471 research outputs found

    Non-magnetic impurity scattering in a dx2−y2d_{x^2 - y^2} superconductor near a van Hove point: Zn versus Ni in the cuprates

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    We consider the effect of non-magnetic impurities in a dx2−y2d_{x^2 - y^2} superconductor with \ef close to a van Hove singularity. It is shown that the non-trivial density of states (DOS) allows for resonant scattering already at intermediate potential strengths ∣u∣≈1−2|u| \approx 1-2eV. The residual DOS at \ef, and the \tc suppression rate are found to strongly depend on the carrier concentration. Quantitative agreement with experiments on Zn and Ni doped cuprates is obtained by adjusting a single parameter, uu.Comment: 4 pages uuencoded compressed Postscript (Minor changes

    Nerve growth factor alters microtubule targeting agent-induced neurotransmitter release but not MTA-induced neurite retraction in sensory neurons

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    Peripheral neuropathy is a dose-limiting side effect of anticancer treatment with the microtubule-targeted agents (MTAs), paclitaxel and epothilone B (EpoB); however, the mechanisms by which the MTAs alter neuronal function and morphology are unknown. We previously demonstrated that paclitaxel alters neuronal sensitivity, in vitro, in the presence of nerve growth factor (NGF). Evidence in the literature suggests that NGF may modulate the neurotoxic effects of paclitaxel. Here, we examine whether NGF modulates changes in neuronal sensitivity and morphology induced by paclitaxel and EpoB. Neuronal sensitivity was assessed using the stimulated release of calcitonin gene-related peptide (CGRP), whereas morphology of established neurites was evaluated using a high content screening system. Dorsal root ganglion cultures, maintained in the absence or presence of NGF, were treated from day 7 to day 12 in culture with paclitaxel (300nM) or EpoB (30nM). Following treatment, the release of CGRP was stimulated using capsaicin or high extracellular potassium. In the presence of NGF, EpoB mimicked the effects of paclitaxel: capsaicin-stimulated release was attenuated, potassium-stimulated release was slightly enhanced and the total peptide content was unchanged. In the absence of NGF, both paclitaxel and EpoB decreased capsaicin- and potassium-stimulated release and the total peptide content, suggesting that NGF may reverse MTA-induced hyposensitivity. Paclitaxel and EpoB both decreased neurite length and branching, and this attenuation was unaffected by NGF in the growth media. These differential effects of NGF on neuronal sensitivity and morphology suggest that neurite retraction is not a causative factor to alter neuronal sensitivity

    Dose Mesurements in SIS18 and in the experimental halls TR, EX, TH

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    Studies for the radioactive waste management of copular air filters

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    Radiation protection related x-ray spectrometry at PHELIX

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    Effect of non-magnetic impurities on the gap of a dx2−y2d_{x^2-y^2} superconductor as seen by angle-resolved photoemission

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    An analysis of angle-resolved photoemission (ARPES) experiments in the superconducting state of the high \tc copper-oxides is presented. It is based on a phenomenological weak-coupling BCS model which incorporates the experimental normal state dispersion extracted from ARPES, and non-magnetic impurity scattering in the presence of a dx2−y2d_{x^2-y^2} order parameter (OP). It is shown, that already in the pure case, the broadening by finite momentum resolution of the analyzer leads to a finite region of apparent `gaplessness' around the true node of the OP. Non-magnetic impurities further amplify this effect by introducing additional spectral weight around zero frequency. At sufficiently large impurity concentrations ni≈0.02−0.05n_i\approx 0.02-0.05, this results in an extended region of `gaplessness' up to δϕ=±7\delta\phi=\pm7 (ϕ\phi the angle on the Fermi surface) around the true node for a large range of moderate to strong impurity potential strengths. Different ways to identify the presence of impurity scattering in the ARPES spectra are proposed.Comment: 8 pages uuencoded gzipped Postscrip

    Paclitaxel alters the evoked release of calcitonin gene-related peptide from rat sensory neurons in culture

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    Peripheral neuropathy (PN) is a debilitating and dose-limiting side effect of treatment with the chemotherapeutic agent, paclitaxel. Understanding the effects of paclitaxel on sensory neuronal function and the signaling pathways which mediate these paclitaxel-induced changes in function are critical for the development of therapies to prevent or alleviate the PN. The effects of long-term administration of paclitaxel on the function of sensory neurons grown in culture, using the release of the neuropeptide calcitonin gene-related peptide (CGRP) as an endpoint of sensory neuronal function, were examined. Dorsal root ganglion cultures were treated with low (10 nM) and high (300 nM) concentrations of paclitaxel for 1, 3, or 5 days. Following paclitaxel treatment, the release of CGRP was determined using capsaicin, a TRPV1 agonist; allyl isothiocyanate (AITC), a TRPA1 agonist; or high extracellular potassium. The effects of paclitaxel on the release of CGRP were stimulant-, concentration-, and time-dependent. When neurons were stimulated with capsaicin or AITC, a low concentration of paclitaxel (10nM) augmented transmitter release, whereas a high concentration (300 nM) reduced transmitter release in a time-dependent manner; however, when high extracellular potassium was used as the evoking stimulus, all concentrations of paclitaxel augmented CGRP release from sensory neurons. These results suggest that paclitaxel alters the function of sensory neurons in vitro, and suggest that the mechanisms by which paclitaxel alters neuronal function may include functional changes in TRP channel activity. The described in vitro model will facilitate future studies to identify the signaling pathways by which paclitaxel alters neuronal sensitivity

    Optical conductivity in the CuO double chains of PrBa_2Cu_4O_8: Consequences of charge fluctuation

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    We calculate the optical conductivity of the CuO double chains of PrBa2_2Cu4_4O8_8 by the mean-field approximation for the coupled two-chain Hubbard model around quarter filling. We show that the ∼\sim40 meV peak structure, spectral shape, and small Drude weight observed in experiment are reproduced well by the present calculation provided that the stripe-type charge ordering presents. We argue that the observed anomalous optical response may be due to the presence of stripe-type fluctuations of charge carriers in the CuO double chains; the fast time scale of the optical measurement should enable one to detect slowly fluctuating order parameters as virtually a long-range order.Comment: 7 pages, 5 eps figure

    On the possibility of superconductivity in PrBa2Cu3O7

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    Recent reports about observations of superconductivity in PrBa2Cu3O7 raise a number of questions: (i) of various theories striving to explain the Tc suppression in PrxY{1-x}Ba2Cu3O7, are there any compatible with possible superconductivity in stoichiometric PrBa2Cu3O7? (ii) if this superconductivity is not an experimental artifact, are the superconducting carriers (holes) of the same character as in the other high-Tc cuprates, or do they represent another electronic subsystem? (iii) is the underlying mechanism the same as in other high-Tc superconductors? I present an answer to the first two questions, while leaving the last one open.Comment: 4 pages 4 eps fig
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