<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0873-2159</journal-id>
<journal-title><![CDATA[Revista Portuguesa de Pneumologia]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Port Pneumol]]></abbrev-journal-title>
<issn>0873-2159</issn>
<publisher>
<publisher-name><![CDATA[Sociedade Portuguesa de Pneumologia]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0873-21592006000400002</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Papel das citocinas proliferativas TGF-&#946; e VEGF no derrame pleural p&#963;s-revascularização do miocárdio]]></article-title>
<article-title xml:lang="en"><![CDATA[The proliferative cytokines TGF-&#946; and VEGF in pleural effusions post-coronary artery bypass graft]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Chibante]]></surname>
<given-names><![CDATA[António MS]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Vaz]]></surname>
<given-names><![CDATA[Marcelo Alexandre C]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Suso]]></surname>
<given-names><![CDATA[Francisco Vargas]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Univesidade do Rio de Janeiro Hospital Gaffrée-Guinle Serviço de Cardiopneumologia]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina Serviço de Pneumologia]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>07</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>07</month>
<year>2006</year>
</pub-date>
<volume>12</volume>
<numero>4</numero>
<fpage>359</fpage>
<lpage>367</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S0873-21592006000400002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S0873-21592006000400002&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S0873-21592006000400002&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="pt"><p><![CDATA[A cirurgia de revascularização do miocárdio envolve o acometimento, tanto do pericárdio como da pleura, conduzindo ao favorecimento de processos inflamatórios responsáveis pelo desenvolvimento de derrames nestes compartimentos. Objectivo: Estudar o comportamento das citocinas proliferativas TGF-&#946; (factor beta de transforma&#951;ão do crescimento) e VEGF (factor de crescimento do endotélio vascular) nos líquidos de 16 transudatos e de 43 derrames pleurais de doentes submetidos a cirurgias de revascularização do miocárdio provenientes do Instituto de Coração e do Serviço de Pneumologia da Universidade do São Paulo nos intervalos de 2, 24 e 48 horas de pós-operatório. Resultados: O derrame pleural pós-revascularização do miocárdio é um exsudato mobilizador de TGF-&#946; e VEGF no pós-operatório imediato. Os níveis de TGF-&#946; apresentam-se elevados nas primeiras 2 horas para caírem progressivamente até se aproximarem dos valores dos transudatos ao fim de 48 horas, enquanto o VEGF se inicia com níveis elevados já nas primeiras 2 horas com tendência a aumento pelo menos até 48 horas de pós-operatório. Conclusões: O TGF-&#946; parece comportar-se como elemento gatilho sobre a c&#953;lula mesotelial pleural para a liberação de VEGF no desenvolvimento de derrame pleural nas cirurgias de revascularização do miocárdio.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Coronary artery bypass graft (CABG) surgeries canimpact on the pericardium and pleural space, leading to inflammation which can cause effusion. Aim: To study the role of the proliferative cytokines TGF-&#946; and VEGF in the fluids of 16 transudates and 43 pleural effusions of patients who underwent CABG at the Heart Unit and Pulmonology Unit of the University Hospital of São Paulo. Levels of cytokines were assessed 2, 24 and 48 hours post-surgery. Results: The pleural effusion after CABG is an exsudative mobilizer of TGF-&#946; and VEGF cytokines immediately after surgery. The TGF-&#946; concentrations were elevated 2 hours after surgery but started to fall soon after, reaching transudate levels after 48 hours. VEGF levels were high in the first 2 hours post surgery and tended to maintain the same concentrations for at least 48 hours after surgery. Conclusions: Based on the results obtained, TGF-&#946; is a cytokine that seems to work as a trigger, leading the pleural mesothelial cell to express VEGF a cause of pleural effusion in CABG surgeries.]]></p></abstract>
<kwd-group>
<kwd lng="pt"><![CDATA[Inflamação]]></kwd>
<kwd lng="pt"><![CDATA[citocinas]]></kwd>
<kwd lng="pt"><![CDATA[derrame pleural]]></kwd>
<kwd lng="pt"><![CDATA[revascularização do miocárdio]]></kwd>
<kwd lng="en"><![CDATA[Inflammation]]></kwd>
<kwd lng="en"><![CDATA[cytokines]]></kwd>
<kwd lng="en"><![CDATA[pleural effusions]]></kwd>
