Análisis semicuantitativo del calcio y fósforo en el esmalte y la dentina

Existe una serie de características comunes asociadas al proceso biológico de formación de los tejidos calcificados a pesar de que los productos finales sean estructuralmente distintos. La presente investigación tiene como propósito determinar si la ratio Ca/P ratio es la misma para los tejidos calcificados dentales tanto del feto como del adulto y si dicha ratio es diferente al valor de la ratio Ca/P de la hidroxiapatita pura calculada por estequiometría. Se escogió como material de observación el esmalte y la dentina, en muestras de fetos humanos y en un total de 30 ratas adultas de raza Wistar y 20 dientes humanos sanos. Las observaciones se llevaron a cabo por medio de Microscopia Electrónica de Barrido y Microanálisis por separación de energía de rayos X. Los valores totales de la ratio Ca/P para el esmalte oscilaron en un intervalo de 0,9 y 1,2, con una media que se encuentra entre 1,07 y 1,08. Los valores totales de la ratio Ca/P para la dentina oscilan entre 1,03 y 1,12 y la media entre 1,07 y 1,075. No se encontraron diferencias estadísticamente significativas entre esmalte fetal y adulto ni entre la dentina fetal y adulta. Aún no pudiendo definir la existencia de precursores específicos en los tejidos calcificados del diente (esmalte y dentina), nuestros resultados sugieren que no toda la cristalización de estos tejidos corre a cargo de la hidroxiapatita sino que deben haber otros compuestos que expliquen la disminución del valor de la ratio Ca/P en las muestras estudiadas

A922 Sequential measurement of 1 hour creatinine clearance (1-CRCL) in critically ill patients at risk of acute kidney injury (AKI)

Meeting abstrac

RICORS2040 : The need for collaborative research in chronic kidney disease

Chronic kidney disease (CKD) is a silent and poorly known killer. The current concept of CKD is relatively young and uptake by the public, physicians and health authorities is not widespread. Physicians still confuse CKD with chronic kidney insufficiency or failure. For the wider public and health authorities, CKD evokes kidney replacement therapy (KRT). In Spain, the prevalence of KRT is 0.13%. Thus health authorities may consider CKD a non-issue: very few persons eventually need KRT and, for those in whom kidneys fail, the problem is 'solved' by dialysis or kidney transplantation. However, KRT is the tip of the iceberg in the burden of CKD. The main burden of CKD is accelerated ageing and premature death. The cut-off points for kidney function and kidney damage indexes that define CKD also mark an increased risk for all-cause premature death. CKD is the most prevalent risk factor for lethal coronavirus disease 2019 (COVID-19) and the factor that most increases the risk of death in COVID-19, after old age. Men and women undergoing KRT still have an annual mortality that is 10- to 100-fold higher than similar-age peers, and life expectancy is shortened by ~40 years for young persons on dialysis and by 15 years for young persons with a functioning kidney graft. CKD is expected to become the fifth greatest global cause of death by 2040 and the second greatest cause of death in Spain before the end of the century, a time when one in four Spaniards will have CKD. However, by 2022, CKD will become the only top-15 global predicted cause of death that is not supported by a dedicated well-funded Centres for Biomedical Research (CIBER) network structure in Spain. Realizing the underestimation of the CKD burden of disease by health authorities, the Decade of the Kidney initiative for 2020-2030 was launched by the American Association of Kidney Patients and the European Kidney Health Alliance. Leading Spanish kidney researchers grouped in the kidney collaborative research network Red de Investigación Renal have now applied for the Redes de Investigación Cooperativa Orientadas a Resultados en Salud (RICORS) call for collaborative research in Spain with the support of the Spanish Society of Nephrology, Federación Nacional de Asociaciones para la Lucha Contra las Enfermedades del Riñón and ONT: RICORS2040 aims to prevent the dire predictions for the global 2040 burden of CKD from becoming true

Preliminary resultsofthe pafeopolinical study of angiosperms coming from the cretaceous formation of Barranco de Patones (Madrid)

Los resultados obtenidos en el estudio paleopalinológico de un tramo muy rico en formas, situado en la parte superior de la formación cretácica del Borde Sur de la Sierra de Guadarramai, evidencia el predominio de las Angiospermas en la paleoasociación. Su análisis induce a situar el nivel estudiado en el Maastrichtiense superior, presentando fuertes afinidades con paleoasociaciones citadas en el Paleoceno-Eocen

Anosmin-1 over-expression regulates oligodendrocyte precursor cell proliferation, migration and myelin sheath thickness

During development of the central nervous system, anosmin-1 (A1) works as a chemotropic cue contributing to axonal outgrowth and collateralization, as well as modulating the migration of different cell types, fibroblast growth factor receptor 1 (FGFR1) being the main receptor involved in all these events. To further understand the role of A1 during development, we have analysed the over-expression of human A1 in a transgenic mouse line. Compared with control mice during development and in early adulthood, A1 over-expressing transgenic mice showed an enhanced oligodendrocyte precursor cell (OPC) proliferation and a higher number of OPCs in the subventricular zone and in the corpus callosum (CC). The migratory capacity of OPCs from the transgenic mice is increased in vitro due to a higher basal activation of ERK1/2 mediated through FGFR1 and they also produced more myelin basic protein (MBP). In vivo, the over-expression of A1 resulted in an elevated number of mature oligodendrocytes with higher levels of MBP mRNA and protein, as well as increased levels of activation of the ERK1/2 proteins, while electron microscopy revealed thicker myelin sheaths around the axons of the CC in adulthood. Also in the mature CC, the nodes of Ranvier were significantly longer and the conduction velocity of the nerve impulse in vivo was significantly increased in the CC of A1 over-expressing transgenic mice. Altogether, these data confirmed the involvement of A1 in oligodendrogliogenesis and its relevance for myelination.This work was supported by grants from the Spanish Ministerio de Economía y Competitividad-MINECO (Grant Numbers SAF2009-07842, SAF2012-40023, RD07-0060-2007 and RD12-0032-12 Red Española de Esclerosis Múltple) and the “Fundación Eugenio Rodríguez Pascual” to FdC; the Fundación para la Investigación Socio-sanitaria de Castilla La-Mancha FISCAM (Grant Number PI2007-66 to FdC and PI2009-29 to PFE); from the Spanish MINECO (Grant Numbers BFU2008-00899 and BFU2008-03390) and the Junta de Andalucía (Grant Numbers BIO-122, CVI-02487 and P07-CVI-02686) to JMDG and AGM; and from the Spanish MINECO (Grant Number BFU-2009-08404) to RL. VMB was hired under FISCAM (MOV2007-JI/19), SAF2009-07842 and RD07-0060-2007; PFE was hired by the Servicio de Salud de Castilla La-Mancha (SESCAM, Gobierno de Castilla-La Mancha) and under grant ADE10-0010 from MINECO to FdC. FdC is a CSIC Staff Scientist on leave of absence and currently hired by SESCAM.Peer reviewe