552 research outputs found

    A Photomicrographic Method for the Detection of Oxygen Content in the Hemoglobin of the Red Blood Cell

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    Previous attempts at photographing the hemoglobin in the red blood cells have been confined to the making of two separate images of the same blood sample; one image is recorded using a wavelength band in the isobestic point region of the spectral distribution of oxygenated and reduced blood, and the other image is made using a wavelength band of radiation in the area of greatest difference in absorption between the two blood states. The method described here attempts to obtain a measurement of oxygenation by means of only one exposure using both regions of wavelengths simultaneously. The response is the density on film of the images of the two blood samples as recorded on color reversal film. A dilute blood sample was deoxygenated with nitrogen gas using a closed chamber. The blood solution was then transfered to a closed 100 micrometer depth chamber through which photomicrographs were made. Fully oxygenated blood was photographed In the same manner. Microdensitometric traces of the Images of individual oxygenated and reduced blood cells show that the meen density of the images of oxygenated hemoglobin in the cells was signifigantly greater than that of the reduced red blood cells

    Stationary Acceleration of Frenet Curves

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    In this paper, the stationary acceleration of the spherical general helix in a 3-dimensional Lie group is studied by using a bi-invariant metric. The relationship between the Frenet elements of the stationary acceleration curve in 4-dimensional Euclidean space and the intrinsic Frenet elements of the Lie group is outlined. As a consequence, the corresponding curvature and torsion of these curves are computed. In Minkowski space, for the curves on a timelike surface to have a stationary acceleration, a necessary and sufficient condition is refined

    Inflationsvolatilitetens samband med sparkvot och humankapital - en studie av upphinnarländer med hög volatil inflation

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    Syftet med studien var att utföra en empirisk undersökning för att ta reda på ifall de teoretiska resonemangen kring inflationsvolatilitetens inverkan på sparkvot och humankapital har stämt överens med verkligheten. Genom att empiriskt undersöka 14 upphinnarländer under 30 år har, sambandet mellan hög volatilitet i inflationsnivåer, sparkvot och humankapital observerats. Urvalet av länder har baserats på tillväxttakt och inflationsvolatilitet, tillgänglig data och kriteriet att landet befunnit sig under sin steady-state nivå i en majoritet av tidsperioden. Enligt det empiriska resultatet går det inte att statistiskt säkerställa att inflationsvolatilitet har någon inverkan på humankapital. Det är därför inte möjligt att dra några slutsatser kring vad den potentiella osäkerheten på arbetsmarknaden har för inverkan på preferenser kring antal utbildningsår. Inflationsvolatilitet har, enligt studiens empiriska undersökning, ett negativt samband med investeringar. För varje enhet inflationsvolatiliteten ökar, minskar sparkvoten med 0,0214 procentenheter. Eftersom sparkvot är en drivande faktor i ekonomisk tillväxt är det motiverat att regeringar och centralbanker lägger energi på att upprätthålla en stabil inflation

    What contributes to an effective mannose recognition domain?

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    In general, carbohydrate-lectin interactions are characterized by high specificity but also low affinity. The main reason for the low affinities are desolvation costs, due to the numerous hydroxy groups present on the ligand, together with the typically polar surface of the binding sites. Nonetheless, nature has evolved strategies to overcome this hurdle, most prominently in relation to carbohydrate-lectin interactions of the innate immune system but also in bacterial adhesion, a process key for the bacterium's survival. In an effort to better understand the particular characteristics, which contribute to a successful carbohydrate recognition domain, the mannose-binding sites of six C-type lectins and of three bacterial adhesins were analyzed. One important finding is that the high enthalpic penalties caused by desolvation can only be compensated for by the number and quality of hydrogen bonds formed by each of the polar hydroxy groups engaged in the binding process. In addition, since mammalian mannose-binding sites are in general flat and solvent exposed, the half-lives of carbohydrate-lectin complexes are rather short since water molecules can easily access and displace the ligand from the binding site. In contrast, the bacterial lectin FimH benefits from a deep mannose-binding site, leading to a substantial improvement in the off-rate. Together with both a catch-bond mechanism (i.e., improvement of affinity under shear stress) and multivalency, two methods commonly utilized by pathogens, the affinity of the carbohydrate-FimH interaction can be further improved. Including those just described, the various approaches explored by nature to optimize selectivity and affinity of carbohydrate-lectin interactions offer interesting therapeutic perspectives for the development of carbohydrate-based drugs

