326 research outputs found
Age, left atrial dimension and arterial stiffness after external cardioversion of atrial fibrillation. A vascular component in arrhythmia maintenance? Results from a preliminary study
The RR Lyrae Distance Scale
We review seven methods of measuring the absolute magnitude M_V of RR Lyrae
stars in light of the Hipparcos mission and other recent developments. We focus
on identifying possible systematic errors and rank the methods by relative
immunity to such errors. For the three most robust methods, statistical
parallax, trigonometric parallax, and cluster kinematics, we find M_V (at
[Fe/H] = -1.6) of 0.77 +/- 0.13, 0.71 +/- 0.15, 0.67 +/- 0.10. These methods
cluster consistently around 0.71 +/- 0.07. We find that Baade-Wesselink and
theoretical models both yield a broad range of possible values (0.45-0.70 and
0.45-0.65) due to systematic uncertainties in the temperature scale and input
physics. Main-sequence fitting gives a much brighter M_V = 0.45 +/- 0.04 but
this may be due to a difference in the metallicity scales of the cluster giants
and the calibrating subdwarfs. White-dwarf cooling-sequence fitting gives 0.67
+/- 0.13 and is potentially very robust, but at present is too new to be fully
tested for systematics. If the three most robust methods are combined with
Walker's mean measurement for 6 LMC clusters, V_{0,LMC} = 18.98 +/- 0.03 at
[Fe/H] = -1.9, then mu_{LMC} = 18.33 +/- 0.08.Comment: Invited review article to appear in: `Post-Hipparcos Cosmic Candles',
A. Heck & F. Caputo (Eds), Kluwer Academic Publ., Dordrecht, in press. 21
pages including 1 table; uses Kluwer's crckapb.sty LaTeX style file, enclose
Fractal assembly of micrometre-scale DNA origami arrays with arbitrary patterns
Self-assembled DNA nanostructures enable nanometre-precise patterning that can be used to create programmable molecular machines and arrays of functional materials. DNA origami is particularly versatile in this context because each DNA strand in the origami nanostructure occupies a unique position and can serve as a uniquely addressable pixel. However, the scale of such structures has been limited to about 0.05 square micrometres, hindering applications that demand a larger layout and integration with more conventional patterning methods. Hierarchical multistage assembly of simple sets of tiles can in principle overcome this limitation, but so far has not been sufficiently robust to enable successful implementation of larger structures using DNA origami tiles. Here we show that by using simple local assembly rules that are modified and applied recursively throughout a hierarchical, multistage assembly process, a small and constant set of unique DNA strands can be used to create DNA origami arrays of increasing size and with arbitrary patterns. We illustrate this method, which we term âfractal assemblyâ, by producing DNA origami arrays with sizes of up to 0.5 square micrometres and with up to 8,704 pixels, allowing us to render images such as the Mona Lisa and a rooster. We find that self-assembly of the tiles into arrays is unaffected by changes in surface patterns on the tiles, and that the yield of the fractal assembly process corresponds to about 0.95^(mâââ1) for arrays containing m tiles. When used in conjunction with a software tool that we developed that converts an arbitrary pattern into DNA sequences and experimental protocols, our assembly method is readily accessible and will facilitate the construction of sophisticated materials and devices with sizes similar to that of a bacterium using DNA nanostructures
Neuroinflammation, Mast Cells, and Glia: Dangerous Liaisons
The perspective of neuroinflammation as an epiphenomenon following neuron damage is being replaced by the awareness of glia and their importance in neural functions and disorders. Systemic inflammation generates signals that communicate with the brain and leads to changes in metabolism and behavior, with microglia assuming a pro-inflammatory phenotype. Identification of potential peripheral-to-central cellular links is thus a critical step in designing effective therapeutics. Mast cells may fulfill such a role. These resident immune cells are found close to and within peripheral nerves and in brain parenchyma/meninges, where they exercise a key role in orchestrating the inflammatory process from initiation through chronic activation. Mast cells and glia engage in crosstalk that contributes to accelerate disease progression; such interactions become exaggerated with aging and increased cell sensitivity to stress. Emerging evidence for oligodendrocytes, independent of myelin and support of axonal integrity, points to their having strong immune functions, innate immune receptor expression, and production/response to chemokines and cytokines that modulate immune responses in the central nervous system while engaging in crosstalk with microglia and astrocytes. In this review, we summarize the findings related to our understanding of the biology and cellular signaling mechanisms of neuroinflammation, with emphasis on mast cell-glia interactions
The stellar and sub-stellar IMF of simple and composite populations
The current knowledge on the stellar IMF is documented. It appears to become
top-heavy when the star-formation rate density surpasses about 0.1Msun/(yr
