Literature DB >> 8743921

Distribution of peptide-containing nerve fibres in achalasia of the oesophagus.

D A Wattchow1, M Costa.   

Abstract

In this study the innervation of the normal human oesophagus was compared with samples taken from 12 patients undergoing Heller's cardiomyotomy for achalasia. The distribution of all nerve fibres in the oesophageal wall was revealed by immunoreactivity to neuron specific enolase and subpopulations of nerve fibres were revealed by immunoreactivity to vasoactive intestinal peptide, neuropeptide Y, enkephalin and substance P. In healthy oesophagus, many nerve fibres immunoreactive for vasoactive intestinal peptide and neuropeptide Y were present in the circular and longitudinal muscle layers of the oesophageal wall and in the cardia of the stomach, whereas fibres immunoreactive for enkephalin and substance P were uncommon. Neuropeptide Y-reactive fibres were commonly seen around blood vessels. In the myenteric plexus cell bodies reactive for vasoactive intestinal peptide and neuropeptide Y were prevalent, as were varicose and non-varicose fibres. In contrast, samples from patients with achalasia revealed few nerve fibres immunoreactive for vasoactive intestinal peptide or neuropeptide Y in either circular or longitudinal muscle, suggesting damage to the inhibitory motor neurons to the muscle layers. Very few fibres were found that were reactive for neuron-specific enolase, indicating that other fibre population (e.g. excitatory cholinergic motor neurons) are also damaged in achalasia. These abnormalities were observed in biopsies from both the constricted and dilated portions of the oesophagus, but the pattern of innervation in the gastric cardia was normal. Myenteric ganglion cells were seen in the oesophagus in only two patients and varicose nerve fibres in the myenteric plexus were uncommon. Neuropeptide Y-reactive perivascular nerve fibres were still found in achalasia as well as non-varicose nerve fibres in the myenteric plexus. These findings indicate damage to all intrinsic neurons in the oesophageal wall in achalasia; however, extrinsic nerve fibres appear to be intact.

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Year:  1996        PMID: 8743921     DOI: 10.1111/j.1440-1746.1996.tb00294.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  6 in total

Review 1.  Pathophysiology of achalasia.

Authors:  I Hirano
Journal:  Curr Gastroenterol Rep       Date:  1999-06

2.  Serum from achalasia patients alters neurochemical coding in the myenteric plexus and nitric oxide mediated motor response in normal human fundus.

Authors:  S Bruley des Varannes; J Chevalier; S Pimont; J-C Le Neel; M Klotz; K-H Schafer; J-P Galmiche; M Neunlist
Journal:  Gut       Date:  2005-08-16       Impact factor: 23.059

3.  Alterations in the density of interstitial cells of Cajal in achalasia.

Authors:  Arman Kilic; James D Luketich; Rodney J Landreneau; Scott R Owens; Alyssa M Krasinskas; Matthew J Schuchert
Journal:  Dig Dis Sci       Date:  2008-06       Impact factor: 3.199

4.  Facioscapulohumeral muscular dystrophy: a radiologic and manometric study of the pharynx and esophagus.

Authors:  Joerg-Patrick Stübgen
Journal:  Dysphagia       Date:  2008-02-08       Impact factor: 3.438

Review 5.  The spectrum of achalasia: lessons from studies of pathophysiology and high-resolution manometry.

Authors:  Peter J Kahrilas; Guy Boeckxstaens
Journal:  Gastroenterology       Date:  2013-08-21       Impact factor: 22.682

Review 6.  The Pathogenesis and Management of Achalasia: Current Status and Future Directions.

Authors:  Fehmi Ates; Michael F Vaezi
Journal:  Gut Liver       Date:  2015-07       Impact factor: 4.519

  6 in total

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