2,567 research outputs found

    The QT interval in lightning injury with implications for the cessation of metabolism hypothesis

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    An hypothesis is presented to provide an alternative to the Cessation of Metabolism hypothesis often invoked in lightning injury. Cessation of Metabolism has been proposed to explain the observation of good recovery after a prolonged period in cardiac arrest in some lightning injured patients. Reevaluation of EEGs from lightning injured patients show a high incidence of QT prolongation. Reexamination of the cases used to support Cessation of Metabolism also reveals little evidence to justify the hypothesis. The finding of QT prolongation coupled with the hyperadrenergic state said to exist in lightning injury, may promote a state of episodic induction of and recovery from Torsade de Pointes Ventricular Tachycardia (VT). Histological examination of the myocardium supports the new hypothesis. This the first concerted description of lightning injury as one of the general causes of QT prolongation. It appears to occur frequently after lightning injury, is a prerequisite of and predisposes to episodes of Torsade de Pointes VT. These electrocardiographic abnormalities explain Cessation of Metabolism and recognition may change management and lead to greater survival

    Francisella infections in farmed and wild aquatic organisms

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    Over the last 10 years or so, infections caused by bacteria belonging to a particular branch of the genus Francisella have become increasingly recognised in farmed fish and molluscs worldwide. While the increasing incidence of diagnoses may in part be due to the development and widespread availability of molecular detection techniques, the domestication of new organisms has undoubtedly instigated emergence of clinical disease in some species. Francisellosis in fish develops in a similar fashion independent of host species and is commonly characterised by the presence of multi-organ granuloma and high morbidity, with varying associated mortality levels. A number of fish species are affected including Atlantic cod, Gadus morhua; tilapia, Oreochromis sp.; Atlantic salmon, Salmo salar; hybrid striped bass, Morone chrysops × M. saxatilis and three-lined grunt, Parapristipoma trilinineatum. The disease is highly infectious and often prevalent in affected stocks. Most, if not all strains isolated from teleost fish belong to either F. noatunensis subsp. orientalis in warm water fish species or Francisella noatunensis subsp. noatunensis in coldwater fish species. The disease is quite readily diagnosed following histological examination and identification of the aetiological bacterium by culture on cysteine rich media or PCR. The available evidence may indicate a degree of host specificity for the various Francisella strains, although this area requires further study. No effective vaccine is currently available. Investigation of the virulence mechanisms and host response shows similarity to those known from Francisella tularensis infection in mammals. However, no evidence exists for zoonotic potential amongst the fish pathogenic Francisella

    B-meson decay constants: a more complete picture from full lattice QCD

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    We extend the picture of BB-meson decay constants obtained in lattice QCD beyond those of the BB, BsB_s and BcB_c to give the first full lattice QCD results for the BB^*, BsB^*_s and BcB^*_c. We use improved NonRelativistic QCD for the valence bb quark and the Highly Improved Staggered Quark (HISQ) action for the lighter quarks on gluon field configurations that include the effect of u/du/d, ss and cc quarks in the sea with u/du/d quark masses going down to physical values. For the ratio of vector to pseudoscalar decay constants, we find fB/fBf_{B^*}/f_B = 0.941(26), fBs/fBsf_{B^*_s}/f_{B_s} = 0.953(23) (both 2σ2\sigma less than 1.0) and fBc/fBcf_{B^*_c}/f_{B_c} = 0.988(27). Taking correlated uncertainties into account we see clear indications that the ratio increases as the mass of the lighter quark increases. We compare our results to those using the HISQ formalism for all quarks and find good agreement both on decay constant values when the heaviest quark is a bb and on the dependence on the mass of the heaviest quark in the region of the bb. Finally, we give an overview plot of decay constants for gold-plated mesons, the most complete picture of these hadronic parameters to date.Comment: 20 pages, 9 figures. Minor updates to the discussion in several places and some additional reference

    Υ and Υ′ leptonic widths, abμ, and mb from full lattice QCD

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    We determine the decay rate to leptons of the ground-state ϒ meson and its first radial excitation in lattice QCD for the first time. We use radiatively improved nonrelativistic QCD for the b quarks and include u, d, s and c quarks in the sea with u=d masses down to their physical values. We find Γðϒ → eþe−Þ ¼ 1.19ð11Þ keV and Γðϒ0 → eþe−Þ ¼ 0.69ð9Þ keV, both in good agreement with experimental results. The decay constants we obtain are included in a summary plot of meson decay constants from lattice QCD given in the Conclusions. We also test time moments of the vector current-current correlator against values determined from the b-quark contribution to σðeþe− → hadronsÞ and calculate the b-quark piece of the hadronic vacuum polarization contribution to the anomalous magnetic moment of the muon, ab μ ¼ 0.271ð37Þ × 10−10. Finally we determine the b-quark mass, obtaining in the MS scheme, ¯ m¯ bðm¯ b; nf ¼ 5Þ ¼ 4.196ð23Þ GeV, the most accurate result from lattice QCD to date

    Ion-channel-like behavior in lipid bilayer membranes at the melting transition

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    It is well known that at the gel-liquid phase transition temperature a lipid bilayer membrane exhibits an increased ion permeability. We analyze the quantized currents in which the increased permeability presents itself. The open time histogram shows a "-3/2" power law which implies an open-closed transition rate that decreases like k(t)t1k(t) \propto t^{-1} as time evolves. We propose a "pore freezing" model to explain the observations. We discuss how this model also leads to the 1/fα1/f^{\alpha} noise that is commonly observed in currents across biological and artificial membranes.Comment: 5 pages, 4 figure
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