Literature DB >> 1594619

Monaural interaction of excitation and inhibition in the medial superior olive of the mustached bat: an adaptation for biosonar.

B Grothe1, M Vater, J H Casseday, E Covey.   

Abstract

In most mammals, the superior olive is the first stage for binaural interaction. Neurons in the medial superior olive (MSO) receive excitatory input from both ears and are sensitive to interaural time or phase differences of low-frequency sounds. The mustached bat (Pteronotus parnellii parnellii), a small echolocating species with high-frequency hearing, probably does not use interaural time or phase differences as cues for sound localization. Although the mustached bat has a large MSO, there is some evidence that it is functionally different from the MSO in nonecholocating mammals. Most MSO neurons in the mustached bat are monaural, excited by a contralateral sound. Their responses are phasic and correlated with either the onset or the offset of a sound. As a first step in determining the origin of these phasic monaural responses, we traced the connections of the MSO by using both retrograde and anterograde transport methods. Excitatory inputs to the MSO originate from spherical cells in the anteroventral cochlear nucleus, almost exclusively from the contralateral side. Glycinergic inhibitory input is relayed from the contralateral cochlear nucleus through the medial nucleus of the trapezoid body. To investigate the interactions of the contralateral excitatory and inhibitory inputs at the level of the MSO cell, we recorded sound-evoked responses and applied glycine or its antagonist by using microiontophoresis. The results show that the phasic response to a contralateral sound is created by interaction of a sustained excitatory input with a sustained inhibitory input, also from the contralateral ear. Whether the response is to the onset or offset of a sound is determined by the relative timing between the excitatory and inhibitory inputs. Thus, in MSO of the mustached bat, the ipsilateral excitatory pathway from the cochlear nucleus seen in animals with low-frequency hearing is virtually absent, and the MSO is adapted for timing analysis by using input from only the contralateral ear.

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Year:  1992        PMID: 1594619      PMCID: PMC49238          DOI: 10.1073/pnas.89.11.5108

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  22 in total

1.  Interaural time sensitivity in medial superior olive of cat.

Authors:  T C Yin; J C Chan
Journal:  J Neurophysiol       Date:  1990-08       Impact factor: 2.714

2.  Functional organization of ascending and descending connections of the cochlear nucleus of horseshoe bats.

Authors:  M Vater; A S Feng
Journal:  J Comp Neurol       Date:  1990-02-15       Impact factor: 3.215

3.  Immunocytochemical evidence for inhibitory and disinhibitory circuits in the superior olive.

Authors:  J C Adams; E Mugnaini
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4.  Binaural properties of single units in the superior olivary complex of the mustached bat.

Authors:  E Covey; M Vater; J H Casseday
Journal:  J Neurophysiol       Date:  1991-09       Impact factor: 2.714

5.  Recordings from cat trapezoid body and HRP labeling of globular bushy cell axons.

Authors:  G A Spirou; W E Brownell; M Zidanic
Journal:  J Neurophysiol       Date:  1990-05       Impact factor: 2.714

6.  Connections of the superior olivary complex in the rufous horseshoe bat Rhinolophus rouxi.

Authors:  J H Casseday; E Covey; M Vater
Journal:  J Comp Neurol       Date:  1988-12-15       Impact factor: 3.215

7.  Characterization of HRP-labeled globular bushy cells in the cat anteroventral cochlear nucleus.

Authors:  P H Smith; W S Rhode
Journal:  J Comp Neurol       Date:  1987-12-15       Impact factor: 3.215

8.  Functional organization of the dog superior olivary complex: an anatomical and electrophysiological study.

Authors:  J M Goldberg; P B Brown
Journal:  J Neurophysiol       Date:  1968-07       Impact factor: 2.714

9.  Interaural time and intensity coding in superior olivary complex and inferior colliculus of the echolocating bat Molossus ater.

Authors:  G Harnischfeger; G Neuweiler; P Schlegel
Journal:  J Neurophysiol       Date:  1985-01       Impact factor: 2.714

10.  The projections of principal cells of the medial nucleus of the trapezoid body in the cat.

Authors:  K M Spangler; W B Warr; C K Henkel
Journal:  J Comp Neurol       Date:  1985-08-15       Impact factor: 3.215

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3.  The functional role of GABA and glycine in monaural and binaural processing in the inferior colliculus of horseshoe bats.

Authors:  M Vater; H Habbicht; M Kössl; B Grothe
Journal:  J Comp Physiol A       Date:  1992-11       Impact factor: 1.836

4.  Functional role of GABAergic and glycinergic inhibition in the intermediate nucleus of the lateral lemniscus of the big brown bat.

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Journal:  J Neurophysiol       Date:  2009-04-15       Impact factor: 2.714

5.  Physiology and anatomy of neurons in the medial superior olive of the mouse.

Authors:  Matthew J Fischl; R Michael Burger; Myriam Schmidt-Pauly; Olga Alexandrova; James L Sinclair; Benedikt Grothe; Ian D Forsythe; Conny Kopp-Scheinpflug
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