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Epoprostenol sodium for treatment of pulmonary arterial hypertension.
Saito, Yukihiro; Nakamura, Kazufumi; Akagi, Satoshi; Sarashina, Toshihiro; Ejiri, Kentaro; Miura, Aya; Ogawa, Aiko; Matsubara, Hiromi; Ito, Hiroshi.
Afiliación
  • Saito Y; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Nakamura K; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Akagi S; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Sarashina T; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Ejiri K; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Miura A; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
  • Ogawa A; Division of Cardiology, National Hospital Organization Okayama Medical Center, Okayama, Japan.
  • Matsubara H; Division of Cardiology, National Hospital Organization Okayama Medical Center, Okayama, Japan.
  • Ito H; Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Vasc Health Risk Manag ; 11: 265-70, 2015.
Article en En | MEDLINE | ID: mdl-25999730
The release of endogenous prostacyclin (PGI2) is depressed in patients with pulmonary arterial hypertension (PAH). PGI2 replacement therapy by epoprostenol infusion is one of the best treatments available for PAH. Here, we provide an overview of the current clinical data for epoprostenol. Epoprostenol treatment improves symptoms, exercise capacity, and hemodynamics, and is the only treatment that has been shown to reduce mortality in patients with idiopathic PAH (IPAH) in randomized clinical trials. We have reported that high-dose epoprostenol therapy (>40 ng/kg/min) also results in marked hemodynamic improvement in some patients with IPAH. High-dose epoprostenol has a pro-apoptotic effect on PAH-PASMCs via the IP receptor and upregulation of Fas ligand (FasL) in vitro. However, long-term intravenous administration of epoprostenol is sometimes associated with catheter-related infections and leads to considerable inconvenience for the patient. In the future, the development of new routes of administration or the development of powerful PGI2 analogs, IP-receptor agonists, and gene and cell-based therapy enhancing PGI2 production with new routes of administration is required.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epoprostenol / Hipertensión Pulmonar / Antihipertensivos Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Vasc Health Risk Manag Asunto de la revista: ANGIOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Epoprostenol / Hipertensión Pulmonar / Antihipertensivos Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Vasc Health Risk Manag Asunto de la revista: ANGIOLOGIA Año: 2015 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Nueva Zelanda