Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Jan, Krusek"'
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
N-methyl-D-aspartate receptors (NMDARs) mediate excitatory synaptic transmission in the central nervous system, underlie the induction of synaptic plasticity, and their malfunction is associated with human diseases. Native NMDARs are tetramers compos
Externí odkaz:
https://doaj.org/article/b7fdc504c10241d1aa8988326b94064a
Autor:
Eva Kudova, Barbora Krausova, Ladislav Vyklicky, Jan Krusek, Tereza Smejkalova, Hana Chodounska, Dragana Hajdukovic, Miriam Candelas Serra, Miloslav Korinek
Publikováno v:
British Journal of Pharmacology
Background and purpose Neurosteroids influence neuronal function and have multiple promising clinical applications. Direct modulation of postsynaptic neurotransmitter receptors by neurosteroids is well characterized, but presynaptic effects remain po
Autor:
Jiri Cerny, Ladislav Vyklicky, Barbora Krausova, Zaneta Naimová, Marek Ladislav, Miloslav Korinek, Jan Krusek, Bohdan Kysilov, Eva Kudova, Pavla Hubalkova, Vojtech Vyklicky, Tereza Smejkalova, Hana Chodounska
Publikováno v:
J Neurosci
NMDARs are ligand-gated ion channels that cause an influx of Na+and Ca2+into postsynaptic neurons. The resulting intracellular Ca2+transient triggers synaptic plasticity. When prolonged, it may induce excitotoxicity, but it may also activate negative
Publikováno v:
Biomedicinepharmacotherapy = Biomedecinepharmacotherapie. 152
Transient receptor potential canonical 5 (TRPC5) is a polymodal, calcium-permeable, nonselective ion channel that is expressed in the brain and 75 % of human sensory neurons. Its pharmacological or genetic inhibition leads to the relief of neuropathi
Autor:
Ladislav Vyklicky, Inmaculada M. Gonzalez-Gonzalez, Martin Horak, Dragana Hajdukovic, Jan Krusek, Tereza Smejkalova, Kristyna Skrenkova, Miloslav Korinek
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-18 (2020)
Scientific Reports
Scientific Reports
Cholesterol is a structural component of cellular membranes particularly enriched in synapses but its role in synaptic transmission remains poorly understood. We used rat hippocampal cultures and their acute cholesterol depletion by methyl-β-cyclode
Publikováno v:
Journal of Cellular and Molecular Medicine
Exposure to repetitive low‐frequency electromagnetic field (LF‐EMF) shows promise as a non‐invasive approach to treat various sensory and neurological disorders. Despite considerable progress in the development of modern stimulation devices, th
Autor:
Martina Kaniakova, Ondrej Soukup, Jan Krusek, Martin Horak, Eugenie Nepovimova, Kristina Holubova, Jan Ricny, Ladislav Vyklicky, Ales Stuchlik, Kamil Kuca, Karel Vales, Jan Korabecny
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 75:54-62
The mechanism of tacrine as a precognitive drug has been considered to be complex and not fully understood. It has been reported to involve a wide spectrum of targets involving cholinergic, gabaergic, nitrinergic and glutamatergic pathways. Here, we
Autor:
Ivan Dittert, Jan Krusek, Vladimira Petrakova, Hana Freislebenová, Kristyna Gottftriedova, Andrew Taylor, Veronika Benson, Tereza Smejkalova, Vaclav Petrak, Eva Neuhöferová, Vincent Mortet, Miloslav Korinek
Publikováno v:
The FASEB Journal. 33
Autor:
Martin Horak, Ales Balik, Jan Krusek, Ladislav Vyklicky, Barbora Krausova, Jirina Borovska, Vojtech Vyklicky, Tereza Smejkalova, Katarina Lichnerova, Martina Kaniakova, Miloslav Korinek
Publikováno v:
The Journal of Physiology. 593:2279-2293
NMDA receptors (NMDARs) are glutamate-gated ion channels that mediate excitatory neurotransmission in the CNS. Although these receptors are in direct contact with plasma membrane, lipid-NMDAR interactions are little understood. In the present study,
Autor:
Vendula Sepsova, Jana Z. Karasova, Gunnar Tobin, Daniel Jun, Jan Korabecny, Pavla Cabelova, Katerina Janska, Jan Krusek, Kristyna Skrenkova, Kamil Kuca, Marian Valko, Ondrej Soukup
Publikováno v:
General physiology and biophysics. 34:189-200
Organophosphorus nerve agents inhibit acetylcholinesterase (AChE) which causes the breakdown of the transmitter acetylcholine (ACh) in the synaptic cleft. Overstimulation of cholinergic receptors (muscarinic and nicotinic) by excessive amounts of ACh