2,031 research outputs found

    Quasi-Two-Body Decays of Nonstrange Baryons

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    We examine the decays of nonstrange baryons to the final states Δπ\Delta\pi, NρN\rho, NηN\eta, NηN\eta^\prime, NωN\omega, N1/2+(1440)πN1/2^+(1440)\pi, and Δ3/2+(1600)π\Delta3/2^+(1600)\pi, in a relativized pair-creation(3P0^3P_0) model which has been developed in a previous study of the NπN\pi decays of the same baryon states. As it is our goal to provide a guide for the possible discovery of new baryon states at CEBAF and elsewhere, we examine the decays of resonances which have already been seen in the partial-wave analyses, along with those of states which are predicted by the quark model but which remain undiscovered. The level of agreement between our calculation and the available widths from the partial-wave analyses is encouraging.Comment: 41 pages, CEBAF-TH-93-1

    New Baryons in the Delta eta and Delta omega Channels

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    The decays of excited nonstrange baryons into the final states Delta eta and Delta omega are examined in a relativized quark pair creation model. The wavefunctions and parameters of the model are fixed by previous calculations of N pi and N pi pi, etc., decays through various quasi-two body channels including N eta and N omega. Our results show that the combination of thresholds just below the region of interest and the isospin selectivity of these channels should allow the discovery of several new baryons in such experiments.Comment: 10 pages, RevTe

    A (p/E) Calculation of Strong Pionic Decays of Baryons

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    Strong pionic decays of baryons are studied in a non-relativistic quark model framework via a convergent (p/E) expansion of the transition operator. Results are compared to the ones obtained within a more conventional (p/m) expansion.Comment: 16 pages, LaTeX, using amssymb.st

    Evidence for the fourth P11 resonance predicted by the constituent quark model

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    It is pointed out that the third of five low-lying P11 states predicted by a constituent quark model can be identified with the third of four states in a solution from a three-channel analysis by the Zagreb group. This is one of the so-called ``missing'' resonances, predicted at 1880 MeV. The fit of the Zagreb group to the pi N -> eta N data is the crucial element in finding this fourth resonance in the P11 partial wave.Comment: 8 pages, revtex; expanded acknowledgement

    Strange Decays of Nonstrange Baryons

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    The strong decays of excited nonstrange baryons into the final states Lambda K, Sigma K, and for the first time into Lambda(1405) K, Lambda(1520) K, Sigma(1385) K, Lambda K*, and Sigma K*, are examined in a relativized quark pair creation model. The wave functions and parameters of the model are fixed by previous calculations of N pi and N pi pi, etc., decays. Our results show that it should be possible to discover several new negative parity excited baryons and confirm the discovery of several others by analyzing these final states in kaon production experiments. We also establish clear predictions for the relative strengths of certain states to decay to Lambda(1405) K and Lambda(1520) K, which can be tested to determine if a three-quark model of the Lambda(1405) K is valid. Our results compare favorably with the results of partial wave analyses of the limited existing data for the Lambda K and Sigma K channels. We do not find large Sigma K decay amplitudes for a substantial group of predicted and weakly established negative-parity states, in contrast to the only previous work to consider decays of these states into the strange final states Lambda K and Sigma K.Comment: 25 pages, 8 figures, RevTe

    Distinguishing Among Strong Decay Models

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    Two competing models for strong hadronic decays, the 3P0^3P_0 and 3S1^3S_1 models, are currently in use. Attempts to rule out one or the other have been hindered by a poor understanding of final state interactions and by ambiguities in the treatment of relativistic effects. In this article we study meson decays in both models, focussing on certain amplitude ratios for which the relativistic uncertainties largely cancel out (notably the S/DS/D ratios in b1πωb_1\rightarrow\pi\omega and a1πρa_1\rightarrow\pi\rho), and using a Quark Born Formalism to estimate the final state interactions. We find that the 3P0^3P_0 model is strongly favoured. In addition, we predict a P/FP/F amplitude ratio of 1.6±.21.6\pm .2 for the decay π2πρ\pi_2\rightarrow\pi\rho. We also study the parameter-dependence of some individual amplitudes (as opposed to amplitude ratios), in an attempt to identify a ``best'' version of the 3P0^3P_0 model.Comment: 20 pages, uuencoded postscript file with 7 figures, MIT-CTP-2295; CMU-HEP94-1

    Structure and Dynamics of the EGF Receptor as Revealed by Experiments and Simulations and Its Relevance to Non-Small Cell Lung Cancer

