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1.
Phys Rev Lett ; 121(5): 052001, 2018 Aug 03.
Article in English | MEDLINE | ID: mdl-30118290

ABSTRACT

Exclusive measurements of the quasifree pp→ppπ^{+}π^{-} reaction have been carried out at WASA@COSY by means of pd collisions at T_{p}=1.2 GeV. Total and differential cross sections have been extracted covering the energy region T_{p}=1.08-1.36 GeV, which is the region of N^{*}(1440) and Δ(1232)Δ(1232) resonance excitations. Calculations describing these excitations by t-channel meson exchange are at variance with the measured differential cross sections and underpredict substantially the experimental total cross section. An isotensor ΔN dibaryon resonance with I(J^{P})=2(1^{+}) produced associatedly with a pion is able to overcome these deficiencies.

2.
Phys Rev Lett ; 120(2): 022002, 2018 Jan 12.
Article in English | MEDLINE | ID: mdl-29376676

ABSTRACT

Taking advantage of the high acceptance and axial symmetry of the WASA-at-COSY detector, and the high polarization degree of the proton beam of COSY, the reaction p[over →]p→ppη has been measured close to threshold to explore the analyzing power A_{y}. The angular distribution of A_{y} is determined with the precision improved by more than 1 order of magnitude with respect to previous results, allowing a first accurate comparison with theoretical predictions. The determined analyzing power is consistent with zero for an excess energy of Q=15 MeV, signaling s-wave production with no evidence for higher partial waves. At Q=72 MeV the data reveal strong interference of Ps and Pp partial waves and cancellation of (Pp)^{2} and Ss^{*}Sd contributions. These results rule out the presently available theoretical predictions for the production mechanism of the η meson.

3.
Phys Rev Lett ; 119(1): 014801, 2017 Jul 07.
Article in English | MEDLINE | ID: mdl-28731757

ABSTRACT

This Letter reports the successful use of feedback from a spin polarization measurement to the revolution frequency of a 0.97 GeV/c bunched and polarized deuteron beam in the Cooler Synchrotron (COSY) storage ring in order to control both the precession rate (≈121 kHz) and the phase of the horizontal polarization component. Real time synchronization with a radio frequency (rf) solenoid made possible the rotation of the polarization out of the horizontal plane, yielding a demonstration of the feedback method to manipulate the polarization. In particular, the rotation rate shows a sinusoidal function of the horizontal polarization phase (relative to the rf solenoid), which was controlled to within a 1 standard deviation range of σ=0.21 rad. The minimum possible adjustment was 3.7 mHz out of a revolution frequency of 753 kHz, which changes the precession rate by 26 mrad/s. Such a capability meets a requirement for the use of storage rings to look for an intrinsic electric dipole moment of charged particles.

11.
Psychopharmacology (Berl) ; 74(2): 187-90, 1981.
Article in English | MEDLINE | ID: mdl-6791225

ABSTRACT

We examined the effects of some atypical antidepressants with central antiserotonergic activity (mianserin, trazodone, danitracen, pizotifen), and 5-HT receptor blocking agents (cyproheptadine and metergoline), on whole rat brain levels of the main noradrenaline (NA) metabolite, 3-methoxy-4-hydroxyphenylglycol (MHPG). In acute experiments, when drugs were injected in a single dose 1, 2, 4, 24 or 48 h before decapitation, only mianserin elevated the MHPG level. In chronic experiments (drugs given b. i. d. for 3 weeks, the last dose being given 4 or 48 h before decapitation), all the drugs significantly increased the concentration of whole brain MHPG. The results indicate that chronic administration of atypical antidepressants leads to activation of the central NA system. It seems, with the exception of mianserin, that this is a secondary phenomenon, resulting from the antiserotonergic activity of the drugs. Our results further corroborate the existence of a serotonergic-noradrenergic interaction, consisting of an inhibitory influence of serotonin on the noradrenergic system.


Subject(s)
Antidepressive Agents/pharmacology , Brain Chemistry/drug effects , Glycols/metabolism , Methoxyhydroxyphenylglycol/metabolism , Animals , Cyproheptadine/pharmacology , Male , Metergoline/pharmacology , Rats , Serotonin Antagonists/pharmacology , Time Factors
12.
J Neural Transm ; 52(3): 189-97, 1981.
Article in English | MEDLINE | ID: mdl-6458665

ABSTRACT

The chronic (10 mg/kg i.p. twice daily, 10 days)-and not the acute-administration of amitriptyline, maprotiline or zimelidine enhances aggressiveness induced by clonidine in mice. An analogous potentiation of clonidine-induced aggressiveness was obtained with chronic administration (the schedule as above) of levomepromazine (2 mg/kg) or thioridazine (5 mg/kg) but not of spiperone (0.2 mg/kg). Fluoxetine (10 mg/kg), atropine (5 mg/kg), propranolol (10 mg/kg) or metergoline (0.5 mg/kg) given chronically (the schedule as above) also had no effect. The enhancement of clonidine aggressiveness induced by prolonged treatment with imipramine (10 mg/kg) was prevented by cycloheximide, an inhibitor of protein synthesis. The results supply further evidence for the previously proposed hypothesis that chronic administration of antidepressants enhances the responsiveness of central postsynaptic noradrenaline receptors.


Subject(s)
Aggression/drug effects , Antidepressive Agents/pharmacology , Clonidine/pharmacology , Amitriptyline/pharmacology , Animals , Brompheniramine/analogs & derivatives , Brompheniramine/pharmacology , Drug Synergism , Fluoxetine/pharmacology , Humans , Male , Maprotiline/pharmacology , Mice , Zimeldine
13.
Pharmacol Biochem Behav ; 13(2): 153-4, 1980 Aug.
Article in English | MEDLINE | ID: mdl-6251483

ABSTRACT

The effects of antidepressant drugs on clonidine-induced aggressive behavior were determined in mice. Imipramine, mianserin and iprindole used in a single dose attenuated clonidine-induced aggression. Their chronic administration enhanced it.


Subject(s)
Aggression/drug effects , Antidepressive Agents/pharmacology , Clonidine/pharmacology , Animals , Drug Interactions , Humans , Male , Mice , Receptors, Neurotransmitter/drug effects , Time Factors
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