The upper frequency range in pigeon hearing: Response properties in auditory nerve and cohlear nucleus—is tuning different in birds?

1999 ◽  
Vol 105 (2) ◽  
pp. 1110-1110
Author(s):  
Jean W. Th. Smolders ◽  
Marcus Mueller ◽  
Rainer Klinke
Keyword(s):  
Auditory Nerve ◽  
Frequency Range ◽  
Response Properties

Response Properties of Single Auditory Nerve Fibers in the Mouse

2005 ◽  
Vol 93 (1) ◽  
pp. 557-569 ◽  
Author(s):  
Annette M. Taberner ◽  
M. Charles Liberman
Keyword(s):  
Auditory Nerve ◽  
Dynamic Range ◽  
Phase Locking ◽  
Nerve Fibers ◽  
Cochlear Function ◽  
Response Properties ◽  
Tuning Curves ◽  
Rate Versus ◽  
Interstrain Difference ◽  
Mutant Lines

The availability of transgenic and mutant lines makes the mouse a valuable model for study of the inner ear, and a powerful window into cochlear function can be obtained by recordings from single auditory nerve (AN) fibers. This study provides the first systematic description of spontaneous and sound-evoked discharge properties of AN fibers in mouse, specifically in CBA/CaJ and C57BL/6 strains, both commonly used in auditory research. Response properties of 196 AN fibers from CBA/CaJ and 58 from C57BL/6 were analyzed, including spontaneous rates (SR), tuning curves, rate versus level functions, dynamic range, response adaptation, phase-locking, and the relation between SR and these response properties. The only significant interstrain difference was the elevation of high-frequency thresholds in C57BL/6. In general, mouse AN fibers showed similar responses to other mammals: sharpness of tuning increased with characteristic frequency, which ranged from 2.5 to 70 kHz; SRs ranged from 0 to 120 sp/s, and fibers with low SR (<1 sp/s) had higher thresholds, and wider dynamic ranges than fibers with high SR. Dynamic ranges for mouse high-SR fibers were smaller (<20 dB) than those seen in other mammals. Phase-locking was seen for tone frequencies <4 kHz. Maximum synchronization indices were lower than those in cat but similar to those found in guinea pig.

Band-Pass Response Properties of Rat SI Neurons

2003 ◽  
Vol 90 (3) ◽  
pp. 1379-1391 ◽  
Author(s):  
Catherine E. Garabedian ◽  
Stephanie R. Jones ◽  
Michael M. Merzenich ◽  
Anders Dale ◽  
Christopher I. Moore
Keyword(s):  
Inhibitory Neuron ◽  
Stimulus Onset ◽  
Spike Timing ◽  
Spike Rate ◽  
Frequency Range ◽  
Response Properties ◽  
Temporal Precision ◽  
Band Pass ◽  
Temporal Measures ◽  
Vector Strength

Rats typically employ 4- to 12-Hz “whisking” movements of their vibrissae during tactile exploration. The intentional sampling of signals in this frequency range suggests that neural processing of tactile information may be differentially engaged in this bandwidth. We examined action potential responses in rat primary somatosensory cortex (SI) to a range of frequencies of vibrissa motion. Single vibrissae were mechanically deflected with 5-s pulse trains at rates ≤40 Hz. As previously reported, vibrissa deflection evoked robust neural responses that consistently adapted to stimulus rates ≥3 Hz. In contrast with this low-pass feature of the response, several other characteristics of the response revealed bandpass response properties. While average evoked response amplitudes measured 0–35 ms after stimulus onset typically decreased with increasing frequency, the later components of the response (>15 ms post stimulus) were augmented at frequencies between 3 and 10 Hz. Further, during the steady state, both rate and temporal measures of neural activity, measured as total spike rate or vector strength (a measure of temporal fidelity of spike timing across cycles), showed peak signal values at 5–10 Hz. A minimal biophysical network model of SI layer IV, consisting of an excitatory and inhibitory neuron and thalamocortical input, captured the spike rate and vector strength band-pass characteristics. Further analyses in which specific elements were selectively removed from the model suggest that slow inhibitory influences give rise to the band-pass peak in temporal precision, while thalamocortical adaptation can account for the band-pass peak in spike rate. The presence of these band-pass characteristics may be a general property of thalamocortical circuits that lead rodents to target this frequency range with their whisking behavior.

