scholarly journals Temporal properties of responses to sound in the ventral nucleus of the lateral lemniscus

2014 ◽  
Vol 111 (4) ◽  
pp. 817-835 ◽  
Author(s):  
Alberto Recio-Spinoso ◽  
Philip X. Joris
Keyword(s):  
Firing Rate ◽  
Modulation Frequency ◽  
Broadband Noise ◽  
Inhibitory Input ◽  
Lateral Lemniscus ◽  
Auditory Midbrain ◽  
Temporal Properties ◽  
Low Pass ◽  
Envelope Spectrum ◽  
Ventral Nucleus

Besides the rapid fluctuations in pressure that constitute the “fine structure” of a sound stimulus, slower fluctuations in the sound's envelope represent an important temporal feature. At various stages in the auditory system, neurons exhibit tuning to envelope frequency and have been described as modulation filters. We examine such tuning in the ventral nucleus of the lateral lemniscus (VNLL) of the pentobarbital-anesthetized cat. The VNLL is a large but poorly accessible auditory structure that provides a massive inhibitory input to the inferior colliculus. We test whether envelope filtering effectively applies to the envelope spectrum when multiple envelope components are simultaneously present. We find two broad classes of response with often complementary properties. The firing rate of onset neurons is tuned to a band of modulation frequencies, over which they also synchronize strongly to the envelope waveform. Although most sustained neurons show little firing rate dependence on modulation frequency, some of them are weakly tuned. The latter neurons are usually band-pass or low-pass tuned in synchronization, and a reverse-correlation approach demonstrates that their modulation tuning is preserved to nonperiodic, noisy envelope modulations of a tonal carrier. Modulation tuning to this type of stimulus is weaker for onset neurons. In response to broadband noise, sustained and onset neurons tend to filter out envelope components over a frequency range consistent with their modulation tuning to periodically modulated tones. The results support a role for VNLL in providing temporal reference signals to the auditory midbrain.

scholarly journals Responses of Neurons in the Rat's Ventral Nucleus of the Lateral Lemniscus to Amplitude-Modulated Tones

2006 ◽  
Vol 96 (6) ◽  
pp. 2905-2914 ◽  
Author(s):  
Huiming Zhang ◽  
Jack B. Kelly
Keyword(s):  
Firing Rate ◽  
Transfer Functions ◽  
Modulation Frequency ◽  
Lateral Lemniscus ◽  
Low Pass ◽  
Band Pass ◽  
Contralateral Ear ◽  
Ventral Nucleus ◽  
Vector Strength ◽  
Onset Responses

Recordings were made from single neurons in the rat's ventral nucleus of the lateral lemniscus (VNLL) to determine responses to amplitude-modulated (AM) tones. The neurons were first characterized on the basis of their response to tone bursts presented to the contralateral ear and a distinction was made between those with transient onset responses and those with sustained responses. Sinusoidal AM tones were then presented to the contralateral ear with a carrier that matched the neuron's characteristic frequency (CF). Modulation transfer functions were generated on the basis of firing rate (MTFFR) and vector strength (MTFVS). Ninety-two percent of onset neurons that responded continuously to AM tones had band-pass MTFFRs with best modulation frequencies from 10 to 300 Hz. Fifty-four percent of sustained neurons had band-pass MTFFRs with best modulation frequencies from 10 to 500 Hz; other neurons had band-suppressed, all-pass, low-pass, or high-pass functions. Most neurons showed either band-pass or low-pass MTFVS. Responses were well synchronized to the modulation cycle with maximum vector strengths ranging from 0.37 to 0.98 for sustained neurons and 0.78 to 0.99 for onset neurons. The upper frequency limit for response synchrony was higher than that reported for inferior colliculus, but lower than that seen in more peripheral structures. Results suggest that VNLL neurons, especially those with onset responses to tone bursts, are sensitive to temporal features of sounds and narrowly tuned to different modulation rates. However, there was no evidence of a topographic relation between dorsoventral position along the length of VNLL and best modulation frequency as determined by either firing rate or vector strength.

