4,446 research outputs found
Quantum dynamical response of ultracold few boson ensembles in finite optical lattices to multiple interaction quenches
The correlated non-equilibrium quantum dynamics following a multiple
interaction quench protocol for few-bosonic ensembles confined in finite
optical lattices is investigated. The quenches give rise to an interwell
tunneling and excite the cradle and a breathing mode. Several tunneling
pathways open during the time interval of increased interactions, while only a
few occur when the system is quenched back to its original interaction
strength. The cradle mode, however, persists during and in between the
quenches, while the breathing mode possesses dinstinct frequencies. The
occupation of excited bands is explored in detail revealing a monotonic
behavior with increasing quench amplitude and a non-linear dependence on the
duration of the application of the quenched interaction strength. Finally, a
periodic population transfer between momenta for quenches of increasing
interaction is observed, with a power-law frequency dependence on the quench
amplitude. Our results open the possibility to dynamically manipulate various
excited modes of the bosonic system.Comment: 13 pages, 9 figure
Possible role of extracellularly released phagocytic proteinases in the coagulation disorder during liver transplantation
Orthotopic liver transplantation is frequently associated with a complex coagulation disorder, influencing the outcome of the procedure. In this respect, disseminated intravascular coagulation (DIC) had been suggested to be of causative importance for bleeding complications after reperfusion of the liver graft. In 10 consecutive patients undergoing orthotopic liver transplantations, we studied the occurrence of two phagocyte proteinases of different origin in the graft liver perfus-ate and in systemic blood during the operation, as well as their effects on hemostasis. As compared with plasma samples taken at the end of the anhepatic phase, highly significant increases of cathepsin B and thrombin-anti-thrombin III complexes (TAT), as well as highly significant decreases in antithrombin III, protein C, and C1-inhibitor were observed in graft liver perfusate. Von Willebrand factor and fibrinogen were slightly decreased, whereas the elastase-alpha1 proteinase inhibitor complexes (EPI) were elevated. In plasma the activity of cathepsin B remained unchanged during the prereperfusion phases, but immediately after revascularization of the graft this cysteine proteinase increased. The EPI showed a gradual increase in plasma during the preanhepatic and anhepatic phases but a more pronounced increase in the reperfusion phase. In parallel with the rise in these two proteinases TAT increased and the activities of antithrombin III and C1-inhibitor in plasma decreased after reperfusion. At 12 hr after revascularization plasma levels of TAT, antithrombin III, and C1-inhibitor had returned to the prereperfusion ranges, whereas cathepsin B and EPI were significantly above the baseline levels. These observations are consistent with the hypothesis that extracellularly released lysosomal proteinases may play a role in the development of a DIC-like constellation, including thrombin formation after revascularization of the liver graft. For the first time we could prove the occurrence of phagocyte proteinases in graft liver perfusate and evaluate the importance of these proteinases for the understanding of the pathophysiology leading to bleeding complications in patients undergoing orthotopic liver transplantation
Xenogeneic, extracorporeal liver perfusion in primates improves the ratio of branched-chain amino acids to aromatic amino acids (Fischer's ratio)
In fulminant hepatic failure (FHF), the development of hepatic encephalopathy is associated with grossly abnormal concentrations of plasma amino acids (PAA). Normalization of the ratio of branched-chain amino acids to aromatic amino acids (Fischer's ratio) correlates with clinical improvement. This study evaluated changes in PAA metabolism during 4 h of isolated, normothermic extracorporeal liver perfusion using a newly designed system containing human blood and a rhesus monkey liver. Bile and urea production were within the physiological range. Release of the transaminases AST, ALT and LDH were minimal. The ratio of branched (valine, leucine, isoleucine) to aromatic (tyrosine, phenylalanine) amino acids increased significantly. These results indicate that a xenogeneic extracorporeal liver perfusion system is capable of significantly increasing Fischer's ratio and may play a role in treating and bridging patients in FHF in the future
Soft repulsive mixtures under gravity: brazil-nut effect, depletion bubbles, boundary layering, nonequilibrium shaking
A binary mixture of particles interacting via long-ranged repulsive forces is
studied in gravity by computer simulation and theory. The more repulsive
A-particles create a depletion zone of less repulsive B-particles around them
reminiscent to a bubble. Applying Archimedes' principle effectively to this
bubble, an A-particle can be lifted in a fluid background of B-particles. This
"depletion bubble" mechanism explains and predicts a brazil-nut effect where
the heavier A-particles float on top of the lighter B-particles. It also
implies an effective attraction of an A-particle towards a hard container
bottom wall which leads to boundary layering of A-particles. Additionally, we
have studied a periodic inversion of gravity causing perpetual mutual
penetration of the mixture in a slit geometry. In this nonequilibrium case of
time-dependent gravity, the boundary layering persists. Our results are based
on computer simulations and density functional theory of a two-dimensional
binary mixture of colloidal repulsive dipoles. The predicted effects also occur
for other long-ranged repulsive interactions and in three spatial dimensions.
