation</subject><subject>Administration, Oral</subject><subject>Adult respiratory distress syndrome</subject><subject>Albumins</subject><subject>Albumins - analysis</subject><subject>Animals</subject><subject>ANTI-INFECTIVE AGENTS</subject><subject>ANTIBIOTICS</subject><subject>ANTIMITOTIC DRUGS</subject><subject>ANTINEOPLASTIC DRUGS</subject><subject>ANTIPYRETICS</subject><subject>BIOLOGICAL EFFECTS</subject><subject>BIOLOGICAL MATERIALS</subject><subject>BLEOMYCIN</subject><subject>Bleomycin - administration & dosage</subject><subject>Bleomycin - toxicity</subject><subject>BLOOD</subject><subject>BLOOD CELLS</subject><subject>BLOOD COUNT</subject><subject>BLOOD PLATELETS</subject><subject>BODY</subject><subject>BODY FLUIDS</subject><subject>CENTRAL NERVOUS SYSTEM DEPRESSANTS</subject><subject>Diterpenes</subject><subject>Dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>DRUGS</subject><subject>EDEMA</subject><subject>ESTERS</subject><subject>Extracellular Space - drug effects</subject><subject>Ginkgolides</subject><subject>Human resources</subject><subject>INFLAMMATION</subject><subject>INHIBITION</subject><subject>Lactones</subject><subject>LIPIDS</subject><subject>Lung Diseases - blood</subject><subject>Lung Diseases - chemically induced</subject><subject>Lung Diseases - pathology</subject><subject>Lung injury</subject><subject>LUNGS</subject><subject>Male</subject><subject>MATERIALS</subject><subject>MEMBRANE PROTEINS</subject><subject>Neutrophils</subject><subject>Organ Size - drug effects</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANIC PHOSPHORUS COMPOUNDS</subject><subject>ORGANS</subject><subject>PATHOLOGICAL CHANGES</subject><subject>PHOSPHOLIPIDS</subject><subject>Platelet Activating Factor - antagonists & inhibitors</subject><subject>Platelet Activating Factor - physiology</subject><subject>Platelet Count - drug effects</subject><subject>Platelets</subject><subject>PROTEINS</subject><subject>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>RECEPTORS</subject><subject>RESPIRATORY SYSTEM</subject><subject>Symposium on Chemicals and Lung Toxicity. To Study the Agent or the Disease. July 24-25, 1988. Cardiff, Wales</subject><subject>SYMPTOMS</subject><subject>TOXICITY</subject><subject>Vehicles</subject><issn>0091-6765</issn><issn>1552-9924</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><recordid>eNp1kd-KEzEUxoMoa63iEwhBBPViNP8mk3ghdNetFooui16HTOZMmzJNyiRd6EP4zmadZdULrw4533d-OZwPoeeUvGOcNO-54ERK-QDNaF2zSmsmHqIZIZpWspH1Y_QkpR0hhCopz9AZlVrWgs7Qz_MB4v7kfKhWoTs66PD6GDZ4FXbH8YR9wHkL-NrmD_iy78HlhGP_u3c12AwD5Grhsr-x2ZeppXU5jvjN1WL5Fl-Dg8PtcxGy3cTgU8bnX3HNCKPYhu6egD_BoRQfw1P0qLdDgmd3dY5-LC-_X3yp1t8-ry4W68oJJXOlWys6ohvBem1bpZSAlnIgWjLFrKSqZ6QTrdMMrLVtbRWhglPa8Fb3XDE-Rx8n7uHY7qFzEPJoB3MY_d6OJxOtN_8qwW_NJt4YWkvFC2uOXk6AmLI3yfkMbutiCOVCpmzRCFUX0-vJ5MaY0gj9_QeUmNvUzF1qxfni733--KaYiv5q0nepHPS_mF8N0Zxx</recordid><startdate>19900401</startdate><enddate>19900401</enddate><creator>Evans, Timothy W.</creator><creator>McAnulty, Robin J.</creator><creator>Rogers, Duncan F.</creator><creator>Chung, K. Fan</creator><creator>Barnes, Peter J.</creator><creator>Laurent, Geoffrey J.