Gastrin-releasing peptide stimulates glycoconjugate release from feline trachea

J. D. Lundgren*, J. N. Baraniuk, N. L. Ostrowski, M. A. Kaliner, J. H. Shelhamer

*Corresponding author af dette arbejde
28 Citationer (Scopus)

Abstract

The effect of gastrin-releasing peptide (GRP) on respiratory glycoconjugate (RGC) secretion was investigated in a feline tracheal organ culture model. RGC secretion was stimulated by GRP in a dose-dependent fashion at concentrations from 10-8 to 10-5 M (range 15-38% increase above control) with a peak effect within 0.5-1 h of incubation. GRP-(14-27), the receptor binding portion of GRP, and the related molecule, bombesin, also stimulated RGC secretion by ~ 20% above control. Acetyl-GRP-(20-27) stimulated RGC release by 10%, whereas GRP-(1-16) was inactie. Autoradiograhic studies with 125I-GRP revealed that specific binding was restricted to the submucosal glands and the surface epithelium. A specific radioimmunoassay showed the content of GRP in feline trachea after extraction with ethanol-acetic acid to be 156 ± 91 fmol/g wet wt. Indirect immunohistochemistry indicated that ganglion cells located just outside the cartilage contained GRP-immunoreactive materials. GRP is a novel mucus secretagogue that may participate in regulating airway mucosal gland secretion.

OriginalsprogEngelsk
TidsskriftAmerican Journal of Physiology - Lung Cellular and Molecular Physiology
Vol/bind258
Udgave nummer2 2-1
Sider (fra-til)L68-L74
ISSN0002-9513
DOI
StatusUdgivet - 1990

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