They are therefore verifiable in settling experiments on dipolar or charged
colloidal mixtures as well as in charged granulates and dusty plasmas.Comment: 10 pages, 11 figure
Mediators of leukocyte yctivation play a role in disseminated intravascular coagulation during orthotopic liver transplantation
Leukocytes play an important role in the development of disseminated intravascular coagulation (DIC). In the reperfusion phase of OLT a DIC-like situation has been described and has been held responsible for the high blood loss during this phase.
We investigated the role of leukocytes in the pathogenesis of DIC in OLT by measuring the leukocytic mediators released upon activation (cathepsin B, elastase, TNF, neopterin) and the levels of thrombin-antithrombin III (TAT) complexes, seen as markers of prothrombin activation. Arterial blood samples were taken at 10 different time points during and after OLT. Samples were also taken of the perfusate released from the liver graft vein during the flushing procedure before the reperfusion phase. Aprotinin was given as a continuous infusion (0.2-0.4 Mill. KlU/hr) and its plasma levels were determined.
Significantly elevated levels of neopterin (15-fold; P<0.01), cathepsin B (440-fold; P<0.01) in the perfusate, as compared with the systemic circulation, as well as their significant increases in the early reperfusion phase suggested that they were released by the graft liver. This was paralleled by elevated levels of elastase (1.3-fold, P<0.05), TNF (1.5-fold, P=NS), and TAT complexes (1.4-fold; P<0.1) in the perfusate. Significant correlations could be identified between the parameters of leukocyte activation and TAT complexes, whereas no correlation was observed between any of the parameters investigated and the aprotinin levels.
Our results strongly indicate a release of leukocytic mediators from the graft liver during its reperfusion which seems to be related to the parallely increased prothrombin activation. No correlation could be seen between levels of aprotinin and levels of leukocytic mediators
Different aprotinin applications influencing hemostatic chances in orthotopic liver transplantation
The effect of different aprotinin applications on hemmtatic changes and blood product requirements in orthotopic liver transplantation was investigated in a prospective, open, and randomized study.
From November 1989 to June 1990, 13 patients received aprotinin as a bolus of 0.5 Mill, kallikrein inac-tivator units (KIU) on three occasions in the course of an OLT, whereas 10 other patients were treated with continuous aprotinin infusion of 0.1-0.4 Mill. KIU/hr. Before and after reperfusion of the graft liver, signs of hyperfibrinolysis, measured by thrombelastography, were significantly lower in the infusion group. Tissue-type plasminogen activator (t-PA) activity increased during the anhepatic phase but to a significantly lesser extent in the infusion group. Blood product requirements during OLT were tendentiously higher in the bolus group but not significantly so. However, the use of packed red blood cells was significantly lower in the postoperative period, whereas there was no significant difference in fresh frozen plasma requirements between the two groups.
All 23 patients have survived, and only one woman of each group required retransplantation due to severe host-versus-graft reactions.
Furthermore, we investigated the perfusate of the graft liver in both groups and detected signs of a decreased t-PA release in the infusion group.
Our results demonstrate an advantage of aprotinin given as continuous infusion over bolus application in OLT
High efficiency deterministic Josephson Vortex Ratchet
We investigate experimentally a Josephson vortex ratchet -- a fluxon in an
asymmetric periodic potential driven by a deterministic force with zero time
average. The highly asymmetric periodic potential is created in an underdamped
annular long Josephson junction by means of a current injector providing
efficiency of the device up to 91%. We measured the ratchet effect for driving
forces with different spectral content. For monochromatic high-frequency drive
the rectified voltage becomes quantized. At high driving frequencies we also
observe chaos, sub-harmonic dynamics and voltage reversal due to the inertial
mass of a fluxon.Comment: accepted by PRL. To see status click on
http://134.2.74.170:88/cnt/cond-mat_0506754.htm
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