Rostislav Tureček, PhD.
Phone: +420 241 062 748
Phone: +420 241 062 748
Morphological and functional characteristics of nerve cells in individual auditory nuclei under normal and pathological conditions are studied in the Department. Electrophysiological and histological data are correlated with changes in the animal behavior evaluated with behavioral tests. Audiological tests and MR imaging are used to characterize age-related changes in hearing in humans.
Jiří Popelář, PhD.
Phone: +420 241 062 689
Assoc. Prof. Zbyněk Bureš, PhD.
Jiří Popelář, PhD.
Oliver Profant, MD., PhD.
Natalia Rybalko, PhD.
Jana Svobodová Burianová, PhD.
Prof. Josef Syka, MD, DSc.
Assoc. Prof. Daniel Šuta, PhD.
Rostislav Tureček, PhD.
Minseok Kang, Ph.D.
Kateryna Pysanenko, PhD.
Ing. Milan Jilek
Dora Čapková, MD.
Jakub Fuksa, MD.
Nataša Jovanović, MSc.
Adolf Melichar, MSc.
Diana Tóthová, MD.
We studied age-, hearing loss-, and tinnitus-related functional and structural changes in cortical and subcortical structures in subjects with varying degrees of presbycusis and tinnitus using audiological examination and MRI scanning. We found that aging was accompanied by a decrease in cortical gray matter thickness; hearing loss led to limited structural modifications and tinnitus caused structural changes occurring predominantly within the limbic system and insula.
Examples of tinnitus related human brain structures scanned with MRI. (A,B) Color-coded regions of interest on the cortical surface: planum temporale (yellow), Heschl gyrus (light blue), anterior insula (green), visual cortex (purple), parahippocampus (red). (C) Localization of tinnitus related limbic structures: hippocampus (blue) and amygdala (orange).
Profant O., Škoch A., Tintěra J., Svobodova V., Tóthová D., Svobodová Burianová J., Syka J. (2020). The influence of aging, hearing loss and tinnitus on the morphology of cortical grey matter, amygdala and hippocampus. Frontiers in Aging Neuroscience. Dec 4;12:553461
The removal of the cochlea during early postnatal development significantly affects the composition and density of presynaptic and postsynaptic inhibitory receptors in the medial nucleus of the trapezoidal body (MNTB) in adult rats. The results suggest that inhibitory transmission in the MNTB is subjected to multiple developmental regulations and support the idea that auditory experience plays a role in the maturation of the brainstem glycinergic circuits.
Bilateral cochleotomy of neonatal rats transiently reduced the number of glycine receptors and inhibitory vGAT-positive terminals in the MNTB. A, B, MNTB sections from 2 week- (2WO) or 2 month-old (Adult) control or cochleotomized rats, stained with antibodies against glycine receptor α1 subunit (A) or vGAT (B). The dashed line indicates the cell surface. The middle columns display cells from the boxes on the left at a higher magnification. C, D, Bar graphs compare the number of α1-positive clusters (C) or vGAT-positive terminals (D) at the somata of MNTB principal cells of the control and cochleotomized rats.
Hrušková, B., Trojanová, J., Kralíková, M., Melichar, A., Suchánková, S., Bartošová, J., Svobodová Burianová, J., Popelář, J., Syka, J., Tureček, R.: (2019) Cochlear ablation in neonatal rats disrupts inhibitory transmission in the medial nucleus of the trapezoid body. Neuroscience Letters. 699: 145-150.
Rearing rat pups in a complex acoustically enriched environment leads to an increased reliability of responses of AC neurons, affecting both the rate and the temporal codes. For a repetitive stimulus, the neurons exhibit a lower spike count variance, indicating a more stable rate coding. Furthermore, the neurons follow more precisely the temporal course of the stimulus, as manifested by improved phase-locking to temporally modulated sounds. The changes are persistent and present up to adulthood.
A. Synchronization of auditory cortex (AC) neuronal responses with amplitude modulated (AM) noise is significantly better in enriched animals than in control rats. B. Better synchronization of neuronal responses to AM noise with 10 Hz modulation frequency is documented in peristimulus time histograms of typical AC neurons recorded from the enriched and control animals.
Bureš Z., Pysanenko K., Lindovský J., Syka J. Acoustical Enrichment during Early Development Improves Response Reliability in the Adult Auditory Cortex of the Rat. Neural Plast. 2018 May 30;2018:5903720. doi: 10.1155/2018/5903720. eCollection 2018.
