345 research outputs found
Rolling Tachyon in Brane World Cosmology from Superstring Field Theory
The pressureless tachyonic matter recently found in superstring field theory
has an over-abundance problem in cosmology. We argue that this problem is
naturally solved in the brane inflationary scenario if almost all of the
tachyon energy is drained (via its coupling to the inflaton and matter fields)
to heating the universe, while the rest of the tachyon energy goes to a network
of cosmic strings (lower-dimensional BPS D-branes) produced during the tachyon
rolling at the end of inflation.Comment: 4 pages, one figure. This version quantifies constraints on various
phenomenological models for tachyon deca
An Attempt to Determine the Largest Scale of Primordial Density Perturbations in the Universe
Inflationary cosmology predicts that the particle horizon should be
generically much bigger than the present-day Hubble radius, . This
implies a special regime of super-Hubble scale energy density fluctuations
imprinted on the cosmic microwave background radiation (CMBR), which from
present theory could only be explained by inflation Causality constraints are
used to determine models for the power spectrum that accommodate a suppression
scale. A three parameter likelihood analysis is performed of the COBE-DMR
4-year data with respect to the amplitude, spectral index, and suppression
scale. It is found that all suppression length scales larger than are
consistent with the data, but that scales of order are slightly
preferred, at roughly the one-sigma level. Many non-inflation models would be
consistent with a small suppression length scale, whereas for standard
inflation models, the duration of the inflation epoch would have to be bounded
by a fairly small upper limit. Suppression scales smaller than are
strongly excluded by the anisotrophy data.Comment: 9 pages, Latex, 1 figure, additional tests reporte
Magnetic Knots as The origin of Spikes in the Gravitational Waves Backgrounds
The dynamical symmetries of hot and electrically neutral plasmas in a highly
conducting medium suggest that, after the epoch of the electron-positron
annihilation, magnetohydrodynamical configurations carrying a net magnetic
helicity can be present. The simultaneous conservation of the magnetic flux and
helicity implies that the (divergence free) field lines will possess
inhomogeneous knot structures acting as source seeds in the evolution equations
of the scalar, vector and tensor fluctuations of the background geometry. We
give explicit examples of magnetic knot configurations with finite energy and
we compute the induced metric fluctuations. Since magnetic knots are
(conformally) coupled to gravity via the vertex dictated by the equivalence
principle, they can imprint spikes in the gravitational wave spectrum for
frequencies compatible with the typical scale of the knot corresponding, in our
examples, to a present frequency range of -- Hertz. At
lower frequencies the spectrum is power-suppressed and well below the COBE
limit. For smaller length scales (i.e. for larger frequencies) the spectrum is
exponentially suppressed and then irrelevant for the pulsar bounds. Depending
upon the number of knots of the configuration, the typical amplitude of the
gravitational wave logarithmic energy spectrum (in critical units) can be even
four orders of magnitude larger than the usual flat (inflationary) energy
spectrum generated thanks to the parametric amplification of the vacuum
fluctuations.Comment: Accepted for publication in Physical Review D, 20 pages in RevTex
style, 4 Encapsulated figure
Skeletal muscle ATP synthesis and cellular H+ handling measured by localized 31P-MRS during exercise and recovery
31P magnetic resonance spectroscopy (MRS) is widely used for non-invasive investigation of muscle metabolism dynamics. This study aims to extend knowledge on parameters derived from these measurements in detail and comprehensiveness: proton (H+) efflux, buffer capacity and the contributions of glycolytic (L) and oxidative (Q) rates to ATP synthesis were calculated from the evolutions of phosphocreatine (PCr) and pH. Data are reported for two muscles in the human calf, for each subject and over a wide range of exercise intensities. 22 subjects performed plantar flexions in a 7T MR-scanner, leading to PCr changes ranging from barely noticeable to almost complete depletion, depending on exercise protocol and muscle studied by localized MRS. Cytosolic buffer capacity was quantified for the first time non-invasively and individually, as was proton efflux evolution in early recovery. Acidification started once PCr depletion reached 60–75%. Initial and end-exercise L correlated with end-exercise levels of PCr and approximately linear with pH. Q calculated directly from PCr and pH derivatives was plausible, requiring fewer assumptions than the commonly used ADP-model. In conclusion, the evolution of parameters describing cellular energy metabolism was measured over a wide range of exercise intensities, revealing a relatively complete picture of muscle metabolism
ATP and its N6-substituted analogues: parameterization, molecular dynamics simulation and conformational analysis
In this work we used a combination of classical molecular dynamics and simulated annealing techniques to shed more light on the conformational flexibility of 12 adenosine triphosphate (ATP) analogues in a water environment. We present simulations in AMBER force field for ATP and 12 published analogues [Shah et al. (1997) Proc Natl Acad Sci USA 94: 3565–3570]. The calculations were carried out using the generalized Born (GB) solvation model in the presence of the cation Mg2+. The ion was placed at a close distance (2 Å) from the charged oxygen atoms of the beta and gamma phosphate groups of the −3 negatively charged ATP analogue molecules. Analysis of the results revealed the distribution of inter-proton distances H8–H1′ and H8–H2′ versus the torsion angle ψ (C4–N9-C1′–O4′) for all conformations of ATP analogues. There are two gaps in the distribution of torsion angle ψ values: the first is between −30 and 30 degrees and is described by cis-conformation; and the second is between 90 and 175 degrees, which mostly covers a region of anti conformation. Our results compare favorably with results obtained in experimental assays [Jiang and Mao (2002) Polyhedron 21:435–438]
C-Jun N-terminal kinase (JNK) isoforms play differing roles in otitis media
BACKGROUND: Innate immunity and tissue proliferation play important roles in otitis media (OM), the most common disease of childhood. CJUN terminal kinase (JNK) is potentially involved in both processes. RESULTS: Genes involved in both innate immune and growth factor activation of JNK are upregulated during OM, while expression of both positive and negative JNK regulatory genes is altered. When compared to wildtypes (WTs), C57BL/6 mice deficient in JNK1 exhibit enhanced mucosal thickening, with delayed recovery, enhanced neutrophil recruitment early in OM, and delayed bacterial clearance. In contrast, JNK2(−/−) mice exhibit delayed mucosal hyperplasia that eventually exceeds that of WTs and is slow to recover, delayed recruitment of neutrophils, and failure of bacterial clearance. CONCLUSIONS: The results suggest that JNK1 and JNK2 play primarily opposing roles in mucosal hyperplasia and neutrophil recruitment early in OM. However, both isoforms are required for the normal resolution of middle ear infection. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12865-014-0046-z) contains supplementary material, which is available to authorized users
Innate Signaling in Otitis Media: Pathogenesis and Recovery
Otitis media (OM) is the most prevalent childhood disease in developed countries. Involvement of innate immunity mediated by Toll-like receptors (TLRs) in OM has been implicated primarily in cell lines and by association studies of innate immune gene polymorphisms with OM prevalence. However, the precise role of innate immunity in OM is incompletely understood. We review recent research that has advanced our understanding of how innate immunity in the middle ear is mediated by the interaction of pathogen molecules with receptors such as the TLRs, leading to the activation of adaptor molecules and production of proinflammatory cytokines. TLR genes and signaling molecules are upregulated in OM in a murine model. Deletion of several key innate immune genes results in persistent OM in mice, coupled with an inability to clear bacterial infection from the middle ear. It is concluded that an intact innate immune signaling system is critical to recovery from bacterial OM
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