<kwd lng="en"><![CDATA[coronary artery bypass grafting]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p><b>Papel das citocinas proliferativas TGF-&#946 e VEGF no derrame pleural pós-revascularização do miocárdio</b></p>       <p><b><em>The proliferative cytokines TGF-&#946 and VEGF in pleural effusions    post-coronary artery bypass graft</em></b></p>      <p>&nbsp;</p>      <p><b>António MS Chibante<sup><a href="#1">1</a><a name="top1"></a></sup></b></p>      <p><b>Marcelo Alexandre C Vaz<sup><a href="#2">2</a><a name="top2"></a></sup></b></p>      <p><b>Francisco Vargas Suso<sup><a href="#2">2</a><a name="top2"></a></sup></b></p>      <p>&nbsp;</p>      <p align="center"><b>Resumo</b></p>      <p>A cirurgia de revascularização do miocárdio envolve o acometimento, tanto do pericárdio como da pleura, conduzindo ao favorecimento de processos inflamatórios responsáveis pelo desenvolvimento de derrames nestes compartimentos.</p>      <p><b>Objectivo:</b> Estudar o comportamento das citocinas proliferativas TGF-&#946    (factor beta de transformação do crescimento) e VEGF (factor de crescimento    do endotélio vascular) nos líquidos de 16 transudatos e de 43 derrames pleurais    de doentes submetidos a cirurgias de revascularização do miocárdio provenientes    do Instituto de Coração e do Serviço de Pneumologia da Universidade do São Paulo    nos intervalos de 2, 24 e 48 horas de pós-operatório.</p>      ]]></body>
<body><![CDATA[<p><b>Resultados:</b> O derrame pleural pós-revascularização do miocárdio é um    exsudato mobilizador de TGF-&#946 e VEGF no pós-operatório imediato. Os níveis    de TGF-&#946 apresentam-se elevados nas primeiras 2 horas para caírem progressivamente    até se aproximarem dos valores dos transudatos ao fim de 48 horas, enquanto    o VEGF se inicia com níveis elevados já nas primeiras 2 horas com tendência    a aumento pelo menos até 48 horas de pós-operatório.</p>      <p><b>Conclusões:</b> O TGF-&#946 parece comportar-se como elemento gatilho sobre    a célula mesotelial pleural para a liberação de VEGF no desenvolvimento de derrame    pleural nas cirurgias de revascularização do miocárdio.</p>        <p><b>Palavras-chave</b>: Inflamação, citocinas, derrame pleural, revascularização    do miocárdio.</p>     <p>&nbsp;</p>      <p>&nbsp;</p>      <p align="center"><b>Abstract</b></p>      <p>Coronary artery bypass graft (CABG) surgeries canimpact on the pericardium and pleural space, leading to inflammation which can cause effusion.</p>      <p><b>Aim: </b>To study the role of the proliferative cytokines TGF-&#946 and    VEGF in the fluids of 16 transudates and 43 pleural effusions of patients who    underwent CABG at the Heart Unit and Pulmonology Unit of the University Hospital    of São Paulo. Levels of cytokines were assessed 2, 24 and 48 hours post-surgery.</p>      <p><b>Results: </b>The pleural effusion after CABG is an exsudative mobilizer of TGF-&#946 and VEGF cytokines immediately after surgery. The TGF-&#946 concentrations were elevated 2 hours after surgery but started to fall soon after, reaching transudate levels after 48 hours. VEGF levels were high in the first 2 hours post surgery and tended to maintain the same concentrations for at least 48 hours after surgery.</p>      <p><b>Conclusions: </b>Based on the results obtained, TGF-&#946 is a cytokine that seems to work as a trigger, leading the pleural mesothelial cell to express VEGF a cause of pleural effusion in CABG surgeries.</p>        ]]></body>
<body><![CDATA[<p><b>Key-words: </b>Inflammation, cytokines, pleural effusions, coronary artery    bypass grafting.</p>     <p>&nbsp;</p>     <p>Texto completo disponível apenas em PDF.</p>     <p>Full text only available in PDF format.</p>      <p>&nbsp;</p>     <p>&nbsp;</p>         <p align="center"><b>Bibliografia/Bibliography</b></p>      <!-- ref --><p>1. Vargas FS, Cukier A, Hueb W, Teixeira LR, Light RW. Relationship between pleural effusions and pericardial involvement after myocardial revascularization. Chest 1994; 105:1738-52.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000030&pid=S0873-2159200600040000200001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>2. Light RW. Pleural effusions after coronary artery bypass graft surgery. Opin Pulm Med 2002; 8:308-11.</p>      <p>3. Vargas FS, Vezhimi KK, Jatene FF, Terra-Filho M, Hueb W, Cukier A, Light RW. Acute pleuropulmonary complications detected by computed tomography following myocardial revascularization. Rev Hosp Clin Fac Med São Paulo. 2002; 57:135-42.</p>      ]]></body>