We provide evidence that GABAB receptors associate with KCTD subunits which hetero-oligomerize through self-interacting T1 and H1 homology domains. KCTD12/16 hetero-oligomers impart unique kinetic properties on GABAB activated Kir3-currents. Our data demonstrate that simultaneous assembly of distinct KCTDs at the receptor increases the molecular and functional repertoire of native GABAB receptors and modulates physiologically induced K+-current responses in the nervous system.
Bidirectional modulation of GABAB-activated Kir3 currents by KCTD hetero-oligomers
A, Baclofen-activated K+ currents recorded from CHO cells expressing GABAB receptors and Kir3.1/3.2 channels without KCTD (w/o), with KCTD12 alone (black), with KCTD16 alone (blue), or with both KCTDs (red). B, GABAB responses recorded from CHO cells expressing KCTD12 (black), a KCTD16 mutant lacking the GABAB-binding T1 domain (blue), or both KCTD isoforms (red). C, Bar graph summarizing the relative desensitization of baclofen-activated K+ currents. D, Representative traces of K+ currents activated by baclofen to CHO cells expressing no KCTD (gray), KCTD12 alone (black), 16ΔT1 alone (blue), or both KCTDs (red). KCTD16 prolongs the deactivation of GABAB responses. KCTD12 neither reduces the effect of 16ΔT1 nor accelerates deactivation of brief current responses. E, Bar graph shows mean time constants obtained from fits of current deactivation to a single exponential function.
Fritzius T., Turecek R., Seddik R., Kobayashi H., Tiao T., Rem P.D., Metz M., Kralikova M., Bouvier M., Gassmann M., Bettler B. (2017) KCTD hetero-oligomers confer unique kinetic properties on hippocampal GABAB receptor-induced K+-currents. J. Neurosci. 37, 1162-1175.
Single-unit electrophysiological recording and two-photon calcium imaging in anaesthetized mice were used to evaluate the effects of acute acoustic trauma on the response properties of neurons in the core auditory cortex. The results demonstrate cell type- and layer-specific changes. The observed changes could play a role in pathogenesis of tinnitus.
An overview of in vivo calcium imaging used for studying effects of acute acoustic trauma in the mouse auditory cortex, with special focus on somatostatin- and parvalbumin-positive (SST+ and PV+) inhibitory interneurons in different cortical layers.
Calcium imaging in the auditory cortex in vivo. A) A scheme of free-field acoustic stimulation under the two-photon microscope. B) Example field of view of layer 2/3 in the auditory cortex. PV+ cells were labeled with tdTomato (red). C) Similar to B, but with labeled SST+ interneurons. All cells in B and C were also loaded with calcium indicator OGB-1 (green). D) Calcium data analysis and spiking activity inference. E) Comparison of coding properties of individual neurons before and after the acoustic trauma.
Publication: Novak O, Zelenka O, Hromadka T, and Syka J. Immediate manifestation of acoustic trauma in the auditory cortex is layer-specific and cell type-dependent. J Neurophysiol jn.00810.02015, 2016. DOI: 10.1152/jn.00810.2015
The responses to aversive 22-kHz vocalization was evaluated by c-Fos mmunolabelling in different brain structures. The natural 22-kHz vocalizations was either played from a recording or produced by a foot-shocked animal located nearby (live vocalizations) or the artificial call-like stimuli was used. The natural 22-kHz vocalizations evoked larger response in auditory and limbic structures, whereas artificial call-like stimuli was less efficient in limbic structures.
Numerical density of c-Fos immunoreactive nuclei in particular brain regions in control non-stimulated rats, animals exposed to playback of 22-kHz vocalizations, animals exposed to artificial stimuli, and animals exposed to natural 22-kHz vocalizations emitted by a nearby rat.
Ouda L, Jilek M, Syka J. Expression of c-Fos in rat auditory and limbic systems following 22-kHz calls. Behav Brain Res. 2016 Jul 15;308:196-204.
Based on the MRI recordings from auditory cortex, it seems that peripheral as well as central components of presbycusis appear to influence each other only to a limited degree. The greater extent of cortical activation in elderly subjects in comparison with young subjects, with an asymmetry towards the right side, may serve as a compensatory mechanism for the impaired processing of auditory information appearing as a consequence of ageing.
