DEPARTMENT OF AUDITORY NEUROSCIENCE

 

Head:

Publications
syka.jpgProf. MUDr. Josef Syka, DrSc.
email: syka@biomed.cas.cz
tel: +420241062787

Laboratory of Auditory Physiology and Pathology

Head:  Prof. MUDr. Josef Syka, DrSc.
email: syka@biomed.cas.cz
tel: +420241062787

Laboratory of Synaptic Physiology

Head:  RNDr. Rostislav Tureček, Ph.D.
email: turecek@biomed.cas.cz
tel: +420241062748

Scientists:

MUDr. Daniela Buckiová, CSc.
Ing. Zbyněk Bureš, Ph.D.
Ing. Milan Jilek
MUDr. Ladislav Ouda, Ph.D.
RNDr. Jiří Popelář, CSc.
RNDr. Natalia Rybalko, CSc.
Ing. Daniel Šuta, Ph.D.

Ph.D. Students:

Mgr. Jana Burianová
Mgr. Jolana Grécová
Mgr. Bohdana Hrušková
MUDr. Tetyana Chumak
Mgr. Kateryna Lomakina
MUDr. Oliver Profant
MUDr. Jana Pelánová
Mgr. Johana Trojanová

Technical Assistants:

Jana Janoušková
Jan Kolář
Jan Setnička
Michal Slavík

Laboratory of Auditory Physiology and Pathology

Structure and function of the auditory system

The main research aim of the Laboratory of Auditory Physiology and Pathology is to investigate the structure and function of the auditory system in animal models under normal conditions, during development and aging, and under different pathological situations such as noise exposure. Using immunohistochemical techniques the expression of calcium binding proteins (calbindin, parvalbumin, calretinin) and GABA precursors GAD 65 and GAD 67 is evaluated in the auditory system in normal and noise-exposed guinea pigs and rats. Recordings of single-unit or multiple-unit extracellular activity with multielectrode probes have revealed basic principles of the processing of complex sounds such as animal vocalizations in the higher auditory centers (auditory cortex, thalamus and tectum). Multielectrode recording combined with immunohistochemical techniques is used for investigation of a detailed parcellation of the auditory cortex. Study of the age-related changes of the hearing function in a fast ageing rat strain Fischer 344 serves as model for understanding mechanisms and progression of the presbycusis in man. The effects of noise exposure on hearing acuity is under evaluation in Long Evans rats with the aid of behavioral operant conditioning procedures, recording of auditory evoked responses and recording of different types of otoacoustic emissions. Behavioral tests are also used to study the lateralization of auditory functions in the rat auditory cortex. Close collaboration with the ENT clinics is oriented to investigation of hearing function in children and adolescents and to characterization of problems of presbycusis.

Current research at the Laboratory of Auditory Physiology and Pathology focuses on the following topics:

  • Processing of simple and complex acoustical signals in the central auditory system of guinea pig 
  • Role of descending pathways in the auditory system
  • Role of the left and right auditory cortices in the processing of acoustical signals in rat 
  • Effect of noise exposure on the function of the auditory system 
  • Development of the auditory system in mouse and rat 
  • Age-related changes in the hearing function
  • Audiological investigation of hearing function in families with the occurrence of connexin 26 related deafness 

Laboratory of Synaptic Physiology

Modulation of excitatory synaptic transmission by GABA and glycine in brainstem auditory nuclei

Rostislav Tureček and his coworkers are interested in the mechanisms of excitatory and inhibitory synaptic transmission. They use electrophysiological and immunohistochemical approaches to study neurons of the medial nucleus of the trapezoid body (MNTB) in rat or mouse brainstem slices. Principal cells of the MNTB play a key role in the acoustic information processing by the brain stem auditory circuitry. These cells accurately convert excitatory signals provided by the ventral cochlear nucleus (AVCN) to inhibitory signals directed to the lateral/medial superior olive (LSO/MSO). Each MNTB principal cell receives the excitatory input forming a giant nerve terminal, the calyx of Held (Fig. 5). This can be directly examined by the patch-clamp recording technique (Fig. 6). Using presynaptic recording we have provided an evidence for the presence of chloride-permeable glycine receptors in the calyx of Held (Fig 7A). These receptors, when activated, potentiate the release of glutamate from the calyx. In addition to the excitatory input, principal cells are innervated by glycinergic inhibitory fibers. Glycine released from the nerve endings of these fibers activates pre- and postsynaptic glycine receptors and generates extremely fast inhibitory postsynaptic currents. The laboratory’s results have shown that the subunit compositions of pre- and postsynaptic glycine receptors differ (Fig. 7B, 8). The presynaptic receptors are homomers composed from α1 subunits, while the postsynaptic receptors are heteromers composed from α1 and β subunits. The results suggest that the postsynaptic phenotype provides receptors with fast kinetics, able to follow repetitive synaptic stimuli at high frequencies, while the presynaptic phenotype is tuned to sense low concentrations of glycine delivered by spillover.

