169 research outputs found

    Acúmulo e distribuição de matéria seca em mandioca submetida a deficiência hídrica

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    Growth of cassava, cultivar M Cal 1684, was evaluated under water stress conditions established over a 100-day period of water exclusion, starting after three and six months from planting. The experiment was carried out in Santander de Quilichao, Colombia, on a lysimeter with 30m x 15m x 2,3m. Accumulation of total dry matter by the plants, measured at regular time intervals, was reduced by water stress, especially in the three month old plants. The same effects were evident on root dry weight. Water stress caused reductions in root dry weights and leaf areas of both groups of plants. In those stressed after three months of growth those reductions were due to lower rates of leaf formation and expansion, contrarily to plants stressed after six months, which reduced shoot weight and leaf area by an increase in leaf fall.Foi avaliado o crescimento da cultivar de mandioca M Col 1684, sob estresse hídrico, por um período de 100 dias, imposto a partir de três e seis meses após o plantio. O experimento foi instalado, em condições de campo, em Santander de Quilichao, Colômbia, em um lisímetro com dimensões de 30m x 15m x 2,3m. A acumulação total de matéria seca, avaliada através de amostragens periódicas de plantas, foi reduzida, em condições de deficiência de água, principalmente em plantas que sofreram essa deficiência após três meses de ciclo. O mesmo comportamento foi observado em relação ao peso de raízes. Reduções no peso seco da parte aérea e da área foliar foram também observadas como resultantes da deficiência hídrica, sendo causadas, nas plantas mais jovens, por menores taxas de expansão das folhas e, nas plantas mais velhas, por aumento significativo do número de folhas caídas

    Accurate and homogeneous abundance patterns in solar-type stars of the solar neighbourhood: a chemo-chronological analysis

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    We report the abundances of C, Na, Mg, Si, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Sr, Y, Zr, Ba, Ce, Nd, and Sm in 25 solar-type stars in the solar neighbourhood, and their correlations with ages, kinematics, and orbital parameters. The spectroscopic analysis, based high resolution and high S/N ratio data, was differential to the Sun and applied to atomic line EWs and to C and C2 spectral synthesis. We performed a statistical study using a tree clustering analysis, searching for groups of stars sharing similar abundance patterns. We derived Teff, log(g), and [Fe/H] with errors of 30 K, 0.13 dex, and 0.05 dex, respectively. The average error in [X/Fe] is 0.06 dex. Ages were derived from theoretical HR diagrams and memberships in kinematical moving groups. We identified four stellar groups: with over-solar abundances ( = +0.26 dex), under-solar abundances ( = -0.24 dex), and intermediate values ( = -0.06 and +0.06 dex) but with distinct chemical patterns. Stars sharing solar metallicity, age, and Galactic orbit possibly have non-solar abundance, an effect either of chemical heterogeneity in their natal clouds or migration. A trend of [Cu/Fe] with [Ba/Fe] seems to exist, in agreement with previous claims in the literature, and maybe also of [Sm/Fe] with [Ba/Fe]. No such correlation involving C, Na, Mn, and Zn is observed. [Mg/Fe], [Sc/Fe], and [Ti/Fe] increase with age. [Mn/Fe] and [Cu/Fe] first increase towards younger stars up to the solar age, and then decrease, a result we interpret as possibly related to time-varying yields of SN Ia and the weak s-process. [Sr/Fe], [Y/Fe], [Sr/Mg], [Y/Mg], [Sr/Zn], and [Y/Zn] linearly increase towards younger stars. [Zr/Fe], [Ce/Fe], [Nd/Fe], [Ba/Mg], [Ba/Zn], and [Sr,Y,Ba/Sm] increase but only for stars younger than the Sun. The steepest negative age relation is due to [Ba/Fe], but only for stars younger than the Sun.Comment: 27 pages, 11 figures, 10 table

    HLA haplotypes associated with hemochromatosis mutations in the Spanish population

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    BACKGROUND: The present study is an analysis of the frequencies of HLA-A and -B antigens and HLA haplotypes in two groups of individuals homozygous for the two main HFE mutations (C282Y and H63D) and a group heterozygous for the S65C mutation. METHODS: The study population includes: 1123 healthy individuals, 100 homozygous for the C282Y mutation, 138 homozygous for the H63D mutation and 17 heterozygous for the S65C mutation. HFE and HLA alleles were detected using DNA-based and microlymphocytotoxicity techniques respectively. RESULTS: An expected significant association between C282Y and the HLA-A3/B7 haplotype was found, but other HLA haplotypes carrying the -A3 antigen were found: HLA-A3/B62 and HLA-A3/B44. Also, a significant association between H63D mutation and HLA-A29/B44 haplotype was found, and again other HLA haplotypes carrying the HLA-A29 antigen were also found: HLA-A29/B14 and HLA-A29/B62. In addition, the S65C mutation seems to be associated with a HLA haplotype carrying the HLA-A26 antigen. CONCLUSION: These findings clearly suggest that HLA-A3/B7 and HLA-A29/B44 are the ancestral haplotypes from which the C282Y and H63D mutations originated, respectively. The frequencies of these mutations in different populations, their geographical distribution, and the degree of the statistical association to the ancestral haplotypes, suggest that the H63D mutation must have occurred earlier than the C282Y mutation

