Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Gabriella Zsilla"'
Autor:
Cecilia Csölle, Mária Baranyi, Gabriella Zsilla, Agnes Kittel, Flóra Gölöncsér, Peter Illes, Edit Papp, E Sylvester Vizi, Beáta Sperlágh
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66547 (2013)
Recent investigations have revealed that the genetic deletion of P2X7 receptors (P2rx7) results in an antidepressant phenotype in mice. However, the link between the deficiency of P2rx7 and changes in behavior has not yet been explored. In the presen
Externí odkaz:
https://doaj.org/article/27382327741b467e8afd60bc1910c122
Publikováno v:
European Journal of Pharmacology. 837:72-80
The addiction-related behavioural effects of drugs of abuse are mediated by the mesocorticolimbic monoamine systems. We investigated the effects of 3,4-methylenedioxymethamphetamine (MDMA), mephedrone, β-phenylethylamine (β-PEA) methylphenidate (MP
Autor:
Balázs Lendvai, Bernadett K. Szasz, E. Sylvester Vizi, Janos P. Kiss, Aliz Mayer, Gabriella Zsilla
Publikováno v:
Neuropharmacology. 49:400-409
We have previously shown that dimethylphenylpiperazinium (DMPP) increases the release of noradrenaline (NA) from rat hippocampal slices via two distinct mechanisms: a nicotinic acetylcholine receptor (nAChR)-mediated exocytosis and a carrier-mediated
Publikováno v:
The Journal of Neuroscience. 24:7888-7894
Our aim was to investigate the functional properties of the noradrenergic system in genetically modified mice lacking the norepinephrine transporter (NET). We measured the uptake and release of [3H]norepinephrine ([3H]NE) from hippocampal and cortica
Publikováno v:
Archiv der Pharmazie. 335:22-26
The synthesis of octahydro-8H-isoquino[2,1-g][1,6]naphthyridine derivatives 2a-f was carried out. These new compounds are selective alpha 2A-adrenoceptor antagonists.
Autor:
Pál Tapolcsányi, Laszlo G. Harsing, Julia Timár, Katalin Nagy, Péter Mátyus, Marko Bernadett Martonne, Andrea Czompa, Szabolcs Udvari, Geza Szabo, Ákos Kocsis, Gabriella Zsilla
Publikováno v:
Current pharmaceutical design. 21(17)
We have synthesized a novel series of N-substituted sarcosines, analogues of NFPS ( N -[3-(biphenyl-4- yloxy)-3-(4-fluorophenyl)propyl]- N -methylglycine), as type-1 glycine transporter (GlyT-1) inhibitors. Several compounds incorporated a diazine ri
Publikováno v:
Brain Research Bulletin. 56:521-524
Using in vitro superfusion techniques and electrical field stimulation, a volatile anesthetic, halothane, decreased impulse-dependent vesicular release, but did not affect amphetamine-induced cytoplasmic release of dopamine (DA) from the rat striatal
Publikováno v:
Neurochemical Research. 26:1095-1100
The alkaloid derivative vinpocetine (14-ethoxycarbonyl-(3α,16α-ethyl)-14,15-eburnamine; Cavinton) has a well known beneficial effect on brain function in hypoxic and ischemic conditions. While it increases CNS blood flow and improves cellular metab
Publikováno v:
Brain Research. 889:63-70
In this study the role of ATP-sensitive K(+) channels (K(ATP) channels) in the A(1) receptor mediated presynaptic inhibitory modulation of acetylcholine release was investigated in the rat hippocampus. N(6)-Cyclohexyladenosine (CHA), the selective A(
Autor:
E. Sylvester Vizi, Andrew L. Salzman, Csaba Szabó, Zoltán Németh, Gabriella Zsilla, György Haskó
Publikováno v:
Brain Research Bulletin. 45:183-187
In a previous study we have demonstrated in conscious endotoxemic mice that isoproterenol, a nonselective agonist of beta-adrenergic receptors, decreased the production of proinflammatory mediators tumor necrosis factor-alpha (TNF-alpha) and nitric o