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Głuch-Lutwin, Monika
2022
Praca doktorska
The first part of the dissertation describes in vitro studies of the functional profile for new selective 5-HT1A receptor ligands. For the first time, they included the parallel characterization of several dozen 5-HT1A receptor ligands in several signaling pathways (cAMP inhibition, ERK1/2 phosphorylation, Ca2+ mobilization, β-arrestin recruitment), which resulted in a pioneering discovery of numerous and diverse functional profiles. Ligands with higher than before functional selectivity for ERK1/2 phosphorylation have been described, as well as for the first time ligands with a clear preference for β-arrestin recruitment. In vivo studies investigated the potential antidepressant properties of four selected 5-HT1A receptor biased agonists, both in the basic forced swimming test in mice and, for the first time, for such ligands, in murine models of corticosterone-induced depression and unpredictable chronic mild stress. The tested compounds showed significant activity after a single administration, which distinguishes them from the currently available antidepressants, and the behavioral effects were correlated with favorable changes in the level of pERK1/2 in the frontal cortex and hippocampus. The impact of the tested compounds on the consolidation process of memory traces in the novel object recognition test was also assessed.
Kraków
2 - studia doktoranckie
farmakologia
Rada Dyscypliny Nauki farmaceutyczne
Kołaczkowski, Marcin ; Pytka, Karolina
oai:dl.cm-uj.krakow.pl:4960
ZB-136385
pol
tylko w bibliotece
Mar 22, 2024
Mar 2, 2023
8
0
http://dl.cm-uj.krakow.pl:8080/publication/4961
RDF
OAI-PMH
Śniecikowska, Joanna
Bugno, Ryszard
Czopek, Anna
Olejarz-Maciej, Agnieszka
Wróbel, Andrzej
Citation style: chicago-author-date iso690-author-date chicago-author-date
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