    Power-to-Syngas: A Parareal Optimal Control Approach

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    A chemical plant layout for the production of syngas from renewable power, H2O and biogas, is presented to ensure a steady productivity of syngas with a constant H2-to-CO ratio under time-dependent electricity provision. An electrolyzer supplies H2 to the reverse water-gas shift reactor. The system compensates for a drop in electricity supply by gradually operating a tri-reforming reactor, fed with pure O2 directly from the electrolyzer or from an intermediate generic buffering device. After the introduction of modeling assumptions and governing equations, suitable reactor parameters are identified. Finally, two optimal control problems are investigated, where computationally expensive model evaluations are lifted viaparareal and necessary objective derivatives are calculated via the continuous adjoint method. For the first time, modeling, simulation, and optimal control are applied to a combination of the reverse water-gas shift and tri-reforming reactor, exploring a promising pathway in the conversion of renewable power into chemicals

    Pharmacodynamic properties for inhibition of cAMP- and cGMP elimination by pentoxifylline remain unaltered in vitro during hypothermia

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    Background - Rewarming from hypothermia is associated with severe complications, one of which is hypothermia-induced cardiac dysfunction. This condition is characterized by decreased cardiac output accompanied by increased total peripheral resistance. This contributes to mortality rate approaching 40%. Despite this, no pharmacological interventions are recommended for these patients below 30 °C. Raising the intracellular levels of cAMP and/or cGMP, through PDE3- and PDE5-inhibitors respectively, have showed the ability to alleviate hypothermia-induced cardiac dysfunction in vivo. Drugs that raise levels of both cAMP and cGMP could therefore prove beneficial in patients suffering from hypothermia-induced cardiac dysfunction. Methods - The unselective PDE-inhibitor pentoxifylline was investigated to determine its ability to reach the intracellular space, inhibit PDE3 and PDE5 and inhibit cellular efflux of cAMP and cGMP at temperatures 37, 34, 30, 28, 24 and 20 °C. Recombinant human PDE-enzymes and human erythrocytes were used in the experiments. IC50-values were calculated at all temperatures to determine temperature-dependent changes. Results - At 20 °C, the IC50-value for PDE5-mediated enzymatic breakdown of cGMP was significantly increased compared to normothermia (IC50: 39.4 µM ± 10.9 µM vs. 7.70 µM ± 0.265 µM, p-value = 0.011). No other significant changes in IC50-values were observed during hypothermia. Conclusions - This study shows that pentoxifylline has minimal temperature-dependent pharmacodynamic changes, and that it can inhibit elimination of both cAMP and cGMP at low temperatures. This can potentially be effective treatment of hypothermia-induced cardiac dysfunction

    Pharmacokinetic study on pradofloxacin in the dog – Comparison of serum analysis, ultrafiltration and tissue sampling after oral administration