Two separate inhibitory mechanisms shape the responses of dorsal cochlear nucleus type IV units to narrowband and wideband stimuli

1994 ◽  
Vol 71 (6) ◽  
pp. 2446-2462 ◽  
Author(s):  
I. Nelken ◽  
E. D. Young
Keyword(s):  
Firing Rate ◽  
Cochlear Nucleus ◽  
Inhibitory Effect ◽  
Broadband Noise ◽  
Dorsal Cochlear Nucleus ◽  
Inhibitory Input ◽  
Inhibitory Influence ◽  
Type Ii ◽  
Rate Level ◽  
Type Iv

1. The principal cells of the dorsal cochlear nucleus (DCN) are mostly inhibited by best frequency (BF) tones but are mostly excited by broadband noise (BBN), producing the so-called type IV response characteristic. The narrowband inhibitory responses can be explained by the inhibitory influence of interneurons with type II response characteristics. However, it is not clear that all the details of the type IV responses can be accounted for by this neural circuit. In particular, many type IV units are inhibited by band-reject noise (notch noise); type II units tend to be only weakly excited by these stimuli, if at all. In this paper we study the relationships between the narrowband, inhibitory and the wideband, excitatory regimens of the type IV responses and present the case for the existence of a second inhibitory source in DCN, called the wideband inhibitor (WBI) below. 2. Type IV units were studied using pure tones, noise bands arithmetically centered on BF, notch noise centered on BF, and BBN. We measured the rate-level function (response rate as function of stimulus level) for each stimulus. This paper is based on the responses of 28 type IV units. 3. Evidence for low-threshold inhibitory input to type IV units is derived from analysis of rate-level functions at sound levels just above threshold. Notch noise stimuli of the appropriate notch width produce inhibition at threshold in this regime. When BBN is presented, this inhibition appears to summate with excitation produced by energy in the band of noise centered on BF, resulting in BBN rate-level functions with decreased slope and maximum firing rate. A range of slopes and maximal firing rates is observed, but these variables are strongly correlated and they are negatively correlated with the strength of the inhibition produced by notch noise; this result supports the conclusion that a single inhibitory source is responsible for these effects. 4. By contrast, there is a weak (nonsignificant) positive correlation between the strength of the inhibitory effect of notch noise and the slope/maximal firing rate in response to narrowband stimuli, including BF tones. The contrast between this positive nonsignificant correlation and the significant negative correlation mentioned above suggests that more than one inhibitory effect operates: specifically, the type II input is responsible for inhibition by narrowband stimuli and a different inhibitory source, the WBI, produces inhibition by notch stimuli. 5. Several lines of evidence are given to show that type II units cannot produce the inhibition seen with notch noise stimuli.(ABSTRACT TRUNCATED AT 400 WORDS)

Responses of Neurons in the Ventral Nucleus of the Lateral Lemniscus to Sinusoidally Amplitude Modulated Tones

2006 ◽  
Vol 96 (5) ◽  
pp. 2388-2398 ◽  
Author(s):  
Ranjan Batra
Keyword(s):  
Spontaneous Activity ◽  
Transfer Functions ◽  
Modulation Frequency ◽  
Auditory Pathway ◽  
Modulation Transfer ◽  
Lateral Lemniscus ◽  
Modulation Transfer Functions ◽  
Band Pass ◽  
Acoustic Space ◽  
Ventral Nucleus

Fluctuations in the amplitude of a sound play an important role in our perception of pitch and acoustic space, but their neural analysis has not been fully elucidated. The ventral nucleus of the lateral lemniscus (VNLL) has been implicated in the processing of such temporal features of a sound. This study examines responses of neurons in the VNLL of unanesthetized rabbits to sinusoidally amplitude modulated tones, a type of stimulus that has often been used to investigate encoding of temporal information. Modulation transfer functions of responses were calculated in two ways: based on discharge rates (rMTFs) and on synchronization to the envelope (tMTFs). Among the variety of rMTFs, two types were readily identifiable: flat and band-pass. The responses of neurons exhibiting these types of rMTF differed in several ways. Neurons with flat rMTFs typically had moderate rates of spontaneous activity, sustained responses to short tone bursts, and low-pass or band-pass tMTFs. Neurons with band-pass rMTFs typically had low spontaneous activity, onset responses to short tone bursts, and flat tMTFs. The vast majority synchronized strongly to the modulation envelope. The best modulation frequencies of neurons with band-pass rMTFs extended from 14 to 283 Hz. The presence of neurons with band-pass rMTFs in the VNLL suggests that this nucleus plays a role in converting the temporal code for modulation frequency used in lower structures into a rate-based code for use higher in the auditory pathway. The substantial number of neurons with more complex modulation transfer functions indicates that the VNLL has other functions.

