Receptor binding sites for substance P in surgical specimens obtained from patients with ulcerative colitis and Crohn disease
Journal Article
·
· Proc. Natl. Acad. Sci. U.S.A.; (United States)
Several lines of evidence indicate that tachykinin neuropeptides (substance P (SP), substance K (SK), and neuromedin K (NK)) play a role in regulating the inflammatory and immune responses. To test this hypothesis in a human inflammatory disease, quantitative receptor autoradiography was used to examine possible abnormalities in tachykinin binding sites in surgical specimens from patients with inflammatory bowel disease. In all cases, specimens were processed for quantitative receptor autoradiography by using /sup 125/I-labeled Bolton-Hunter conjugates of NK, SK, and SP. In colon tissue obtained from ulcerative colitis and Crohn disease patients, very high concentrations of SP receptor binding sites are expressed by arterioles and venules located in the submucosa, muscalairs mucosa, external circular muscle, external longitudinal muscle, and serosa, in contrast to control patients. These results demonstrate that receptor binding sites for SP, but not SK or NK, are ectopically expressed in high concentrations by cells involved in mediating inflammatory and immune responses. These data suggest that SP may be involved in the pathophysiology of inflammatory bowel disease and might provide some insight into the interaction between the nervous system and the regulation of inflammation and the immune response in human inflammatory disease.
- Research Organization:
- Veterans Administration Wadsworth Medical Center, Los Angeles, CA (USA)
- OSTI ID:
- 6142248
- Journal Information:
- Proc. Natl. Acad. Sci. U.S.A.; (United States), Journal Name: Proc. Natl. Acad. Sci. U.S.A.; (United States) Vol. 85:9; ISSN PNASA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550501* -- Metabolism-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ARTERIES
AUTORADIOGRAPHY
BETA DECAY RADIOISOTOPES
BLOOD VESSELS
BODY
CARDIOVASCULAR SYSTEM
CHEMICAL REACTIONS
CROSS-LINKING
DAYS LIVING RADIOISOTOPES
DIGESTIVE SYSTEM
DIGESTIVE SYSTEM DISEASES
DISEASES
ELECTRON CAPTURE RADIOISOTOPES
GASTROINTESTINAL TRACT
IMMUNOLOGY
INFLAMMATION
INTERMEDIATE MASS NUCLEI
INTESTINES
IODINE 125
IODINE ISOTOPES
ISOTOPES
KININS
LABELLED COMPOUNDS
LARGE INTESTINE
LYMPH NODES
LYMPHATIC SYSTEM
MEMBRANE PROTEINS
MUSCLES
NERVE CELLS
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
ORGANS
PATHOLOGICAL CHANGES
PEPTIDES
POLYMERIZATION
POLYPEPTIDES
PROTEINS
RADIOISOTOPES
RECEPTORS
SOMATIC CELLS
SYMPTOMS
TRITIUM COMPOUNDS
VEINS
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ARTERIES
AUTORADIOGRAPHY
BETA DECAY RADIOISOTOPES
BLOOD VESSELS
BODY
CARDIOVASCULAR SYSTEM
CHEMICAL REACTIONS
CROSS-LINKING
DAYS LIVING RADIOISOTOPES
DIGESTIVE SYSTEM
DIGESTIVE SYSTEM DISEASES
DISEASES
ELECTRON CAPTURE RADIOISOTOPES
GASTROINTESTINAL TRACT
IMMUNOLOGY
INFLAMMATION
INTERMEDIATE MASS NUCLEI
INTESTINES
IODINE 125
IODINE ISOTOPES
ISOTOPES
KININS
LABELLED COMPOUNDS
LARGE INTESTINE
LYMPH NODES
LYMPHATIC SYSTEM
MEMBRANE PROTEINS
MUSCLES
NERVE CELLS
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
ORGANS
PATHOLOGICAL CHANGES
PEPTIDES
POLYMERIZATION
POLYPEPTIDES
PROTEINS
RADIOISOTOPES
RECEPTORS
SOMATIC CELLS
SYMPTOMS
TRITIUM COMPOUNDS
VEINS