Examples of different types of electrophysiological recording used to study ion channel function.
Research of the Laboratory of Cellular Neurophysiology focuses on the function and pharmacology of ionotropic receptors (ligand-activated ion channels), specifically ionotropic glutamate receptors (iGluRs) and transient receptor potential (TRP) channels. iGluRs mediate the majority of excitatory signaling in the central nervous system, are essential for normal brain development and function, and their dysfunction leads to serious neurological and psychiatric disorders, including many forms of neurodegeneration. TRP channels are present in both the peripheral and the central nervous system, and they play a fundamental role in the detection and transmission of painful stimuli and participate in signaling associated with chronic inflammation.
The goal of our research is to better characterize the relationship between ionotropic receptor structure and function, to identify molecular mechanisms of ionotropic receptor modulation by different chemical compounds or physical variables, and to describe the consequences of mutations of human ionotropic receptors for the function of synapses, neurons and neuronal networks. Obtained results deepen our basic understanding of the mechanisms of ionotropic receptor function, and inform the development of novel receptor modulators with therapeutic potential in the treatment of neurodevelopmental and neurodegenerative disorders.
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Glutamate is the main excitatory neurotransmitter in the central nervous system. It activates specific membrane proteins known as glutamate receptors. Our studies focus on ionotropic glutamate receptors, which, when activated, allow ions to flow across the cell membrane.
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We investigate molecular mechanisms of nociception and thermosensation by focusing on transient receptor potential (TRP) ion channels. These channels are specifically expressed in primary nociceptive neurones and work in concert to detect potentially damaging stimuli and transduce them into pain signalling.
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Publications
Míková; H. - Kuchtiak; Viktor - Svobodová; Irena - Spišská; V. - Pačesová; D. - Balík; Aleš - Bendová; Z.
Circadian Regulation of GluA2 mRNA Processing in the Rat Suprachiasmatic Nucleus and Other Brain Structures
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Molecular Neurobiology. 2021; 58(1); 439-449
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IF = 4.500
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Konečný; J. - Misiachna; Anna - Hrabinová; M. - Pulkrábková; L. - Benková; M. - Prchal; L. - Kučera; T. - Kobrlová; T. - Finger; V. - Kolcheva; Marharyta - Kortus; Štěpán - Jun; D. - Valko; M. - Horák; Martin - Soukup; O. - Korábečný; J.
Pursuing the Complexity of Alzheimer's Disease: Discovery of Fluoren-9-Amines as Selective Butyrylcholinesterase Inhibitors and N-Methyl-d-Aspartate Receptor Antagonists
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Biomolecules. 2021; 11(1)); 3
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IF = 4.082
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Hubálková; Pavla - Ladislav; Marek - Vyklický; Vojtěch - Smejkalová; Tereza - Hrčka Krausová; Barbora - Kysilov; Bohdan - Krůšek; Jan - Naimová; Žaneta - Kořínek; Miloslav - Chodounská; Hana - Kudová; Eva - Černý; Jiří - Vyklický ml.; Ladislav
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Palmitoylation Controls NMDA Receptor Function and Steroid Sensitivity
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Journal of Neuroscience. 2021; 41(10); 2119-2134
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IF = 5.674
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Bernal; L. - Sotelo-Hitschfeld; P. - König; Ch. - Sinica; Viktor - Wyatt; A. - Winter; Z. - Hein; A. - Touška; Filip - Reinhardt; S. - Tragl; A. - Kusuda; R. - Wartenberg; P. - Sclaroff; A. - Pfeifer; J. D. - Ectors; F. - Dahl; A. - Freichel; M. - Vlachová; Viktorie - Brauchi; S. - Roza; C. - Boehm; U. - Clapham; D. E. - Lennerz; J. K. - Zimmermann; K.
Odontoblast TRPC5 channels signal cold pain in teeth
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Science Advances. 2021; 7(13)); eabf5567
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IF = 13.117
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Zímová; Lucie - Barvíková; Kristýna - Máčiková; Lucie - Vyklická; Lenka - Sinica; Viktor - Barvík; I. - Vlachová; Viktorie
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Proximal C-Terminus Serves as a Signaling Hub for TRPA1 Channel Regulation via Its Interacting Molecules and Supramolecular Complexes
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Frontiers in physiology. 2020; 11(Mar 12)); 189
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IF = 3.367
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