3,199 research outputs found
Centrality dependence of the ratios and - a test of thermalization in Au+Au collisions at RHIC
We present the centrality dependence of the ratios and
measured in Au+Au collisions at GeV by the
STAR experiment at RHIC. The results are compared to measurements of other
identified particles and recombination model expectations in order to gain
insight into the partonic collectivity and possible thermalization of the
produced medium.Comment: 4 pages, 2 figures, Quark Matter 2006 conference proceeding
Patterns of recruitment and injury in a heterogeneous airway network model
In respiratory distress, lung airways become flooded with liquid and may collapse due
to surface-tension forces acting on air-liquid interfaces, inhibiting gas exchange. This pa-
per proposes a mathematical multiscale model for the mechanical ventilation of a network
of occluded airways, where air is forced into the network at a fixed tidal volume, allowing
investigation of optimal recruitment strategies. The temporal response is derived from
mechanistic models of individual airway reopening, incorporating feedback on the airway
pressure due to recruitment. The model accounts for stochastic variability in airway di-
ameter and stiffness across and between generations. For weak heterogeneity, the network
is completely ventilated via one or more avalanches of recruitment (with airways recruited
in quick succession), each characterised by a transient decrease in the airway pressure;
avalanches become more erratic for airways that are initially more flooded. However, the
time taken for complete ventilation of the network increases significantly as the network
becomes more heterogeneous, leading to increased stresses on airway walls. The model
predicts that the most peripheral airways are most at risk of ventilation-induced damage.
A positive-end-expiratory pressure (PEEP) reduces the total recruitment time but at the
cost of larger stresses exerted on airway walls
Endoplasmic reticulum stress induces ligand-independent TNFR1-mediated necroptosis in L929 cells
Endoplasmic reticulum (ER) stress-induced cellular dysfunction and death is associated with several human diseases. It has been widely reported that ER stress kills through activation of the intrinsic mitochondrial apoptotic pathway. Here we demonstrate that ER stress can also induce necroptosis, an receptor-interacting protein kinase 1 (RIPK1)/RIPK3/mixed lineage kinase domain-like protein (MLKL)-dependent form of necrosis. Remarkably, we observed that necroptosis induced by various ER stressors in L929 cells is dependent on tumor necrosis factor receptor 1 (TNFR1), but occurs independently of autocrine TNF or lymphotoxin α production. Moreover, we found that repression of either TNFR1, RIPK1 or MLKL did not protect the cells from death but instead allowed a switch to ER stress-induced apoptosis. Interestingly, while caspase inhibition was sufficient to protect TNFR1- or MLKL-deficient cells from death, rescue of the RIPK1-deficient cells additionally required RIPK3 depletion, indicating a switch back to RIPK3-dependent necroptosis in caspase-inhibited conditions. The finding that ER stress also induces necroptosis may open new therapeutic opportunities for the treatment of pathologies resulting from unresolved ER stress
Phi-meson Production in Heavy-Ion Collisions at RHIC
We present the first elliptic flow, , measurement for the -meson
in Au+Au collisions at =200 GeV. At low (<2 GeV/c), the
is consistent with mass ordering expected from hydrodynamics, while at
higher (>4 GeV/c), it follows the same trend as the
and a parameterization for number of quarks = 2. The nuclear modification
factor, , has also been measured and it follows the same trend as the
rather than the which confirms the baryon/meson-type
dependence of at RHIC. A model based on the recombination of thermal
s-quarks describes the central -meson spectrum as well as the
baryon/meson ratio of up to ~4 GeV/c.Comment: Submitted to J. Phys. G (Proceedings of the 9th International
Conference on Strangeness in Quark Matter, Los Angeles, USA, March 26-31) 4
pages, 3 figure
The effect of a monetary incentive on return of a postal health and development questionnaire: a randomised trial [ISRCTN53994660]
BACKGROUND: Postal questionnaires are widely used to collect data in healthcare research but a poor response rate may reduce the validity and reliability of results. There was a lack of evidence available relating to use of a monetary incentive to improve the response rate in the healthcare setting. METHODS: The MRC ORACLE Children Study is assessing the health and development of nearly 9000 seven year old children whose mothers' joined the MRC ORACLE Trial. We carried out a randomised controlled trial of inclusion of monetary incentive (five pound voucher redeemable at many high street stores) with the reminder questionnaire to parents. This trial took place between April 2002 and November 2003. When the parents were sent the reminder questionnaire about their child's health and development they were randomly assigned by concealed computer-generated allocation stratified by week of birthday to receive a five pound voucher or no incentive. The population were 722 non-responders to the initial mailing of a 12-page questionnaire. Main outcome measures: Difference in response rate between the two groups. RESULTS: Inclusion of the voucher with the reminder questionnaire resulted in a 11.7%(95% CI 4.7% to 18.6%) improvement in the response rate between the two groups. CONCLUSION: This improvement in response rate and hence the validity and reliability of results obtained appears to be justified ethically and financially
Quality of private and public ambulatory health care in low and middle income countries: systematic review of comparative studies
Paul Garner and colleagues conducted a systematic review of 80 studies to compare
the quality of private versus public ambulatory health care in low- and
middle-income countries
Free energy for parameterized Polyakov loops in SU(2) and SU(3) lattice gauge theory