pc^3) on a pc scale and it may become increasingly bottom-heavy with increasing
metallicity and in increasingly massive early-type galaxies. It declines quite
steeply below about 0.07Msun with brown dwarfs (BDs) and very low mass stars
having their own IMF. The most massive star of mass mmax formed in an embedded
cluster with stellar mass Mecl correlates strongly with Mecl being a result of
gravitation-driven but resource-limited growth and fragmentation induced
starvation. There is no convincing evidence whatsoever that massive stars do
form in isolation. Various methods of discretising a stellar population are
introduced: optimal sampling leads to a mass distribution that perfectly
represents the exact form of the desired IMF and the mmax-to-Mecl relation,
while random sampling results in statistical variations of the shape of the
IMF. The observed mmax-to-Mecl correlation and the small spread of IMF
power-law indices together suggest that optimally sampling the IMF may be the
more realistic description of star formation than random sampling from a
universal IMF with a constant upper mass limit. Composite populations on galaxy
scales, which are formed from many pc scale star formation events, need to be
described by the integrated galactic IMF. This IGIMF varies systematically from
top-light to top-heavy in dependence of galaxy type and star formation rate,
with dramatic implications for theories of galaxy formation and evolution.Comment: 167 pages, 37 figures, 3 tables, published in Stellar Systems and
Galactic Structure, Vol.5, Springer. This revised version is consistent with
the published version and includes additional references and minor additions
to the text as well as a recomputed Table 1. ISBN 978-90-481-8817-
The Near-Infrared Spectrograph (NIRSpec) on the James Webb Space Telescope II. Multi-object spectroscopy (MOS)
We provide an overview of the capabilities and performance of the
Near-Infrared Spectrograph (NIRSpec) on the James Webb Space Telescope (JWST)
when used in its multi-object spectroscopy (MOS) mode employing a novel Micro
Shutter Array (MSA) slit device. The MSA consists of four separate 98 arcsec
91 arcsec quadrants each containing individually
addressable shutters whose open areas on the sky measure 0.20 arcsec
0.46 arcsec on a 0.27 arcsec 0.53 arcsec pitch. This is the first time
that a configurable multi-object spectrograph has been available on a space
mission. The levels of multiplexing achievable with NIRSpec MOS mode are
quantified and we show that NIRSpec will be able to observe typically fifty to
two hundred objects simultaneously with the pattern of close to a quarter of a
million shutters provided by the MSA. This pattern is fixed and regular, and we
identify the specific constraints that it yields for NIRSpec observation
planning. We also present the data processing and calibration steps planned for
the NIRSpec MOS data. The significant variation in size of the mostly
diffraction-limited instrument point spread function over the large wavelength
range of 0.6-5.3 m covered by the instrument, combined with the fact that
most targets observed with the MSA cannot be expected to be perfectly centred
within their respective slits, makes the spectrophotometric and wavelength
calibration of the obtained spectra particularly complex. These challenges
notwithstanding, the sensitivity and multiplexing capabilities anticipated of
NIRSpec in MOS mode are unprecedented, and should enable significant progress
to be made in addressing a wide range of outstanding astrophysical problems
Recommended from our members
The Near-Infrared Spectrograph (NIRSpec) on the James Webb Space Telescope II. Multi-object spectroscopy (MOS)
We provide an overview of the capabilities and performance of the
Near-Infrared Spectrograph (NIRSpec) on the James Webb Space Telescope (JWST)
when used in its multi-object spectroscopy (MOS) mode employing a novel Micro
Shutter Array (MSA) slit device. The MSA consists of four separate 98 arcsec
91 arcsec quadrants each containing individually
addressable shutters whose open areas on the sky measure 0.20 arcsec
0.46 arcsec on a 0.27 arcsec 0.53 arcsec pitch. This is the first time
that a configurable multi-object spectrograph has been available on a space
mission. The levels of multiplexing achievable with NIRSpec MOS mode are
quantified and we show that NIRSpec will be able to observe typically fifty to
two hundred objects simultaneously with the pattern of close to a quarter of a
million shutters provided by the MSA. This pattern is fixed and regular, and we
identify the specific constraints that it yields for NIRSpec observation
planning. We also present the data processing and calibration steps planned for
the NIRSpec MOS data. The significant variation in size of the mostly
diffraction-limited instrument point spread function over the large wavelength
range of 0.6-5.3 m covered by the instrument, combined with the fact that
most targets observed with the MSA cannot be expected to be perfectly centred
within their respective slits, makes the spectrophotometric and wavelength
calibration of the obtained spectra particularly complex. These challenges
notwithstanding, the sensitivity and multiplexing capabilities anticipated of
NIRSpec in MOS mode are unprecedented, and should enable significant progress
