Abstract
The efficacy of a new class of drugs for Pneumocystis carinii pneumonitis was demonstrated. 566C80, a hydroxynaphthoquinone, administered orally in a dose of greater than or equal to 100 mg/kg of body weight per day prophylactically prevented P. carinii pneumonitis in 90% or more of rats, while all untreated control animals developed pneumonitis. When 566C80 (100 mg/kg per day) was administered for 3 weeks after P. carinii pneumonitis was established, therapy was totally effective and all of the untreated controls had progressive P. carinii pneumonitis. A dose of 566C80 of between 25 and 50 mg/kg per day protected 50% of the rats from P. carinii pneumonitis, and a dose of between 50 and 100 mg/kg per day cured 50% of those treated for P. carinii pneumonitis. Both prophylaxis and treatment with 566C80 were at least as effective as with trimethoprim-sulfamethoxazole. Animals maintained on immunosuppression after completion of treatment remained free of P. carinii, suggesting a killing effect. Clearance of P. carinii was associated with levels of 60 micrograms or more of 566C80 per ml of plasma. This hydroxynaphthoquinone offers promise as an anti-P. carinii drug.
MeSH Terms
Animals
Anti-Infective Agents/pharmacokinetics,therapeutic use
Atovaquone
Dexamethasone/therapeutic use
Lung/pathology
Male
Naphthoquinones/pharmacokinetics,therapeutic use
Pneumonia, Pneumocystis/drug therapy,microbiology,pathology
Rats
Rats, Inbred Strains
Tetracyclines/therapeutic use
Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
Chemicals
Anti-Infective Agents
Naphthoquinones
Tetracyclines
Dexamethasone
Trimethoprim, Sulfamethoxazole Drug Combination
Atovaquone
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hughes W T
Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee 38101.
Gray V L
Gutteridge W E
Latter V S
Pudney M
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