Literature DB >> 1864326

Vocalization-correlated single-unit activity in the brain stem of the squirrel monkey.

A Kirzinger1, U Jürgens.   

Abstract

The brain stems of 17 squirrel monkeys (Saimiri sciureus) were systematically explored for vocalization-related single-unit activity during calls electrically elicited from the periaqueductal grey. Of 12,280 cells tested, 1151 fired in relation to vocalization. Of these, 587 reacted to external acoustic stimuli and started firing after vocalization onset. As most of these cells were located in classical auditory relay structures, they probably represent auditory neurones reacting indirectly to self-produced vocalization due to auditory feedback. Seven cells reacted to acoustic stimuli but fired in advance of self-produced vocalization. These cells were located in the pericentral inferior colliculus, dorsal nucleus of the lateral lemniscus, dorsomedial to the ventral nucleus of the lateral lemniscus and immediately lateral to the central grey. They are probably engaged in tuning the auditory system to process self-generated sounds differently from external sounds. 261 neurones reacted to nonphonatory oral movements (chewing, swallowing) and started firing after vocalization onset. These neurones were widely distributed within the brain stem, with the highest density in the spinal trigeminal nucleus and medially adjacent reticular formation. The majority of these cells seem to react to proprioceptive and tactile stimuli generated by phonatory and nonphonatory oral activities. Some of them may exert motor control on muscles that come into play at later stages of phonation. 57 neurones reacted to nonphonatory oral movements but fired in advanced of vocalization onset. These neurones were located mainly in the trigeminal motor nucleus, nucl. ambiguous, reticular formation around these nuclei, parabrachial region and lateral vestibular nucleus. Their role in motor control seems to be related to specific muscles rather than specific functions. 100 of the vocalization-related cells showed a correlation with respiration. Expiration-related cells were found in and around the rostral nucl. ambiguous and in the reticular formation dorsal to the facial nucleus. Inspiration-related cells were located in the rostral and caudal nucl. ambiguous regions, ventrolateral solitary tract nucleus and the lateral reticular formation below the trigeminal motor nucleus. Most of these cells probably represent premotor neurones of respiratory muscles and laryngeal motoneurones of the cricothyroid and posterior cricoarytenoid muscles. Finally, a last group of cells was found that was unresponsive to chewing and swallowing movements, quiet breathing and acoustic stimuli, but changed activity during vocalization. 38 of them became active before vocalization and cricothyroid activity, and 101 afterward.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1864326     DOI: 10.1007/bf00230967

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  78 in total

1.  Monosynaptic excitation of thoracic motoneurones by inspiratory neurones of the nucleus tractus solitarius in the cat.

Authors:  J Duffin; J Lipski
Journal:  J Physiol       Date:  1987-09       Impact factor: 5.182

2.  Projections of the internal branch of the superior laryngeal nerve of the cat.

Authors:  G E Lucier; R Egizii; J O Dostrovsky
Journal:  Brain Res Bull       Date:  1986-05       Impact factor: 4.077

3.  Respiratory neurones of the ventrolateral nucleus of the solitary tract of cat: vagal input, spinal connections and morphological identification.

Authors:  C von Euler; J N Hayward; I Marttila; R J Wyman
Journal:  Brain Res       Date:  1973-10-26       Impact factor: 3.252

4.  Parabrachial nucleus neurons projecting to the lower brain stem and the spinal cord. A study in the cat by the Fink-Heimer and the horseradish peroxidase methods.

Authors:  Y Takeuchi; M Uemura; K Matsuda; R Matsushima; N Mizuno
Journal:  Exp Neurol       Date:  1980-11       Impact factor: 5.330

5.  Respiratory activity of the cricothyroid muscle.

Authors:  O P Mathew; F B Sant'Ambrogio; G E Woodson; G Sant'Ambrogio
Journal:  Ann Otol Rhinol Laryngol       Date:  1988 Nov-Dec       Impact factor: 1.547

6.  Single-unit activity in bulbar reticular formation during food ingestion in chronic cats.

Authors:  K Hiraba; M Taira; Y Sahara; Y Nakamura
Journal:  J Neurophysiol       Date:  1988-10       Impact factor: 2.714

7.  Somatotopic organization of the hypoglossal nucleus: a HRP study in the rat.

Authors:  E B Krammer; T Rath; M F Lischka
Journal:  Brain Res       Date:  1979-07-20       Impact factor: 3.252

8.  Somatotopic representation of facial muscles within the facial nucleus of the mouse. A study using the retrograde horseradish peroxidase and cell degeneration techniques.

Authors:  M Komiyama; H Shibata; T Suzuki
Journal:  Brain Behav Evol       Date:  1984       Impact factor: 1.808

9.  Periaqueductal gray neuronal activity associated with laryngeal EMG and vocalization in the awake monkey.

Authors:  C R Larson; M K Kistler
Journal:  Neurosci Lett       Date:  1984-05-18       Impact factor: 3.046

10.  Somatotopic representation of the laryngeal motoneurons in the medulla of monkeys.

Authors:  Y Yoshida; T Mitsumasu; M Hirano; T Kanaseki
Journal:  Acta Otolaryngol       Date:  1985 Sep-Oct       Impact factor: 1.494

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  16 in total

1.  Speaking modifies voice-evoked activity in the human auditory cortex.

Authors:  G Curio; G Neuloh; J Numminen; V Jousmäki; R Hari
Journal:  Hum Brain Mapp       Date:  2000-04       Impact factor: 5.038

2.  Regional differences in length change and electromyographic heterogeneity in sternohyoid muscle during infant mammalian swallowing.

Authors:  Nicolai Konow; Allan Thexton; A W Crompton; Rebecca Z German
Journal:  J Appl Physiol (1985)       Date:  2010-06-10

Review 3.  Inspiring song: The role of respiratory circuitry in the evolution of vertebrate vocal behavior.

Authors:  Charlotte L Barkan; Erik Zornik
Journal:  Dev Neurobiol       Date:  2020-05-19       Impact factor: 3.964

Review 4.  Corollary discharge inhibition and audition in the stridulating cricket.

Authors:  J F A Poulet
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2005-11-04       Impact factor: 1.836

5.  Brain stimulation-induced changes of phonation in the squirrel monkey.

Authors:  J Dressnandt; U Jürgens
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 6.  Corollary Discharge Mechanisms During Vocal Production in Marmoset Monkeys.

Authors:  Steven J Eliades; Xiaoqin Wang
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2019-06-29

7.  Projections of the ventrolateral pontine vocalization area in the squirrel monkey.

Authors:  Stefanie Hannig; Uwe Jürgens
Journal:  Exp Brain Res       Date:  2005-11-16       Impact factor: 1.972

Review 8.  Laryngeal motor cortex and control of speech in humans.

Authors:  Kristina Simonyan; Barry Horwitz
Journal:  Neuroscientist       Date:  2011-02-28       Impact factor: 7.519

9.  Multi-sensory integration in brainstem and auditory cortex.

Authors:  Gregory J Basura; Seth D Koehler; Susan E Shore
Journal:  Brain Res       Date:  2012-08-24       Impact factor: 3.252

10.  Functional neuroanatomy of human voluntary cough and sniff production.

Authors:  Kristina Simonyan; Ziad S Saad; Torrey M J Loucks; Christopher J Poletto; Christy L Ludlow
Journal:  Neuroimage       Date:  2007-05-24       Impact factor: 6.556

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