221 research outputs found

    CD-62°1346: An extreme halo or hypervelocity CH star?

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    High-velocity halo stars provide important information about the properties of the extreme Galactic halo. The study of unbound and bound Population II stars permits us to better estimate the mass of the halo. Aims: We carried out a detailed spectroscopic and kinematic study and have significantly refined the distance and the evolutionary state of the star. Methods: Its atmospheric parameters, chemical abundances and kinematical properties were determined using high-resolution optical spectroscopy and employing the local-thermodynamic-equilibrium model atmospheres of Kurucz and the spectral analysis code moog. Results: We found that CD-62°1346 is a metal-poor ([Fe/H] = -1.6) evolved giant star with Teff = 5300 K and log g = 1.7. The star exhibits high carbon and s-element abundances typical of CH stars. It is also a lead star. Our kinematic analysis of its 3D space motions shows that this star has a highly eccentric (e = 0.91) retrograde orbit with an apogalactic distance of ~100 kpc, exceeding by a factor of two the distance of the Magellanic Clouds. The star travels with very high velocity relative to the Galactocentric reference frame (VGRF = 570 km s-1). Conclusions: CD-62°1346 is an evolved giant star and not a subgiant star, as was considered earlier. Whether it is bound or unbound to the Galaxy depends on the assumed mass and on the adopted Galactic potential. We also show that the star HD 5223 is another example of a high-velocity CH star that exceeds the Galactic escape velocity. Possible origins of these two high-velocity stars are briefly discussed. CD-62°1346 and HD 5223 are the first red giant stars to join the restricted group of hypervelocity stars.Fil: Pereira, C. B.. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; BrasilFil: Jilinski, E.. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; Brasil. Universidade do Estado de Rio do Janeiro; Brasil. Russian Academy of Sciences. Pulkovo Observatory; RusiaFil: Drake, N. A.. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; Brasil. Russian Academy of Sciences. Pulkovo Observatory; RusiaFil: de Castro, D. B.. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; BrasilFil: Ortega, V. G.. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; BrasilFil: Chavero, Carolina Andrea. Universidad Nacional de Córdoba. Observatorio Astronómico de Córdoba; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Roig, Fernando Virgilio. Ministério de Ciencia, Tecnologia e Innovacao. Observatorio Nacional; Brasi

    Influence of the adherence to the Mediterranean diet on the effect of smoking on genomewide methylation among subjects with metabolic syndrome

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    PĂČster presentat al congrĂ©s " Epigenetics: Playing with the Gameof Life" celebrat al University Hospital Halle (Saale) entre els dies 13-15 de 2019.Tobacco smoking is an important risk factor for lung cancer, respiratory diseases and cardiovascular diseases, among others. Moreover, smoking can speed up the normal aging process of several tissues increasing the biological age. Changes in methylation due to smoking have been demonstrated at several loci across the genome, particularly in long-term smokers (Figure 1). The most consistent association reported in different populations has been decreased methylation in smokers in comparison with non-smokers at the CpG cg05575921, located in the gene for the aryl hydrocarbon receptor repressor (AHRR) located in chromosome 5

    The Gln241His polymorphism in the carbohydrate response element binding protein (MLXIPL) gene

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    ComunicaciĂł presentada com a pĂČster a European Association of Human Genetics Conference, May 23-26, 2009, Vien

    Estructura factorial de la escala DREEM en estudiantes de medicina chilenos

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    IndexaciĂłn: ScieloBackground: The entry to a University requires an adaptation process that not all students solve with the same kind of success. Even though students’ social adaptation and emotional skills are essential, the educational environmental that they perceive has a significant influence in their academic life. Aim: To describe the changes in the perception about academic environment that medical students experience during the first three years of undergraduate career. Material and Methods: The Dundee Ready Education Environment Measure (DREEM) scale was applied to 525 first to third year medical students and an exploratory factorial analysis was made. Results: Four factors were identified: Academic Perception: academic quality that students attribute to the process in which they take part, as well as to the assessment that they do of their learning outcomes (coefficient α = 0.85); Academic Experience: refers to positive emotions that students experience during the career such as confidence, pleasure and energy (coefficient α = 0.76); Atmosphere Perception, comfort and calm that students experiment during their academic activities (coefficient α = 0.79); Teachers Perception: the perception that students have of teachers about their interest and disposition towards students (coefficient α = 0.50). Conclusions: The assessment of academic environment quality is inversely associated with the lapse that the students have spent in their undergraduate careers. Key words: Education, Medical; Psychometrics; Students, medical; Undergraduate

    Assessment of psychometric properties of the academic involvement questionnaire, expectations version

