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 inJournal of Comparative Physiology Vol. 197; no. 1; pp. 97 - 108
Main Authors Rose, Gary J, Leary, Christopher J, Edwards, Christofer J
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Berlin/Heidelberg : Springer-Verlag 01.01.2011
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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.
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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SSID ssj0002121
ssj0036119
Score 2.1558373
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....
SourceID pubmedcentral
proquest
crossref
pubmed
springer
fao
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 97
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
URI https://link.springer.com/article/10.1007/s00359-010-0591-8
https://www.ncbi.nlm.nih.gov/pubmed/20931335
https://www.proquest.com/docview/821743478
https://search.proquest.com/docview/822360969
https://search.proquest.com/docview/869580905
https://pubmed.ncbi.nlm.nih.gov/PMC3111073
Volume 197
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