to be made in addressing a wide range of outstanding astrophysical problems
The effect of electrical neurostimulation on collateral perfusion during acute coronary occlusion
<p>Abstract</p> <p>Background</p> <p>Electrical neurostimulation can be used to treat patients with refractory angina, it reduces angina and ischemia. Previous data have suggested that electrical neurostimulation may alleviate myocardial ischaemia through increased collateral perfusion. We investigated the effect of electrical neurostimulation on functional collateral perfusion, assessed by distal coronary pressure measurement during acute coronary occlusion. We sought to study the effect of electrical neurostimulation on collateral perfusion.</p> <p>Methods</p> <p>Sixty patients with stable angina and significant coronary artery disease planned for elective percutaneous coronary intervention were split in two groups. In all patients two balloon inflations of 60 seconds were performed, the first for balloon dilatation of the lesion (first episode), the second for stent delivery (second episode). The Pw/Pa ratio (wedge pressure/aortic pressure) was measured during both ischaemic episodes. Group 1 received 5 minutes of active neurostimulation before plus 1 minute during the first episode, group 2 received 5 minutes of active neurostimulation before plus 1 minute during the second episode.</p> <p>Results</p> <p>In group 1 the Pw/Pa ratio decreased by 10 ± 22% from 0.20 ± 0.09 to 0.19 ± 0.09 (p = 0.004) when electrical neurostimulation was deactivated. In group 2 the Pw/Pa ratio increased by 9 ± 15% from 0.22 ± 0.09 to 0.24 ± 0.10 (p = 0.001) when electrical neurostimulation was activated.</p> <p>Conclusion</p> <p>Electrical neurostimulation induces a significant improvement in the Pw/Pa ratio during acute coronary occlusion.</p
Presynaptic Nicotinic α7 and Non-α7 Receptors Stimulate Endogenous GABA Release from Rat Hippocampal Synaptosomes through Two Mechanisms of Action
BACKGROUND: Although converging evidence has suggested that nicotinic acetylcholine receptors (nAChR) play a role in the modulation of GABA release in rat hippocampus, the specific involvement of different nAChR subtypes at presynaptic level is still a matter of debate. In the present work we investigated, using selective α7 and α4ÎČ2 nAChR agonists, the presence of different nAChR subtypes on hippocampal GABA nerve endings to assess to what extent and through which mechanisms they stimulate endogenous GABA release. METHODOLOGY/FINDINGS: All agonists elicited GABA overflow. Choline (Ch)-evoked GABA overflow was dependent to external Ca(2+), but unaltered in the presence of Cd(2+), tetrodotoxin (TTX), dihydro-ÎČ-erythroidine (DHÎČE) and 1-(4,4-Diphenyl-3-butenyl)-3-piperidinecarboxylic acid hydrochloride SKF 89976A. The effect of Ch was blocked by methyllycaconitine (MLA), α-bungarotoxin (α-BTX), dantrolene, thapsigargin and xestospongin C, suggesting that GABA release might be triggered by Ca(2+) entry into synaptosomes through the α7 nAChR channel with the involvement of calcium from intracellular stores. Additionally, 5-Iodo-A-85380 dihydrochloride (5IA85380) elicited GABA overflow, which was Ca(2+) dependent, blocked by Cd(2+), and significantly inhibited by TTX and DHÎČE, but unaffected by MLA, SKF 89976A, thapsigargin and xestospongin C and dantrolene. These findings confirm the involvement of α4ÎČ2 nAChR in 5IA85380-induced GABA release that seems to occur following membrane depolarization and opening calcium channels. CONCLUSIONS/SIGNIFICANCE: Rat hippocampal synaptosomes possess both α7 and α4ÎČ2 nAChR subtypes, which can modulate GABA release via two distinct mechanisms of action. The finding that GABA release evoked by the mixture of sub-maximal concentration of 5IA85380 plus sub-threshold concentrations of Ch was significantly larger than that elicited by the sum of the effects of the two agonists is compatible with the possibility that they coexist on the same nerve terminals. These findings would provide the basis for possible selective pharmacological strategies to treat neuronal disorders that involve the dysfunction of hippocampal cholinergic system
The Near-Infrared Spectrograph (NIRSpec) on the James Webb Space Telescope: IV. Capabilities and predicted performance for exoplanet characterization
The Near-Inrared Spectrograph (NIRSpec) on the James Webb Space Telescope
(JWST) is a very versatile instrument, offering multiobject and integral field
spectroscopy with varying spectral resolution (30 to 3000) over a
wide wavelength range from 0.6 to 5.3 micron, enabling scientists to study many
science themes ranging from the first galaxies to bodies in our own Solar
System. In addition to its integral field unit and support for multiobject
spectroscopy, NIRSpec features several fixed slits and a wide aperture
specifically designed to enable high precision time-series and transit as well
as eclipse observations of exoplanets. In this paper we present its
capabilities regarding time-series observations, in general, and transit and
eclipse spectroscopy of exoplanets in particular. Due to JWST's large
collecting area and NIRSpec's excellent throughput, spectral coverage, and
detector performance, this mode will allow scientists to characterize the
atmosphere of exoplanets with unprecedented sensitivity
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