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    Indexación: Web of Science; Scielo.Background: Academic Involvement Questionnaire, Expectations version (CIA-A), assesses the expectations of involvement in studies. It is a relevant predictor of student success. However, the evidence of its validity and reliability in Chile is low, and in the case of Medical students, there is no evidence at all. Aim: To evaluate the factorial structure and internal consistency of the CIA-A in Chilean Medical school freshmen. Material and Methods: The survey was applied to 340 Medicine freshmen, chosen by non-probability quota sampling. They answered a back-translated version of CIA-A from Portuguese to Spanish, plus a sociodemographic questionnaire. For psychometric analysis of the CIA-A, an exploratory factor analysis was carried on, the reliability of the factors was calculated, a descriptive analysis was conducted and their correlation was assessed. Results: Five factors were identified: vocational, institutional and social involvement, use of resources and student participation. Their reliabilities ranged between Cronbach’s alpha values of 0.71 to 0.87. Factors also showed statistically significant correlations between each other. Conclusions: Identified factor structure is theoretically consistent with the structure of original version. It just disagrees in one factor. In addition, the factors’ internal consistency were adequate for using them in research. This supports the construct validity and reliability of the CIA-A to assess involvement expectations in medical school freshmen.http://ref.scielo.org/r2sn6

    Chronological age interacts with the circadian melatonin receptor 1b gene variation, determining fasting glucose concentrations in mediterranean populations. Additional analyses on type-2 diabetes risk

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    Gene-age interactions have not been systematically investigated on metabolic phenotypes and this modulation will be key for a better understanding of the temporal regulation in nutrigenomics. Taking into account that aging is typically associated with both impairment of the circadian system and a decrease in melatonin secretion, we focused on the melatonin receptor 1B (MTNR1B)-rs10830963 C>G variant that has been associated with fasting glucose concentrations, gestational diabetes, and type-2 diabetes. Therefore, our main aim was to investigate whether the association between the MTNR1B-rs10830963 polymorphism and fasting glucose is age dependent. Our secondary aims were to analyze the polymorphism association with type-2 diabetes and explore the gene-pregnancies interactions on the later type-2 diabetes risk. Three Mediterranean cohorts (n = 2823) were analyzed. First, a cross-sectional study in the discovery cohort consisting of 1378 participants (aged 18 to 80 years; mean age 41 years) from the general population was carried out. To validate and extend the results, two replication cohorts consisting of elderly individuals were studied. In the discovery cohort, we observed a strong gene-age interaction (p = 0.001), determining fasting glucose in such a way that the increasing effect of the risk G-allele was much greater in young (p = 5.9 × 10−10) than in elderly participants (p = 0.805). Consistently, the association of the MTNR1B-rs10830963 polymorphism with fasting glucose concentrations in the two replication cohorts (mean age over 65 years) did not reach statistical significance (p > 0.05 for both). However, in the elderly cohorts, significant associations between the polymorphism and type-2 diabetes at baseline were found. Moreover, in one of the cohorts, we obtained a statistically significant interaction between the MTNR1B polymorphism and the number of pregnancies, retrospectively assessed, on the type-2 diabetes risk. In conclusion, the association of the MTNR1B-rs10830963 polymorphism with fasting glucose is age-dependent, having a greater effect in younger people. However, in elderly subjects, associations of the polymorphism with type-2 diabetes were observed and our exploratory analysis suggested a modulatory effect of the number of past pregnancies on the future type-2 diabetes genetic risk

    Chronological Age Interacts with the Circadian Melatonin Receptor 1B Gene Variation, Determining Fasting Glucose Concentrations in Mediterranean Populations. Additional Analyses on Type-2 Diabetes Risk

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    Gene-age interactions have not been systematically investigated on metabolic phenotypes and this modulation will be key for a better understanding of the temporal regulation in nutrigenomics. Taking into account that aging is typically associated with both impairment of the circadian system and a decrease in melatonin secretion, we focused on the melatonin receptor 1B (MTNR1B)-rs10830963 C>G variant that has been associated with fasting glucose concentrations, gestational diabetes, and type-2 diabetes. Therefore, our main aim was to investigate whether the association between the MTNR1B-rs10830963 polymorphism and fasting glucose is age dependent. Our secondary aims were to analyze the polymorphism association with type-2 diabetes and explore the gene-pregnancies interactions on the later type-2 diabetes risk. Three Mediterranean cohorts (n = 2823) were analyzed. First, a cross-sectional study in the discovery cohort consisting of 1378 participants (aged 18 to 80 years; mean age 41 years) from the general population was carried out. To validate and extend the results, two replication cohorts consisting of elderly individuals were studied. In the discovery cohort, we observed a strong gene-age interaction (p = 0.001), determining fasting glucose in such a way that the increasing effect of the risk G-allele was much greater in young (p = 5.9 × 10-10) than in elderly participants (p = 0.805). Consistently, the association of the MTNR1B-rs10830963 polymorphism with fasting glucose concentrations in the two replication cohorts (mean age over 65 years) did not reach statistical significance (p > 0.05 for both). However, in the elderly cohorts, significant associations between the polymorphism and type-2 diabetes at baseline were found. Moreover, in one of the cohorts, we obtained a statistically significant interaction between the MTNR1B polymorphism and the number of pregnancies, retrospectively assessed, on the type-2 diabetes risk. In conclusion, the association of the MTNR1B-rs10830963 polymorphism with fasting glucose is age-dependent, having a greater effect in younger people. However, in elderly subjects, associations of the polymorphism with type-2 diabetes were observed and our exploratory analysis suggested a modulatory effect of the number of past pregnancies on the future type-2 diabetes genetic risk

    gh/igf axis gene expression profile in developing atlantic bluefin tuna (Thunnus thynnus).

