Chaos, Fractals and Inflation

In order to draw out the essential behavior of the universe, investigations of early universe cosmology often reduce the complex system to a simple integrable system. Inflationary models are of this kind as they focus on simple scalar field scenarios with correspondingly simple dynamics. However, we can be assured that the universe is crowded with many interacting fields of which the inflaton is but one. As we describe, the nonlinear nature of these interactions can result in a complex, chaotic evolution of the universe. Here we illustrate how chaotic effects can arise even in basic models such as homogeneous, isotropic universes with two scalar fields. We find inflating universes which act as attractors in the space of initial conditions. These universes display chaotic transients in their early evolution. The chaotic character is reflected by the fractal border to the basin of attraction. The broader implications are likely to be felt in the process of reheating as well as in the nature of the cosmic background radiation.Comment: 16 pages, RevTeX. See published version for fig

Fractal Spin Glass Properties of Low Energy Configurations in the Frenkel-Kontorova chain

We study numerically and analytically the classical one-dimensional Frenkel-Kontorova chain in the regime of pinned phase characterized by phonon gap. Our results show the existence of exponentially many static equilibrium configurations which are exponentially close to the energy of the ground state. The energies of these configurations form a fractal quasi-degenerate band structure which is described on the basis of elementary excitations. Contrary to the ground state, the configurations inside these bands are disordered.Comment: revtex, 9 pages, 9 figure

Collimation of a Circulating Beam in the U_70 Synchrotron by Use of Reflections in Axially - Oriented Crystals

The possibilities of the extraction and collimation of a circulating beam by a new method due to the reflection of particles in crystals with axial orientation were experimentally investigated in the Fall-2010 run at the U_70 synchrotron. Such crystals have positive features, because the axial potential is five times larger than the planar potential. It has been shown that the collimation efficiency can reach 90% due to axial effects in the crystal. Losses of the circulating beam on a collimator have been reduced by several times; this makes it possible to suppress the muon jet near the steel collimator of the circulating beam.Comment: 6 pages, 7 figure

Nitrite circumvents platelet resistance to nitric oxide in patients with heart failure preserved ejection fraction and chronic atrial fibrillation

Aims: Heart failure (HF) is a pro-thrombotic state. Both platelet and vascular responses to nitric oxide (NO) donors are impaired in HF patients with reduced ejection fraction (HFrEF) compared to healthy volunteers (HV) due to scavenging of NO, and possibly also reduced activity of the principal NO sensor, soluble guanylate cyclase (sGC), limiting the therapeutic potential of NO donors as anti-aggregatory agents. Previous studies have shown that nitrite inhibits platelet activation presumptively after its reduction to NO, but the mechanism(s) involved remain poorly characterized. Our aim was to compare the effects of nitrite on platelet function in HV vs. HF patients with preserved ejection fraction (HFpEF) and chronic atrial fibrillation (HFpEF-AF), vs. patients with chronic AF without HF, and to assess whether these effects occur independent of the interaction with other formed elements of blood. Methods and Results: Platelet responses to nitrite and the NO donor sodium nitroprusside (SNP) were compared in age-matched HV controls (n = 12), HFpEF-AF patients (n = 29) and chronic AF patients (n = 8). Anti-aggregatory effects of nitrite in the presence of NO scavengers/sGC inhibitor were determined and vasodilator-stimulated phosphoprotein (VASP) phosphorylation was assessed using Western blotting. In HV and chronic AF, both nitrite and SNP inhibited platelet aggregation in a concentration-dependent manner. Inhibition of platelet aggregation by the NO donor SNP was impaired in HFpEF-AF patients compared to healthy and chronic AF individuals, but there was no impairment of the anti-aggregatory effects of nitrite. Nitrite circumvented platelet NO resistance independently of other blood cells by directly activating sGC and phosphorylating VASP. Conclusion: We here show for the first time that HFpEF-AF (but not chronic AF without HF) is associated with marked impairment of platelet NO responses due to sGC dysfunction and nitrite circumvents the “platelet NO resistance” phenomenon in human HFpEF, at least partly, by acting as a direct sGC activator independent of NO

Fluorescence Dequenching Makes Haem-Free Soluble Guanylate Cyclase Detectable in Living Cells

In cardiovascular disease, the protective NO/sGC/cGMP signalling-pathway is impaired due to a decreased pool of NO-sensitive haem-containing sGC accompanied by a reciprocal increase in NO-insensitive haem-free sGC. However, no direct method to detect cellular haem-free sGC other than its activation by the new therapeutic class of haem mimetics, such as BAY 58-2667, is available. Here we show that fluorescence dequenching, based on the interaction of the optical active prosthetic haem group and the attached biarsenical fluorophor FlAsH can be used to detect changes in cellular sGC haem status. The partly overlap of the emission spectrum of haem and FlAsH allows energy transfer from the fluorophore to the haem which reduces the intensity of FlAsH fluorescence. Loss of the prosthetic group, e.g. by oxidative stress or by replacement with the haem mimetic BAY 58-2667, prevented the energy transfer resulting in increased fluorescence. Haem loss was corroborated by an observed decrease in NO-induced sGC activity, reduced sGC protein levels, and an increased effect of BAY 58-2667. The use of a haem-free sGC mutant and a biarsenical dye that was not quenched by haem as controls further validated that the increase in fluorescence was due to the loss of the prosthetic haem group. The present approach is based on the cellular expression of an engineered sGC variant limiting is applicability to recombinant expression systems. Nevertheless, it allows to monitor sGC's redox regulation in living cells and future enhancements might be able to extend this approach to in vivo conditions

Choosing Dimensions: The Capability Approach and Multidimensional Poverty

N/

Reversal of acute hyperglycemia restores tissue responsiveness to nitric oxide and improves endothelial progenitor cell function without downregulating platelet thioredoxin interacting protein

Abstract 15725Cher-Rin Chong, Saifei Liu, Giovanni Licari, Yuliy Chirkov, Doan T Ngo, John D Horowit

Reversal of hyperglycemia: effects on nitric oxide signaling

Abstract not availableCher-Rin Chong, Saifei Liu, Giovanni Licari, Tamila Heresztyn, Yuliy Y. Chirkov, Doan T. Ngo, John D. Horowit