Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros

Bases de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Fitoterapia ; 172: 105719, 2024 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-37931717

RESUMEN

Red yeast rice (RYR) is an entirely natural product that originates from the fermentation of white rice (Oryza sativa) with a yeast, mainly Monascus Purpureus, and has been part of traditional Chinese medicine and diet since ancient times. It has generated great interest in recent years in the context of cardiovascular (CV) prevention due to its ability to inhibit endogenous cholesterol production, helping to achieve and maintain optimal plasma lipid concentrations. This review aims to make an extensive 360-degree assessment and summary of the whole currently available scientific evidence about RYR, starting with its biochemical composition, passing through a historical reconstruction of all the studies that have evaluated its efficacy and safety in cholesterol-lowering action, with a focus on CV outcomes, and ultimately addressing its other relevant clinical effects. We also discuss its possible therapeutic role, alone or in combination with other nutraceuticals, in different clinical scenarios, taking into account the positions of major scientific documents on the issue, and describe the articulate legal controversies that have characterized the regulation of its use up to the present day. RYR preparations have been proven safe and effective in improving lipid profile, with a potential role in reducing cardiovascular risk. They can be considered as additional supportive agents in the armamentarium of lipid-modifying therapies.


Asunto(s)
Productos Biológicos , Colesterol , Estructura Molecular , Suplementos Dietéticos , Productos Biológicos/farmacología
2.
Artículo en Inglés | MEDLINE | ID: mdl-25548520

RESUMEN

Regenerative or stem cell therapy is an emerging field of treatment based on stimulation of endogenous resident stem cells or administration of exogenous stem cells to treat diseases or injury and to replace malfunctioning or damaged tissues. Current evidence suggests that in the lung, these cells may participate in tissue homeostasis and regeneration after injury. Animal and human studies have demonstrated that tissue-specific stem cells and bone marrow-derived cells contribute to lung tissue regeneration and protection, and thus administration of exogenous stem/progenitor cells or humoral factors responsible for the activation of endogenous stem/progenitor cells may be a potent next-generation therapy for chronic obstructive pulmonary disease. The use of bone marrow-derived stem cells could allow repairing and regenerate the damaged tissue present in chronic obstructive pulmonary disease by means of their engraftment into the lung. Another approach could be the stimulation of resident stem cells by means of humoral factors or photobiostimulation.


Asunto(s)
Pulmón/fisiopatología , Enfermedad Pulmonar Obstructiva Crónica/terapia , Regeneración , Medicina Regenerativa/métodos , Trasplante de Células Madre , Animales , Humanos , Terapia por Luz de Baja Intensidad , Pulmón/patología , Enfermedad Pulmonar Obstructiva Crónica/patología , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Recuperación de la Función , Resultado del Tratamiento
3.
Expert Rev Respir Med ; 8(6): 665-71, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25312239

RESUMEN

Umeclidinium is a novel inhaled long-acting muscarinic receptor antagonist (LAMA) approved for treatment of chronic obstructive pulmonary disease (COPD). It provides a bronchodilation of at least 24 h, is well tolerated and has a safe profile. In this article, we describe its pharmacokinetic and pharmacodynamic characteristics. Moreover, we present a meta-analysis of randomized clinical trials carried out in COPD patients, in which the change of forced expiratory volume in 1 s (FEV1) induced by umeclidinium has been compared with that elicited by placebo or the active compound tiotropium. The data generated by the pivotal trials indicate that umeclidinium bromide delivered once-daily via the Ellipta™ inhaler is an effective and well-tolerated treatment for COPD. Therefore, it could to be used as an alternative to LAMAs already in the market, although substantial information is still lacking. It is likely that in the future, umeclidinium will be used frequently, mainly in combination with vilanterol, which is a new once-daily long-acting ß2-agonist (LABA).


Asunto(s)
Broncodilatadores/uso terapéutico , Antagonistas Muscarínicos/uso terapéutico , Enfermedad Pulmonar Obstructiva Crónica/tratamiento farmacológico , Quinuclidinas/uso terapéutico , Broncodilatadores/farmacología , Volumen Espiratorio Forzado/efectos de los fármacos , Humanos , Antagonistas Muscarínicos/farmacología , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Quinuclidinas/farmacología , Resultado del Tratamiento
4.
Drug Des Devel Ther ; 7: 1201-8, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24143077

RESUMEN

An increasing body of evidence suggests that the long-acting muscarinic antagonist (LAMA)/long-acting ß2-agonist (LABA) combination appears to play an important role in maximizing bronchodilation, with studies to date indicating that combining different classes of bronchodilators may result in significantly greater improvements in lung function compared to the use of a single drug, and that these combinations are well tolerated in patients with moderate-to-severe chronic obstructive pulmonary disease (COPD). An inhaled, fixed-dose combination of two 24-hour bronchodilators, the LAMA umeclidinium and the LABA vilanterol, is under development as a once-daily treatment for COPD. The efficacy of both mono-components has already been demonstrated. The information currently available suggests that umeclidinium/vilanterol is an effective once-daily dual bronchodilator fixed-dose combination in the treatment of COPD. However, it remains to be seen if it compares favorably with current therapies. Moreover, the question remains whether umeclidinium/vilanterol fixed-dose combination, which significantly improves FEV1, is also associated with improvements in other outcome measures that are important to COPD patients.


Asunto(s)
Alcoholes Bencílicos/uso terapéutico , Clorobencenos/uso terapéutico , Enfermedad Pulmonar Obstructiva Crónica/tratamiento farmacológico , Quinuclidinas/uso terapéutico , Administración por Inhalación , Agonistas de Receptores Adrenérgicos beta 2/administración & dosificación , Agonistas de Receptores Adrenérgicos beta 2/farmacología , Agonistas de Receptores Adrenérgicos beta 2/uso terapéutico , Alcoholes Bencílicos/administración & dosificación , Alcoholes Bencílicos/farmacología , Broncodilatadores/administración & dosificación , Broncodilatadores/farmacología , Broncodilatadores/uso terapéutico , Clorobencenos/administración & dosificación , Clorobencenos/farmacología , Preparaciones de Acción Retardada , Combinación de Medicamentos , Volumen Espiratorio Forzado , Humanos , Antagonistas Muscarínicos/administración & dosificación , Antagonistas Muscarínicos/farmacología , Antagonistas Muscarínicos/uso terapéutico , Evaluación de Resultado en la Atención de Salud , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Quinuclidinas/administración & dosificación , Quinuclidinas/farmacología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA