| Literature DB >> 26183422 |
Marco Túlio Alves da Silva1, Izaltina Silva-Jardim1, Gisele Bulhões Portapilla1, Gustavo Machado Alvares de Lima1, Fernanda Cristina Costa2, Fernanda de Freitas Anibal3, Otavio Henrique Thiemann4.
Abstract
Chagas disease, Sleeping Sickness, Nagana and Leishmaniasis are serious infections caused by protozoa of the order Kinetoplastidae. They were described over a century ago by seminal work of different physician-researchers and, despite the initial discoveries, few drugs have been made available for the treatment of these infections. The drugs available present serious efficacy and toxicity problems. Moreover, the emergence of resistant strains has rendered the development of novel chemotherapeutic strategies a priority. Auranofin is currently in use to treat rheumatoid arthritis in humans. Previous reports showed that this compound presents activity against Trypanosoma brucei and Leishmania cells. In Trypanosoma cruzi cells, auranofin resulted in a more potent compound than benznidazole in vitro when tested in different DTUs. In vivo experiments, although not decreasing T. cruzi parasitemia, decreases host mortality. Therefore, we propose auranofin as a potential alternative for a new chemotherapy in Chagas disease with the added advantage of already being approved for use in humans.Entities:
Keywords: Auranofin; Chemotherapy; Trypanosoma cruzi
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Year: 2015 PMID: 26183422 DOI: 10.1016/j.exppara.2015.05.012
Source DB: PubMed Journal: Exp Parasitol ISSN: 0014-4894 Impact factor: 2.011