234 research outputs found
A CASE OF CONSTRICTIVE PERICARDITIS IN A PATIENT WITH GRANULOMATOSIS WITH POLYANGIITIS (WEGENER'S GRANULOMATOSIS)
The lower mass function of the young open cluster Blanco 1: from 30 Mjup to 3 Mo
We performed a deep wide field optical survey of the young (~100-150 Myr)
open cluster Blanco1 to study its low mass population well down into the brown
dwarf regime and estimate its mass function over the whole cluster mass
range.The survey covers 2.3 square degrees in the I and z-bands down to I ~ z ~
24 with the CFH12K camera. Considering two different cluster ages (100 and 150
Myr), we selected cluster member candidates on the basis of their location in
the (I,I-z) CMD relative to the isochrones, and estimated the contamination by
foreground late-type field dwarfs using statistical arguments, infrared
photometry and low-resolution optical spectroscopy. We find that our survey
should contain about 57% of the cluster members in the 0.03-0.6 Mo mass range,
including 30-40 brown dwarfs. The candidate's radial distribution presents
evidence that mass segregation has already occured in the cluster. We took it
into account to estimate the cluster mass function across the
stellar/substellar boundary. We find that, between 0.03Mo and 0.6Mo, the
cluster mass distribution does not depend much on its exact age, and is well
represented by a single power-law, with an index alpha=0.69 +/- 0.15. Over the
whole mass domain, from 0.03Mo to 3Mo, the mass function is better fitted by a
log-normal function with m0=0.36 +/- 0.07Mo and sigma=0.58 +/- 0.06. Comparison
between the Blanco1 mass function, other young open clusters' MF, and the
galactic disc MF suggests that the IMF, from the substellar domain to the
higher mass part, does not depend much on initial conditions. We discuss the
implications of this result on theories developed to date to explain the origin
of the mass distribution.Comment: 18 pages, 15 figures and 5 tables accepted in A&
Treatment in the context of confinement: – understanding the barriers and possibilities for facilitating change in at-risk youth
AbstractIn this article the authors present a meta-synthesis of their studies on secure institutions in Sweden and Denmark. The aim of the metasynthesis is to explore how the context of confinement shapes the possibilities for providing treatment and positive change for at-risk youth. Drawing on meta-synthesis methodology the authors extract content from nine studies published in 20 articles. We highlight three dimensions, which are a) treatment practices and behavioural regulation, b) the carceral materialities and sociomaterial practices, and c) relations. We argue that while treatment is curtailed by confinement, improvements can be made to support more successful change among at-risk youth and smooth their transition into adulthood.
Artiklen præsenterer en metasyntese af ni studier om sikrede institutioner i Danmark og Sverige. Formålet med metasyntesen er at undersøge, hvordan frihedsberøvelse rammesætter behandling og forandringsarbejde med unge i udsatte positioner. Forfatterne analyserer 20 artikler fordelt på ni studier, de selv har gennemført. Analysen har fokus på tre centrale forhold; a) behandlingsarbejde og adfærdsregulering, b) materialitet og sociomaterielle praktikker, og c) relationer. Vi argumenterer for, at behandling påvirkes af frihedsberøvelse, men med forbedringer kan behandling på sikret institution bidrage til at skabe positiv forandring og sikre de unges overgang til voksenliv
c-Fos induction by gut hormones and extracellular ATP in osteoblastic-like cell lines
It is widely accepted that the c-Fos gene has a role in proliferation and differentiation of bone cells. ATP-induced c-Fos activation is relevant to bone homeostasis, because nucleotides that are present in the environment of bone cells can contribute to autocrine/paracrine signalling. Gut hormones have previously been shown to have an effect on bone metabolism. In this study, we used the osteoblastic Saos-2 cell line transfected with a c-Fos-driven reporter stimulated with five gut hormones: glucose inhibitory peptide (GIP), glucagon-like peptide-1 (GLP-1), glucagon-like peptide-2 (GLP-2), ghrelin and obestatin, in the presence or absence of ATP. In addition, TE-85 cells were used to determine the time course of c-Fos transcript induction following stimulation with GLP-1, and GLP-2 with or without ATP, using reverse transcription qPCR. The significant results from the experiments are as follows: higher level of c-Fos induction in presence of GIP, obestatin (p = 0.019 and p = 0.011 respectively), and GIP combined with ATP (p < 0.001) using the luciferase assay; GLP-1 and GLP-2 combined with ATP (p = 0.034 and p = 0.002, respectively) and GLP-2 alone (p < 0.001) using qPCR. In conclusion, three of the gut peptides induced c-Fos, providing a potential mechanism underlying the actions of these hormones in bone which can be directed or enhanced by the presence of ATP
Ferumoxytol-enhanced magnetic resonance imaging in acute myocarditis
Objectives Ultrasmall superparamagnetic particles of iron oxide (USPIO)-enhanced MRI can detect tissue-resident macrophage activity and identify cellular inflammation within tissues. We hypothesised that USPIO-enhanced MRI would provide a non-invasive imaging technique that would improve the diagnosis and management of patients with acute myocarditis. Methods Ten volunteers and 14 patients with suspected acute myocarditis underwent T2, T2* and late gadolinium enhancement (LGE) 3T MRI, with further T2* imaging at 24 hours after USPIO (ferumoxytol, 4 mg/kg) infusion, at baseline and 3 months. Myocardial oedema and USPIO enhancement were determined within areas of LGE as well as throughout the myocardium. Results Myocarditis was confirmed in nine of the 14 suspected cases of myocarditis. There was greater myocardial oedema in regions of LGE in patients with myocarditis when compared with healthy volunteer myocardium (T2 value, 57.1±5.3 vs 46.7±1.6 ms, p0.05). Imaging after 3 months in patients with myocarditis revealed a reduction in volume of LGE, a reduction in oedema measures within regions displaying LGE and improvement in ejection fraction (mean −19.7 mL, 95% CI (−0.5 to −40.0)), −5.8 ms (−0.9 to −10.7) and +6% (0.5% to 11.5%), respectively, p<0.05 for all). Conclusion In patients with acute myocarditis, USPIO-enhanced MRI does not provide additional clinically relevant information to LGE and T2 mapping MRI. This suggests that tissue-resident macrophages do not provide a substantial contribution to the myocardial inflammation in this condition. Clinical trial registration NCT02319278; Results
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