MR Unit, Department of Diagnostic and Interventional Radiology, Institute for Clinical and Experimental Medicine, Prague
Department of Otorhinolaryngology and Head and Neck Surgery, 1st Faculty of Medicine, Charles University in Prague, University Hospital Motol, Prague
Averaged cortical activity evoked by acoustic stimulation examined by fMRI in all 3 groups. YC – young controls, MP – mild presbycusis, EP – expressed presbycusis. Red colour – stimulation with pink noise centered at 350 Hz and 700 Hz; blue colour – stimulation with pink noise centered at 1.5 kHz, 3 kHz and 8 kHz. The arrowheads accentuate an increase in the right AC activation in both elderly groups.
Publication: Profant O., Tintěra J., Balogová Z., Ibrahim I., Jilek M., Syka J. (2015) Functional changes in the human auditory cortex in ageing. PLoS One. 2015 Mar 3;10(3):e0116692.
Overexpression of transcription factor ISLET1 under the Pax2 promoter in mice manifested in hyperactivity, circling behavior, and early onset of progressive age-related hearing loss. Early age related reduction of otoacoustic emissions (DPOAEs) was found to be conditioned by deterioration of cochlear efferent terminals. Our data provide the first evidence that the alternation of MOC efferent system accelerates the age-related functional decline of hearing without the loss of OHCs.
Gabriela Pavlínková Ph.D., Laboratory of Molecular Pathogenetics, Institute of Biotechnology CAS, Prague
Prof. Bernd Fritzsch, Department of Biology, University of Iowa, Iowa City, IA, USA
Altered efferent innervations. Despite visible similarities, the quantitative analysis shows a decrease in the volume of MOC terminals of OHCs (A, C, arrows; quantified in M) and efferent vesiculated fibers in the region of Deiters’ cells (B, D, arrows; quantified in N) in young Tg+/− mice (I, M) than in WT animals (G, M). The progressive loss of efferent fibers is visible in older Tg+/− (J) compared toWT (H). In both WT and Tg+/− groups, efferent endings are missing if the OHC is lost (G, I; stars). Side view (E, F, K, L) represents the maximum projection of a focal series through the thickness of one OHC, arrows here and in B, D, H, J point out ChAT positive particles in the region of Deiters’ cells. MOC medial olivocochlear eferent system, IHC inner hair cells, OHC outer hair cells, DC Deiters’ cells, ChAT cholin acetyltransferaza.
Publication: Chumak T., Bohuslavova R., Macova I., Dodd N., Buckiova D., Fritzsch B., Syka J., Pavlinkova G. (2015) Deterioration of the Medial Olivocochlear Efferent System Accelerates Age-Related Hearing Loss in Pax2-Isl1 Transgenic Mice. Mol Neurobiol, [Epub ahead of print] DOI 10.1007/s12035-015-9215-1
GABAB receptors are the G-protein coupled receptors for the main inhibitory neurotransmitter in the brain, γ-aminobutyric acid (GABA). GABAB receptors regulate the excitability of most neurons in the central nervous system by modulating the activity of enzymes and ion channels. GABAB receptors associate with homo-oligomers of auxiliary KCTD 8, 12, 12b and 16 subunits that differentially regulate the receptor response by directly binding to the G-protein. We have shown distinct regulatory effects on G-protein signaling exerted by KCTD12 and 16 and provided evidence that GABAB/KCTD16 complexes regulate the kinetics of late inhibitory postsynaptic currents in hippocampal neurons. In summary, our data demonstrate that simultaneous assembly of distinct KCTDs at the receptor increases the molecular complexity of native GABAB receptors.
Collaboration: Prof. Bernhard Bettler, Department of Biomedicine, Institute of Physiology, Pharmazentrum, University of Basel, Basel, Switzerland
A, GABAB receptor subunit compositions in neurons. The principal subunits of GABAB receptors - GABAB1 (black) and GABAB2 (white) - have the prototypical seven transmembrane domains of G protein-coupled receptors. GABAB2 associates with auxiliary KCTD12 (red) or 16 (blue) subunits. B, Altered GABAB receptor responses in neurons with deleted KCTD proteins. Representative traces of GABAB agonist baclofen-evoked K+ currents recorded from cultured hippocampal neurons of WT (black), KCTD16 (red) or KCTD12 (blue) knockout mice. Deletion of KCTD12 reduces desensitization of the responses while deletion of KCTD16 leads to slightly elevated desensitization due to higher occupancy of the receptor by KCTD12. C, Superimposed traces show K+ currents evoked by 1 s-long application of baclofen to cultured hippocampal neurons isolated from WT, KCTD12 KO or KCTD16 KO mice. Bar graph summarizes the time constants obtained from a fit of the deactivation decay to a single exponential function. Note that the decay time course of the currents was significantly reduced in KCTD16 KO and unchanged in KCTD12 KO neurons, compared to WT. D, Examples of inhibitory postsynaptic currents (IPSCs) recorded from CA1 hippocampal neurons of WT or KCTD16 KO mice. Note faster decay kinetics of the currents obtained from KCTD16 KO neurons. Bar graph summarizes the time constants obtained from a fit of the deactivation decay of IPSCs to a single exponential function.
