The Brazilian Toxoplasma gondii strain BRI caused greater inflammation and impairment in anxiogenic behavior in mice, which was reverted by rosuvastatin treatment

Author:

Evangelista Fernanda Ferreira1,Sant’Ana Priscilla de Laet1,Ferreira Willian Costa2,Ferreira Thaisa Andreia3,Santos Milena Lopes dos3,de Souza Amanda Hinobu4,de Andrade Felipe Aparecido Lacerda3,Silva Douglas Aparecido da5,de Barros Luiz Daniel5,Colli Cristiane Maria6,de Melo Gessilda Ancântara Nogueira7,Costa Idessania Nazareth8,Falavigna-Guilherme Ana Lúcia1

Affiliation:

1. Department of Health Sciences, State University of Maringá (UEM), Maringá, PR

2. Department of Health Sciences, Unicesumar, Maringá, PR

3. Pharmacy student, State University of Maringá (UEM), Maringá, PR

4. Pharmaceutical Sciences Program, State University of Maringá (UEM), Maringá, PR

5. Department of Preventive Veterinary Medicine, State University of Londrina (UEL), Londrina, PR

6. Federal University of Grande Dourados (UFGD), Dourados, MS

7. Department of Clinical Analysis and Biomedicine, State University of Maringá (UEM), Maringá, PR

8. Department of Pathological Sciences, State University of Londrina (UEL), Londrina, PR

Abstract

Abstract This study aimed to investigate the effect of rosuvastatin treatment on anxiety-related behavior and short- and long-term memory impairment in mice infected with acute RH and BRI strains of Toxoplasma gondii. Balb/C mice were infected intraperitoneally and after two hours, oral treatment with rosuvastatin (40 mg/kg/day) was initiated for four days. Behaviors related to anxiety and locomotion were evaluated in the open field (OF), and short- and long-term memory through the novel object recognition test (NOR). At the end of the experiments, peritoneal fluid, brain, liver, and lung were collected for T. gondii DNA quantification and histopathological analysis. Infection with BRI strain reduced the dwell time and central locomotion in the OF (p < 0.05), indicating anxiogenic type behavior, while treatment with rosuvastatin reversed this response (p < 0.05). RH strain infection did not alter any behavior in the OF (p > 0.05) and both strains impaired short- and long-term memory (NOR test), but with no significant treatment effect (p > 0.05). The BRI strain was shown to be more damaging in relation to anxiogenic type behavior when compared to the RH strain (p < 0.05), whereas rosuvastatin reduced this damaging effect in BRI. The treatment reduced the parasite load in the peritoneal lavage, liver, and lung of animals infected with both acute strains, however, it significantly (p < 0.05) attenuated the inflammatory process only in BRI-infected and treated animals, showing that non-archetypal genotypes are more damaging in rodents. This suggests that rosuvastatin may be a drug with great therapeutic potential against T. gondii mainly to reduce damage from virulent strains.

Publisher

Research Square Platform LLC

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