</creator><general>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</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>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>19900401</creationdate><title>Bleomycin-Induced Lung Injury in the Rat: Effects of the Platelet-Activating Factor (PAF) Receptor Antagonist BN 52021 and Platelet Depletion</title><author>Evans, Timothy W. ; McAnulty, Robin J. ; Rogers, Duncan F. ; Chung, K. Fan ; Barnes, Peter J. ; Laurent, Geoffrey J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-9ba4d09742f9ab8884eb13e096282a618f20d4bc92eaaab5a801431173b9f3823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>560300 - Chemicals Metabolism & Toxicology</topic><topic>Administration, Inhalation</topic><topic>Administration, Oral</topic><topic>Adult respiratory distress syndrome</topic><topic>Albumins</topic><topic>Albumins - analysis</topic><topic>Animals</topic><topic>ANTI-INFECTIVE AGENTS</topic><topic>ANTIBIOTICS</topic><topic>ANTIMITOTIC DRUGS</topic><topic>ANTINEOPLASTIC DRUGS</topic><topic>ANTIPYRETICS</topic><topic>BIOLOGICAL EFFECTS</topic><topic>BIOLOGICAL MATERIALS</topic><topic>BLEOMYCIN</topic><topic>Bleomycin - administration & dosage</topic><topic>Bleomycin - toxicity</topic><topic>BLOOD</topic><topic>BLOOD CELLS</topic><topic>BLOOD COUNT</topic><topic>BLOOD PLATELETS</topic><topic>BODY</topic><topic>BODY FLUIDS</topic><topic>CENTRAL NERVOUS SYSTEM DEPRESSANTS</topic><topic>Diterpenes</topic><topic>Dosage</topic><topic>Dose-Response Relationship, Drug</topic><topic>DRUGS</topic><topic>EDEMA</topic><topic>ESTERS</topic><topic>Extracellular Space - drug effects</topic><topic>Ginkgolides</topic><topic>Human resources</topic><topic>INFLAMMATION</topic><topic>INHIBITION</topic><topic>Lactones</topic><topic>LIPIDS</topic><topic>Lung Diseases - blood</topic><topic>Lung Diseases - chemically induced</topic><topic>Lung Diseases - pathology</topic><topic>Lung injury</topic><topic>LUNGS</topic><topic>Male</topic><topic>MATERIALS</topic><topic>MEMBRANE PROTEINS</topic><topic>Neutrophils</topic><topic>Organ Size - drug effects</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANIC PHOSPHORUS COMPOUNDS</topic><topic>ORGANS</topic><topic>PATHOLOGICAL CHANGES</topic><topic>PHOSPHOLIPIDS</topic><topic>Platelet Activating Factor - antagonists & inhibitors</topic><topic>Platelet Activating Factor - physiology</topic><topic>Platelet Count - drug effects</topic><topic>Platelets</topic><topic>PROTEINS</topic><topic>RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>RECEPTORS</topic><topic>RESPIRATORY SYSTEM</topic><topic>Symposium on Chemicals and Lung Toxicity. To Study the Agent or the Disease. July 24-25, 1988. Cardiff, Wales</topic><topic>SYMPTOMS</topic><topic>TOXICITY</topic><topic>Vehicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evans, Timothy W.</creatorcontrib><creatorcontrib>McAnulty, Robin J.</creatorcontrib><creatorcontrib>Rogers, Duncan F.</creatorcontrib><creatorcontrib>Chung, K. Fan</creatorcontrib><creatorcontrib>Barnes, Peter J.</creatorcontrib><creatorcontrib>Laurent, Geoffrey J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Environmental health perspectives</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evans, Timothy W.</au><au>McAnulty, Robin J.</au><au>Rogers, Duncan F.</au><au>Chung, K. Fan</au><au>Barnes, Peter J.