Publication: Raveh A, Turecek R and Bettler B (2015) Mechanisms of Fast Desensitization of GABAB Receptor-Gated Currents. Adv. Pharmacol. 73C:145-165.
Hearing thresholds were examined using pure-tone audiometry over the extended frequency range 0.125–16 kHz in a large sample of men and women aged 16–70 years The results could be used to normalize hearing thresholds when comparing participants differing in age and to prepare an international standard. Magnetic resonance morphometry was used to study the state of the central auditory system in a group of elderly subjects with different degree of presbycusis. The results demonstrate significant atrophy in the auditory cortex of elderly subjects.
The MR Unit, Department of Diagnostic and Interventional Radiology of the Institute for Clinical and Experimental Medicine (IKEM), Prague
Department of Otorhinolaryngology and Head and Neck Surgery, 1st Medical Faculty of Charles University, University Hospital Motol, Prague
Audiograms. Average pure-tone audiograms in men (top) and women (bottom) grouped by their age in decades (the parameter is age group in years). The extended high-frequency range is zoomed for clarity.
Jilek M., Šuta D., Syka J. (2014) Reference hearing thresholds in an extended frequency range as a function of age and their mathematical approximation. J Acoust Soc Am. 136(4):1821- 1830. IF1.555
Profant, O., Škoch, A., Balogová, Z., Tintěra, J., Hlinka, J., Syka, J.: (2014) Diffusion tensor imaging and MR morphometry of the central auditory pathway and auditory cortex in aging. Neuroscience 260: 87-97. IF3.327
The study explores the effects of an acoustically enriched environment applied during the critical period of development on the responsiveness of auditory neurons in rats resulting in lower excitatory thresholds at neuronal characteristic frequency, an increased frequency selectivity, larger response magnitudes, steeper rate-intensity functions and an increased spontaneous activity. Acoustically enriched environment may permanently affect signal processing in the subcortical auditory nuclei.
Collaboration: Department of Electrical Engineering and Computer Science, College of Polytechnics, Jihlava
Neuronal excitatory thresholds and tuning bandwidth. Top – scatter diagrams showing the dependence of the excitatory threshold on the characteristic frequency (CF) of the neurons in the control and enriched groups of rats along with fifth-order polynomial regression curves. Bottom – scatter diagrams showing the dependence of the Q30 parameter on the CF of the neurons in the control and enriched groups of rats along with fifth-order polynomial regression curves.
Publication: Bureš Z., Bartošová J., Lindovský J., Chumak T., Popelář J., Syka J. (2014) Acoustical enrichment during early postnatal development changes response properties of inferior colliculus neurons in rats. Eur. J. Neurosci 2014, Vol. 40, pp. 3674–3683. IF 3.669
We studied mechanisms of KCTD12-induced desensitization of GABAB receptor activated K+ currents. We show that the desensitization results from a dual interaction of KCTD12 with the G protein: constitutive binding stabilizes the heterotrimeric G protein at the receptor, whereas dynamic binding to the receptor-activated Gbg subunits induces desensitization by uncoupling Gbg from the effector K+ channel. Our results show that GABAB receptors are endowed with fast and reversible desensitization by harnessing KCTD12 that intercepts Gbg signaling.
Molecular mechanism of KCTD12-induced desensitization of GABAB responses.
