Activity of the new triazole derivative albaconazole against Trypanosoma (Schizotrypanum) cruzi in dog hosts.
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2004
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Abstract
Albaconazole is an experimental triazole derivative with potent and broad-spectrum antifungal activity and
a remarkably long half-life in dogs, monkeys, and humans. In the present work, we investigated the in vivo
activity of this compound against two strains of the protozoan parasite Trypanosoma (Schizotrypanum) cruzi, the
causative agent of Chagas’ disease, using dogs as hosts. The T. cruzi strains used in the study were previously
characterized (murine model) as susceptible (strain Berenice-78) and partially resistant (strain Y) to the drugs
currently in clinical use, nifurtimox and benznidazole. Our results demonstrated that albaconazole is very
effective in suppressing the proliferation of the parasite and preventing the death of infected animals. Furthermore,
the parasitological, PCR, serological, and proliferative assay results indicated parasitological cure
indices of 25 and 100% among animals inoculated with T. cruzi strain Y when they were treated with
albaconazole at 1.5 mg/kg of body weight/day for 60 and 90 days, respectively. On the other hand, although
albaconazole given at 1.5 mg/kg/day was very effective in suppressing the proliferation of the parasite in
animals infected with the Berenice-78 T. cruzi strain, no parasitological cure was observed among them, even
when a longer treatment period (150 doses) was used. In conclusion, our results demonstrate that albaconazole
has trypanocidal activity in vivo and is capable of inducing radical parasitological cure, although natural
resistance to this compound was also indicated. Furthermore, the compound can be used in long-term
treatment schemes (60 to 150 days) with minimal toxicity and thus represents a potentially useful candidate
for the treatment of human Chagas’ disease.
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GUEDES, P. M. da M. et al. Activity of the new triazole derivative albaconazole against Trypanosoma (Schizotrypanum) cruzi in dog hosts. Antimicrobial Agents and Chemotherapy, v. 48, p. 4286-4292, 2004. Disponível em: <http://aac.asm.org/content/48/11/4286.long>. Acesso em: 20 jan. 2017.