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Rychlik, Michał
2022
Praca doktorska
In the mammalian brains synaptic zinc acts as a neuromodulator and a neurotransmitter. Synapses are also where toxic forms of amyloid beta (Aβ) are formed, which is the first step of a pathological cascade leading to Alzheimer’s dementia (AD) in humans. Evidence gathered over the span of last 25 years shows that synaptic zinc exacerbates the effects of Aβ; and, that by binding zinc Aβ disrupts the physiological functions of the ion. One of the most understudied physiological functions in this regard is neurotransmission through the zincergic GPR39 receptor. The main aim of this work was to establish whether GPR39 modulates memory in mice, especially: an analogue of declarative memory affected in early stages of AD in humans i.e. episodic memory. Secondly, the effects of both acute and chronic pharmacological manipulations of GPR39 with its agonist (TC-G 1008) on declarative memory of mice were investigated; as well as, the effect of GPR39 knock-out (KO) on the action of memantine – a drug used in pharmacotherapy of AD. Lastly, the procognitive potential of both drugs was tested in a model of neurodegeneration – the constitutive heterozygous KO of brain-derived neurotropic factor (Bdnf).
Kraków
2 - studia doktoranckie
farmakologia ; neurologia
Rada Dyscypliny Nauki farmaceutyczne
Młyniec, Katarzyna
2021
oai:dl.cm-uj.krakow.pl:4906
ZB-135618
eng
nieograniczony
Apr 8, 2024
Dec 13, 2022
104
63
http://www.dl.cm-uj.krakow.pl:8080/publication/4907
RDF
OAI-PMH
Nowak, Barbara
Bober-Płonka, Bogusława
Fijałkowska, Agata
Stochel-Gaudyn, Anna
Szlósarczyk, Marek
Klimkowicz-Mrowiec, Aleksandra
Ostrowska, Monika
Citation style: chicago-author-date iso690-author-date chicago-author-date
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