Current research at the Laboratory of Synaptic Physiology focuses on the following topics:

  • Subunit composition and localization of glycine and GABAB receptors in the medial nucleus of the trapezoid body (MNTB) 
  • Role of cochlear activity in the postnatal development of glycinergic synaptic transmission in the MNTB
  • Interactive effects of Ca2+-activated potassium channels and GABAB receptors on excitatory synaptic transmission in the MNTB

Fig. 1 The function of the cortico-thalamic pathway

Fig_01
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(A) The neuronal response in the medial geniculate body (MGB) to acoustic stimulation (AS) can be influenced by prior local electrical stimulation (ES) of the auditory cortex (AC) (panel A). (B) A multielectrode probe enables us to evaluate the effects of ES on neuronal responses simultaneously from up to 16 electrode positions in the MGB. (C) The modulatory effects of the cortical ES according to the characteristic frequencies (CF) of units in the MGB and the site of stimulation in the AC.

Fig. 2 Avoidance conditioning behavioral procedures on rats

Fig_02
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Avoidance conditioning behavioral procedures on rats are performed in modified Skinner box.
Discrimination of frequency-modulated sounds is significantly worsened after lesion of the right auditory cortex (filled green squares), whereas lesion of the left auditory cortex (filled red diamonds) has only negligible effect. Discrimination of pure tones (3 and 6 kHz) is not affected by lesion of the auditory cortex (open symbols).


Fig. 3 The effects of noise exposure on the central auditory nuclei

Fig_03
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The amplitudes of middle latency responses (MLR), recorded in the auditory cortex are significantly enhanced after intense noise exposure (broad-band noise, 120 dB SPL, 1 hour), whereas the responses recorded from the brain stem (ABR) are suppressed. The results point point to a specific effect of noise exposure on neural activity in the central auditory nuclei.

Fig. 4  Age-related changes in hearing in Fischer 344 rats

Fig_04
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Age-related changes in hearing are studied in the fast aging Fischer 344 rat strain. In contrast to the standard Long Evans rat strain, Fischer 344 rats develop a pronounced hearing loss and an almost full diminution of distortion product otoacoustic emissions during the second year of life. Because the hair cell loss in aged Fischer 344 rats is relatively small, the hearing deterioration is probably caused by the dysfunction of other inner ear structures (tectorial membrane, stria vascularis).


Fig. 5 The calyx of Held

Fig_05
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The calyx of Held, a giant glutamate-releasing nerve terminal, stained with specific antibodies raised against the calcium-binding protein, calretinin.

 


Fig. 6 Cells and patch-clamp recordings from the calyx of Held in MNTB supravital slices

Fig_06
zoom figure

Cells and patch-clamp electrodes recording from the calyx of Held in MNTB supravital slices can be viewed with differential interference contrast (upper photograph). The recording electrode contains fluorescent dyes (e.g. lucifer yellow) to visualize the calyx (lower photograph).


Fig. 7 Current responses of chloride-permeable glycine receptors

Fig_07
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Current responses of chloride-permeable glycine receptors expressed in a calyx (A) or in a principal cell (B). The responses were evoked by the application of exogenous glycine and recorded by the patch-clamp technique from neurons held at the membrane potentials indicated. The presynaptic responses were sensitive to picrotoxin, a selective inhibitor of the α-homomeric form of the receptor. The postsynaptic responses were potentiated by 3-tropanylindole-3-carboxylate, a selective modulator of αβ-heteromeric form of the receptor.


Fig. 8 An imaging of MNTB cells labelled with antibodies directed against the glycine receptor α1-subunit.

Fig_08
zoom figure

A confocal image of an MNTB principal cell labelled with antibodies directed against the glycine receptor α1-subunit. The α1-positive clusters often form rosette-like structures.


List of current grants:

Name of the grant

Grant agency

Number of the grant

Principal investigator

Duration of the grant

Plasticity of hearing and sensorineural hearing impairment - from early development to presbycusis

IGA MZ

NR/8113 - 4

Prof. Syka

2004-07

Center of neuroscience

MŠMT ČR

LC554

Prof. Syka

2005-09

Nanotechnology-based targeted drug delivery (NANOEAR)

FP6 framework

NMP-2004-3.4.1.5-1 -1

Prof. Syka

2006-10

Acoustical signal processing in the neuronal circuits of the auditory system

GAČR

309/07/1336

Dr. Popelář

2007-11

The role of GABA-B receptors in the mammalian MNTB

GAČR

309/06/1304

Dr. Tureček

2006-08

From molecules to networks: understanding synaptic physiology and pathology in the brain through mouse models

Integrated FP6 Project

LSHM-CT-
2005-019055

Dr. Tureček

2005-09

The role of inhibition in mammalian MNTB

Wellcome Trust

073966

Dr. Tureček

2004-09


List of publications in impacted journals and books

1977 | 1978 | 1979 | 1980 | 1981 | 1982 | 1984 | 1985 | 1987
1988 | 1989 | 1990 | 1992 | 1993 | 1994 | 1995 | 1996 | 1997
1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006
2007 | 2008 | 2009

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