| Literature DB >> 26025154 |
Luciana Dalla Rosa1, Aleksandro S Da Silva2, Camila B Oliveira3, Lucas T Gressler3, Caroline B Arnold3, Matheus D Baldissera3, Michele Sagrillo4, Manuela Sangoi3, Rafael Moresco3, Ricardo E Mendes5, Paulo E Weiss2, Luiz C Miletti2, Silvia G Monteiro6.
Abstract
The aim of this study was to evaluate the therapeutic efficacy and safety of using 3'deoxyadenosine (Cordycepin - adenosine analogue) combined with deoxycoformycin (Pentostatin - an adenosine deaminase inhibitor) in mice infected with Trypanosoma evansi. We show that the combination of Cordycepin (2.0 mg kg(-1)) and Pentostatin (0.2, 0.5, 1.0, 2.0 mg kg(1)) is effective in the clearance of T. evansi, although at the higher concentrations of Pentostatin 2 mg kg(-1) some toxicity was observed in the liver and kidney. Since the Cordycepin 2.0 mg kg(-1) and Pentostatin 0.2 mg kg(-1) combination was effective and had low toxicity, we recommend this as a therapeutic option for a T. evansi mouse model.Entities:
Keywords: Adenosine; Cordycepin; Pentostatin; Toxicity; Trypanosomiasis
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Year: 2015 PMID: 26025154 DOI: 10.1016/j.micpath.2015.05.005
Source DB: PubMed Journal: Microb Pathog ISSN: 0882-4010 Impact factor: 3.738