RESUMEN
Summary In this randomised controlled trial we examined the effects of four different levels of positive end expiratory pressure (PEEP at 0, 5, 8 or 10 cmH(2)O), added to the dependent lung, on respiratory profile and oxygenation during one lung ventilation. Forty-six patients were recruited to receive one of the randomised PEEP levels during one lung ventilation. We did not find significant differences in lung compliance, intra-operative or postoperative oxygenation amongst the four different groups. However, the physiological deadspace to tidal volume ventilation ratio was significantly lower in the 8 cmH(2)O PEEP group compared with the other levels of PEEP (p < 0.0001). We concluded that the use of PEEP (< or =10 cmH(2)O) during one lung ventilation does not clinically improve lung compliance, intra-operative or postoperative oxygenation despite a statistically significant reduction in the physiological deadspace to tidal volume ratio.
Asunto(s)
Pulmón/fisiopatología , Respiración con Presión Positiva/métodos , Toracotomía/métodos , Anciano , Femenino , Humanos , Periodo Intraoperatorio , Rendimiento Pulmonar/fisiología , Masculino , Persona de Mediana Edad , Oxígeno/fisiología , Periodo Posoperatorio , Espacio Muerto Respiratorio/fisiología , Volumen de Ventilación Pulmonar/fisiologíaAsunto(s)
Fundoplicación/efectos adversos , Complicaciones Intraoperatorias/terapia , Laparoscopía/efectos adversos , Neumotórax/terapia , Dióxido de Carbono , Femenino , Humanos , Complicaciones Intraoperatorias/etiología , Persona de Mediana Edad , Neumotórax/etiología , Reoperación , Succión/métodosRESUMEN
Nkx2.5 is expressed in the cardiogenic mesoderm of avian, mouse, and amphibian embryos. To understand how various cardiac fates within this domain are apportioned, we fate mapped the mesodermal XNkx2.5 domain of neural tube stage Xenopus embryos. The lateral portions of the XNkx2.5 expression domain in the neural tube stage embryo (stage 22) form the dorsal mesocardium and roof of the pericardial cavity while the intervening ventral region closes to form the myocardial tube. XNkx2.5 expression is maintained throughout the period of heart tube morphogenesis and differentiation of myocardial, mesocardial, and pericardial tissues. A series of microsurgical experiments showed that myocardial differentiation in the lateral portion of the field is suppressed during normal development by signals from the prospective myocardium and by tissues located more dorsally in the embryo, in particular the neural tube. These signals combine to block myogenesis downstream of XNkx2.5 and at or above the level of contractile protein gene expression. We propose that the entire XNkx2.5/heart field is transiently specified as cardiomyogenic. Suppression of this program redirects lateral cells to adopt dorsal mesocardial and dorsal pericardial fates and subdivides the field into distinct myogenic and nonmyogenic compartments.
Asunto(s)
Corazón/embriología , Proteínas de Homeodominio/genética , Miocardio/metabolismo , Factores de Transcripción , Proteínas de Xenopus , Animales , Biomarcadores , Regulación del Desarrollo de la Expresión Génica , Proteína Homeótica Nkx-2.5 , Mesodermo/metabolismo , Ratones , XenopusRESUMEN
We have used serial histological sections to document heart formation in Xenopus laevis, from the formation of a linear heart tube to the appearance of morphologically distinct atrial and ventricular chambers. 3D reconstruction techniques have been used to derive accurate models from digital images, revealing the morphological changes that accompany heart differentiation. To demonstrate the utility of this approach in analysing cardiac gene expression, we have reexamined the distribution of Hand1 transcripts in the linear and looped heart tube. Our results demonstrate that prior to looping, an initial asymmetric, left-sided pattern is replaced by more symmetrical localisation of transcripts to the ventral portion of the myocardium. After the onset of looping, Hand1 expression is restricted to the ventral ventricular myocardium and extends along the entire length of the single ventricle.
Asunto(s)
Corazón/embriología , Xenopus laevis/embriología , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico , Diferenciación Celular , Proteínas de Unión al ADN/aislamiento & purificación , Atrios Cardíacos/embriología , Ventrículos Cardíacos/embriología , Microtomía/métodos , Modelos Estructurales , Morfogénesis , Miocardio/citología , Factores de Transcripción/aislamiento & purificaciónRESUMEN
Bone morphogenic protein-4 (BMP-4) is one of nine structurally related BMPs belonging to the transforming growth factor-beta (TGF-beta) superfamily of secreted proteins. Mature BMP-4 is a dimer that binds to a multimeric transmembrane receptor with serine/threonine kinase activity. Although discovered because it stimulates bone formation in adult mammals, BMP-4 has important roles as a signalling molecule in embryonic tissues, including the developing central and peripheral nervous system, musculature and skeleton. It participates in an ancient signalling pathway also found in insects and worms. Nevertheless, the main practical application of BMPs is for stimulating repair of bone, and their use in humans is currently being assessed.
Asunto(s)
Proteínas Morfogenéticas Óseas/fisiología , Receptores de Factores de Crecimiento , Animales , Proteína Morfogenética Ósea 4 , Receptores de Proteínas Morfogenéticas Óseas , Proteínas Morfogenéticas Óseas/química , Proteínas Morfogenéticas Óseas/genética , Desarrollo Embrionario y Fetal/fisiología , Humanos , Estructura Molecular , Mutación , Receptores de Superficie Celular/fisiología , Transducción de SeñalRESUMEN
Nonheme iron proteins can be visualized as blue bands in native polyacrylamide gels using a staining method that is both simple and rapid. The reaction of potassium ferricyanide with protein-bound iron atoms to form royal blue complexes occurs almost instantaneously and is sensitive enough to detect 1 microgram of analytical-grade ferritin and 2 micrograms of purified ferredoxin from cyanobacteria. No special treatment of reagents or apparatus was necessary. On comparison, this stain was found to be more specific than the Ferene S stain, not detecting bovine serum albumin even when present as a hundredfold excess over ferritin. The method was found to be effective for isoelectric focusing gels as well.