Abstract
We have investigated the effect of rolipram, a type IV phosphodiesterase inhibitor, on Pseudomonas aeruginosainfection 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-actingbeta-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.
Footnotes
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Send reprint requests to: Dr. R. Wilson, M.D., FRCP, Host Defence Unit, National Heart and Lung Institute, Emmanuel Kaye Building, Manresa Road, London SW3 6LR, UK.
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↵1 Present address: Glaxo Wellcome Research and Development, Stockley Park West, Uxbridge, Middlesex, UB11 1BU, UK.
- Abbreviations:
- PDE
- phosphodieterase
- BHI
- brain heart infusion
- PBS
- phosphate-buffered saline
- MEM
- minimal essential medium
- BAL
- bronchoalveolar lavage
- IL-8
- interleukin-8
- TNF
- tumor necrosis factor
- IBMX
- 3-isobutyl-1-methylxanthine
- Received October 9, 1996.
- Accepted May 6, 1997.
- The American Society for Pharmacology and Experimental Therapeutics
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