A, Scheme illustrates the patch-clamp recording of membrane currents mediated by G-protein activated inwardly rectifying K+ channels (GIRK) from CHO cells. B, Representative traces of K+ currents activated by GABAB agonist baclofen in CHO cells expressing GABAB receptors and GIRK channels either with or without (w/o) KCTD12. KCTD12 induces pronounced and rapid desensitization of the K+ currents. C, Scheme illustrating a mechanism for fast desensitization of GABAB-activated GIRK currents. Resting (left), active (middle), and desensitized (right) states of the current response are shown. KCTD12 constitutively assembles with GABAB receptors and the G-protein into a signaling complex (inactive state). Constitutive binding of KCTD12 to activated Gβγ allows for a transient activation of GIRK channels (active state). An activity-dependent rearrangement of KCTD12 at Gβγ leads to a shielding of the GIRK-binding site on Gβγ by KCTD12 and induces current desensitization (desensitized state).
Publication: Tureček R, Schwenk J, Fritzius T, Ivánková K, Zolles G, Adelfinger L, Jacquier V, Besseyrias V, Gassmann M, Schulte U, Fakler B, Bettler B, (2014): Auxiliary GABAB Receptor Subunits Uncouple G Protein βγ Subunits from Effector Channels to Induce Desensitization. Neuron 82(5): 1032-1044. IF 15.982
Software generator for spectrotemporal receptive field (STRF) measurement.
Bureš, Z., Rybalko, N.
Software system for controlling and evaluation of behavioral experiments.
Bureš, Z., Popelář, J.
Software system for evaluation of neuronal responses.
The miniature ballpoint wire electrode technology.
Jilek, M., Popelář, J.
Brain cortex cooling and temperature measuring device.
Rybalko N, Popelář J, Šuta D, Svobodová Burianová J, Alvaro GS, Large CH, Syka J (2020) Effect of Kv3 channel modulators on auditory temporal resolution in aged Fischer 344 rats. Hear. Res. IN PRESS
Svobodová Burianová J, Syka J (2020) Postnatal exposure to an acoustically enriched environment alters the morphology of neurons in the adult rat auditory system. Brain Struct. Funct. 225(7): 1979-1995.
Bureš Z, Pysanenko K, Syka J (2020) Age-related changes in the temporal processing of acoustical signals in the auditory cortex of rats. Hear Res. 108025. doi: 10.1016/j.heares.2020.108025.
Profant O, Škoch A, Tintěra J, Svobodová V, Tóthová D, Svobodová Burianová J, Syka J (2020) The influence of aging, hearing and tinnitus on the morphology of cortical grey matter, amygdala and hippocampus. Front. Aging Neurosci. 12:553461. doi: 10.3389/fnagi.2020.553461.
Syka J (2020) Age-Related Changes in the Auditory Brainstem and Inferior Colliculus. In: Aging and Hearing. Springer Handbook of Auditory Research, Vol. 72, Eds.: K.S. Helfer, E.L. Bartlett, A.N. Popper, R.R. Fay. Springer Nature Switzerland AG, pp. 67-96.
Chang TR, Šuta D, Chiu TW (2020) Responses of midbrain auditory neurons to two different environmental sounds-A new approach on cross-sound modeling. Biosystems. 187: 104021. doi: 10.1016/j.biosystems.2019.104021.
Abdelfattah AS, Kawashima T, Singh A, Novák O, Liu H, Shuai YC, Huang YC, Campagnola L, Seeman SC, Yu J, Zheng JH, Grimm JB, Patel R, Friedrich J, Mensh BD, Paninski L, Macklin JJ, Murphy GJ, Podgorski K, Lin BJ, Chen TW, Turner GC, Liu Z, Koyama M, Svoboda K, Ahrens MB, Lavis LD, Schreiter ER (2019) Bright and photostable chemigenetic indicators for extended in vivo voltage imaging. Science 365(6454): 699-704.
Bureš Z, Profant O, Svobodová V, Tothová D, Vencovský V, Syka J (2019) Speech Comprehension and Its Relation to Other Auditory Parameters in Elderly Patients With Tinnitus. Front. Aging Neurosci. 11: 219.
Dinamarca MC, Raveh A, Schneider A, Fritzius T, Fruh S, Rem PD, Stawarski M, Lalanne T, Tureček R, Choo M, Besseyrias V, Bildl V, Bentrop D, Staufenbiel M, Gassmann M, Fakler B, Schwenk J, Bettler B (2019) Complex formation of APP with GABA(B) receptors links axonal trafficking to amyloidogenic processing. Nat. Commun. 10: 1331. doi: 10.1038/s41467-019-09164-3.
