neuropeptide-y has been researched along with Esophageal-Achalasia* in 2 studies
2 other study(ies) available for neuropeptide-y and Esophageal-Achalasia
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Innervation of an esophageal ectatic submucosal blood vessel in achalasia and a comparison with normals.
Achalasia is a disease of the esophagus characterized by incomplete relaxation of the lower esophageal sphincter, resulting in obstruction. Aperistalsis and dilation of the esophageal body occurs later, contributing to the esophageal dysfunction. Gastrointestinal bleeding in achalasia is an infrequent complication usually caused by stasis ulcer, esophageal varices, carcinoma, or pneumatic dilation of the sphincter. We describe here a patient with longstanding achalasia who bled vigorously from a proximal esophageal site that can be identified as arterial bleeding by endoscopy. Subsequent esophageal resection allowed detailed histological and immunohistochemical examination, which revealed a vascular ectasia. This lesion was associated with an unusually rich network of nerve fibers containing calcitonin gene-related peptide. Neuropeptide Y- and substance P-containing fibers were found to be decreased in this lesion as compared with controls. On the other hand vasoactive intestinal peptide- and nitric oxide synthase-containing fibers appeared quantitatively similar to those of controls. Calcitonin gene-related peptide is known to be involved in angiogenesis and may have played a causative role in the development of this lesion. Vascular ectasia may represent a hitherto unreported complication of achalasia. Topics: Blood Vessels; Calcitonin Gene-Related Peptide; Dilatation, Pathologic; Esophageal Achalasia; Esophagus; Female; Fluorescent Antibody Technique; Gastrointestinal Hemorrhage; Humans; Middle Aged; Mucous Membrane; Nerve Fibers; Neuropeptide Y; Neuropeptides; Substance P | 1994 |
Distribution and content of neuropeptide Y in the human lower esophageal sphincter.
The occurrence and distribution of neuropeptide Y (NPY) was studied in smooth-muscle specimens from the human lower esophageal sphincter region by immunocytochemistry and immunochemistry. Normal individuals and patients suffering from achalasia or hiatus hernia with severe gastroesophageal reflux were examined. NPY fibers were found within and around smooth-muscle bundles of the longitudinal and the circular muscle layers and within the myenteric ganglia. Smooth-muscle specimens from patients with hiatus hernia and gastroesophageal reflux displayed numerous NPY fibers and an increased content of NPY. Specimens from patients with achalasia contained only few NPY fibers and had a decreased content of NPY as compared to specimens from control patients. Conceivably, NPY may play a role in the regulation of the lower esophageal sphincter. Topics: Adolescent; Adult; Aged; Esophageal Achalasia; Esophageal Diseases; Esophageal Neoplasms; Esophagogastric Junction; Gastroesophageal Reflux; Hernia, Hiatal; Histocytochemistry; Humans; Middle Aged; Neuropeptide Y; Radioimmunoassay | 1987 |