Microbial pathogenesis · 2025
Rutin inhibits inflammatory responses by modulating purinergic enzymes and purine metabolism in Cryptococcus neoformans var. grubii-infected rats.
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Fernandes Colvero Rita Laine, Tamiosso Raquel Tusi, Biscarra Bortolotto Paz Maria Fernanda, da Silva de Oliveira Laís Suarez, De Paula Martins Teodoro Trevisan, Nicaretta Júlia Salvagni, Vieira Isabela Maraschin, Leite da Veiga Marcelo, Baldissera Matheus Dellaméa
Аннотация
The aim of this study was to evaluate whether intraperitoneally administration of 50 mg rutin/kg body weight exerts a protective effect against Cryptococcus neoformans var. grubii-induced inflammatory damage by modulating serum purinergic enzymes and molecules. In a study, rats treated with a saline solution and infected with C. neoformans var. grubii demonstrated significant reductions (p < 0.05) in E-nucleoside triphosphate diphosphohydrolase (E-NTPDase) activity using adenosine triphosphate (ATP) as a substrate, as well as E-adenosine deaminase (E-ADA) activity, compared to the saline-treated uninfected group. Elevated extracellular ATP and adenosine (Ado) levels, along with increased serum interleukin-6 (IL-6) levels were observed (p < 0.05) in the C. neoformans var. grubii-infected group compared to the saline-treated uninfected group. No significant differences (p > 0.05) were noted in E-NTPDase activity for adenosine diphosphate (ADP), E-5'-nucleotidase activity, or levels of ADP and adenosine monophosphate between the groups. Treatment with rutin in infected animals effectively prevented these alterations (p > 0.05) when compared to the saline-infected group. In conclusion, purinergic signalling is involved in the pathogenesis of disseminated cryptococcosis, triggering different immunological responses depending on the specific enzyme involved, i.e., a pro-inflammatory response due to inhibition on E-NTPDase activity and an anti-inflammatory response due to inhibition on E-ADA activity. The intraperitoneal administration of 50 mg rutin/kg body weight exerted protective effects on purinergic signalling, preventing impairment on E-NTPDase and E-ADA activities and on ATP and Ado levels, thereby contributing to an improved immune response during disseminated cryptococcosis.