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Review Article
Experimental Models for the Study of Pulmonary Fibrosis: Current Usefulness and Future Promise
María Molina-Molina
Corresponding author
mariamolinamolina@hotmail.com

Correspondence: Dra. M. Molina-Molina. Unidad de Endoscopia Respiratoria. Servicio de Neumología. Hospital Clínic. Villarroel, 170. Barcelona. España
, Javier Pereda, Antoni Xaubet
Instituto de Investigaciones Agustí Pi i Sunyer (IDIBAPS), Unidad de Endoscopia Respiratoria, CIBER, Enfermedades Respiratorias, Servicio de Neumología, Instituto Clínico del Tórax, Hospital Clínic, Barcelona, Spain
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        "autoresLista" => "Mar&#237;a Molina-Molina, Javier Pereda, Antoni Xaubet"
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            "entidad" => "Instituto de Investigaciones Agust&#237; Pi i Sunyer &#40;IDIBAPS&#41;&#44; Unidad de Endoscopia Respiratoria&#44; CIBER&#44; Enfermedades Respiratorias&#44; Servicio de Neumolog&#237;a&#44; Instituto Cl&#237;nico del T&#243;rax&#44; Hospital Cl&#237;nic&#44; Barcelona&#44; Spain"
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    "fechaRecibido" => "2006-09-12"
    "fechaAceptado" => "2006-09-19"
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          "clase" => "keyword"
          "titulo" => "Key words"
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          "palabras" => array:3 [
            0 => "Pulmonary fibrosis"
            1 => "Experimental studies"
            2 => "Interstitial lung disease"
          ]
        ]
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          "clase" => "keyword"
          "titulo" => "Palabras clave"
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          "palabras" => array:3 [
            0 => "Fibrosis pulmonar"
            1 => "Estudio experimental"
            2 => "Enfermedad pulmonar intersticial"
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      "en" => array:1 [
        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">Diffuse interstitial lung diseases form a group of respiratory diseases about which many questions remain to be answered&#46; In recent years there have been major advances in the correct diagnostic classification of each disease&#44; and therefore&#44; the essential foundations have been laid for investigation of their pathophysiology&#46; However&#44; both the triggers and the precise mechanisms that lead to irreversible changes in the lung parenchyma remain to be identified&#46; Idiopathic pulmonary fibrosis is the most common diffuse interstitial lung disease and has the worst prognosis&#46; Current treatments are empirical and the response is random&#59; furthermore&#44; they do not improve survival&#46; Consequently&#44; most basic research has focused on the pathophysiology of the disease and on identifying an effective therapeutic approach&#46; The aim of this review is to describe the experimental studies that have begun to open the way towards an understanding of the complex process of fibrosis&#46;</p>"
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      "es" => array:1 [
        "resumen" => "<p class="elsevierStyleSimplePara elsevierViewall">Las enfermedades pulmonares intersticiales difusas son un grupo de enfermedades respiratorias con m&#250;ltiples inc&#243;gnitas por resolver&#46; En los &#250;ltimos a&#241;os se ha asistido a un gran avance en la clasificaci&#243;n para el diagn&#243;stico correcto de cada una de ellas&#44; con lo que se han sentado las bases indispensables para el estudio del proceso fisiopatol&#243;gico en cada entidad&#46; Sin embargo&#44; resultan desconocidos tanto la causa desencadenante como los mecanismos exactos que llevan a la alteraci&#243;n irreversible del par&#233;nquima&#46; Dentro de las enfermedades pulmonares intersticiales difusas&#44; la m&#225;s frecuente y de peor pron&#243;stico es la fibrosis pulmonar idiop&#225;tica&#46; Los tratamientos actuales son emp&#237;ricos&#44; con respuesta aleatoria&#44; e incapaces de mejorar la supervivencia&#46; Por este motivo la mayor&#237;a de los estudios b&#225;sicos se han centrado en buscar respuestas sobre su fisiopatolog&#237;a y un abordaje terap&#233;utico efectivo&#46; El objetivo de esta revisi&#243;n es dar a conocer los estudios experimentales que han empezado a abrir caminos hacia la comprensi&#243;n del complejo proceso fibr&#243;tico&#46;</p>"
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ISSN: 15792129
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