Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Jerzy Vetulani"'
Autor:
Irena Nalepa, Katarzyna Rafa-Zabłocka, Agnieszka Zelek-Molik, Jerzy Vetulani, Adam Roman, Clelia Rossi-Arnaud, Marco Costanzi, Vincenzo Cestari, Grzegorz Kreiner
Publikováno v:
Progress in neuro-psychopharmacologybiological psychiatry. 93
Disturbances in fear-evoked signal transduction in the hippocampus (HP), the nuclei of the amygdala (AMY), and the prefrontal cortex (PFC) underlie anxiety-related disorders. However, the molecular mechanisms underlying these effects remain elusive.
Autor:
Jerzy Vetulani
Publikováno v:
Pharmacological Reports. 65:1451-1461
The early life of most mammals is spent in close contact with the mother, and for the neonate, early maternal separation is a traumatic event that, depending on various conditions, may shape its behavioral and neurochemical phenotype in adulthood. St
Autor:
Jerzy Vetulani, Irena Romańska, Jerzy Michaluk, Lucyna Antkiewicz-Michaluk, Krystyna Ossowska
Publikováno v:
European Journal of Pharmacology. 599:32-35
3-Methoxytyramine (3-MT), an extraneuronal metabolite of dopamine, present in the synaptic cleft at a very low amount (low nanomolar range), comparable to dopamine concentration, is generally regarded as a biologically inactive compound. We have show
Autor:
Jerzy Vetulani, Małgorzata Filip, Edmund Przegaliński, Lucyna Antkiewicz-Michaluk, Irena Romańska, Jerzy Michaluk
Publikováno v:
Journal of Neural Transmission. 114:307-317
Drug abuse disorder is induced by a variety of substances and results from their interaction with the brain reward system. It is characterized by a high frequency of relapse, usually associated with to craving. In this study we investigated the effec
Autor:
Elzbieta Salinska, Elzbieta Zieminska, Jerzy Vetulani, Jerzy W. Lazarewicz, Krystyna Gołembiowska, Małgorzata Kajta, Antoni Patsenka, A. Wasik, Lucyna Antkiewicz-Michaluk
Publikováno v:
Journal of Neurochemistry. 97:846-856
1-Methyl-1,2,3,4-tetrahydroisoquinoline (1MeTIQ), unlike several other tetrahydroisoquinolines, displays neuroprotective properties. To elucidate this action we compared the effects of 1MeTIQ with 1,2,3,4-tetrahydroisoquinoline (TIQ), a compound shar
Publikováno v:
Journal of Pharmacy and Pharmacology. 56:1429-1434
A carane derivative, KP-23 [RS](–)-4-(2-hydroxy-3)N-isopropylamino)-propoxyimino)-cis-carane, was earlier described as a potential local anaesthetic and antiplatelet agent, and the following studies revealed that its R and S stereoisomers, KP-23R a
Autor:
Jadwiga Wardas, Jerzy Vetulani, Lucyna Antkiewicz-Michaluk, Andrzej J. Bojarski, Jerzy Michaluk, Irena Romańska
Publikováno v:
The International Journal of Neuropsychopharmacology. 7:155-163
The aim of this paper was to investigate whether rotenone, a pesticide causing experimental parkinsonism, causes direct damage to dopaminergic structure when injected intracerebrally and whether this action may be prevented by peripheral administrati
Autor:
Jerzy Michaluk, Irena Romańska, Jerzy Vetulani, Lucyna Antkiewicz-Michaluk, Andrzej J. Bojarski, Beata Karolewicz
Publikováno v:
European Journal of Pharmacology. 466:263-269
The effect of single and multiple administration of the neurotoxic pesticide, rotenone, and the potentially neuroprotective compound, 1-methyl-1,2,3,4-tetrahydroisoquinoline (1MeTIQ), on the concentration of dopamine and its metabolites (homovanillic
Publikováno v:
Neurotoxicity Research. 5:147-155
Tetrahydroisoquinolines present in the mammalian brain, 1,2,3,4-tetrahydroisoquinoline (TIQ) and salsolinol, suspected to cause neurodegeneration leading to Parkinson's disease, were investigated to find their possible physiological role. To this aim
Autor:
Shigeru Ohta, Jerzy Vetulani, Lucyna Antkiewicz-Michaluk, Jerzy Michaluk, Irena Romańska, Elbieta Lorenc-Koci, Maria J. Mokrosz
Publikováno v:
Journal of Neurochemistry. 78:100-108
The effect of single and multiple 1-methyl-1,2,3,4-tetrahydroisoquinoline (1MeTIQ) and 1-benzyl-1,2,3,4-tetrahydroisoquinoline (1BnTIQ) administration on concentrations of dopamine and its metabolites: homovanillic acid (HVA) and 3,4-dihydroxyphenyla