15 research outputs found
Genomic Ancestry, CYP2D6, CYP2C9, and CYP2C19 Among Latin Americans
We present the distribution of CYP2D6, CYP2C9, and CYP2C19 variants and predicted phenotypes in 33 native and
admixed populations from Ibero-America (n > 6,000) in the context of genetic ancestry (n = 3,387). Continental
ancestries are the major determinants of frequencies of the increased-activity allele CYP2C19*17 and CYP2C19
gUMs (negatively associated with Native American ancestry), decreased-activity alleles CYP2D6*41 and CYP2C9*2
(positively associated with European ancestry), and decreased-activity alleles CYP2D6*17 and CYP2D6*29 (positively
associated with African ancestry). For the rare alleles, CYP2C9*2 and CYPC19*17, European admixture accounts
for their presence in Native American populations, but rare alleles CYP2D6*5 (null-activity), CYP2D6-multiplication
alleles (increased activity), and CYP2C9*3 (decreased-activity) were present in the pre-Columbian Americas.
The study of a broad spectrum of Native American populations from different ethno-linguistic groups show how
autochthonous diversity shaped the distribution of pharmaco-alleles and give insights on the prevalence of clinically
relevant phenotypes associated with drugs, such as paroxetine, tamoxifen, warfarin, and clopidogrel
Influence of gender on carcass yield of twin lambs Blackbelly x Pelibuey at 56 days of age
Nanomechanical properties of molecular organic thin films
Using atomic force microscopy we have studied the nanomechanical response to nanoindentations of surfaces of highly oriented molecular organic thin films (thickness¿1000¿nm). The Young¿s modulus E can be estimated from the elastic deformation using Hertzian mechanics. For the quasi-one-dimensional metal tetrathiafulvalene tetracyanoquinodimethane E~20¿GPa and for the ¿ phase of the p-nitrophenyl nitronyl nitroxide radical E~2GPa. Above a few GPa, the surfaces deform plastically as evidenced by discrete discontinuities in the indentation curves associated to molecular layers being expelled by the penetrating tip
Regulation of the Micromechanical Properties of Pulmonary Endothelium by S1P and Thrombin: Role of Cortactin
Disruption of pulmonary endothelial cell (EC) barrier function is a critical pathophysiologic event in highly morbid inflammatory conditions such as sepsis and acute respiratory disease stress syndrome. Actin cytoskeleton, an essential regulator of endothelial permeability, is a dynamic structure whose stimuli-induced rearrangement is linked to barrier modulation. Here, we used atomic force microscopy to characterize structural and mechanical changes in the F-actin cytoskeleton of cultured human pulmonary artery EC in response to both barrier-enhancing (induced by sphingosine 1-phosphate (S1P)) and barrier-disrupting (induced by thrombin) conditions. Atomic force microscopy elasticity measurements show differential effects: for the barrier protecting molecule S1P, the elastic modulus was elevated significantly on the periphery; for the barrier-disrupting molecule thrombin, on the other hand, it was elevated significantly in the central region of the cell. The force and elasticity maps correlate with F-actin rearrangements as identified by immunofluorescence analysis. Significantly, reduced expression (via siRNA) of cortactin, an actin-binding protein essential to EC barrier regulation, resulted in a shift in the S1P-mediated elasticity pattern to more closely resemble control, unstimulated endothelium
La Rábida : Revista Colombina Iberoamericana. Número 85 - Año VIII
16 páginasMarchena Colombo, José: Nuestras fiestas de Agosto.- Barras de Aragón, Francisco de las: Noticias americanas restrospectivas.- Oviedo y Arce, Eladio: ¿Colón español?. Informe que presenta a la Real Academia Gallega de La Coruña (continuación del número anterior).- Del Senado (intervención del Sr. Antonio López Muñoz sobre el proyecto de jubilación del profesorado).- J.D. Roqueta: Cancionero de mi tierra (libro de Casilda de Antón del Olmet).- Terán, Eugenio: Pro patria.- Beltrán y Rozpide, Ricardo: La fiesta de la Raza. El Hispanismo de Cristóbal Colón.- Causerie pour les réfugiés belges de Pau.- López Canto, F.: Carta al Director.- Del diario vivir (un onubense).- Las Fiestas Patrioticas Colombinas. Programa general
On the Thermodynamic Stability of (√3 × √3)R30° Methanethiolate Lattice on Reconstructed Au(111) Surface Models
Relevance of the ancestry for the variability of the Drug-Metabolizing Enzymes CYP2C9, CYP2C19 and CYP2D6 polymorphisms in a multiethnic Costa Rican population
CYP2C9, CYP2C19 and CYP2D6 metabolize around 40 % of drugs and their genes vary across populations. The Costa Rican population has a trihybrid ancestry and its key geographic location turns it into a suitable scenario to evaluate interethnic differences across populations. This study aims to describe the diversity of CYP2C9, CYP2C19 and CYP2D6 polymorphisms in Costa Rican populations in the context of their ancestry. A total of 448 healthy individuals were included in the study: Bribri (n= 47), Cabécar (n= 27), Maleku (n= 16), Guaymí (n= 30), Huetar (n= 48), Chorotega (n= 41), Admixed/Mestizos from the Central Valley/Guanacaste (n= 189), and Afro-Caribbeans (n= 50) from Limón. CYP2C9 (alleles *2, *3, *6) and CYP2C19 (*2, *3, *4, *5, *17) genotypes were determined by Real-Time PCR. African, European and Native American ancestry were inferred using 87 ancestry informative markers. The frequency of the decreased activity allele CYP2C9*2 is lower in the self-reported Amerindian groups compared to the admixed population, and the highest frequencies of CYP2C19*2 (null activity) and the CYP2C19*17 (increased activity) were found in the self-reported Afro- Caribbean population. Moreover, a frequency of 0.7 % CYP2C9 gPMs in the Admixed population and a variable frequency of CYP2C19 gUMs (0.0-32.6 %, more prevalent in Afro-Caribbeans) in Costa Rican populations, was found. Finally, the following alleles were positively correlated with genomic African ancestry and negatively correlated with genomic Native American ancestry: CYP2D6*5 (null activity), CYP2D6*17 (decreased activity), CYP2D6*29 (decreased activity) and CYP2C19*17 (increased activity). No correlation for CYP2C9 polymorphisms and genomic ancestry was found. Further studies assessing the CYP2C9 and CYP2C19 sequence in these populations, preferentially by sequencing these genes, are warranted