    Interaction Pattern of Arg 62 in the A-Pocket of Differentially Disease-Associated HLA-B27 Subtypes Suggests Distinct TCR Binding Modes

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    The single amino acid replacement Asp116His distinguishes the two subtypes HLA-B*2705 and HLA-B*2709 which are, respectively, associated and non-associated with Ankylosing Spondylitis, an autoimmune chronic inflammatory disease. The reason for this differential association is so far poorly understood and might be related to subtype-specific HLA:peptide conformations as well as to subtype/peptide-dependent dynamical properties on the nanoscale. Here, we combine functional experiments with extensive molecular dynamics simulations to investigate the molecular dynamics and function of the conserved Arg62 of the α1-helix for both B27 subtypes in complex with the self-peptides pVIPR (RRKWRRWHL) and TIS (RRLPIFSRL), and the viral peptides pLMP2 (RRRWRRLTV) and NPflu (SRYWAIRTR). Simulations of HLA:peptide systems suggest that peptide-stabilizing interactions of the Arg62 residue observed in crystal structures are metastable for both B27 subtypes under physiological conditions, rendering this arginine solvent-exposed and, probably, a key residue for TCR interaction more than peptide-binding. This view is supported by functional experiments with conservative (R62K) and non-conservative (R62A) B*2705 and B*2709 mutants that showed an overall reduction in their capability to present peptides to CD8+ T cells. Moreover, major subtype-dependent differences in the peptide recognition suggest distinct TCR binding modes for the B*2705 versus the B*2709 subtype

    Fusion and Binary-Decay Mechanisms in the 35^{35}Cl+24^{24}Mg System at E/A \approx 8 MeV/Nucleon

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    Compound-nucleus fusion and binary-reaction mechanisms have been investigated for the 35^{35}Cl+24^{24}Mg system at an incident beam energy of ELab_{Lab}= 282 MeV. Charge distributions, inclusive energy spectra, and angular distributions have been obtained for the evaporation residues and the binary fragments. Angle-integrated cross sections have been determined for evaporation residues from both the complete and incomplete fusion mechanisms. Energy spectra for binary fragment channels near to the entrance-channel mass partition are characterized by an inelastic contribution that is in addition to a fully energy damped component. The fully damped component which is observed in all the binary mass channels can be associated with decay times that are comparable to, or longer than the rotation period. The observed mass-dependent cross sections for the fully damped component are well reproduced by the fission transition-state model, suggesting a fusion followed by fission origin. The present data cannot, however, rule out the possibility that a long-lived orbiting mechanism accounts for part or all of this yield.Comment: 41 pages standard REVTeX file, 14 Figures available upon request -

    Serum Neurotrophin Profile in Systemic Sclerosis

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    International audienceBACKGROUND: Neurotrophins (NTs) are able to activate lymphocytes and fibroblasts; they can modulate angiogenesis and sympathic vascular function. Thus, they can be implicated in the three pathogenic processes of systemic sclerosis (SSc). The aims of this study are to determine blood levels of Nerve Growth Factor (NGF), Brain-Derived Neurotrophic Factor (BDNF) and Neurotrophin-3 (NT-3) in SSc and to correlate them with clinical and biological data.METHODS: Serum samples were obtained from 55 SSc patients and 32 control subjects to measure NTs levels by ELISA and to determine their relationships with SSc profiles. FINDINGS: Serum NGF levels were higher in SSc patients (288.26 ± 170.34 pg/mL) than in control subjects (170.34 ± 50.8 pg/mL, p<0.001) and correlated with gammaglobulins levels and the presence of both anti-cardiolipin and anti-Scl-70 antibodies (p<0.05). In contrast, BDNF levels were lower in SSc patients than in controls (1121.9 ± 158.1 vs 1372.9 ± 190.9 pg/mL, p<0.0001), especially in pulmonary arterial hypertension and diffuse SSc as compared to limited forms (all p<0.05). NT-3 levels were similar in SSc and in the control group (2657.2 ± 2296 vs 2959.3 ± 2555 pg/mL, NS). BDNF levels correlated negatively with increased NGF levels in the SSc group (and not in controls). CONCLUSION: Low BDNF serum levels were not previously documented in SSc, particularly in the diffuse SSc subset and in patients with pulmonary hypertension or anti-Scl-70 antibodies. The negative correlation between NGF and BDNF levels observed in SSc and not in healthy controls could be implicated in sympathic vascular dysfunction in SSc