Hruskova B , Trojanova J, Kralikova M, Melichar A, Suchankova S, Bartosova J, Svobodova Burianova J, Popelar J, Syka J, Turecek R (2019) Cochlear ablation in neonatal rats disrupts inhibitory transmission in the medial nucleus of the trapezoid body. Neurosci. Lett. 699,145-150. doi: 10.1016/j.neulet.2019.01.058.
Macová I, Pysaněnko K, Chumak T, Dvořáková M, Bohuslavová R, Syka J, Fritzsch B, Pavlinková G (2019) Neurod1 Is Essential for the Primary Tonotopic Organization and Related Auditory Information Processing in the Midbrain. J. Neurosci. 39(6): 984-1004. doi: 10.1523/JNEUROSCI.2557-18.2018.
Profant O , Jilek M, Bures Z, Vencovsky V, Kucharova D, Svobodova V , Korynta J, Syka J (2019) Functional Age-Related Changes Within the Human Auditory System Studied by Audiometric Examination. Front. Aging Neurosci. 11:26. doi: 10.3389/fnagi.2019.00026.
Rybalko N , Mitrovic D, Suta D, Bures Z, Popelar J, Syka J (2019) Behavioral evaluation of auditory function abnormalities in adult rats with normal hearing thresholds that were exposed to noise during early development. Physiol. Behav. 210:112620. doi: 10.1016/j.physbeh.2019.112620
Stříteská M, Profant O, Trnková K, Laboš M, Weichet J, Dědková J, Vališ M, Chrobok V, Chovanec M (2019) Superior semicircular canal dehiscence. Česká a Slovenská Neurologie a Neurochirurgie 115: 461– 463.
Shen TW, Liu TJ, Šuta D, Lee ChCH (2018) Acoustic Perturbation of Breathing: A Newly Discovered Response to Soft Sounds in Rats Using an Approach of Image Analysis. Journal of Medical and Biological Engineering 39: 43–53.
Balogova Z , Popelar J, Chiumenti F, Chumak T, Svobodova Burianova J, Rybalko N, Syka J (2018) Age-related differences in hearing function and cochlear morphology between male and female Fischer 344 rats. Front. Aging Neurosci. 9:428. doi: 10.3389/fnagi.2017.00428.
Bureš Z , Pysaněnko K, Lindovský J, Syka J (2018) Acoustical Enrichment during Early Development Improves Response Reliability in the Adult Auditory Cortex of the Rat. Neural Plasticity 5903720. doi: 10.1155/2018/5903720.
Hod D, Novák O, Guardado-Montesino M, Fransen JW, Hu A, Borghuis BG, Guo C, Kim DS, Svoboda K (2018) Thy1 transgenic mice expressing the red fluorescent calcium indicator jRGECO1a for neuronal population imaging in vivo. PLoS One 13(10):e0205444. doi: 10.1371/journal.pone.0205444
Lindovský J , Pysaněnko K, Popelář J, Syka J (2018) Fast tonotopy mapping of the rat auditory cortex with a custom-made electrode array. Physiol. Res. 67(6):993-998.
Pysanenko K , Bureš Z, Lindovský J, Syka J: (2018) The effect of complex acoustic environment during early development on the responses of auditory cortex neurons in rats. Neuroscience 371:221-228. doi: 10.1016/j.neuroscience.2017.11.049.
Školoudík L, Chrobok V, Kočí Z, Popelář J, Syka J, Laco J, Filipová A, Syková E, Filip S (2018) The Transplantation of hBM-MSCs Increases Bone Neo-Formation and Preserves Hearing Function in the Treatment of Temporal Bone Defects - on the Experience of Two Month Follow Up. Stem Cell Rev. Rep. 14: 860-870.
Zarska M, Sramek M, Novotny F, Havel F, Babelova A, Mrazkova B, Benada O, Reinis M, Stepanek I, Musilek K, Bartek J, Ursinyova M, Novak O, Dzijak R, Kuca K, Proska J, Hodny Z (2018) Biological safety and tissue distribution of (16-mercaptohexadecyl) trimethylammonium bromidemodified cationic gold nanorods. Biomaterials 154:275-290. doi: 10.1016/j.biomaterials.2017.10.044.
Fík Z, Chovanec M, Zvěřina E, Kluh J, Profant O, Kraus J, Hrubá S, Čada Z, Procházková K, Plzák J, Betka J (2017) Funkce lícního nervu po mikrochirurgické léčbě vestibulárního schwannomu. Česká a Slovenská neurologie a neurochirurgie 80(5): 545-551.