scholarly journals Intrinsic Dynamics in Neuronal Networks. I. Theory

2000 ◽  
Vol 83 (2) ◽  
pp. 808-827 ◽  
Author(s):  
P. E. Latham ◽  
B. J. Richmond ◽  
P. G. Nelson ◽  
S. Nirenberg
Keyword(s):  
Firing Rate ◽  
Firing Pattern ◽  
Neuronal Networks ◽  
Network Connectivity ◽  
Excitatory Input ◽  
High Rate ◽  
Inhibitory Neurons ◽  
Inhibitory Input ◽  
Dynamic Interactions ◽  
Firing Patterns

Many networks in the mammalian nervous system remain active in the absence of stimuli. This activity falls into two main patterns: steady firing at low rates and rhythmic bursting. How are these firing patterns generated? Specifically, how do dynamic interactions between excitatory and inhibitory neurons produce these firing patterns, and how do networks switch from one firing pattern to the other? We investigated these questions theoretically by examining the intrinsic dynamics of large networks of neurons. Using both a semianalytic model based on mean firing rate dynamics and simulations with large neuronal networks, we found that the dynamics, and thus the firing patterns, are controlled largely by one parameter, the fraction of endogenously active cells. When no endogenously active cells are present, networks are either silent or fire at a high rate; as the number of endogenously active cells increases, there is a transition to bursting; and, with a further increase, there is a second transition to steady firing at a low rate. A secondary role is played by network connectivity, which determines whether activity occurs at a constant mean firing rate or oscillates around that mean. These conclusions require only conventional assumptions: excitatory input to a neuron increases its firing rate, inhibitory input decreases it, and neurons exhibit spike-frequency adaptation. These conclusions also lead to two experimentally testable predictions: 1) isolated networks that fire at low rates must contain endogenously active cells and 2) a reduction in the fraction of endogenously active cells in such networks must lead to bursting.

Periodicity coding in the inferior colliculus of the cat. I. Neuronal mechanisms

1988 ◽  
Vol 60 (6) ◽  
pp. 1799-1822 ◽  
Author(s):  
G. Langner ◽  
C. E. Schreiner
Keyword(s):  
Firing Rate ◽  
Inferior Colliculus ◽  
Amplitude Modulation ◽  
Transfer Functions ◽  
Modulation Frequency ◽  
Temporal Structure ◽  
Stimulus Frequency ◽  
Single Units ◽  
Central Nucleus ◽  
Multiple Unit

1. Temporal properties of single- and multiple-unit responses were investigated in the inferior colliculus (IC) of the barbiturate-anesthetized cat. Approximately 95% of recording sites were located in the central nucleus of the inferior colliculus (ICC). Responses to contralateral stimulation with tone bursts and amplitude-modulated tones (100% sinusoidal modulation) were recorded. Five response parameters were determined for neurons at each location: 1) characteristic frequency (CF); 2) onset latency of responses to CF-tones 60 dB above threshold; 3) Q10 dB (CF divided by bandwidth of tuning curve 10 dB above threshold); 4) best modulation frequency for firing rate (rBMF or BMF; amplitude modulation frequency that elicited the highest firing rate); and 5) best modulation frequency for synchronization (sBMF; amplitude modulation frequency that elicited the highest degree of phase-locking to the modulation frequency). 2. Response characteristics for single units and multiple units corresponded closely. A BMF was obtained at almost all recording sites. For units with a similar CF, a range of BMFs was observed. The upper limit of BMF increased approximately proportional to CF/4 up to BMFs as high as 1 kHz. The lower limit of encountered BMFs for a given CF also increased slightly with CF. BMF ranges for single-unit and multiple-unit responses were similar. Twenty-three percent of the responses revealed rBMFs between 10 and 30 Hz, 51% between 30 and 100 Hz, 18% between 100 and 300 Hz, and 8% between 300 and 1000 Hz. 3. For single units with modulation transfer functions of bandpass characteristics, BMFs determined for firing rate and synchronization were similar (r2 = 0.95). 4. Onset latencies for responses to CF tones 60 dB above threshold varied between 4 and 120 ms. Ninety percent of the onset latencies were between 5 and 18 ms. A range of onset latencies was recorded for different neurons with any given CF. The onset response latency of a given unit or unit cluster was significantly correlated with the period of the BMF and the period of the CF (P less than 0.05). 5."Intrinsic oscillations" of short duration, i.e., regularly timed discharges of units in response to stimuli without a corresponding temporal structure, were frequently observed in the ICC. Oscillation intervals were commonly found to be integer multiples of 0.4 ms. Changes of stimulus frequency or intensity had only minor influences on these intrinsic oscillations.(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals Effect of sinusoidally amplitude modulated broadband noise stimuli on stream segregation in individuals with sensorineural hearing loss