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    Background: Pradofloxacin, a newly developed 8-cyano-fluoroquinolone, show enhanced activity against Grampositive organisms and anaerobes to treat canine and feline bacterial infections. The purpose of this cross-over study was to measure the unbound drug concentration of pradofloxacin in the interstitial fluid (ISF) using ultrafiltration and to compare the kinetics of pradofloxacin in serum, ISF and tissue using enrofloxacin as reference. Results: After oral administration of enrofloxacin (5 mg/kg) and pradofloxacin (3 mg/kg and 6 mg/kg, respectively), serum collection and ultrafiltration in regular intervals over a period of 24 h were performed, followed by tissue sampling at the end of the third dosing protocol (pradofloxacin 6 mg/kg). Peak concentrations of pradofloxacin (3 mg/kg) were 1.55±0.31 μg/ml in the ISF and 1.85±0.23 μg/ml in serum and for pradofloxacin (6 mg/kg) 2.71±0.81 μg/kg in the ISF and 2.77±0.64 μg/kg in serum; both without a statistical difference between ISF and serum. Comparison between all sampling approaches showed no consistent pattern of statistical differences. Conclusions: Despite some technical shortcomings the ultrafiltration approach appears to be the most sensitive sampling technique to estimate pharmacokinetic values of pradofloxacin at the infection site. Pharmacokinetics – Pradofloxacin – Ultrafiltration – Dog – Oral Administration

    Copper-nickel-rich, amalgamated ferromanganese crust-nodule deposits from Shatsky Rise, NW Pacific

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    A unique set of ferromanganese crusts and nodules collected from Shatsky Rise (SR), NW Pacific, were analyzed for mineralogical and chemical compositions, and dated using Be isotopes and cobalt chronometry. The composition of these midlatitude, deep-water deposits is markedly different from northwest-equatorial Pacific (PCZ) crusts, where most studies have been conducted. Crusts and nodules on SR formed in close proximity and some nodule deposits were cemented and overgrown by crusts, forming amalgamated deposits. The deep-water SR crusts are high in Cu, Li, and Th and low in Co, Te, and Tl concentrations compared to PCZ crusts. Thorium concentrations (ppm) are especially striking with a high of 152 (mean 56), compared to PCZ crusts (mean 11). The deep-water SR crusts show a diagenetic chemical signal, but not a diagenetic mineralogy, which together constrain the redox conditions to early oxic diagenesis. Diagenetic input to crusts is rare, but unequivocal in these deep-water crusts. Copper, Ni, and Li are strongly enriched in SR deep-water deposits, but only in layers older than about 3.4 Ma. Diagenetic reactions in the sediment and dissolution of biogenic calcite in the water column are the likely sources of these metals. The highest concentrations of Li are in crust layers that formed near the calcite compensation depth. The onset of Ni, Cu, and Li enrichment in the middle Miocene and cessation at about 3.4 Ma were accompanied by changes in the deep-water environment, especially composition and flow rates of water masses, and location of the carbonate compensation depth. Key Points - Fe-Mn crusts can have a diagenetic component - Mid-latitude N. Pacific deep-water Fe-Mn crusts are uniquely enriched in Cu, Th, Li - Temporal changes in deep-ocean geochemical processes are recorde

    Moderate but not severe hypothermia increases intracellular cyclic AMP through preserved production and reduced elimination

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    Rewarming from accidental hypothermia could be complicated by acute cardiac dysfunction but providing supportive pharmacotherapy at low core temperatures is challenging. Several pharmacological strategies aim to improve cardiovascular function by increasing cAMP in cardiomyocytes as well as cAMP and cGMP levels in vascular smooth muscle, but it is not clear what effects temperature has on cellular elimination of cAMP and cGMP. We therefore studied the effects of differential temperatures from normothermia to deep hypothermia (37 ◦C–20 ◦C) on cAMP levels in embryonic H9c2 cardiac cells and elimination of cAMP and cGMP by PDEenzymes and ABC-transporter proteins. Our experiments showed significant elevation of intracellular cAMP in H9c2-cells at 30 ◦C but not 20 ◦C. Elimination of both cAMP and cGMP through ABC transport-proteins and PDEenzymes showed a temperature dependent reduction. Accordingly, the increased cardiomyocyte cAMP-levels during moderate hypothermia appears an effect of preserved production and reduced elimination at 30 ◦C. This correlates with earlier in vivo findings of a positive inotropic effect of moderate hypothermia
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