Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Piotr Rafalski"'
Publikováno v:
Chemical Speciation & Bioavailability. 23:61-70
Medicinal plants originating from different natural locations in Northern Poland representing four different plant species: Betula pubescens Ehr., Achillea millefolium L., Urtica dioica L. and Hype...
Autor:
Jerzy Silberring, J. Wichmann, Tomasz Dylag, Krzysztof Rolka, Piotr Rafalski, Jolanta Kotlinska, Sylwia Talarek
Publikováno v:
Behavioural Pharmacology. 16:101-106
In the present study we investigated whether synthetic agonists of the nociceptin (NOP) receptors, Ro 64-6198 {(1 S,3aS)-8-(2,3,3a,4,5,6-hexahydro-1 H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro[4,5]decan-4-one} and Ro 65-6570 (8-acenaphthen-1-yl-1 -p
Publikováno v:
European Journal of Pharmacology. 503:95-98
It has been suggested that drugs modulating the glutamate/N-methyl-D-aspartate (NMDA) receptor system may be useful in the treatment of alcohol dependence. The effect of neramexane, a low-to-moderate affinity uncompetitive NMDA receptor antagonist, w
Autor:
Sylwia Talarek, Piotr Rafalski, Jerzy Silberring, Tomasz Dylag, Jolanta Kotlinska, Maria Kosior
Publikováno v:
Neuropeptides. 38:277-282
Our previous studies demonstrated that endogenous ligand of nociceptin (NOP) receptor, nociceptin(1-17) (also known as orphanin FQ), inhibits morphine-withdrawal syndrome measured as wet dog shakes in rats [Life Sci. 66 (2000) PL119]. This peptide is
Autor:
Tomasz Dylag, Juergen Wichmann, Piotr Rafalski, Jolanta Kotlinska, Sylwia Talarek, Jerzy Silberring
Publikováno v:
NeuroReport. 14:601-604
The non-peptidergic opioid receptor-like 1 (ORL1, OP4) receptor ligand, Ro 64-6198 [(1S,3aS)-8-(2,3,3a,4,5,6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-spiro[4,5]decan-4-one], is a full agonist of the OP4 receptor. The aim of this study was to
Synthetic derivative of C-terminal fragment of CART (55–102) with reduced thiol groups, [Abu 86,94 ]CART (85–102) red , given together with amphetamine (5 mg/kg, s.c.) or cocaine (15 mg/kg, s.c.), reversed hyperlocomotion induced by these drugs a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c4cbb05fa3f694a65306507da36fc82
https://ruj.uj.edu.pl/xmlui/handle/item/88606
https://ruj.uj.edu.pl/xmlui/handle/item/88606
Autor:
Jolanta, Kotlińska, Piotr, Rafalski
Publikováno v:
Postepy higieny i medycyny doswiadczalnej (Online). 58
Nociceptin/orphanin FQ (N/OFQ) is a neuropeptide discovered in the middle of the 1990. It possesses an amino acid sequence very similar to those of endogenous opioid peptides (particularly dynorphin A). However, N/OFQ lacks the N-terminal tyrosine ne
Autor:
Tomasz Dylag, Jerzy Silberring, Grazyna Biala, Piotr Rafalski, Krzysztof Rolka, Jolanta Kotlinska
Publikováno v:
European journal of pharmacology. 474(2-3)
Nociceptin (also called orphanin FQ), a 17-amino-acid peptide, is the natural ligand of the nociceptin opioid peptide (NOP) receptor. This peptide shows similarities, in its structure, to opioid peptides, mainly to dynorphin A. However, unlike opioid
Publikováno v:
European Neuropsychopharmacology. 14:S350