Literature DB >> 8576432

Auditory thalamocortical pathways defined in monkeys by calcium-binding protein immunoreactivity.

M Molinari1, M E Dell'Anna, E Rausell, M G Leggio, T Hashikawa, E G Jones.   

Abstract

This study investigated differentiation of Macaca fuscata auditory thalamus into chemically defined nuclei forming relays to auditory cortical areas. The thalamus was stained immunocytochemically for parvalbumin and 28 kDa calbindin in normals and in brains in which retrogradely transported tracers were injected into middle layers of auditory cortical areas or applied to the cortical surface. Parvalbumin- and calbindin-immunoreactive cells show a complementary distribution in ventral, anterodorsal, posterodorsal, and magnocellular medial geniculate nuclei. The ventral nucleus has a high density of parvalbumin cells and few calbindin cells, and the anterodorsal nucleus has a high density of parvalbumin cells and moderate numbers of calbindin cells. Both nuclei have a dense parvalbumin-immunoreactive neuropil formed by terminations of fibers ascending in the brachium of the inferior colliculus. The posterodorsal nucleus has approximately equal proportions of parvalbumin and calbindin cells; neuropil staining is weak but contains terminations of calbindin-immunoreactive fibers ascending in the midbrain tegmentum. The magnocellular nucleus contains domains of parvalbumin and calbindin cells. Parvalbumin cells in the ventral nucleus project to a central core of auditory cortex with densest parvalbumin immunoreactivity. Those in anterodorsal and posterodorsal nuclei project to surrounding auditory fields with less dense parvalbumin immunoreactivity; those in the magnocellular nucleus project widely to auditory and other fields. Injections of middle cortical layers label a large majority of parvalbumin cells in the ventral, anterodorsal, or posterodorsal nuclei and in the magnocellular nucleus. Superficial deposits label calbindin cells only, usually in more than one nucleus, implying a widespread projection system.

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Year:  1995        PMID: 8576432     DOI: 10.1002/cne.903620203

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


  38 in total

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2.  Mechanisms and streams for processing of "what" and "where" in auditory cortex.

Authors:  J P Rauschecker; B Tian
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3.  Laminar and columnar auditory cortex in avian brain.

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4.  Transformation of temporal processing across auditory cortex of awake macaques.

Authors:  Brian H Scott; Brian J Malone; Malcolm N Semple
Journal:  J Neurophysiol       Date:  2010-11-24       Impact factor: 2.714

Review 5.  Thalamic and cortical pathways supporting auditory processing.

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6.  Neuronal oscillations and multisensory interaction in primary auditory cortex.

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Review 7.  The biological basis of audition.

Authors:  Gregg H Recanzone; Mitchell L Sutter
Journal:  Annu Rev Psychol       Date:  2008       Impact factor: 24.137

8.  Parvalbumin and calbindin expression in parallel thalamocortical pathways in a gleaning bat, Antrozous pallidus.

Authors:  Heather Martin del Campo; Kevin Measor; Khaleel A Razak
Journal:  J Comp Neurol       Date:  2014-07-01       Impact factor: 3.215

9.  Drivers of the primate thalamus.

Authors:  Zita Rovó; István Ulbert; László Acsády
Journal:  J Neurosci       Date:  2012-12-05       Impact factor: 6.167

10.  Thalamic connections of architectonic subdivisions of temporal cortex in grey squirrels (Sciurus carolinensis).

Authors:  Peiyan Wong; Omar A Gharbawie; Lynn E Luethke; Jon H Kaas
Journal:  J Comp Neurol       Date:  2008-10-01       Impact factor: 3.215

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