We present a study of the free energy of parameterized Polyakov loops P in
SU(2) and SU(3) lattice gauge theory as a function of the parameters that
characterize P. We explore temperatures below and above the deconfinement
transition, and for our highest temperatures T > 5 T_c we compare the free
energy to perturbative results.Comment: Minor changes. Final version to appear in JHE
Piperidinols that show anti-tubercular activity as inhibitors of arylamine N-acetyltransferase: an essential enzyme for mycobacterial survival inside macrophages
Latent M. tuberculosis infection presents one of the major obstacles in the global eradication of tuberculosis (TB). Cholesterol plays a critical role in the persistence of M. tuberculosis within the macrophage during latent infection. Catabolism of cholesterol contributes to the pool of propionyl-CoA, a precursor that is incorporated into cell-wall lipids. Arylamine N-acetyltransferase (NAT) is encoded within a gene cluster that is involved in the cholesterol sterol-ring degradation and is essential for intracellular survival. The ability of the NAT from M. tuberculosis (TBNAT) to utilise propionyl-CoA links it to the cholesterol-catabolism pathway. Deleting the nat gene or inhibiting the NAT enzyme prevents intracellular survival and results in depletion of cell-wall lipids. TBNAT has been investigated as a potential target for TB therapies. From a previous high-throughput screen, 3-benzoyl-4-phenyl-1-methylpiperidinol was identified as a selective inhibitor of prokaryotic NAT that exhibited antimycobacterial activity. The compound resulted in time-dependent irreversible inhibition of the NAT activity when tested against NAT from M. marinum (MMNAT). To further evaluate the antimycobacterial activity and the NAT inhibition of this compound, four piperidinol analogues were tested. All five compounds exert potent antimycobacterial activity against M. tuberculosis with MIC values of 2.3-16.9 µM. Treatment of the MMNAT enzyme with this set of inhibitors resulted in an irreversible time-dependent inhibition of NAT activity. Here we investigate the mechanism of NAT inhibition by studying protein-ligand interactions using mass spectrometry in combination with enzyme analysis and structure determination. We propose a covalent mechanism of NAT inhibition that involves the formation of a reactive intermediate and selective cysteine residue modification. These piperidinols present a unique class of antimycobacterial compounds that have a novel mode of action different from known anti-tubercular drugs
Drug-resistant genotypes and multi-clonality in Plasmodium falciparum analysed by direct genome sequencing from peripheral blood of malaria patients.
Naturally acquired blood-stage infections of the malaria parasite Plasmodium falciparum typically harbour multiple haploid clones. The apparent number of clones observed in any single infection depends on the diversity of the polymorphic markers used for the analysis, and the relative abundance of rare clones, which frequently fail to be detected among PCR products derived from numerically dominant clones. However, minority clones are of clinical interest as they may harbour genes conferring drug resistance, leading to enhanced survival after treatment and the possibility of subsequent therapeutic failure. We deployed new generation sequencing to derive genome data for five non-propagated parasite isolates taken directly from 4 different patients treated for clinical malaria in a UK hospital. Analysis of depth of coverage and length of sequence intervals between paired reads identified both previously described and novel gene deletions and amplifications. Full-length sequence data was extracted for 6 loci considered to be under selection by antimalarial drugs, and both known and previously unknown amino acid substitutions were identified. Full mitochondrial genomes were extracted from the sequencing data for each isolate, and these are compared against a panel of polymorphic sites derived from published or unpublished but publicly available data. Finally, genome-wide analysis of clone multiplicity was performed, and the number of infecting parasite clones estimated for each isolate. Each patient harboured at least 3 clones of P. falciparum by this analysis, consistent with results obtained with conventional PCR analysis of polymorphic merozoite antigen loci. We conclude that genome sequencing of peripheral blood P. falciparum taken directly from malaria patients provides high quality data useful for drug resistance studies, genomic structural analyses and population genetics, and also robustly represents clonal multiplicity
Subbarrel patterns in somatosensory cortical barrels can emerge from local dynamic instabilities
Complex spatial patterning, common in the brain as well as in other biological systems, can emerge as a result of dynamic interactions that occur locally within developing structures. In the rodent somatosensory cortex, groups of neurons called "barrels" correspond to individual whiskers on the contralateral face. Barrels themselves often contain subbarrels organized into one of a few characteristic patterns. Here we demonstrate that similar patterns can be simulated by means of local growth-promoting and growth-retarding interactions within the circular domains of single barrels. The model correctly predicts that larger barrels contain more spatially complex subbarrel patterns, suggesting that the development of barrels and of the patterns within them may be understood in terms of some relatively simple dynamic processes. We also simulate the full nonlinear equations to demonstrate the predictive value of our linear analysis. Finally, we show that the pattern formation is robust with respect to the geometry of the barrel by simulating patterns on a realistically shaped barrel domain. This work shows how simple pattern forming mechanisms can explain neural wiring both qualitatively and quantitatively even in complex and irregular domains. © 2009 Ermentrout et al
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