Response selectivity for multiple dimensions of frequency sweeps in the pallid bat inferior colliculus

1994 ◽  
Vol 72 (3) ◽  
pp. 1061-1079 ◽  
Author(s):  
Z. M. Fuzessery
Keyword(s):  
Inferior Colliculus ◽  
High Frequency ◽  
Low Frequency ◽  
Central Nucleus ◽  
Frequency Change ◽  
Frequency Range ◽  
Low Frequencies ◽  
Response Properties ◽  
Sweep Direction ◽  
Pallid Bat

1. While hunting, the pallid bat uses passive sound localization at low frequencies to find terrestrial prey, and echolocation for general orientation. It must therefore process two different types of acoustic input at the same time. The pallid bat's echolocation pulse is a downward frequency-modulated (FM) sweep from 60 to 30 kHz. This study examined the response selectivity of single neurons in the pallid bat's central nucleus of the inferior colliculus (ICC) for FM sweeps, comparing the response properties of the high-frequency population, tuned to the biosonar pulse, with the low-frequency population, tuned below the pulse. The working hypothesis was that the high-frequency population would exhibit a response selectivity for downward FM sweeps that was not present in the low-frequency population. 2. Neurons were tested for their selectivity for FM sweep direction, duration, frequency range and bandwidth, and rate of frequency change. The extent to which they responded exclusively to tones, noise, and FM sweeps was also examined. Significant differences in the response properties of neurons in the two populations were found. In the low-frequency population, all neurons responded to tones, but only 50% responded to FM sweeps. Only 23% were selective for sweep direction. In the high-frequency population, all neurons responded to FM sweeps, but 31% did not respond to tones. Over one-half of this population was selective for sweep direction, and of those that were selective, all preferred the downward sweep direction of the biosonar pulse. A large percentage (31%) responded exclusively to downward sweeps, and not to tones or upward sweeps. None of the cells in either population responded to noise, or did so only at very high relative thresholds. 3. Both populations contained neurons that were selective for short stimulus durations that approximated the duration of the biosonar pulse, although the percentage was greater in the high-frequency population (58% vs. 20%). In the high-frequency population, 31% of the neurons tested for duration responded exclusively to both the sweep direction and duration of the biosonar pulse. 4. Downward FM-selective neurons, with one exception, were generally insensitive to the rate of frequency change of the FM sweep, as well as the frequency range and bandwidth of the sweep. They responded similarly to both the full 60- to 30-kHz sweep and to 5-kHz bandwidth portions of the full sweep.(ABSTRACT TRUNCATED AT 400 WORDS)

Functional Imaging of the Human Lateral Geniculate Nucleus and Pulvinar

2004 ◽  
Vol 91 (1) ◽  
pp. 438-448 ◽  
Author(s):  
Sabine Kastner ◽  
Daniel H. O'Connor ◽  
Miki M. Fukui ◽  
Hilda M. Fehd ◽  
Uwe Herwig ◽  
...  
Keyword(s):  
Human Brain ◽  
Lateral Geniculate Nucleus ◽  
Functional Anatomy ◽  
Extrastriate Cortex ◽  
Anatomical Location ◽  
Stimulus Contrast ◽  
Frequency Range ◽  
Response Properties ◽  
Contrast Gain ◽  
Lateral Geniculate

In the human brain, little is known about the functional anatomy and response properties of subcortical nuclei containing visual maps such as the lateral geniculate nucleus (LGN) and the pulvinar. Using functional magnetic resonance imaging (fMRI) at 3 tesla (T), collective responses of neural populations in the LGN were measured as a function of stimulus contrast and flicker reversal rate and compared with those obtained in visual cortex. Flickering checkerboard stimuli presented in alternation to the right and left hemifields reliably activated the LGN. The peak of the LGN activation was found to be on average within ±2 mm of the anatomical location of the LGN, as identified on high-resolution structural images. In all visual areas except the middle temporal (MT), fMRI responses increased monotonically with stimulus contrast. In the LGN, the dynamic response range of the contrast function was larger and contrast gain was lower than in the cortex. Contrast sensitivity was lowest in the LGN and V1 and increased gradually in extrastriate cortex. In area MT, responses were saturated at 4% contrast. Response modulation by changes in flicker rate was similar in the LGN and V1 and occurred mainly in the frequency range between 0.5 and 7.5 Hz; in contrast, in extrastriate areas V4, V3A, and MT, responses were modulated mainly in the frequency range between 7.5 and 20 Hz. In the human pulvinar, no activations were obtained with the experimental designs used to probe response properties of the LGN. However, regions in the mediodorsal right and left pulvinar were found to be consistently activated by bilaterally presented flickering checkerboard stimuli, when subjects attended to the stimuli. Taken together, our results demonstrate that fMRI at 3 T can be used effectively to study thalamocortical circuits in the human brain.

scholarly journals Response Properties of the Refractory Auditory Nerve Fiber

2001 ◽  
Vol 2 (3) ◽  
pp. 216-232 ◽  
Author(s):  
Charles A. Miller ◽  
Paul J. Abbas ◽  
Barbara K. Robinson
Keyword(s):  
Nerve Fiber ◽  
Auditory Nerve ◽  
Auditory Nerve Fiber ◽  
Response Properties
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