Fritzius T, Tureček R, Seddik R, Kobayashi H, Tiao J, Rem PD, Metz M, Králíková M, Bouvier M, Gassmann M, Bettler B (2017) KCTD Hetero-oligomers Confer Unique Kinetic Properties on Hippocampal GABA(B) Receptor-Induced K+ Currents. J. Neurosci. 37(5): 1162-1175.
Kratochvílová B, Profant O, Astl J, Holý R (2017) Our experience in the treatment of idiopathic sensorineural hearing loss (ISNHL): Effect of combination therapy with HBO2 and vasodilator infusion therapy. Undersea & Hyperbaric Medicine 43(7): 771-780.
Popelář J, Gómez MD, Lindovský J, Rybalko N, Burianová J, Oohashi T, Syka J (2017) The absence of brain-specific link protein Bral2 in perineuronal nets hampers auditory temporal resolution and neural adaptation in mice. Physiol. Res. 66, 867-880.
Profant O , Roth J, Bureš Z, Balogová Z, Lišková I, Betka J, Syka J (2017) Auditory dysfunction in patients with Huntington's disease. Clin. Neurophysiol. 128(10): 1946-1953.
Bohuslavová R, Dodd N, Macová I, Chumak T, Horák M, Syka J, Fritzsch B, Pavlínková G (2017) Pax2-Islet1 Transgenic Mice Are Hyperactive and Have Altered Cerebellar Foliation. Mol. Neurobiol. 54(2):1352-1368. doi: 10.1007/s12035-016-9716-6.
Bureš Z, Popelář J, Syka J (2017) The effect of noise exposure during the developmental period on the function of the auditory system. Hear. Res. 352:1-11. doi: 10.1016/j.heares.2016.03.008.
Dvořáková, M., Jahan, I., Macová, I., Chumak, T., Bohuslavová, R., Syka, J., Fritzsch, B., Pavlinková, G.: (2016) Incomplete and delayed Sox2 deletion defines residual ear neurosensory development and maintenance. Scientific Reports 6: 38253.
Jírů, F., Skoch, A., Wagnerová, D., Dezortová, M., Visková, J., Profant, O., Syka, J., Hájek, M.: (2016) The age dependence of T2 relaxation times of N-acetyl aspartate, creatine and choline in the human brain at 3 and 4T. NMR Biomed., 29(3): 284-92.
Novák, O. , Zelenka, O., Hromádka, T., Syka, J.: (2016) Immediate manifestation of acoustic trauma in the auditory cortex is layer specific and cell type dependent. J. Neurophysiol, 115(4): 1860-74.
Ouda, L. , Jilek, M., Syka, J.: (2016) Expression of c-Fos in rat auditory and limbic systems following 22-kHz calls. Behav. Brain Res., 308: 196-204.
Školoudik, L., Chrobok, V., Kalfert, D., Koči, Z., Syková, E., Chumak, T., Popelář, J., Syka. J., Laco, J., Dědková, J., Dayanithi, G., Filip, S.:(2016) Human multipotent mesenchymal stromal cells in the treatment of postoperative temporal bone defect: an animal model. Cell Transplant., 25(7): 1405-1414.
Burianová, J. , Ouda, L., Syka, J.: (2015) The influence of aging on the number of neurons and levels of non-phosporylated neurofilament proteins in the central auditory system of rats. Front Aging Neurosci. 7: 27.
Chovanec, M., Zvěřina, E., Profant, O., Balogová, Z., Kluh, J, Syka, J., Lisý, J., Merunka, I., Skřivan, J., Betka, J.: (2015) Does attempt at hearing preservation microsurgery of vestibular schwannoma affect postoperative tinnitus? Biomed Res. Int. 2015: 783169.
Ouda, L. , Profant, O., Syka, J.: (2015) Age-related changes in the central auditory system. Cell Tissue Res. 361(1): 337-358.
Profant, O. , Tintěra, J., Balogová, Z., Ibrahim, I., Jilek, M., Syka, J.: (2015) Functional changes in the human auditory cortex in ageing. PLoS One 10(3):e0116692.
Raveh, A., Tureček, R., Bettler, B.: (2015) Mechanisms of fast desensitization of GABA(B) receptor-gated currents. Adv Pharmacol. 73:145-165.
Rybalko, N. , Chumak, T., Bureš, Z., Popelář, J., Šuta, D., Syka, J.: (2015) Development of the acoustic startle response in rats and its change after early acoustic trauma. Behav. Brain Res. 286: 212-221.