2020 ◽  
Author(s):  
Jawahar Antony P ◽  
Animesh Barman
Keyword(s):  
Hearing Loss ◽  
Sensorineural Hearing Loss ◽  
Amplitude Modulation ◽  
Modulation Frequency ◽  
Study Groups ◽  
Normal Hearing ◽  
Broadband Noise ◽  
Sensorineural Hearing ◽  
Stream Segregation ◽  
Temporal Cues

Background and Aim: Auditory stream segre­gation is a phenomenon that splits sounds into different streams. The temporal cues that contri­bute for stream segregation have been previ­ously studied in normal hearing people. In peo­ple with sensorineural hearing loss (SNHL), the cues for temporal envelope coding is not usually affected, while the temporal fine structure cues are affected. These two temporal cues depend on the amplitude modulation frequency. The present study aimed to evaluate the effect of sin­usoidal amplitude modulated (SAM) broadband noises on stream segregation in individuals with SNHL. Methods: Thirty normal hearing subjects and 30 subjects with mild to moderate bilateral SNHL participated in the study. Two experi­ments were performed; in the first experiment, the AB sequence of broadband SAM stimuli was presented, while in the second experiment, only B sequence was presented. A low (16 Hz) and a high (256 kHz) standard modulation fre­quency were used in these experiments. The subjects were asked to find the irregularities in the rhythmic sequence. Results: Both the study groups could identify the irregularities similarly in both the experi­ments. The minimum cumulative delay was sli­ghtly higher in the SNHL group. Conclusion: It is suggested that the temporal cues provided by the broadband SAM noises for low and high standard modulation frequencies were not used for stream segregation by either normal hearing subjects or those with SNHL. Keywords: Stream segregation; sinusoidal amplitude modulation; sensorineural hearing loss

scholarly journals Specific loss of neural sensitivity to interaural time difference of unmodulated noise stimuli following noise-induced hearing loss

2020 ◽  
Vol 124 (4) ◽  
pp. 1165-1182
Author(s):  
Hariprakash Haragopal ◽  
Ryan Dorkoski ◽  
Austin R. Pollard ◽  
Gareth A. Whaley ◽  
Timothy R. Wohl ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Interaural Time Difference ◽  
Acoustic Trauma ◽  
Sound Level ◽  
Broadband Noise ◽  
Neural Responses ◽  
Auditory Midbrain ◽  
Midbrain Neurons ◽  
Perceptual Abilities ◽  
Encode Time

Sensorineural hearing loss compromises perceptual abilities that arise from hearing with two ears, yet its effects on binaural aspects of neural responses are largely unknown. We found that, following severe hearing loss because of acoustic trauma, auditory midbrain neurons specifically lost the ability to encode time differences between the arrival of a broadband noise stimulus to the two ears, whereas the encoding of sound level differences between the two ears remained uncompromised.

Envelope Coding in the Lateral Superior Olive. III. Comparison With Afferent Pathways

1998 ◽  
Vol 79 (1) ◽  
pp. 253-269 ◽  
Author(s):  
Philip X. Joris ◽  
Tom C. T. Yin
Keyword(s):  
Firing Rate ◽  
Auditory Nerve ◽  
Modulation Frequency ◽  
Nerve Fibers ◽  
Cell Populations ◽  
Average Firing Rate ◽  
Afferent Pathways ◽  
Lateral Superior Olive ◽  
Superior Olive ◽  
Auditory Nerve Fibers

