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The Journal of Neurophysiology Vol. 87 No. 6 June 2002, pp. 2915-2928
Copyright ©2002 by the American Physiological Society
Max-Planck-Institute of Neurobiology, D-82152 Martinsried, Germany
Behrend, Oliver,
Antje Brand,
Christoph Kapfer, and
Benedikt Grothe.
Auditory Response Properties in the Superior Paraolivary Nucleus
of the Gerbil. J. Neurophysiol. 87: 2915-2928, 2002. The ascending auditory pathway is characterized
by parallel processing. At the brain stem level, several structures are
involved that are known to serve different well-defined functions.
However, the function of one prominent brain stem nucleus, the rodent
superior paraolivary nucleus (SPN) and its putative homologue in other mammals, the dorsomedial periolivary nucleus, is unknown. Based on
extracellular recordings from anesthetized gerbils, we tested the role
of the SPN in sound localization and temporal processing. First, the
existence of binaural inputs indicates that the SPN might be involved
in sound localization. Although almost half of the neurons exhibited
binaural interactions (most of them excited from both sides), effects
of interaural time and intensity differences (ITD; IID) were weak and
ambiguous. Thus a straightforward function of SPN in sound localization
appears to be implausible. Second, inputs from octopus and
multipolar/stellate cells of the cochlear nucleus and from principal
cells of the medial nucleus of the trapezoid body could relate to
precise temporal processing in the SPN. Based on discharge types, two
subpopulations of SPN cells were observed: about 60% of the neurons
responded to pure tones with sustained discharges, with irregular spike
patterns and no phase-locking. Only four neurons showed a regular spike
pattern ("chopping"). About 40% of the neurons responded with
phasic ON or OFF discharges. Average first
spike latency observed in neurons with sustained discharges was
significantly shorter than that of ON responders, but had a
considerably higher trial-to-trial variation ("jitter"). A
subpopulation of ON responders showed a jitter of less than
±0.1 ms. Most neurons (66%) responded to sinusoidally
amplitude-modulated sounds (SAM) with an ongoing response, phase-locked
to the stimulus envelope. Again, ON responders showed a
significantly higher temporal precision in the phase-locked discharge
compared with the sustained responders. High variability was observed
among spike-rate-based modulation transfer functions. Histologically, a
massive concentration of cytochemical markers for glycinergic input to
SPN cells was demonstrated. Application of glycine or its blockade
revealed profound effects of glycinergic inhibition on the auditory
responses of SPN neurons. The existence of at least two subpopulations
of neurons is in line with different subsets of SPN cells that can be
distinguished morphologically. One temporally less precise population
might modulate the processing of its target structures by providing a
rather diffuse inhibition. In contrast, precise ON
responders might provide a short, initial inhibitory pulse to its targets.
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