Serum and brain purine levels in an experimental systemic infection of mice by Cryptococcus neoformans: Purinergic immunomodulatory effects

The aim of this study was to evaluate the purine levels in serum and brains of mice experimentally infected by Cryptococcus neoformans. Twenty-four mice were divided into the following groups: a control group (n = 12; Group A) and an infection group with animals that were infected (n = 12; Group B)...

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Veröffentlicht in:Microbial pathogenesis 2017-12, Vol.113, p.124-128
Hauptverfasser: de Azevedo, Maria Isabel, Da Silva, Aleksandro S., Ferreiro, Laerte, Doleski, Pedro H., Tonin, Alexandre A., Casali, Emerson A., Moritz, Cesar E.J., Schirmbeck, Gabriel H., Cardoso, Valesca V., Flores, Mariana M., Fighera, Rafael, Santurio, Janio M.
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Sprache:eng
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Zusammenfassung:The aim of this study was to evaluate the purine levels in serum and brains of mice experimentally infected by Cryptococcus neoformans. Twenty-four mice were divided into the following groups: a control group (n = 12; Group A) and an infection group with animals that were infected (n = 12; Group B) with a 0.3-mL intraperitoneal injection containing 1.7 × 107C. neoformans cells. Blood and brains were collected on days 20 (n = 6 per group) and 50 (n = 6 per group) post-infection (PI). Histopathology and lung and brain cultures were performed to confirm fungal infection and tissue injuries. The levels of adenosine triphosphate (ATP), adenosine diphosphate (ADP), adenosine monophosphate (AMP), adenosine (ADO), inosine (INO), hypoxanthine (HYPO), xanthine (XAN) and uric acid (UA) in brains and serum were measured by high-performance liquid chromatography (HPLC) analysis. At both time points, histopathology analysis revealed inflammatory infiltrates in the brains and lungs of infected mice; clinical signs, such as piloerection and clinical respiratory distress, were also observed. ATP levels were significantly increased on days 20 and 50 PI (P  0.05). Serum levels of INO of infected mice increased only on day 50 PI (P 
ISSN:0882-4010
1096-1208
DOI:10.1016/j.micpath.2017.10.012