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Antimicrobial Agents and Chemotherapy, Aug 1995, 1784-1789, Vol 39, No. 8
MB Kurtz, EM Bernard, FF Edwards, JA Marrinan, J Dropinski, CM Douglas and D Armstrong
The pneumocandins are semisynthetic analogs of echinocandin-like compounds
that have shown efficacy in animal models of systemic candidiasis,
disseminated aspergillosis, and pneumocystis pneumonia. However, the most
common form of Aspergillus infection in susceptible patients is pulmonary
aspergillosis, which was not directly tested in the mouse models used in
the past. We have evaluated three pneumocandins, L-693,989, L-731,373, and
L-733,560, in a rat model of pulmonary aspergillosis. Male Sprague-Dawley
rats were treated for 2 weeks with cortisone and tetracycline and fed a
low-protein diet before being inoculated via the trachea with 10(6) conidia
of Aspergillus fumigatus H11-20. In the absence of drug treatment, the
animals developed a progressive, rapidly fatal bronchopneumonia. All three
pneumocandins at doses of 5 mg/kg (intraperitoneally [i.p.] every 12 h
[q12h]) were effective in delaying mortality in this model. Survival at day
7 postinfection was 20% among controls (n = 10 for all groups), while it
was 60, 80, and 90% in groups that were treated with L- 693,989, L-731,373,
and L-733,560, respectively. In another trial, survival at day 7
postinfection was 25% among controls (n = 8 for all groups); it was 87.5%
in a group treated with amphotericin B (0.5 mg/kg i.p. q12h) and was 100%
in a group treated with L-733,560 (0.625 mg/kg i.p. q12h). In a separate
trial, aerosol L-693,989 administered 2 h before infection (5 mg/kg)
delayed mortality. Eight of the 10 animals treated with aerosol L-693,989
survived for 7 days, whereas only 2 of 10 control animals
survived.(ABSTRACT TRUNCATED AT 250 WORDS)
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Aerosol and parenteral pneumocandins are effective in a rat model of pulmonary aspergillosis
Merck Research Laboratories, Rahway, New Jersey 07065, USA.
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