6,066 research outputs found

    Gravitomagnetism in superconductors and compact stars

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    There are three experimentally observed effects in rotating superconductors that are so far unexplained. Some authors have tried to interpret such a phenomena as possible new gravitational properties of coherent quantum systems: in particular, they suggest that the gravitomagnetic field of that kind of matter may be many orders of magnitude stronger than the one expected in the standard theory. Here I show that this interpretation would be in conflict with the common belief that neutron stars have neutrons in superfluid state and protons in superconductive one.Comment: 9 pages, no figur

    On the time delay in binary systems

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    The aim of this paper is to study the time delay on electromagnetic signals propagating across a binary stellar system. We focus on the antisymmetric gravitomagnetic contribution due to the angular momentum of one of the stars of the pair. Considering a pulsar as the source of the signals, the effect would be manifest both in the arrival times of the pulses and in the frequency shift of their Fourier spectra. We derive the appropriate formulas and we discuss the influence of different configurations on the observability of gravitomagnetic effects. We argue that the recently discovered PSR J0737-3039 binary system does not permit the detection of the effects because of the large size of the eclipsed region.Comment: 7 pages, 2 eps figures, RevTex, to appear in Physical Review

    A post-Keplerian parameter to test gravito-magnetic effects in binary pulsar systems

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    We study the pulsar timing, focusing on the time delay induced by the gravitational field of the binary systems. In particular, we study the gravito-magnetic correction to the Shapiro time delay in terms of Keplerian and post-Keplerian parameters, and we introduce a new post-Keplerian parameter which is related to the intrinsic angular momentum of the stars. Furthermore, we evaluate the magnitude of these effects for the binary pulsar systems known so far. The expected magnitude is indeed small, but the effect is important per se.Comment: 6 pages, RevTeX, 1 eps figure, accepted for publication in Physical Review D; references adde

    Gravitomagnetic time-varying effects on the motion of a test particle

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    We study the effects of a time-varying gravitomagnetic field on the motion of test particles. Starting from recent results, we consider the gravitomagnetic field of a source whose spin angular momentum has a linearly time-varying magnitude. The acceleration due to such a time-varying gravitomagnetic field is considered as a perturbation of the Newtonian motion, and we explicitly evaluate the effects of this perturbation on the Keplerian elements of a closed orbit. The theoretical predictions are compared with actual astronomical and astrophysical scenarios, both in the solar system and in binary pulsars systems, in order to evaluate the impact of these effects on real systems.Comment: 8 pages, RevTeX; revised to match the version accepted for publication in General Relativity and Gravitatio

    Targeting the Toll-like receptor/interleukin 1 receptor pathway in human diseases: rational design of MyD88 inhibitors

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    Toll-like receptor (TLR)/interleukin (IL) 1 receptor (IL-1R) play a fundamental role in the immune response. These receptors are distributed in various cellular compartments and recognize different components of pathogens. All TLR/IL-1Rs, with the exception of TLR3, interact with MyD88, an intracellular adapter protein that triggers a signaling cascade that culminates in the expression of inflammatory genes. Because aberrant activation of TLR/IL-1Rs can promote the onset of inflammatory or autoimmune diseases and malignancies, this pathway has attracted considerable interest as a potential therapeutic target. Given the central role of MyD88 in TLR/IL-1R signaling, we set out different strategies to develop drugs that can block its function. Structural and functional analysis of the MyD88 domains allowed us to identify crucial residues required for MyD88 homodimerization. Moreover, we developed small cell-permeable peptides and peptidomimetic agents that inhibit MyD88 homodimerization and function. Our results pave the way for the development of new therapeutic drugs for the inhibition of MyD88-dependent signaling
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