Literature DB >> 8653176

Neural control of vocalization: respiratory and emotional influences.

P J Davis1, S P Zhang, A Winkworth, R Bandler.   

Abstract

Previous research has shown that a region of the midbrain, the periaqueductal gray matter (PAG), is critical for vocalization. In this review, we describe the results of previous investigations in which we sought to find out how PAG neurons integrate the activity and precise timing of respiratory, laryngeal, and oral muscle activity for natural-sounding vocalization using the technique of excitatory amino acid microinjections in cats. In these studies, all surgical procedures were carried out under deep anaesthesia. In the precollicular decerebrate cat two general types of vocalization, classified as voiced and unvoiced, could be evoked by exciting neurons in the lateral part of the intermediate part of the PAG. The patterns of evoked electromyographic activity were strikingly similar to previously reported patterns of human muscle activity. Coordinated patterns of activity were evoked with just-threshold excitation leading to the conclusion that patterned muscle activity corresponding to the major categories of voiced and voiceless sound production are represented in the PAG. In a parallel series of human and animal experiments, we also determined that the speech and vocalization respiratory patterns are integrated and coordinated with afferent signals related to lung volume. These data have led to the proposal of a new hypothesis for the neural control of vocalization: that the PAG is a crucial brain site for mammalian voice production, not only in the production of emotional or involuntary sounds, but also as a generator of specific respiratory and laryngeal motor patterns essential for human speech and song.

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Year:  1996        PMID: 8653176     DOI: 10.1016/s0892-1997(96)80016-6

Source DB:  PubMed          Journal:  J Voice        ISSN: 0892-1997            Impact factor:   2.009


  11 in total

1.  Projections of preBötzinger complex neurons in adult rats.

Authors:  Wenbin Tan; Silvia Pagliardini; Paul Yang; Wiktor A Janczewski; Jack L Feldman
Journal:  J Comp Neurol       Date:  2010-05-15       Impact factor: 3.215

2.  Functional connectivity of PAG with core limbic system and laryngeal cortico-motor structures during human phonation.

Authors:  Jessica Galgano; Spiro Pantazatos; Kachina Allen; Ted Yanagihara; Joy Hirsch
Journal:  Brain Res       Date:  2018-11-27       Impact factor: 3.252

3.  Modification of spectral features by nonhuman primates.

Authors:  Daniel J Weiss; Cara F Hotchkin; Susan E Parks
Journal:  Behav Brain Sci       Date:  2014-12       Impact factor: 12.579

4.  Trigeminal and telencephalic projections to jaw and other upper vocal tract premotor neurons in songbirds: sensorimotor circuitry for beak movements during singing.

Authors:  J M Wild; N E O Krützfeldt
Journal:  J Comp Neurol       Date:  2012-02-15       Impact factor: 3.215

5.  Brainstem regions involved in the expiration reflex. A c-fos study in anesthetized cats.

Authors:  Ivan Poliacek; Erika Halasova; Jan Jakus; Peter Murin; Helena Barani; Albert Stransky; Donald C Bolser
Journal:  Brain Res       Date:  2007-10-02       Impact factor: 3.252

Review 6.  The respiratory-vocal system of songbirds: anatomy, physiology, and neural control.

Authors:  Marc F Schmidt; J Martin Wild
Journal:  Prog Brain Res       Date:  2014       Impact factor: 2.453

7.  Human brain activation during phonation and exhalation: common volitional control for two upper airway functions.

Authors:  Torrey M J Loucks; Christopher J Poletto; Kristina Simonyan; Catherine L Reynolds; Christy L Ludlow
Journal:  Neuroimage       Date:  2007-03-12       Impact factor: 6.556

8.  Humans identify negative (but not positive) arousal in silver fox vocalizations: implications for the adaptive value of interspecific eavesdropping.

Authors:  Piera Filippi; Svetlana S Gogoleva; Elena V Volodina; Ilya A Volodin; Bart de Boer
Journal:  Curr Zool       Date:  2017-06-20       Impact factor: 2.624

9.  A challenge to human evolution-cognitive dissonance.

Authors:  Leonid Perlovsky
Journal:  Front Psychol       Date:  2013-04-10

10.  Eliminating the VGlut2-Dependent Glutamatergic Transmission of Parvalbumin-Expressing Neurons Leads to Deficits in Locomotion and Vocalization, Decreased Pain Sensitivity, and Increased Dominance.

Authors:  Diana M Roccaro-Waldmeyer; Franck Girard; Daniele Milani; Elisabetta Vannoni; Laurent Prétôt; David P Wolfer; Marco R Celio
Journal:  Front Behav Neurosci       Date:  2018-07-18       Impact factor: 3.558

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