Šuta, D. , Rybalko, N., Shen, D. W., Popelář, J., Poon, P. W., Syka J.: (2015) Frequency discrimination in rats exposed to noise as juveniles. Physiol. Behav. 144: 60-65.
Tomková, M., Tomek, J., Novák, O., Zelenka, O., Syka, J., Brom, C.: (2015) Formation and disruption of tonotopy in a large-scale model of the auditory cortex. J Comput Neurosci. 39(2):131-153.
Adelfinger, L., Tureček, R., Ivankova, K., Jensen, A. A., Moss, S. J., Gassmann, M., Bettler, B.: (2014) GABAB receptor phosphorylation regulates KCTD12-induced K+ current desensitization. Biochem. Pharmacol. 91(3): 369-379.
Betka, J., Zvěřina, E., Balogová, Z., Profant, O., Skřivan, J., Kraus, J., Lisý, J., Syka, J., Chovanec, A.: (2014) Complications of microsurgery of vestibular schwannoma. Biomed. Res. Int. 2014: 315952.
Bureš, Z. , Bartošová, J., Lindovský, J., Chumak, T., Popelář, J., Syka, J.: (2014) Acoustical enrichment during early postnatal development changes response properties of inferior colliculus neurons in rats. Eur. J. Neurosci. 40(11): 3674-3683.
Jilek, M. , Šuta, D., Syka, J.: (2014) Reference hearing thresholds in an extended frequency range as a function of age. J. Acoust. Soc. Am. 136(4): 1821.
Profant, O. , Škoch, A., Balogová, Z., Tintěra, J., Hlinka, J., Syka, J.: (2014) Diffusion tensor imaging and MR morphometry of the central auditory pathway and auditory cortex in aging. Neurosci. 260: 87-97.
Lu, H. P., Syka, J., Chiu, T. W., Poon, P. W.: (2014) Prolonged sound exposure has different effects on increasing neuronal size in the auditory cortex and brainstem. Hear. Res. 314: 42-50.
Trojanová, J. , Kulík, A., Janacek, J., Králíková, M., Syka, J., Tureček, R.: (2014) Distribution of glycine receptors on the surface of the mature calyx of Held nerve terminal. Front. Neural Circuits. 8: 120.
Tureček, R. , Schwenk, J., Fritzius, T., Ivankova, K., Zolles, G., Adelfinger, L., Jacquier, V., Besseyrias, V., Gassmann, M., Schulte U., Fakler, B., Bettler, B.: (2014) Auxiliary GABAB Receptor Subunits Uncouple G Protein βγ Subunits from Effector Channels to Induce Desensitization. Neuron. 82(5): 1032-1044.
Functional changes of the auditory system associated with auditory experience and aging
Czech Science Foundation, 18-09692S, 2018–2021
GABAB receptor dysfunction and the pathophysiology of tinnitus
Czech Science Foundation, 19-09283S, 2019–2021
Changes in the auditory cortex in patients with single sided deafness
Czech Science Foundation, 19-08241S, 2019–2021
Modulation of excitatory and inhibitory synaptic transmission by KCTD proteins and the role of the modulation in coding of sound stimuli by the auditory cortex in mice (GAUK, 42119, 2019-2021)
Center of Reconstruction Neuroscience – NEURORECON
Ministry of Education, Youth and Sports, CZ.02.1.01/0.0/0.0/15_003/0000419, 2017–2022
The role of NEUROD1 and ISL1 in neuronal development of the inner ear
Czech Science Foundation, 20-06927S, 2020–2022
Processing of complex acoustical signals including vocalizations in inhibitory circuits of the central auditory system in mice models of autism and different types of sensorineural hearing loss
Ministry of Education, Youth and Sports, INTER-ACTION, 2019LTAIN, 2020–2022
Novel diagnostic methods in examination of age related changes of the auditory system
Czech health research council, NU20-08-00311, 2020-2023
The role of GABAB receptor-associated KCTD proteins in the sensory nervous system
Czech Science Foundation, 21-17085S, 2021–2023
Institute for Clinical and Experimental Medicine, Prague
Institute of Biotechnology Czech Academy of Science
University of Basel, Basel, Switzerland
National Chiao Tung University, Taiwan
The Czech Institute of Informatics, Robotics and Cybernetics, Czech Technical University in Prague
Motol University Hospital, Prague
Université de Bordeaux, France