Abstract
Rats immunosuppressed by the administration of cyclophosphamide and cortisone acetate and then infected with Aspergillus fumigatus were treated with an antifungal drug, EDTA, or a combination of one of the antifungal agents, amphotericin B lipid complex (ABLC; 5 mg/kg of body weight/day for 7 days), and EDTA (30 mg/kg/day for 7 days). The mortality rate was reduced, the duration of survival was increased, fewer A. fumigatus organisms were recovered from the lungs, and less-severe lung lesions were seen histopathologically in the rats receiving the combination treatment than in the rats receiving either an antifungal agent or EDTA alone. Further studies regarding the mechanisms of EDTA and its interactions with ABLC are warranted, and further studies are needed to more fully examine the safety, tolerance, and optimal dosing of EDTA in the treatment of this and other fungal infections.
Publication types
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Comparative Study
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Evaluation Study
MeSH terms
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Amphotericin B / pharmacology
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Animals
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Antifungal Agents / pharmacokinetics
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Antifungal Agents / pharmacology*
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Aspergillosis / blood
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Aspergillosis / drug therapy*
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Aspergillus fumigatus / drug effects*
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Aspergillus fumigatus / genetics
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Aspergillus fumigatus / growth & development
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Calcium / analysis
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Colony Count, Microbial
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Confidence Intervals
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Creatinine / blood
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Disease Models, Animal
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Drug Combinations
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Drug Evaluation, Preclinical
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Drug Therapy, Combination
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Edetic Acid / pharmacokinetics
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Edetic Acid / pharmacology*
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Lung Diseases, Fungal / drug therapy*
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Lung Diseases, Fungal / pathology
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Male
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Phosphatidylcholines / pharmacology
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Phosphatidylglycerols / pharmacology
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Rats
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Rats, Sprague-Dawley
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Survival Analysis
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Time Factors
Substances
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Antifungal Agents
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Drug Combinations
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Phosphatidylcholines
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Phosphatidylglycerols
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liposomal amphotericin B
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Amphotericin B
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Edetic Acid
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Creatinine
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Calcium