Literature DB >> 105921

The cingular vocalization pathway in the squirrel monkey.

U Jürgens, R Pratt.   

Abstract

In 39 squirrel monkeys (Saimiri sciureus), the effects of various brain lesions on vocalizations elicited from the precallosal cingulate gyrus were tested. It was found that lesions abolishing the "cingular vocalization" completely can be traced from the stimulation site continuously down to the laryngeal motoneurons in the nucleus ambiguus. The pathway thus determined (Fig. 4) travels from the precallosal cingulate gyrus through the frontal white matter and enters the internal capsule from a dorsolateral position. The pathway then follows this structure in a medio-caudal direction down to the caudal diencephalon. Here, the effective lesions leave the corticospinal tract and ascend dorsally into the periaqueductal grey. The pathway follows this structure to its end where it sweeps lateral through the parabrachial area and then descends through the lateral pons and ventrolateral medulla to the nucleus ambiguus. In nine of the animals, in addition, the effects of bilateral anterior cingular lesions on vocalizations elicited in other brain areas were tested. It was found that the only vocalization-eliciting area which becomes ineffective after destruction of the anterior cingulate gyrus is the postero-medial orbital cortex.

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Year:  1979        PMID: 105921     DOI: 10.1007/bf00239145

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


  21 in total

1.  Role of the periaqueductal grey in vocal expression of emotion.

Authors:  U Jürgens; R Pratt
Journal:  Brain Res       Date:  1979-05-11       Impact factor: 3.252

2.  Organization of the subcortical system governing defence and flight reactions in the cat.

Authors:  A FERNANDEZ DE MOLINA; R W HUNSPERGER
Journal:  J Physiol       Date:  1962-02       Impact factor: 5.182

3.  Experimental mutism resulting from periaqueductal lesions in cats.

Authors:  J ADAMETZ; J L O'LEARY
Journal:  Neurology       Date:  1959-10       Impact factor: 9.910

4.  Studies on the supracallosal mesial cortex of unanesthetized, conscious mammals. II. Monkey. A. Movements elicited by electrical stimulation.

Authors:  J R HUGHES; J A MAZUROWSKI
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1962-08

5.  Somatic and visceral responses from the cingulate gyrus.

Authors:  M J SHOWERS; E C CROSBY
Journal:  Neurology       Date:  1958-07       Impact factor: 9.910

6.  Somato-motor, autonomic and electrocorticographic responses to electrical stimulation of rhinencephalic and other structures in primates, cat, and dog; a study of responses from the limbic, subcallosal, orbito-insular, piriform and temporal cortex, hippocampus-fornix and amygdala.

Authors:  B R KAADA
Journal:  Acta Physiol Scand Suppl       Date:  1951

7.  Reinforcing concomitants of electrically elicited vocalizations.

Authors:  U Jürgens
Journal:  Exp Brain Res       Date:  1976-09-24       Impact factor: 1.972

8.  Aphasia with infarction in the territory of the anterior cerebral artery.

Authors:  A B Rubens
Journal:  Cortex       Date:  1975-09       Impact factor: 4.027

9.  Projections from the cortical larynx area in the squirrel monkey.

Authors:  U Jürgens
Journal:  Exp Brain Res       Date:  1976-06-30       Impact factor: 1.972

10.  Vocal repertoire of the squirrel monkey (Saimiri sciureus), its analysis and significance.

Authors:  P Winter; D Ploog; J Latta
Journal:  Exp Brain Res       Date:  1966       Impact factor: 1.972

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  16 in total

1.  Factors influencing neural activity in parabrachial regions during cat vocalizations.

Authors:  G R Farley; S M Barlow; R Netsell
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

2.  The relationship of periaqueductal gray neurons to vocalization and laryngeal EMG in the behaving monkey.

Authors:  C R Larson; M K Kistler
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

3.  The squirrel monkey as an experimental model in the study of cerebral organization of emotional vocal utterances.

Authors:  U Jürgens
Journal:  Eur Arch Psychiatry Neurol Sci       Date:  1986

4.  Reduced speech activity and hypokinetic phonation in communicating hydrocephalus following subarachnoid hemorrhage.

Authors:  S Gackenholz; D von Cramon
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

5.  Cooperative vocal control in marmoset monkeys via vocal feedback.

Authors:  Jung Yoon Choi; Daniel Y Takahashi; Asif A Ghazanfar
Journal:  J Neurophysiol       Date:  2015-04-29       Impact factor: 2.714

6.  Pitch underlies activation of the vocal system during affective vocalization.

Authors:  Michel Belyk; Steven Brown
Journal:  Soc Cogn Affect Neurosci       Date:  2015-06-15       Impact factor: 3.436

7.  Topographic representation of vocal frequency demonstrated by microstimulation of anterior cingulate cortex in the echolocating bat, Pteronotus parnelli parnelli.

Authors:  D M Gooler; W E O'Neill
Journal:  J Comp Physiol A       Date:  1987-08       Impact factor: 1.836

8.  In vivo animation of auditory-language-induced gamma-oscillations in children with intractable focal epilepsy.

Authors:  Erik C Brown; Robert Rothermel; Masaaki Nishida; Csaba Juhász; Otto Muzik; Karsten Hoechstetter; Sandeep Sood; Harry T Chugani; Eishi Asano
Journal:  Neuroimage       Date:  2008-03-20       Impact factor: 6.556

9.  The laryngeal sensory pathway and its role in phonation. A brain lesioning study in the squirrel monkey.

Authors:  U Jürgens; A Kirzinger
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

10.  Activation of frontal neocortical areas by vocal production in marmosets.

Authors:  Cristiano S Simões; Paulo V R Vianney; Marco Marcondes de Moura; Marco A M Freire; Luiz E Mello; Koichi Sameshima; John F Araújo; Miguel A L Nicolelis; Claudio V Mello; Sidarta Ribeiro
Journal:  Front Integr Neurosci       Date:  2010-09-23
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