1,027 research outputs found
Core Polarization and Tensor Coupling Effects on Magnetic Moments of Hypernuclei
The effects of core polarization and tensor coupling on the magnetic moments
in C, O, and Ca
-hypernuclei are studied in the Dirac equation with scalar, vector and
tensor potentials. It is found that the effect of core polarization on the
magnetic moments is suppressed by tensor coupling. The
tensor potential reduces the spin-orbit splitting of states
considerably. However, almost the same magnetic moments are obtained using the
hyperon wave function obtained via the Dirac equation either with or without
the tensor potential in the electromagnetic current vertex. The
deviations of magnetic moments for states from the Schmidt values
are found to increase with nuclear mass number.Comment: 10 pages, 2 figures, 2 table
A systematic study on the binding energy of hypernuclei
In this paper, we calculated the binding energy per baryon of the
hypernuclei systemically, using the relativistic mean field theory (RMF) in a
statistic frame. Some resemble properties are found among most of the
hypernuclei found in experiments. The data show that a hypernucleus
will be more stable, if it is composed of a hyperon adding to a
stable normal nuclear core, or a hyperon replacing a neutron in a
stable normal nuclear core. According to our calculations, existences of some
new hypernuclei are predicted under the frame of RMF.Comment: 8 pages, 6 figures, 3 table
Pharmacodynamics of Memantine: An Update
Memantine received marketing authorization from the European Agency for the Evaluation of Medicinal Products (EMEA) for the treatment of moderately severe to severe Alzheimer´s disease (AD) in Europe on 17th May 2002 and shortly thereafter was also approved by the FDA for use in the same indication in the USA. Memantine is a moderate affinity, uncompetitive N-methyl-D-aspartate (NMDA) receptor antagonist with strong voltage-dependency and fast kinetics. Due to this mechanism of action (MOA), there is a wealth of other possible therapeutic indications for memantine and numerous preclinical data in animal models support this assumption. This review is intended to provide an update on preclinical studies on the pharmacodynamics of memantine, with an additional focus on animal models of diseases aside from the approved indication. For most studies prior to 1999, the reader is referred to a previous review [196]
Double and the Interaction
The - effective interaction, in the channel , in the
nuclear medium is fitted to the available binding energies,
, of double hypernuclei:
He, Be and
B. The mesonic decay of these hypernuclei is also
investigated. Finally, this effective interaction is used to predict the
binding energies and mesonic decays widths of heavier double
hypernuclei.Comment: 4 pages, (latex file, postscript-file and 3 Postscript-figures
included
Observation of hypertritons in Au+Au collisions at \sqrt{s_{NN}} = 200 GeV
We report preliminary results of hypertriton observation in heavy-ion
collisions at RHIC. We have identified 157 +- 30 candidates in the current
sample containing ~10^8 Au+Au events at \sqrt{s_{NN}} = 200 GeV. The production
rate of hypertriton is close to that of helium 3. No extra penalty factor is
observed for hypertriton, in contrast to results observed at the AGS.Comment: Turn off the line number package for QM09 proceeding publicatio
Memantine and Cholinesterase Inhibitors: Complementary Mechanisms in the Treatment of Alzheimer’s Disease
This review describes the preclinical mechanisms that may underlie the increased therapeutic benefit of combination therapy—with the N-methyl-d-aspartate receptor antagonist, memantine, and an acetylcholinesterase inhibitor (AChEI)—for the treatment of Alzheimer’s disease (AD). Memantine, and the AChEIs target two different aspects of AD pathology. Both drug types have shown significant efficacy as monotherapies for the treatment of AD. Furthermore, clinical observations indicate that their complementary mechanisms offer superior benefit as combination therapy. Based on the available literature, the authors have considered the preclinical mechanisms that could underlie such a combined approach. Memantine addresses dysfunction in glutamatergic transmission, while the AChEIs serve to increase pathologically lowered levels of the neurotransmitter acetylcholine. In addition, preclinical studies have shown that memantine has neuroprotective effects, acting to prevent glutamatergic over-stimulation and the resulting neurotoxicity. Interrelations between the glutamatergic and cholinergic pathways in regions of the brain that control learning and memory mean that combination treatment has the potential for a complex influence on disease pathology. Moreover, studies in animal models have shown that the combined use of memantine and the AChEIs can produce greater improvements in measures of memory than either treatment alone. As an effective approach in the clinical setting, combination therapy with memantine and an AChEI has been a welcome advance for the treatment of patients with AD. Preclinical data have shown how these drugs act via two different, but interconnected, pathological pathways, and that their complementary activity may produce greater effects than either drug individually
Further pharmacological characterization of eltoprazine: focus on its anxiolytic, anorexic, and adverse‑effect potential
Eltoprazine, a drug that had previously been developed for aggression, has recently been investigated for L‑DOPA‑induced dyskinesia in animal models of Parkinson´s disease (PD) and in dyskinetic PD patients. Much less is known about effects of eltoprazine in other therapeutic indications. Indeed, the pharmacological profile of eltoprazine might suggest its effects on anxiety and food intake, but also adverse effect potential, which is the focus of the present study. Given for 2 weeks either as infusion or as twice‑daily treatment, eltoprazine produced a decrease in food intake and body weight at doses leading to 200–500 nM plasma concentrations. In the elevated plus maze eltoprazine increased anxiety‑like behavior. On the other hand, it induced a clear‑cut anxiolytic effect in context fear conditioning test starting at ca. 0.3 mg/kg, and failed to produce any significant effect in fear potentiated startle test. Regarding adverse effects, eltoprazine was found to produce hypothermia starting from 1 mg/kg. At similar doses it also increased locomotion in the open field. However, eltoprazine failed to affect acquisition in context fear conditioning paradigm, which may indicate lack of its detrimental effect on learning at the doses tested (i.e., up to 5 mg/kg). In summary, effects of eltoprazine in different anxiety tests were equivocal while its effect on body weight seems robust and requires further investigation. It is to be determined whether these effects can be expected at the doses free of adverse effects
Hypernuclear physics legacy and heritage of Dick Dalitz
The major contributions of Richard H. Dalitz to hypernuclear physics, since
his first paper in 1955 to his last one in 2005 covering a span of 50 years
during which he founded and led the theoretical study of hypernuclei, are
reviewed from a personal perspective. Topical remarks on the search for
quasi-bound antikaon-nuclear states and on kaon condensation are made.Comment: prepared for NPA vol. 804 (2008), Recent Advances in Strangeness
Nuclear Physics, edited by A. Gal and R.S. Hayano; a preliminary version
appeared in the proceedings of HYP0
Antimatter production in proton-proton and heavy-ion collisions at ultrarelativistic energies
One of the striking features of particle production at high beam energies is
the near equal abundance of matter and antimatter in the central rapidity
region. In this paper we study how this symmetry is reached as the beam energy
is increased. In particular, we quantify explicitly the energy dependence of
the approach to matter/antimatter symmetry in proton-proton and in heavy-ion
collisions. Expectations are presented also for the production of more complex
forms of antimatter like antihypernuclei.Comment: 7 pages, 5 figure
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