Literature DB >> 7636017

GABA and glycine in the central auditory system of the mustache bat: structural substrates for inhibitory neuronal organization.

J A Winer1, D T Larue, G D Pollak.   

Abstract

The distribution and morphology of neurons and axonal endings (puncta) immunostained with antibodies to gamma-aminobutyric acid (GABA) and glycine (Gly) were analyzed in auditory brainstem, thalamic, and cortical centers in the mustache bat. The goals of the study were (1) to compare and contrast the location of GABAergic and glycinergic neurons and puncta, (2) to determine whether nuclei containing immunoreactive neurons likewise have a similar concentration of puncta, (3) to assess the uniformity of immunostaining within a nucleus and to consider regional differences that were related to or independent of cytoarchitecture, and (4) to compare the patterns recognized in this bat with those in other mammals. There are nine major conclusions. (1) Glycinergic immunostaining is most pronounced in the hindbrain. (2) In the forebrain, GABA alone is present. (3) Some nuclei have GABAergic or glycinergic neurons exclusively; a few have neither. (4) Although there is sometimes a close relationship between the relative number of immunopositive neurons and the density of the puncta, just as often there is no particular correlation between them; this reflects the fact that many GABAergic and glycinergic neurons project beyond their nucleus of origin. (5) Even nuclei devoid of or with few GABAergic or glycinergic neurons contain relatively abundant numbers of puncta; some neurons receive axosomatic terminals of each type. (6) In a few nuclei there are physiological subregions with specific local patterns of immunostaining. (7) The patterns of immunostaining resemble those in other mammals; the principal exceptions are in nuclei that, in the bat, are hypertrophied (such as those of the lateral lemniscus) and in the medial geniculate body. (8) Cellular colocalization of GABA and Gly is specific to only a few nuclei. (9) GABA and glutamic acid decarboxylase (GAD) immunostaining have virtually identical distributions in each nucleus. Several implications follow. First, the arrangements of GABA and Gly in the central auditory system represent all possible patterns, ranging from mutually exclusive to overlapping within a nucleus to convergence of both types of synaptic endings on single neurons. Second, although both transmitters are present in the hindbrain, glycine appears to be dominant, and it is often associated with circuitry in which precise temporal control of aspects of neuronal discharge is critical. Third, the auditory system, especially at or below the level of the midbrain, contains significant numbers of GABAergic or glycinergic projection neurons. The latter feature distinguishes it from the central visual and somatic sensory pathways.

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Year:  1995        PMID: 7636017     DOI: 10.1002/cne.903550302

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  41 in total

1.  Afferent regulation of inhibitory synaptic transmission in the developing auditory midbrain.

Authors:  C Vale; D H Sanes
Journal:  J Neurosci       Date:  2000-03-01       Impact factor: 6.167

2.  Spectral integration in the inferior colliculus of the mustached bat.

Authors:  S A Leroy; J J Wenstrup
Journal:  J Neurosci       Date:  2000-11-15       Impact factor: 6.167

3.  Reversible inactivation of the dorsal nucleus of the lateral lemniscus reveals its role in the processing of multiple sound sources in the inferior colliculus of bats.

Authors:  R M Burger; G D Pollak
Journal:  J Neurosci       Date:  2001-07-01       Impact factor: 6.167

Review 4.  Inhibitory projections from the ventral nucleus of the lateral lemniscus and superior paraolivary nucleus create directional selectivity of frequency modulations in the inferior colliculus: a comparison of bats with other mammals.

Authors:  George D Pollak; Joshua X Gittelman; Na Li; Ruili Xie
Journal:  Hear Res       Date:  2010-05-06       Impact factor: 3.208

5.  Substrates of auditory frequency integration in a nucleus of the lateral lemniscus.

Authors:  A Yavuzoglu; B R Schofield; J J Wenstrup
Journal:  Neuroscience       Date:  2010-05-06       Impact factor: 3.590

6.  Inhibitory and excitatory response areas of neurons in the central nucleus of the inferior colliculus in unanesthetized chinchillas.

Authors:  Ala Alkhatib; Ulrich W Biebel; Jean W T Smolders
Journal:  Exp Brain Res       Date:  2006-03-31       Impact factor: 1.972

7.  Neural rate and timing cues for detection and discrimination of amplitude-modulated tones in the awake rabbit inferior colliculus.

Authors:  Paul C Nelson; Laurel H Carney
Journal:  J Neurophysiol       Date:  2006-11-01       Impact factor: 2.714

8.  The role of broadband inhibition in the rate representation of spectral cues for sound localization in the inferior colliculus.

Authors:  Bradford J May; Michael Anderson; Matthew Roos
Journal:  Hear Res       Date:  2008-01-26       Impact factor: 3.208

9.  GABA immunoreactivity in auditory and song control brain areas of zebra finches.

Authors:  Raphael Pinaud; Claudio V Mello
Journal:  J Chem Neuroanat       Date:  2007-03-27       Impact factor: 3.052

10.  Rethinking tuning: in vivo whole-cell recordings of the inferior colliculus in awake bats.

Authors:  Ruili Xie; Joshua X Gittelman; George D Pollak
Journal:  J Neurosci       Date:  2007-08-29       Impact factor: 6.167

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