    Inflammasome-Mediated IL-1β Production in Humans with Cystic Fibrosis

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    Inflammation and infection are major determinants of disease severity and consequently, the quality of life and outcome for patients with cystic fibrosis (CF). Interleukin-1 beta (IL-1β) is a key inflammatory mediator. Secretion of biologically active IL-1β involves inflammasome-mediated processing. Little is known about the contribution of IL-1β and the inflammasomes in CF inflammatory disease. This study examines inflammasome-mediated IL-1β production in CF bronchial epithelial cell lines and human patients with CF.Bronchial epithelial cell lines were found to produce negligible amounts of basal or stimulated IL-1β compared to hematopoeitic cells and they did not significantly upregulate caspase-1 activity upon inflammasome stimulation. In contrast, peripheral blood mononuclear cells (PBMCs) from both CF and healthy control subjects produced large amounts of IL-1β and strongly upregulated caspase-1 activity upon inflammasome stimulation. PBMCs from CF patients and controls displayed similar levels of caspase-1 activation and IL-1β production when stimulated with inflammasome activators. This IL-1β production was dependent on NF-κB activity and could be enhanced by priming with LPS. Finally, chemical inhibition of CFTR activity in control PBMCs and THP-1 cells did not significantly alter IL-1β or IL-8 production in response to P. aeruginosa.Hematopoeitic cells appear to be the predominant source of inflammasome-induced pro-inflammatory IL-1β in CF. PBMCs derived from CF subjects display preserved inflammasome activation and IL-1β secretion in response to the major CF pathogen Pseudomonas aeruginosa. However, our data do not support the hypothesis that increased IL-1β production in CF subjects is due to an intrinsic increase in NF-κB activity through loss of CFTR function

    Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries.

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    BACKGROUND: As global initiatives increase patient access to surgical treatments, there remains a need to understand the adverse effects of surgery and define appropriate levels of perioperative care. METHODS: We designed a prospective international 7-day cohort study of outcomes following elective adult inpatient surgery in 27 countries. The primary outcome was in-hospital complications. Secondary outcomes were death following a complication (failure to rescue) and death in hospital. Process measures were admission to critical care immediately after surgery or to treat a complication and duration of hospital stay. A single definition of critical care was used for all countries. RESULTS: A total of 474 hospitals in 19 high-, 7 middle- and 1 low-income country were included in the primary analysis. Data included 44 814 patients with a median hospital stay of 4 (range 2-7) days. A total of 7508 patients (16.8%) developed one or more postoperative complication and 207 died (0.5%). The overall mortality among patients who developed complications was 2.8%. Mortality following complications ranged from 2.4% for pulmonary embolism to 43.9% for cardiac arrest. A total of 4360 (9.7%) patients were admitted to a critical care unit as routine immediately after surgery, of whom 2198 (50.4%) developed a complication, with 105 (2.4%) deaths. A total of 1233 patients (16.4%) were admitted to a critical care unit to treat complications, with 119 (9.7%) deaths. Despite lower baseline risk, outcomes were similar in low- and middle-income compared with high-income countries. CONCLUSIONS: Poor patient outcomes are common after inpatient surgery. Global initiatives to increase access to surgical treatments should also address the need for safe perioperative care. STUDY REGISTRATION: ISRCTN5181700

    Essential Medicines at the National Level : The Global Asthma Network's Essential Asthma Medicines Survey 2014

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    Patients with asthma need uninterrupted supplies of affordable, quality-assured essential medicines. However, access in many low- and middle-income countries (LMICs) is limited. The World Health Organization (WHO) Non-Communicable Disease (NCD) Global Action Plan 2013-2020 sets an 80% target for essential NCD medicines' availability. Poor access is partly due to medicines not being included on the national Essential Medicines Lists (EML) and/or National Reimbursement Lists (NRL) which guide the provision of free/subsidised medicines. We aimed to determine how many countries have essential asthma medicines on their EML and NRL, which essential asthma medicines, and whether surveys might monitor progress. A cross-sectional survey in 2013-2015 of Global Asthma Network principal investigators generated 111/120 (93%) responses41 high-income countries and territories (HICs); 70 LMICs. Patients in HICs with NRL are best served (91% HICs included ICS (inhaled corticosteroids) and salbutamol). Patients in the 24 (34%) LMICs with no NRL and the 14 (30%) LMICs with an NRL, however no ICS are likely to have very poor access to affordable, quality-assured ICS. Many LMICs do not have essential asthma medicines on their EML or NRL. Technical guidance and advocacy for policy change is required. Improving access to these medicines will improve the health system's capacity to address NCDs.Peer reviewe
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