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    The epidermal growth factor receptor (EGFR) is historically the prototypical receptor tyrosine kinase, being the first cloned and the first where the importance of ligand-induced dimer activation was ascertained. However, many years of structure determination has shown that EGFR is not completely understood. One challenge is that the many structure fragments stored at the PDB only provide a partial view because full-length proteins are flexible entities and dynamics play a key role in their functionality. Another challenge is the shortage of high-resolution data on functionally important higher-order complexes. Still, the interest in the structure/function relationships of EGFR remains unabated because of the crucial role played by oncogenic EGFR mutants in driving non-small cell lung cancer (NSCLC). Despite targeted therapies against EGFR setting a milestone in the treatment of this disease, ubiquitous drug resistance inevitably emerges after one year or so of treatment. The magnitude of the challenge has inspired novel strategies. Among these, the combination of multi-disciplinary experiments and molecular dynamic (MD) simulations have been pivotal in revealing the basic nature of EGFR monomers, dimers and multimers, and the structure-function relationships that underpin the mechanisms by which EGFR dysregulation contributes to the onset of NSCLC and resistance to treatment

    Ethanol reversal of tolerance to the respiratory depressant effects of morphine

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    Opioids are the most common drugs associated with unintentional drug overdose. Death results from respiratory depression. Prolonged use of opioids results in the development of tolerance but the degree of tolerance is thought to vary between different effects of the drugs. Many opioid addicts regularly consume alcohol (ethanol), and post-mortem analyses of opioid overdose deaths have revealed an inverse correlation between blood morphine and ethanol levels. In the present study, we determined whether ethanol reduced tolerance to the respiratory depressant effects of opioids. Mice were treated with opioids (morphine, methadone, or buprenorphine) for up to 6 days. Respiration was measured in freely moving animals breathing 5% CO(2) in air in plethysmograph chambers. Antinociception (analgesia) was measured as the latency to remove the tail from a thermal stimulus. Opioid tolerance was assessed by measuring the response to a challenge dose of morphine (10 mg/kg i.p.). Tolerance developed to the respiratory depressant effect of morphine but at a slower rate than tolerance to its antinociceptive effect. A low dose of ethanol (0.3 mg/kg) alone did not depress respiration but in prolonged morphine-treated animals respiratory depression was observed when ethanol was co-administered with the morphine challenge. Ethanol did not alter the brain levels of morphine. In contrast, in methadone- or buprenorphine-treated animals no respiratory depression was observed when ethanol was co-administered along with the morphine challenge. As heroin is converted to morphine in man, selective reversal of morphine tolerance by ethanol may be a contributory factor in heroin overdose deaths

    Phenomenological study of hadron interaction models

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    We present a phenomenological study of three models with different effective degrees of freedom: a Goldstone Boson Exchange (GBE) model which is based on quark-meson couplings, the quark delocalization, color screening model (QDCSM) which is based on quark-gluon couplings with delocalized quark wavefunctions, and the Fujiwara-Nijmegen (FN) mixed model which includes both quark-meson and quark-gluon couplings. We find that for roughly two-thirds of 64 states consisting of pairs of octet and decuplet baryons, the three models predict similar effective baryon-baryon interactions. This suggests that the three very different models, based on different effective degrees of freedom, are nonetheless all compatible with respect to baryon spectra and baryon-baryon interactions. We also discuss the differences between the three models and their separate characteristics.Comment: 30 pages latex, 7 tables, 12 figs; submitted to Phys. Rev.

    Simulation of propofol anaesthesia for intracranial decompression using brain hypothermia treatment

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    <p>Abstract</p> <p>Background</p> <p>Although propofol is commonly used for general anaesthesia of normothermic patients in clinical practice, little information is available in the literature regarding the use of propofol anaesthesia for intracranial decompression using brain hypothermia treatment. A novel propofol anaesthesia scheme is proposed that should promote such clinical application and improve understanding of the principles of using propofol anaesthesia for hypothermic intracranial decompression.</p> <p>Methods</p> <p>Theoretical analysis was carried out using a previously-developed integrative model of the thermoregulatory, hemodynamic and pharmacokinetic subsystems. Propofol kinetics is described using a framework similar to that of this model and combined with the thermoregulation subsystem through the pharmacodynamic relationship between the blood propofol concentration and the thermoregulatory threshold. A propofol anaesthesia scheme for hypothermic intracranial decompression was simulated using the integrative model.</p> <p>Results</p> <p>Compared to the empirical anaesthesia scheme, the proposed anaesthesia scheme can reduce the required propofol dosage by more than 18%.</p> <p>Conclusion</p> <p>The integrative model of the thermoregulatory, hemodynamic and pharmacokinetic subsystems is effective in analyzing the use of propofol anaesthesia for hypothermic intracranial decompression. This propofol infusion scheme appears to be more appropriate for clinical application than the empirical one.</p
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