Alterations inN-methyl-d-aspartate receptor subunits in primary sensory neurons following acid-induced esophagitis in cats
Male
0301 basic medicine
Eosinophil Peroxidase
Neutrophils
Blotting, Western
Immunohistochemistry
Receptors, N-Methyl-D-Aspartate
Disease Models, Animal
Protein Subunits
03 medical and health sciences
Esophagus
Neutrophil Infiltration
Ganglia, Spinal
Cats
Gastroesophageal Reflux
Animals
Esophagitis
Protein Isoforms
Female
Nodose Ganglion
Hydrochloric Acid
Peroxidase
DOI:
10.1152/ajpgi.90419.2008
Publication Date:
2008-10-31T01:09:06Z
AUTHORS (7)
ABSTRACT
The excitatory amino acid glutamate plays an important role in the development of neuronal sensitization and the ionotropic N-methyl-d-aspartate receptor (NMDAR) is one of the major receptors involved. The objective of this study was to use a cat model of gastroesophageal reflux disease (GERD) to investigate the expression of the NR1 and NR2A subunits of NMDAR in the vagal and spinal afferent fibers innervating the esophagus. Two groups of cats (Acid-7D and PBS-7D) received 0.1 N HCl (pH 1.2) or 0.1 M PBS (pH 7.4) infusion in the esophagus (1 ml/min for 30 min/day for 7 days), respectively. NR1 splice variants (both NH2and COOH terminals) and NR2A in the thoracic dorsal root ganglia (DRGs), nodose ganglia (NGs), and esophagus were evaluated by RT-PCR, Western blot, and immunohistochemistry. Acid produced marked inflammation and a significant increase in eosinophil peroxidase and myeloperoxidase contents compared with PBS-infused esophagus. The NR1-4 splice variant gene exhibited a significant upregulation in DRGs and esophagus after acid infusion. In DRGs, NGs, and esophagus, acid infusion resulted in significant upregulation of NR1 and downregulation of NR2A subunit gene expression. A significant increase in NR1 polypeptide expression was observed in DRGs and NGs from Acid-7D compared with control. In conclusion, long-term acid infusion in the cat esophagus resulted in ulcerative esophagitis and differential expressions of NR1 and NR2A subunits. It is possible that these changes may in part contribute to esophageal hypersensitivity observed in reflux esophagitis.
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