Interval-counting neurons in the anuran auditory midbrain: factors underlying diversity of interval tuning
In anurans, the temporal patterning of sound pulses is the primary information used for differentiating between spectrally similar calls. One class of midbrain neurons, referred to as ‘interval-counting' cells, appears to be particularly important for discriminating among calls that differ in p...
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Published in | Journal of Comparative Physiology Vol. 197; no. 1; pp. 97 - 108 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Berlin/Heidelberg : Springer-Verlag
01.01.2011
Springer-Verlag Springer Nature B.V |
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Abstract | In anurans, the temporal patterning of sound pulses is the primary information used for differentiating between spectrally similar calls. One class of midbrain neurons, referred to as ‘interval-counting' cells, appears to be particularly important for discriminating among calls that differ in pulse repetition rate (PRR). These cells only respond after several pulses are presented with appropriate interpulse intervals. Here we show that the range of selectivity and sharpness of interval tuning vary considerably across neurons. Whole-cell recordings revealed that neurons showing temporally summating excitatory postsynaptic potentials (EPSPs) with little or no inhibition or activity-dependent enhancement of excitation exhibited low-pass or band-pass tuning to slow PRRs. Neurons that showed inhibition and rate-dependent enhancement of excitation, however, were band-pass or high-pass to intermediate or fast PRRs. Surprisingly, across cells, interval tuning based on membrane depolarization and spike rate measures were not significantly correlated. Neurons that lacked inhibition showed the greatest disparities between these two measures of interval tuning. Cells that showed broad membrane potential-based tuning, for example, varied considerably in their spike rate-based tuning; narrow spike rate-based tuning resulted from ‘thresholding' processes, whereby only the largest depolarizations triggered spikes. The potential constraints associated with generating interval tuning in this manner are discussed. |
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AbstractList | In anurans, the temporal patterning of sound pulses is the primary information used for differentiating between spectrally similar calls. One class of midbrain neurons, referred to as 'interval-counting' cells, appears to be particularly important for discriminating among calls that differ in pulse repetition rate (PRR). These cells only respond after several pulses are presented with appropriate interpulse intervals. Here we show that the range of selectivity and sharpness of interval tuning vary considerably across neurons. Whole-cell recordings revealed that neurons showing temporally summating excitatory postsynaptic potentials (EPSPs) with little or no inhibition or activity-dependent enhancement of excitation exhibited low-pass or band-pass tuning to slow PRRs. Neurons that showed inhibition and rate-dependent enhancement of excitation, however, were band-pass or high-pass to intermediate or fast PRRs. Surprisingly, across cells, interval tuning based on membrane depolarization and spike rate measures were not significantly correlated. Neurons that lacked inhibition showed the greatest disparities between these two measures of interval tuning. Cells that showed broad membrane potential-based tuning, for example, varied considerably in their spike rate-based tuning; narrow spike rate-based tuning resulted from 'thresholding' processes, whereby only the largest depolarizations triggered spikes. The potential constraints associated with generating interval tuning in this manner are discussed. Many anurans use primarily the temporal patterning of sound pulses for differentiating between spectrally similar conspecific and heterospecific call types. ‘Interval-counting’ midbrain neurons appear to be particularly important for discriminating among calls that differ in pulse repetition rate (PRR). These cells respond selectively over a particular range of PRRs and only after several pulses have occurred with the appropriate timing; single, brief sound pulses do not elicit spikes. Although most interval-counting cells examined thus far are tuned to PRRs of approximately 30 to 100 pulses/s, some are selective for slower PRRs. In addition to differences in best rate, we show that the sharpness of interval tuning varies considerably across interval-counting neurons. To further investigate the processes that determine interval tuning, we made whole-cell recordings from cells of this type. Neurons that showed temporally summating EPSPs, with little or no inhibition or activity-dependent enhancement of excitation, exhibited low-pass or band-pass tuning to slow PRRs. Neurons that were band-pass or high-pass to intermediate or fast PRRs, however, showed inhibition and rate-dependent enhancement of excitation ( Edwards et al., 2007 ). Surprisingly, across cells, interval tuning values calculated from membrane depolarization and spike rate measures were not significantly correlated. Neurons that showed sharp membrane depolarization-based tuning generally showed sharp spike-rate-based tuning. However, cells that showed broader membrane potential-based tuning varied considerably in their spike rate-based tuning; narrow spike-rate tuning resulted from ‘thresholding’ processes, whereby only the largest depolarizations triggered spikes. Neurons that lacked inhibition showed the greatest disparities between these two measures of interval tuning. In anurans, the temporal patterning of sound pulses is the primary information used for differentiating between spectrally similar calls. One class of midbrain neurons, referred to as 'interval-counting' cells, appears to be particularly important for discriminating among calls that differ in pulse repetition rate (PRR). These cells only respond after several pulses are presented with appropriate interpulse intervals. Here we show that the range of selectivity and sharpness of interval tuning vary considerably across neurons. Whole-cell recordings revealed that neurons showing temporally summating excitatory postsynaptic potentials (EPSPs) with little or no inhibition or activity-dependent enhancement of excitation exhibited low-pass or band-pass tuning to slow PRRs. Neurons that showed inhibition and rate-dependent enhancement of excitation, however, were band-pass or high-pass to intermediate or fast PRRs. Surprisingly, across cells, interval tuning based on membrane depolarization and spike rate measures were not significantly correlated. Neurons that lacked inhibition showed the greatest disparities between these two measures of interval tuning. Cells that showed broad membrane potential-based tuning, for example, varied considerably in their spike rate-based tuning; narrow spike rate-based tuning resulted from 'thresholding' processes, whereby only the largest depolarizations triggered spikes. The potential constraints associated with generating interval tuning in this manner are discussed.[PUBLICATION ABSTRACT] |
Author | Leary, Christopher J Edwards, Christofer J Rose, Gary J |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20931335$$D View this record in MEDLINE/PubMed |
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Keywords | Whole-cell Temporal processing Midbrain Amplitude modulation Auditory |
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Snippet | In anurans, the temporal patterning of sound pulses is the primary information used for differentiating between spectrally similar calls. One class of midbrain... Many anurans use primarily the temporal patterning of sound pulses for differentiating between spectrally similar conspecific and heterospecific call types.... |
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SubjectTerms | Acoustic Stimulation - methods Animal Physiology Animals Anura Auditory Pathways - physiology Auditory Perception - physiology Biomedical and Life Sciences Excitatory Postsynaptic Potentials - physiology Life Sciences Mesencephalon - cytology Neural Inhibition - physiology Neurons - physiology Neurosciences Original Paper Patch-Clamp Techniques Psychoacoustics Reaction Time - physiology Time Factors Zoology |
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Title | Interval-counting neurons in the anuran auditory midbrain: factors underlying diversity of interval tuning |
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