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Biomedical subjects

G Seibold

Publications and source records attributed to G Seibold.

17 recordsLinked to original sources

Magnetic fluctuations of stripes in the high temperature cuprate superconductors.

Within the time-dependent Gutzwiller approximation for the Hubbard model we compute the magnetic fluctuations of vertical metallic stripes with parameters appropriate for La(1.875)Ba(0.125)CuO(4) (LBCO). For bond- and site-centered stripes the excitation spectra are similar, consisting of a low-energy incommensurate acoustic branch which merges into a "resonance peak" at the antiferromagnetic wave vector and several high-energy optical branches. The acoustic branch is similar to the result of theories assuming localized spins whereas the optical branches are significantly different. Results are in good agreement with a recent inelastic neutron study of LBCO.

Journal Article↗

Outpatient parenteral antibiotic therapy (OPAT) in different countries: a comparison.

In order to assess how outpatient parenteral antibiotic therapy (OPAT) is managed in different countries, we analyzed the data collected in the USA, UK and Italy by the International OPAT Registry using an ad hoc Access/Excel Microsoft program. The analysis of data concerned 9826 patients in the USA, 981 in the UK and 620 in Italy. Differences were observed in several aspects of OPAT management such as the infections treated and the antibiotics utilized. The duration of therapy also differed: it was much longer in Italy (56.0 average days), than in the USA (22.5 days) and UK (19.9 days). Delivery model, delivery route and infusion devices show substantial differences. The present analysis shows that OPAT is carried out with substantial differences in different countries probably according to different programmes and guidelines adopted.

Ambulatory Care↗

Dynamics of metallic stripes in cuprates.

We study the dynamics of metallic vertical stripes in cuprates within the three-band Hubbard model based on a recently developed time-dependent Gutzwiller approximation. As doping increases, the optical conductivity shows transfer of spectral weight from the charge-transfer band towards (i) an incoherent band centered at 1.3 eV, (ii) a Drude peak, due mainly to motion along the stripe, and (iii) a low-energy collective mode which softens with doping and merges with (ii) at optimum doping in good agreement with experiment. The softening is related to the quasidegeneracy between Cu-centered and O-centered mean-field stripe solutions close to optimal doping.

Journal Article↗

Metallic mean-field stripes, incommensurability, and chemical potential in cuprates.

We perform a systematic slave-boson mean-field analysis of the three-band model for cuprates with first-principle parameters. Contrary to widespread belief based on earlier mean-field computations low doping stripes have a linear density close to 1/2 added hole per lattice constant. We find a dimensional crossover from 1D to 2D at doping approximately 0.1 followed by a breaking of particle-hole symmetry around doping 1/8 as doping increases. Our results explain in a simple way the behavior of the chemical potential, the magnetic incommensurability, and transport experiments as a function of doping. Bond centered and site-centered stripes become degenerate for small overdoping.

Journal Article↗

Time-dependent Gutzwiller approximation for the Hubbard model.

We develop a time-dependent Gutzwiller approximation (GA) for the Hubbard model analogous to the time-dependent Hartree-Fock (HF) method. This new formalism incorporates ground state correlations of the random phase approximation (RPA) type beyond the GA. Static quantities like ground state energy and double occupancy are in excellent agreement with exact results in one dimension up to moderate coupling and in two dimensions for all couplings. We find a substantial improvement over traditional GA and HF+RPA treatments. Dynamical correlation functions can be computed and are also substantially better than HF+RPA ones and obey well behaved sum rules.

Journal Article↗

Altered immune response (humoral and delayed-type hypersensitivity reactions) to sheep red blood cells in the course of experimental filarial infections (Litomosoides carinii, Brugia malayi, Acanthocheilonema viteae) of Mastomys natalensis.

