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Vol. 282, Issue 3, 1565-1571, 1997
Host Defence Unit, Imperial College of Science, Technology and
Medicine, National Heart and Lung Institute, London, United Kingdom
We have investigated the effect of rolipram, a type IV
phosphodiesterase inhibitor, on Pseudomonas aeruginosa
infection of the respiratory mucosa of an organ culture model and on
the reduction in intracellular cAMP levels seen in human nasal
epithelial cells incubated with P. aeruginosa culture
filtrate. We have compared rolipram with salmeterol, a long-acting
beta-2 agonist, and have also studied the effect of the two
agents together. Infected organ cultures had significantly (P
.05) increased epithelial damage. Rolipram significantly (P
.05) reduced P. aeruginosa-induced epithelial damage and
reduced the total number of bacteria adhering to the respiratory mucosa
(P
.04) in a concentration-dependent manner, although neither
rolipram nor salmeterol affected P. aeruginosa growth in
broth cultures. Rolipram reduced P. aeruginosa-induced mucosal damage more than salmeterol (P
.03). The effect of the two agents was neither additive nor synergistic. Rolipram, salmeterol and both agents together significantly (P
.01) increased
intracellular cAMP levels in epithelial cells treated with P. aeruginosa culture filtrate. Rolipram alone increased cAMP more
than salmeterol or both agents together (P
.01), probably
because of an interaction between the two agents. These results suggest
that agents that elevate intracellular cAMP protect the epithelium
during bacterial infection. Rolipram is more effective than salmeterol
in preventing P. aeruginosa-induced epithelial damage.