</au><au>Laurent, Geoffrey J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bleomycin-Induced Lung Injury in the Rat: Effects of the Platelet-Activating Factor (PAF) Receptor Antagonist BN 52021 and Platelet Depletion</atitle><jtitle>Environmental health perspectives</jtitle><addtitle>Environ Health Perspect</addtitle><date>1990-04-01</date><risdate>1990</risdate><volume>85</volume><spage>65</spage><epage>69</epage><pages>65-69</pages><issn>0091-6765</issn><eissn>1552-9924</eissn><abstract>Bleomycin is a highly effective antitumor agent, but pulmonary toxicity, characterized by an acute inflammatory reaction and associated pulmonary edema, limits clinical use of the drug. Platelets and platelet-activating factor (PAF), a membrane-derived phospholipid, have been implicated in the mechanisms that can mediate pulmonary microvascular injury. We sought to investigate the role of PAF in bleomycin-induced lung injury in the rat, using the PAF receptor antagonist BN 52021; and the role of platelets though the use of an anti-platelet antibody. Lung injury was induced by intratracheal bleomycin (1.5 mg) and assessed by measurements of lung wet weight and total pulmonary extravascular albumin space (TPEAS). Bleomycin caused a significant increase in both indices after 48 hr, compared with control animals (p < 0.05). A single dose of BN 52021 (20 mg/kg orally) significantly reduced the bleomycin-induced increase in lung weight, but not the rise in TPEAS (p > 0.05). Increasing the dose of BN 52021 (20 mg/kg/12 hr, orally) had no additional effect. Reducing circulating platelet numbers by approximately 75% had no effect on either the increase in lung weight or TPEAS, observed 48 hr after bleomycin (p > 0.05). PAF may partially contribute to the acute inflammatory reaction seen after intratracheal bleomycin in rats.</abstract><cop>United States</cop><pub>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</pub><pmid>1696541</pmid><doi>10.2307/3430666</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 560300 - Chemicals Metabolism & Toxicology Administration, Inhalation Administration, Oral Adult respiratory distress syndrome Albumins Albumins - analysis Animals ANTI-INFECTIVE AGENTS ANTIBIOTICS ANTIMITOTIC DRUGS ANTINEOPLASTIC DRUGS ANTIPYRETICS BIOLOGICAL EFFECTS BIOLOGICAL MATERIALS BLEOMYCIN Bleomycin - administration & dosage Bleomycin - toxicity BLOOD BLOOD CELLS BLOOD COUNT BLOOD PLATELETS BODY BODY FLUIDS CENTRAL NERVOUS SYSTEM DEPRESSANTS Diterpenes Dosage Dose-Response Relationship, Drug DRUGS EDEMA ESTERS Extracellular Space - drug effects Ginkgolides Human resources INFLAMMATION INHIBITION Lactones LIPIDS Lung Diseases - blood Lung Diseases - chemically induced Lung Diseases - pathology Lung injury LUNGS Male MATERIALS MEMBRANE PROTEINS Neutrophils Organ Size - drug effects ORGANIC COMPOUNDS ORGANIC PHOSPHORUS COMPOUNDS ORGANS PATHOLOGICAL CHANGES PHOSPHOLIPIDS Platelet Activating Factor - antagonists & inhibitors Platelet Activating Factor - physiology Platelet Count - drug effects Platelets PROTEINS RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT Rats Rats, Inbred Lew RECEPTORS RESPIRATORY SYSTEM Symposium on Chemicals and Lung Toxicity. To Study the Agent or the Disease. July 24-25, 1988. Cardiff, Wales SYMPTOMS TOXICITY Vehicles |
title | Bleomycin-Induced Lung Injury in the Rat: Effects of the Platelet-Activating Factor (PAF) Receptor Antagonist BN 52021 and Platelet Depletion |
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