Literature DB >> 6745343

Medullary control of the pontine swallowing neurones in sheep.

M Amri, A Car, A Jean.   

Abstract

The origin of the inputs from the medullary swallowing centre (dorsal region including the nucleus of the solitary tract, or ventral region corresponding to the reticular formation surrounding the nucleus ambigous) to the pontine swallowing neurones (PSNs) was studied in sheep anaesthetized with halothane. Out of 101 PSNs located in the posterior part of the trigeminal (Vth) motor nucleus, 46 were activated by stimulating either the dorsal (21 neurones) or the ventral (25 neurones) region of the ipsilateral medullary swallowing centre, 3-4 mm rostral from the obex. Thirty-one neurones out of the 46 were identified as alpha motoneurones supplying swallowing muscles (mylohyoïd, anterior body of digastric and medial pterygoïd). Their average activation latency through stimulation of the dorsal medullary region was about 1 ms longer than through stimulation of the ventral region (3.63 ms +/- 0.81 versus 2.72 ms +/- 0.32). To determine the origin of the medullary input to the PSNs, we tried to activate the medullary swallowing neurones (MSNs) antidromically through stimulating the posterior part of the Vth motor nucleus, which contains the swallowing motoneurones. Seventy-three MSNs were tested (25 located in the dorsal and 48 in the ventral region). None of the dorsal neurones tested could be antidromically activated by pontine stimulation: 15 ventral neurones showed a clear antidromic response (collision test) with an average latency of 2.5 ms +/- 0.73. These neurones, which send their axons into the pons, were all located in the reticular formation, above the nucleus ambiguus, 3-4 mm rostral from the obex.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1984        PMID: 6745343     DOI: 10.1007/BF00240503

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


  22 in total

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Authors:  M K Warren Cottle; F R Calaresu
Journal:  J Comp Neurol       Date:  1975-05-15       Impact factor: 3.215

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Authors:  A Car; C Roman
Journal:  Exp Brain Res       Date:  1970       Impact factor: 1.972

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Authors:  A Jean
Journal:  J Physiol (Paris)       Date:  1978

Review 6.  Deglutition.

Authors:  A J Miller
Journal:  Physiol Rev       Date:  1982-01       Impact factor: 37.312

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Authors:  A L Bianchi; W M St John
Journal:  Respir Physiol       Date:  1981-08

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Authors:  R Norgren
Journal:  Neuroscience       Date:  1978       Impact factor: 3.590

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Journal:  J Comp Neurol       Date:  1980-06-15       Impact factor: 3.215

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Authors:  D K Morest
Journal:  J Comp Neurol       Date:  1967-08       Impact factor: 3.215

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  16 in total

1.  Central projections of the nodose ganglion and the origin of vagal efferents in the lamb.

Authors:  J M Wild; B M Johnston; P D Gluckman
Journal:  J Anat       Date:  1991-04       Impact factor: 2.610

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Journal:  Dysphagia       Date:  1996       Impact factor: 3.438

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Authors:  A J Miller
Journal:  Dysphagia       Date:  1987       Impact factor: 3.438

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Journal:  Dysphagia       Date:  1989       Impact factor: 3.438

6.  Excitatory and inhibitory postsynaptic potentials in cat hypoglossal motoneurons during swallowing.

Authors:  N Tomomune; M Takata
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

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8.  Neuronal activity in nucleus ambiguous during deglutition and vocalization in conscious monkeys.

Authors:  G Z Chiao; C R Larson; Y Yajima; P Ko; P J Kahrilas
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

9.  Activity of bulbar respiratory neurons during fictive coughing and swallowing in the decerebrate cat.

Authors:  Y Oku; I Tanaka; K Ezure
Journal:  J Physiol       Date:  1994-10-15       Impact factor: 5.182

10.  Evaluating the tongue-hold maneuver using high-resolution manometry and electromyography.

Authors:  Michael J Hammer; Corinne A Jones; Corrine A Jones; Jason D Mielens; Chloe H Kim; Timothy M McCulloch
Journal:  Dysphagia       Date:  2014-06-27       Impact factor: 3.438

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