Litomosoides carinii-, Acanthocheilonema viteae- or Brugia malayi-infected Mastomys natalensis were sensitised against sheep red blood cells (SRBC) on various occasions after infection to determine the effect of filarial infections on the immune response to a non-filarial antigen. The phagocytic activity of the reticuloendothelial system (RES) was controlled in vivo by the elimination of 51Cr-labelled SRBC. Antibody titres against SRBC (agglutinating and lytic antibodies) were similar to those of uninfected controls in L. carinii- or B. malayi-infected Mastomys sensitised during prepatency or early patency up to 90 days post infection (p.i.) but were reduced in animals sensitised during patency. A significant inverse correlation existed between anti-SRBC antibody titres and microfilaraemia levels. In contrast, A. viteae-infected Mastomys showed reduced humoral anti-SRBC responses at the end of prepatency, whereas the response tended towards normal with increasing parasitaemia. Delayed-type hypersensitivity (DTH) against SRBC was measured as footpad swelling after sensitisation by the s.c. or i.v. route and intraplantar challenge. DTH reactions were reduced during prepatency in all infections after s.c. sensitisation. During patency, 24-h reactions were similar to those of age-matched controls but the swelling persisted 24 or 48 h longer than in the latter. In A. viteae infections, even enhanced 24-h reactions were found during patency. Histological investigations did not reveal differences in the type of cell infiltrations between infected and control animals. After i.v. sensitisation with SRBC, L. carinii- and A. viteae-infected animals showed weaker DTH reactions than the controls, independent of the period after infection. In the case of B. malayi infections, DTH reactions were similar to those of controls during early prepatency, whereas reduced DTH responses were observed later than 50 days p.i. As shown in L. carinii-infected animals, depressed DTH reactions after i.v. sensitisation did not depend on an altered expression phase but rather on an altered regulation during the inductive phase of the response: increases in the sensitising SRBC doses that caused decreasing DTH reactions in uninfected animals led to enhanced reactions in infected animals. Phagocytosis of i.v. injected 51Cr-labelled SRBC was enhanced during prepatency in L. carinii infection and during patency in all infections.

Animals↗

Lamin disassembly kinetics: a cell-free system with extracts from mitotic HeLa cells.

We describe a cell-free system in which a postribosomal supernatant from metaphase HeLa cells induces prophase-like changes in permeabilized HeLa cell populations as evidenced by the nuclear lamin disassembly and chromatin condensation. We have attempted to characterize the cell-free system with permeabilized HeLa cells. First, by extracting lamins with agents known to disrupt the noncovalent interactions in the supramolecular lamin aggregate in interphase using polyclonal and a newly established monoclonal anti-lamin Ab 2E3, uniform extraction of lamins was achieved with urea and deoxycholate whereas the cation Mg2+ and 2-mercaptoethanol had little effect on the disassembly of interphase lamins. Second, cytoplasmic extract from mitotic HeLa cells, synchronized by a nitrous oxide metaphase arrest, was tested. It had a differential effect on interphase lamin depolymerization. Nuclei in G1 phase of the cell cycle were more resistant against the mitotic extracts than cells in S and G2 phase. The results are discussed in terms of a possible inactivation of mitotic extracts by factors present in nuclei in early interphase.

Adenosine Triphosphate↗

Quantitative autoradiography of [125I] apamin binding sites in the central nervous system.

The binding sites for [125I] apamin in the central nervous system of rat, guinea-pig, chicken and frog were assessed by quantitative autoradiography on X-ray film. In rat and guinea-pig brain apamin labels preferentially the limbic-olfactory system, i.e. nucleus olfactorius, nuclei septi, habenula and hippocampus. In the rat spinal cord the peptide binds preferentially to the substantia gelatinosa. Tectum opticum and nuclei isthmi are labelled in chicken brain. In frog brain no preferentially "apamin-stained" area was found. The role of the cerebral binding sites is still unknown, whereas the spinal sites may be involved in apamin poisoning.

Animals↗

Use of a PDP-12 computer for an on-line analysis of TC-chromatograms by a scanning system.

A software system, Chromscan, has been developed on a PDP-12 computer for quantitative analysis of TC-chromatograms and correlated problems in an on-line scanning system. The program controls a one- or two-dimensional scanning process of either a microscope stage or a modified TC-chromatogram photometer (Zeiss) storing the data on tape. The results can be obtained directly or in an off-line calculation by different Focal-12 programs. For spot evaluations a two-dimensional scan is performed with an aperture. The area of spots is measured and the integrated values of absorbed or remitted light represent the amount of separated substances. For line-scans slits are used. The pherogram is displayed on the scope to keep for baseline corrections peak-integration and some other handling under operators control.

Chromatography, Thin Layer↗

Computer assisted quantitative densitometric analysis of 125I-apamin binding sites in the central nervous system.

The binding sites for 125I-monoiododerivative of apamin in the central nervous system of rat, guinea-pig, chicken and frog were analysed and compared by computer assisted quantitative densitometric autoradiography on X-ray film. The highest level of binding sites in the rat and guinea-pig brain was found in the limbic-olfactory system and in the substantia gelatinosa of the spinal cord. In the chicken brain apamin binds preferentially to the tectum opticum and nuclei isthmi. In the frog brain no specific apamin binding sites were found. The role of presented topography for apamin binding sites is discussed in relation to neurotoxic properties of apamin.

Animals↗