<body><![CDATA[<p>4. Dinarello CA. Proinflammatory Cytokines. Chest 2000; 118:503-8.</p>      <p>5. Kroegel C, Anthony VB. Immunobiology of pleural inflammation: potential implications for pathogenesis, diagnosis and therapy. Eur Respir J 1997; 10:2411-18. 6. Areno JP, McCarteney JP, Eggerstedt J, Grafton W, George R. Persistent pleural effusions following coronary bypass surgery. Chest 1998; 114:311-4.</p>      <p>7. Lee YC, Vaz Mac, Ely KA <i>et al</i>. Symptomatic persistent post-coronary artery bypass graft pleural effusion requiring treatment-clinical and histologic features. Chest 2001; 119:795-800.</p>      <p>8. Chung CL, Chen CH, Sheu JR, Chen YC, Chang SC. Proinflammatory cytokines, transforming growth factorbeta1, and fibrinolytic enzymes in loculated and free-flowing pleural exudates. Chest 2005; 128:690-7.</p>      <p>9. Kelly BM, Nicholas JJ, Chhablani R, Kavinsky CJ. The postpericardiotomy syndrome as a cause of pleurisy in rehabilitation patients. Arch Phys Med Rehabil 2000; 81:517-8.</p>      <p>10. De Souza Pereira. Morphofunctions study of rat pleural mesothelial cells exposed to low frequency noise. Aviat Space Environ Med 1999; 70:A-78-85.</p>      <p>11. Michailova KN. Electronmicroscopic observations on the visceral and parietal rat&#8217;s pleura after contralateral pneumonectomy. Eur J Morphol 2001; 39:47-56 </p>      <p>12. Mohammed KA, Nasreen N, Hardwick J, Logie CS, Patterson CE, Anthony VB. Bacterial induction of pleural mesothelial monolayer barrier dysfunction. AmJ Physiol Lung Cell Mol Physiol 2001; 281:119-25.</p>      <p>13. Gary-Lee YC, Melkerneker D, Thompson PJ, Light WR, Lane KB. Transforming growth factor beta induces VEGF elaboration from pleural mesothelial cell in vivo and in vitro. Am J Respir Crit Care Med 2002; 165:88-94.</p>      <p>14. Weatherhead M; Antunes G. Chemotherapeutic management of malignant pleural effusion. Expert Opin Pharmacother 2004; 5:1233-42.</p>      ]]></body>
<body><![CDATA[<p>15. Gary-Lee YC, Lane KB. The many faces of transforming growth factor- beta in pleural diseases. Curr Opin Pulm Med 2001; 7:173-9.</p>      <p>16. Grove CS, Lee YC. Vascular endothelial growth factor: the key mediator in pleural effusion formation. Curr Opin Pulm Med 2002; 8:294-301.</p>      <p>17. Aoki Y, Tosato G. Vascular endothelial growth factor/vascular permeability factor in the pathogenesis of primary effusion lymphomas. Leuk Lymphoma 2001; 41:229-37.</p>      <p>18. Kishiro I, Kato D, Fuse D, Yoshida T, Machida S, Kaneko N. Clinical significance of vascular endothelial growth factor in patient with primary lung cancer. Respirology 2002; 7:93-8.</p>      <p>19. Naim R; Tolnay E; Mueller KM; Kuhnen C. Co-expression of VEGF, c-Met and HGF/SF in secondary pleural tumors. Int J Mol Med 2004; 14:787-91.</p>      <p>20. Mohammed KA; Nasreen N; Hardwick J; Van Horn RD; Sanders KL; Antony VB. Mycobacteria induces pleural mesothelial permeability by down-regulating beta-catenin expression. Lung 2003; 181:57-66.</p>      <p>21. Roberts WG, Palade GE. Increased microvascular permeability and endothelial fenestration induced by vascular endothelial growth factor. J Cell Sci 1995; 108:2369-79.</p>      <p>22. Grove CS, Lee YC. Vascular endothelial growth factor: the key mediator in pleural effusion formation. Curr Opin Pulm Med 2002; 8:294-301.</p>      <p>23. Chibante AMS. Análise do processo inflamatório agudo no líquido pleural    pós-cirurgias de revascularização do miocárdio. Tese para obtenção do Título    de Doutor em Ciências pela Faculdade de Medicina da Universidade de São Paulo/Brasil    2004.</p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p>         <p><sup><a href="#top1">1</a><a name="1"></a></sup> Serviço de Cardiopneumologia,    Hospital Gaffrée-Guinle. Univesidade do Rio de Janeiro/ Cardiopulmonology Unit,    Hospital Gaffrée-Guinle. Universidade do Rio de Janeiro</p>     <p><sup><a href="#top2">2</a><a name="2"></a></sup> Serviço de Pneumologia, Hospital    das Clínicas da Faculdade de Medicina da Universidade de São Paulo/ Pulmonolgy    Unit, Hospital das Clínicas da Faculdade de Medicina da Universidade de São    Paulo</p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p align="right">Recebido para publica&ccedil;&atilde;o/<em>received for publication</em>:    05.11.11</p>     <p align="right">Aceite para publica&ccedil;&atilde;o/<em>accepted for publication</em>:    06.04.26 </p>     <p>&nbsp;</p>         ]]></body><back>
<ref-list>
<ref id="B1">
<nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Vargas]]></surname>
<given-names><![CDATA[FS]]></given-names>
</name>
<name>
<surname><![CDATA[Cukier]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Hueb]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
<name>
<surname><![CDATA[Teixeira]]></surname>
<given-names><![CDATA[LR]]></given-names>
</name>
<name>
<surname><![CDATA[Light]]></surname>
<given-names><![CDATA[RW]]></given-names>
</name>
</person-group>
<article-title xml:lang="en"><![CDATA[Relationship between pleural effusions and pericardial involvement after myocardial revascularization.]]></article-title>
<source><![CDATA[Chest]]></source>
<year>1994</year>
<volume>105</volume>
<page-range>1738-52</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