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    Atlantic bluefin tuna (ABFT), Thunnus thynnus (Linnaeus, 1758), is a large migratory oceanic top predator, considered as an important worldwide fishery source and a key species in pelagic ecosystems. Survival during the early life stages is crucial for future recruitment success, with larval growth being a determining process. Fish growth and development are mainly controlled by the GH/IGF axis, being involved in skeletal and soft tissue growth, as well as in immune function, appetite control, behavior (including foraging, aggression, and predator avoidance). To characterize the ontogenetic development profile of the GH/IGF axis at the level of gene expression, an ABFT larval rearing experiment (under controlled feeding conditions) was performed in the aquaculture facilities of the Spanish Institute of Oceanography (IEO), in MazarrĂłn during June 2019. Eggs and larvae from 3 replicates were collected regularly every 2-3 days from 0 until 30 days post-hatching (dph). In a total of 14 sampling points (n = 6-12 larvae) along the ontogeny, growth hormone (gh) and two forms of insulin growth factor (igf1 and igf2) were analyzed by real-time RT-PCR. A sigmoidal gh expression profile was observed, with higher values at 5 and 23 (maximum) dph, and lower values at 0 (minimum), 12 and 30 dph. Nevertheless, igf1 and igf2 showed a gradual increase from early days, also with lower values at 0 and 12 dph, but with maximum levels at 30 dph. Results are discussed considering growing rates and transition from larvae to juvenile, underlining the importance of gh/ igf axis during the ABFT early development and growth

    GH/IGF AXIS GENE EXPRESSION PROFILE IN DEVELOPING ATLANTIC BLUEFIN TUNA (Thunnus thynnus)

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    Atlantic bluefin tuna (ABFT), Thunnus thynnus (Linnaeus, 1758), is a large migratory oceanic top predator, considered as an important worldwide fishery source and a key species in pelagic ecosystems. Survival during the early life stages is crucial for future recruitment success, with larval growth being a determining process. Fish growth and development are mainly controlled by the GH/IGF axis, being involved in skeletal and soft tissue growth, as well as in immune function, appetite control, behavior (including foraging, aggression, and predator avoidance). To characterize the ontogenetic development profile of the GH/IGF axis at the level of gene expression, an ABFT larval rearing experiment (under controlled feeding conditions) was performed in the aquaculture facilities of the Spanish Institute of Oceanography (IEO), in MazarrĂłn during June 2019. Eggs and larvae from 3 replicates were collected regularly every 2-3 days from 0 until 30 days post-hatching (dph). In a total of 14 sampling points (n = 6-12 larvae) along the ontogeny, growth hormone (gh) and two forms of insulin growth factor (igf1 and igf2) were analyzed by real-time RT-PCR. A sigmoidal gh expression profile was observed, with higher values at 5 and 23 (maximum) dph, and lower values at 0 (minimum), 12 and 30 dph. Nevertheless, igf1 and igf2 showed a gradual increase from early days, also with lower values at 0 and 12 dph, but with maximum levels at 30 dph. Results are discussed considering growing rates and transition from larvae to juvenile, underlining the importance of gh/ igf axis during the ABFT early development and growth

    Autophagy and Apoptosis Have a Role in the Survival or Death of Stallion Spermatozoa during Conservation in Refrigeration

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    Apoptosis has been recognized as a cause of sperm death during cryopreservation and a cause of infertility in humans, however there is no data on its role in sperm death during conservation in refrigeration; autophagy has not been described to date in mature sperm. We investigated the role of apoptosis and autophagy during cooled storage of stallion spermatozoa. Samples from seven stallions were split; half of the ejaculate was processed by single layer centrifugation, while the other half was extended unprocessed, and stored at 5°C for five days. During the time of storage, sperm motility (CASA, daily) and membrane integrity (flow cytometry, daily) were evaluated. Apoptosis was evaluated on days 1, 3 and 5 (active caspase 3, increase in membrane permeability, phosphatidylserine translocation and mitochondrial membrane potential) using flow cytometry. Furthermore, LC3B processing was investigated by western blotting at the beginning and at the end of the period of storage. The decrease in sperm quality over the period of storage was to a large extent due to apoptosis; single layer centrifugation selected non-apoptotic spermatozoa, but there were no differences in sperm motility between selected and unselected sperm. A high percentage of spermatozoa showed active caspase 3 upon ejaculation, and during the period of storage there was an increase of apoptotic spermatozoa but no changes in the percentage of live sperm, revealed by the SYBR-14/PI assay, were observed. LC3B was differentially processed in sperm after single layer centrifugation compared with native sperm. In processed sperm more LC3B-II was present than in non-processed samples; furthermore, in non-processed sperm there was an increase in LC3B-II after five days of cooled storage. These results indicate that apoptosis plays a major role in the sperm death during storage in refrigeration and that autophagy plays a role in the survival of spermatozoa representing a new pro-survival mechanism in spermatozoa not previously described
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