scholarly journals Sound Localization Ability and Glycinergic Innervation of the Superior Olivary Complex Persist after Genetic Deletion of the Medial Nucleus of the Trapezoid Body

2013 ◽  
Vol 33 (38) ◽  
pp. 15044-15049 ◽  
Author(s):  
W. Jalabi ◽  
C. Kopp-Scheinpflug ◽  
P. D. Allen ◽  
E. Schiavon ◽  
R. R. DiGiacomo ◽  
...  
2019 ◽  
Vol 597 (8) ◽  
pp. 2269-2295 ◽  
Author(s):  
Alexander U. Fischer ◽  
Nicolas I. C. Müller ◽  
Thomas Deller ◽  
Domenico Del Turco ◽  
Jonas O. Fisch ◽  
...  

2005 ◽  
Vol 94 (6) ◽  
pp. 3826-3835 ◽  
Author(s):  
Joshua S. Green ◽  
Dan H. Sanes

Despite the peripheral and central immaturities that limit auditory processing in juvenile animals, they are able to lateralize sounds using binaural cues. This study explores a central mechanism that may compensate for these limitations during development. Interaural time and level difference processing by neurons in the superior olivary complex depends on synaptic inhibition from the medial nucleus of the trapezoid body (MNTB), a group of inhibitory neurons that is activated by contralateral sound stimuli. In this study, we examined the maturation of coding properties of MNTB neurons and found that they receive an inhibitory influence from the ipsilateral ear that is modified during the course of postnatal development. Single neuron recordings were obtained from the MNTB in juvenile (postnatal day 15–19) and adult gerbils. Approximately 50% of all recorded MNTB neurons were inhibited by ipsilateral sound stimuli, but juvenile neurons displayed a much greater suppression of firing as compared with those in adults. A comparison of the prepotential and postsynaptic action potential indicated that inhibition occurred at the presynaptic level, likely within the cochlear nucleus. A simple linear model of level difference detection by lateral superior olivary neurons that receive input from MNTB suggested that inhibition of the MNTB may expand the response of LSO neurons to physiologically realistic level differences, particularly in juvenile animals, at a time when these cues are reduced.


1994 ◽  
Vol 110 (1) ◽  
pp. 84-92 ◽  
Author(s):  
Chiyeko Tsuchitani

Single-unit responses of cat superior olivary complex neurons to acoustic stimuli were examined to determine whether the units' action potentials were sufficiently synchronized to contribute to the brain stem evoked response. The medial nucleus of the trapezoid body and lateral superior olive are two major nuclei within the cat superior olivary complex. The first-spike discharge latencies of medial nucleus of the trapezoid body and lateral superior olivary neurons to monaural presentations of tone burst stimuli were measured as a function of stimulus level. Evidence is provided to support the hypotheses that in cat the medial nucleus of the trapezoid body may contribute directly to the monaural brain stem evoked response by producing action potentials synchronized to stimulus onset and may also contribute indirectly to the brain stem evoked response binaural difference wave bc by inhibiting the lateral superior olive unit excitatory responses synchronized to stimulus onset.


2021 ◽  
Vol 15 ◽  
Author(s):  
Nichole L. Beebe ◽  
Chao Zhang ◽  
R. Michael Burger ◽  
Brett R. Schofield

The superior olivary complex (SOC) is a major computation center in the brainstem auditory system. Despite previous reports of high expression levels of cholinergic receptors in the SOC, few studies have addressed the functional role of acetylcholine in the region. The source of the cholinergic innervation is unknown for all but one of the nuclei of the SOC, limiting our understanding of cholinergic modulation. The medial nucleus of the trapezoid body, a key inhibitory link in monaural and binaural circuits, receives cholinergic input from other SOC nuclei and also from the pontomesencephalic tegmentum. Here, we investigate whether these same regions are sources of cholinergic input to other SOC nuclei. We also investigate whether individual cholinergic cells can send collateral projections bilaterally (i.e., into both SOCs), as has been shown at other levels of the subcortical auditory system. We injected retrograde tract tracers into the SOC in gerbils, then identified retrogradely-labeled cells that were also immunolabeled for choline acetyltransferase, a marker for cholinergic cells. We found that both the SOC and the pontomesencephalic tegmentum (PMT) send cholinergic projections into the SOC, and these projections appear to innervate all major SOC nuclei. We also observed a small cholinergic projection into the SOC from the lateral paragigantocellular nucleus of the reticular formation. These various sources likely serve different functions; e.g., the PMT has been associated with things such as arousal and sensory gating whereas the SOC may provide feedback more closely tuned to specific auditory stimuli. Further, individual cholinergic neurons in each of these regions can send branching projections into both SOCs. Such projections present an opportunity for cholinergic modulation to be coordinated across the auditory brainstem.