Joris, Philip X. and Tom C. T. Yin. Envelope coding in the lateral superior olive. III. Comparison with afferent pathways. J. Neurophysiol. 79: 253–269, 1998. Binaural cues for spatial localization of complex high-frequency sounds are interaural level and time differences (ILDs and ITDs). We previously showed that cells in the lateral superior olive (LSO) are sensitive to ITDs in the envelope of sinusoidally amplitude-modulated (AM) signals up to a modulation frequency of only ∼800 Hz. To understand the limitations in this ITD-sensitivity, we here compare responses to monaural modulation in LSO and its input pathways, derived from cochlear nucleus and medial nucleus of the trapezoid body. These pathways have marked functional and morphological specializations, suggestive of adaptations for timing. Afferent cell populations were identified on the basis of electrophysiological signatures, and for each population, average firing rate and synchronization to AM tones were compared with auditory-nerve fibers and LSO cells. Except for an increase in modulation gain in some subpopulations, synchronization of LSO afferents was very similar to that in auditory nerve fibers in its dependency on sound pressure level (SPL), modulation depth, and modulation frequency. Distributions of cutoff frequencies of modulation transfer functions were largely coextensive with the distribution in auditory nerve. Group delays, measured from the phase of the response modulation as a function of modulation frequency, showed an orderly dependence on characteristic frequency and cell type and little dependence on SPL. Similar responses were obtained to a modulated broadband carrier. Compared with their afferents, LSO cells synchronized to monaurally modulated stimuli with a higher gain but often over a narrower range of modulation frequencies. Considering the scatter in afferent and LSO cell populations, ipsi- and contralateral responses were well matched in cutoff frequency and magnitude of delays. In contrast to their afferents, LSO cells show a decrease in average firing rate at high modulation frequencies. We conclude that the restricted modulation frequency range over which LSO cells show ITD-sensitivity does not result from loss of envelope information along the afferent pathway but is due to convergence or postsynaptic effects at the level of the LSO. The faithful transmission of envelope phase-locking in LSO afferents is consistent with their physiological and morphological adaptations, but these adaptations are not commensurate with the rather small effects of physiological ITDs reported previously, especially when compared with effects of ILDs. We suggest that these adaptations have evolved to allow a comparison of instantaneous amplitude fluctuations at the two ears rather than to extract interaural timing information per se.

Differential Response Properties to Amplitude Modulated Signals in the Dorsal Nucleus of the Lateral Lemniscus of the Mustache Bat and the Roles of GABAergic Inhibition

1997 ◽  
Vol 77 (1) ◽  
pp. 324-340 ◽  
Author(s):  
Lichuan Yang ◽  
George D. Pollak
Keyword(s):  
Phase Locking ◽  
Modulation Frequency ◽  
Tone Burst ◽  
Differential Response ◽  
Gabaergic Inhibition ◽  
Lateral Lemniscus ◽  
Response Properties ◽  
Dorsal Nucleus ◽  
Modulated Signals ◽  
Onset Response

Yang, Lichuan and George D. Pollak. Differential response properties to amplitude modulated signals in the dorsal nucleus of the lateral lemniscus of the mustache bat and the roles of GABAergic inhibition. J. Neurophysiol. 77: 324–340, 1997. We studied the phase-locking of 89 neurons in the dorsal nucleus of the lateral lemniscus (DNLL) of the mustache bat to sinusoidally amplitude modulated (SAM) signals and the influence that GABAergic inhibition had on their response properties. Response properties were determined with tone bursts at each neuron's best frequency and then with a series of SAM signals that had modulation frequencies ranging from 50–100 to 800 Hz in 100-Hz steps. DNLL neurons were divided into two principal types: sustained neurons (55%), which responded throughout the duration of the tone burst, and onset neurons (45%), which responded only at the beginning of the tone burst. Sustained and onset neurons responded differently to SAM signals. Sustained neurons responded with phase-locked discharges to modulation frequencies ≤400–800 Hz. In contrast, 70% of the onset neurons phase-locked only to low modulation frequencies of 100–300 Hz, whereas 30% of the onset neurons did not phase-lock to any modulation frequency. Signal intensity differentially affected the phase-locking of sustained and onset neurons. Sustained neurons exhibited tight phase-locking only at low intensities, 10–30 dB above threshold. Onset neurons, in contrast, maintained strong phase-locking even at relatively high intensities. Blocking GABAergic inhibition with bicuculline had different effects on the phase-locking of sustained and onset neurons. In sustained neurons, there was an overall decline in phase-locking at all modulation frequencies. In contrast, 70% of the onset neurons phase-locked to much higher modulation frequencies than they did when inhibition was intact. The other 30% of onset neurons phase-locked to SAM signals, although they fired only with an onset response to the same signals before inhibition was blocked. In both cases, blocking GABAergic inhibition transformed their responses to SAM signals into patterns that were more like those of sustained neurons. We also propose mechanisms that could explain the differential effects of GABAergic inhibition on onset neurons that locked to low modulation frequencies and on onset neurons that did not lock to any SAM signals before inhibition was blocked. The key features of the proposed mechanisms are the absolute latencies and temporal synchrony of the excitatory and inhibitory inputs.

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