Objective and Design: Currently no method is available for measurement of m
ediator release from intact human lung. In this study, a microdialysis tech
nique was used to measure histamine release from mast cells in human lung t
issue ex vivo.
Material: Microdialysis fibers of 216 mu m were inserted into lung tissue a
nd perfused with Krebs Ringer buffer at a rate of 3 mu l/min. After a 15 mi
n period of steady-state perfusion, anti-IgE and vehicle were injected into
the lung tissue above individual fibers. Samples from each fibre were coll
ected for 20 min at 2 min intervals. Histamine was assayed fluorometrically
.
Results: Anti-IgE concentrations of 40-40,000 U/ml dose-dependently release
d histamine, significant histamine release being demonstrated with anti-IgE
concentrations of 400 U/ml and greater. The kinetics of histamine release
showed peak values 2-8 min after the injection. Great individual responses
were observed but data could be reproduced within individual donors. Monocy
te chemoattractant protein-1, a potent basophil secretagogue, did not induc
e histamine release in lung tissue which indicated mast cells to be the his
tamine source. Substance P did not release histamine in the lung tissue.
Conclusions: The microdialysis technique allowed measurements of histamine
release from mast cells in intact lung ex vivo. The method may prove useful
since a number of experiments can be performed in a few hours in intact lu
ng tissue without any dispersion or enzymatic treatment.