Literature DB >> 6520630

Swallow-evoked action potentials in vagal preganglionic efferents.

J S Gidda, R K Goyal.   

Abstract

Swallow-evoked potentials in the preganglionic vagal fibers were studied using the single-fiber recording technique in anesthetized opossums. Swallows were evoked by tactile pharyngeal stimulation or electrical stimulation of the cut central end of the superior laryngeal nerve (SLN). Swallowing activity was recorded by the mylohyoid electromyogram and esophageal motility. Sixty-six fibers were studied in which swallowing evoked action potentials. The latencies (from the onset of mylohyoid activity) of evoked responses in different fibers varied from 100 ms to 5 s. The discharge rate of the evoked response was 3-8 action potentials per burst. Each burst lasted 1.1 +/- 0.02 (SE)s. The latencies of evoked spike bursts showed a bimodal distribution. In 34 fibers the latencies were less than 1 s, and in 32 fibers the latencies ranged between 1 and 5 s; these are the short- and long-latency fibers, respectively. Short-latency fibers could easily be distinguished from long-latency fibers based on the influence of SLN-stimulus frequency. Short-latency discharges had low thresholds of activation and were sensitive to changes in the frequency of SLN stimulation, since their latencies decreased and their discharge rate increased with increasing SLN-stimulus frequency. On the other hand, the latencies and discharge rates of long-latency discharges were not modified with changing SLN stimulus frequencies. The conduction velocities of 6 short- and 9 long-latency fibers were 5.64 +/- 0.12 and 5.78 +/- 0.12 (SE) m/s, respectively (P greater than 0.05). The relationship between the latencies of swallow-evoked discharges in the short- and long-latency fibers and the esophageal smooth muscle responses suggested that the short-latency discharges may correlate with the latency of initial inhibition, and the long-latency fibers may correlate with latencies of peristaltic contractions. Based on these temporal relationships, we speculate that vagal efferent fibers showing swallow-evoked, short-latency discharges make contact with intramural inhibitory neurons. They may mediate deglutitive inhibition in the body of the esophagus, relaxation of the lower esophageal sphincter, and receptive relaxation of the fundus of the stomach. The fibers showing late discharges make contact with intramural excitatory neurons and participate in their sequential activation. This dual pathway of activation may be responsible for physiological esophageal peristalsis.

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Year:  1984        PMID: 6520630     DOI: 10.1152/jn.1984.52.6.1169

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  14 in total

Review 1.  Neuronal Control of Esophageal Peristalsis and Its Role in Esophageal Disease.

Authors:  K Nikaki; A Sawada; A Ustaoglu; D Sifrim
Journal:  Curr Gastroenterol Rep       Date:  2019-11-23

Review 2.  Physiology of normal esophageal motility.

Authors:  Raj K Goyal; Arun Chaudhury
Journal:  J Clin Gastroenterol       Date:  2008 May-Jun       Impact factor: 3.062

Review 3.  Swallowing: neurophysiologic control of the esophageal phase.

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

Review 4.  Regulation and dysregulation of esophageal peristalsis by the integrated function of circular and longitudinal muscle layers in health and disease.

Authors:  Ravinder K Mittal
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-07-21       Impact factor: 4.052

5.  Experimental induction of isolated lower esophageal sphincter relaxation in anesthetized opossums.

Authors:  W G Paterson; S Rattan; R K Goyal
Journal:  J Clin Invest       Date:  1986-04       Impact factor: 14.808

6.  Atropine inhibits gastric distension and pharyngeal receptor mediated lower oesophageal sphincter relaxation.

Authors:  R K Mittal; C Chiareli; J Liu; R H Holloway; W Dixon
Journal:  Gut       Date:  1997-09       Impact factor: 23.059

Review 7.  Coordination of peristalsis in pharynx and esophagus.

Authors:  T R Hendrix
Journal:  Dysphagia       Date:  1993       Impact factor: 3.438

Review 8.  Central neural control of esophageal motility: a review.

Authors:  E T Cunningham; P E Sawchenko
Journal:  Dysphagia       Date:  1990       Impact factor: 3.438

9.  Impairment of deglutition reflex by acid-induced esophageal mucosal injury.

Authors:  R J White; G P Morris; W G Paterson
Journal:  Dig Dis Sci       Date:  2001-04       Impact factor: 3.199

10.  A mouse model of pharyngeal dysphagia in amyotrophic lateral sclerosis.

Authors:  Teresa E Lever; Emmanuelle Simon; Kathleen T Cox; Norman F Capra; Kevin F O'Brien; Monica S Hough; Alexander K Murashov
Journal:  Dysphagia       Date:  2009-06-03       Impact factor: 3.438

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