2018 ◽  
Author(s):  
Mariano N. Di Guilmi ◽  
Luis E. Boero ◽  
Valeria C. Castagna ◽  
Adrián Rodríguez-Contreras ◽  
Carolina Wedemeyer ◽  
...  

AbstractThe auditory system in many mammals is immature at birth but precisely organized in adults. Spontaneous activity in the inner ear plays a critical role in guiding this process. This is shaped by an efferent pathway that descends from the brainstem and makes transient direct synaptic contacts with inner hair cells (IHCs). In this work, we used an α9 cholinergic receptor knock-in mouse model (of either sex) with enhanced medial efferent activity (Chrna9L9’T, L9’T) to understand the role of the olivocochlear system in the correct establishment of auditory circuits. Wave III of auditory brainstem responses (which represents synchronized activity of synapses within the superior olivary complex) were smaller in L9’T mice, suggesting a central dysfunction. The mechanism underlying this functional alteration was analysed in brain slices containing the medial nucleus of the trapezoid body (MNTB), where neurons are topographically organized along a medio-lateral axis. The topographic organization of MNTB physiological properties observed in WT mice was abolished in the L9’T mice. Additionally, electrophysiological recordings in slices evidenced MNTB synaptic alterations, which were further supported by morphological alterations. The present results suggest that the transient cochlear efferent innervation to IHCs during the critical period before the onset of hearing is involved in the refinement of topographic maps as well as in setting the correct synaptic transmission at central auditory nuclei.Significance StatementCochlear inner hair cells of altricial mammals display spontaneous electrical activity before hearing onset. The pattern and firing rate of these cells is crucial for the correct maturation of the central auditory pathway. A descending efferent innervation from the central nervous system contacts hair cells during this developmental window. The function of this transient efferent innervation remains an open question. The present work shows that the genetic enhancement of efferent function disrupts the orderly topographic distribution at the medial nucleus of the trapezoid body level and causes severe synaptic dysfunction. Thus, the transient efferent innervation to the cochlea is necessary for the correct establishment of the central auditory circuitry.


2006 ◽  
Vol 95 (3) ◽  
pp. 1499-1508 ◽  
Author(s):  
Alexander Kadner ◽  
Randy J. Kulesza ◽  
Albert S. Berrebi

We describe neurons in two nuclei of the superior olivary complex that display differential sensitivities to sound duration. Single units in the medial nucleus of the trapezoid body (MNTB) and superior paraolivary nucleus (SPON) of anesthetized rats were studied. MNTB neurons produced primary-like responses to pure tones and displayed a period of suppressed spontaneous activity after stimulus offset. In contrast, neurons of the SPON, which receive a strong glycinergic input from MNTB, showed very little or no spontaneous activity and responded with short bursts of action potentials after the stimulus offset. Because SPON spikes were restricted to the same time window during which suppressed spontaneous activity occurs in the MNTB, we presume that SPON offset activity represents a form of postinhibitory rebound. Using characteristic frequency tones of 2- to 1,000-ms duration presented 20 dB above threshold, we show that the profundity and duration of the suppression of spontaneous activity in MNTB as well as the magnitude and first spike latency of the SPON offset response depend on stimulus duration as well as on stimulus intensity, showing a tradeoff between intensity and duration. Pairwise comparisons of the responses to stimuli of various durations revealed that the duration sensitivity in both nuclei is sharpest for stimuli <50 ms.


Author(s):  
Anna K. Magnusson ◽  
Marcelo Gómez-Álvarez

This chapter summarizes the current concepts of the superior paraolivary nucleus (SPON)—a structure embedded in the superior olivary complex in the mammalian auditory brainstem. SPON is driven by input pathways from two of the most temporally secure neurons in the brain: the octopus cells in the cochlear nucleus and the neurons of the medial nucleus of the trapezoid body. These inputs activate spiking activity that marks the onset and offset of sound, the latter based on a rebound depolarization mechanism. This makes the SPON an excellent detector of transient sound energy. Robust detection of the coarse sound pattern over time further gives SPON the capacity to track the temporal envelope of complex sounds with supreme precision. Since the SPON circuitry is constant in mammals and resilient to sensory perturbation, it indicates its high survival value. A possible neuroevolutionary role of SPON in the processing of vocalizations is discussed.


