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Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 36(4): 322-329, Oct-Dec/2014. graf
Article in English | LILACS | ID: lil-730589

ABSTRACT

Objective: To evaluate the influence of environmental enrichment (EE) on memory, cytokines, and brain-derived neurotrophic factor (BDNF) in the brain of adult rats subjected to experimental pneumococcal meningitis during infancy. Methods: On postnatal day 11, the animals received either artificial cerebrospinal fluid (CSF) or Streptococcus pneumoniae suspension intracisternally at 1 × 106 CFU/mL and remained with their mothers until age 21 days. Animals were divided into the following groups: control, control + EE, meningitis, and meningitis + EE. EE began at 21 days and continued until 60 days of age (adulthood). EE consisted of a large cage with three floors, ramps, running wheels, and objects of different shapes and textures. At 60 days, animals were randomized and subjected to habituation to the open-field task and the step-down inhibitory avoidance task. After the tasks, the hippocampus and CSF were isolated for analysis. Results: The meningitis group showed no difference in performance between training and test sessions of the open-field task, suggesting habituation memory impairment; in the meningitis + EE group, performance was significantly different, showing preservation of habituation memory. In the step-down inhibitory avoidance task, there were no differences in behavior between training and test sessions in the meningitis group, showing aversive memory impairment; conversely, differences were observed in the meningitis + EE group, demonstrating aversive memory preservation. In the two meningitis groups, IL-4, IL-10, and BDNF levels were increased in the hippocampus, and BDNF levels in the CSF. Conclusions: The data presented suggest that EE, a non-invasive therapy, enables recovery from memory deficits caused by neonatal meningitis. .


Subject(s)
Animals , Male , Brain-Derived Neurotrophic Factor/blood , Cognition Disorders/therapy , Cytokines/blood , Environmental Exposure , Memory Disorders/therapy , Meningitis, Pneumococcal/therapy , Brain/physiopathology , Disease Models, Animal , Enzyme-Linked Immunosorbent Assay , Neurogenesis/physiology , Neuronal Plasticity/physiology , Rats, Wistar , Recovery of Function , Reproducibility of Results , Treatment Outcome
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