Effect of a New Anti-Inflammatory Drug, Fenoprofen, on Platelet Aggregation and Thrombus Formation

Summary Fenoprofen sodium (a new antiinflammatory drug), aspirin, and phenylbutazone were compared with respect to their inhibitory activity on platelet function. These compounds inhibit collagen-induced platelet aggregation both in vitro (human, rabbit, and guinea pig) and in vivo (rabbit and guine...

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Veröffentlicht in:Experimental biology and medicine (Maywood, N.J.) N.J.), 1972-02, Vol.139 (2), p.548-552
Hauptverfasser: Herrmann, Roy G., Marshall, W. S., Crowe, V. Gail, Frank, J. D., Marlett, D. L., Lacefield, W. B.
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container_end_page 552
container_issue 2
container_start_page 548
container_title Experimental biology and medicine (Maywood, N.J.)
container_volume 139
creator Herrmann, Roy G.
Marshall, W. S.
Crowe, V. Gail
Frank, J. D.
Marlett, D. L.
Lacefield, W. B.
description Summary Fenoprofen sodium (a new antiinflammatory drug), aspirin, and phenylbutazone were compared with respect to their inhibitory activity on platelet function. These compounds inhibit collagen-induced platelet aggregation both in vitro (human, rabbit, and guinea pig) and in vivo (rabbit and guinea pig). In an extracorporeal shunt experiment in the rabbit, both fenoprofen sodium and aspirin inhibited thrombus formation. Of the three compounds tested, fenoprofen sodium appears to be the most active inhibitor of platelet function.
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S.</creatorcontrib><creatorcontrib>Crowe, V. Gail</creatorcontrib><creatorcontrib>Frank, J. D.</creatorcontrib><creatorcontrib>Marlett, D. L.</creatorcontrib><creatorcontrib>Lacefield, W. B.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herrmann, Roy G.</au><au>Marshall, W. S.</au><au>Crowe, V. Gail</au><au>Frank, J. D.</au><au>Marlett, D. L.</au><au>Lacefield, W. B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of a New Anti-Inflammatory Drug, Fenoprofen, on Platelet Aggregation and Thrombus Formation</atitle><jtitle>Experimental biology and medicine (Maywood, N.J.)</jtitle><addtitle>Proc Soc Exp Biol Med</addtitle><date>1972-02</date><risdate>1972</risdate><volume>139</volume><issue>2</issue><spage>548</spage><epage>552</epage><pages>548-552</pages><issn>0037-9727</issn><issn>1535-3702</issn><eissn>1535-3699</eissn><abstract>Summary Fenoprofen sodium (a new antiinflammatory drug), aspirin, and phenylbutazone were compared with respect to their inhibitory activity on platelet function. These compounds inhibit collagen-induced platelet aggregation both in vitro (human, rabbit, and guinea pig) and in vivo (rabbit and guinea pig). In an extracorporeal shunt experiment in the rabbit, both fenoprofen sodium and aspirin inhibited thrombus formation. Of the three compounds tested, fenoprofen sodium appears to be the most active inhibitor of platelet function.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>5059045</pmid><doi>10.3181/00379727-139-36183</doi><tpages>5</tpages></addata></record>
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ispartof Experimental biology and medicine (Maywood, N.J.), 1972-02, Vol.139 (2), p.548-552
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subjects Adenosine Diphosphate - antagonists & inhibitors
Analysis of Variance
Animals
Anti-Inflammatory Agents - pharmacology
Aspirin - pharmacology
Blood Platelets - drug effects
Collagen - antagonists & inhibitors
Depression, Chemical
Drug Antagonism
Ethers - pharmacology
Extracorporeal Circulation
Humans
In Vitro Techniques
Mesentery - blood supply
Microcirculation - drug effects
Phenylbutazone - pharmacology
Platelet Adhesiveness - drug effects
Propionates - pharmacology
Rabbits
Thrombosis - prevention & control
title Effect of a New Anti-Inflammatory Drug, Fenoprofen, on Platelet Aggregation and Thrombus Formation
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