2004 ◽  
Vol 92 (1) ◽  
pp. 545-552 ◽  
Author(s):  
Jeremy B. Bergsman ◽  
Pietro De Camilli ◽  
David A. McCormick

The calyx of Held is a giant nerve terminal that forms a synapse directly onto the principal cells of the medial nucleus of the trapezoid body (MNTB) in the mammalian auditory brain stem. This central synapse, which is involved in sound localization, has become widely used for studying synaptic transmission. Anatomical studies of this nucleus have indicated that each principal cell is innervated by only one calyx. Here we use previously established electrophysiological criteria of excitatory postsynaptic current amplitude, kinetics, and transmitter type, as well as other characteristics commonly reported for this synapse, to examine the input properties of principal neurons. Our findings indicate that some principal cells receive more than one strong excitatory input. These inputs meet previously established electrophysiological criteria for identification as calyceal nerve terminals. Implications for the execution and analysis of experiments to avoid errors due to such multiple inputs are discussed.


1990 ◽  
Vol 63 (5) ◽  
pp. 1169-1190 ◽  
Author(s):  
G. A. Spirou ◽  
W. E. Brownell ◽  
M. Zidanic

1. Recordings were made from single nerve fibers in barbiturate-anesthetized cats in the midline trapezoid body, a location that permits selective sampling of efferent cells of the ventral cochlear nucleus. Single units were localized to either the dorsal or ventral components of the trapezoid body. The fibers were physiologically classified on the basis of their peristimulus time histograms (PSTH) and receptive-field properties. In addition, low characteristic frequency (CF) units were probed for rapid rate and phase shifts with increases in intensity. The projection patterns of some fibers were traced by iontophoresing horseradish peroxidase (HRP) into their axons. 2. HRP-labeled fibers most likely originated from globular bushy cells of the ventral cochlear nucleus in that they sent a large branch into the contralateral medial nucleus of the trapezoid body which terminated in a calyceal ending and an ipsilateral branch into the lateral nucleus of the trapezoid body. A thin branch, usually starting from the large branch, wound its way through the medial nucleus of the trapezoid body to its termination in the ventral nucleus of the trapezoid body. Additional branches from the parent axon could pass through medial periolivary groups throughout the rostrocaudal extent of the superior olivary complex. The parent fiber was traced as far as the ventral lateral lemniscus where it faded before reaching its termination. 3. The majority of units were recorded in the ventral component of the trapezoid body. Although the ventral component is comprised of both large and small diameter fibers, our sample was biased to the larger diameter fibers representing the activity of axons originating from globular bushy cells in the ventral cochlear nucleus. Ventral component units were not tonotopically arrayed and had CFs that spanned the audible range for cats. HRP labeling of ventral component axons revealed that the section of the axon traveling through the midline shifted its dorsal-ventral location. This pattern was compatible with the lack of tonotopy found in the ventral component. Recordings were also made from the dorsal component of the trapezoid body, which contained medium diameter axons. These axons originated from spherical bushy cells in the ventral cochlear nucleus. Dorsal component units were tonotopically arrayed and had CFs less than 7 kHz. 4. Cells were characterized by their PSTH at CF. Primary-like and phase-locked units constituted most of the dorsal component units.(ABSTRACT TRUNCATED AT 400 WORDS)


1979 ◽  
Vol 88 (5) ◽  
pp. 684-688 ◽  
Author(s):  
Douglas B. Webster ◽  
Molly Webster

Both postnatal auditory deprivation and experimentally produced conductive hearing losses in mice result in incomplete maturation of most brain stem auditory neurons. The affected groups are: octopus cell, globular cell, small spherical cell, and large spherical cell groups in ventral cochlear nuclei; and the lateral superior olive and medial nucleus of the trapezoid body of the superior olivary complex. When 45 days of auditory deprivation are followed by 45 days of normal acoustic stimulation, there is incomplete maturation of neurons in: multipolar cell, globular cell, small spherical cell, and large spherical cell groups in ventral cochlear nuclei; lateral superior olive and medial nucleus of trapezoid body in superior olivary complex; and central nucleus of inferior colliculus. A critical period exists when adequate sound stimulation is needed for full development of these neurons.


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