Laboratory of Experimental Microbiology, Universidade do Extremo Sul Catarinense (UNESC), Criciúma, SC, Brazil.
Department of Animal Biology, Universidade Federal de Viçosa (UFV), Viçosa, MG, Brazil.
Braz J Psychiatry. 2014 Oct-Dec;36(4):322-9. doi: 10.1590/1516-4446-2014-1443. Epub 2014 Jul 25.
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.
On postnatal day 11, the animals received either artificial cerebrospinal fluid (CSF) or Streptococcus pneumoniae suspension intracisternally at 1 × 10(6) 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.
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.
The data presented suggest that EE, a non-invasive therapy, enables recovery from memory deficits caused by neonatal meningitis.
评估环境富集(EE)对婴儿期实验性肺炎球菌性脑膜炎后成年大鼠记忆、细胞因子和脑源性神经营养因子(BDNF)的影响。
在出生后第 11 天,动物通过脑室内给予人工脑脊液(CSF)或肺炎链球菌悬浮液(1×106 CFU/mL),并与母亲一起生活至 21 天。动物分为以下几组:对照组、对照组+EE、脑膜炎组和脑膜炎+EE。EE 从 21 天开始,持续到 60 天(成年)。EE 包括一个有三层、斜坡、跑步轮和不同形状和质地物体的大笼子。在 60 天时,动物被随机分为习惯化到旷场任务和跳下抑制性回避任务。任务完成后,分离海马体和 CSF 进行分析。
脑膜炎组在旷场任务的训练和测试阶段表现无差异,提示习惯化记忆受损;在脑膜炎+EE 组中,表现明显不同,习惯化记忆得到保留。在跳下抑制性回避任务中,脑膜炎组在训练和测试阶段的行为无差异,提示厌恶记忆受损;相反,脑膜炎+EE 组观察到差异,表现出厌恶记忆的保留。在两个脑膜炎组中,IL-4、IL-10 和 BDNF 水平在海马体中增加,CSF 中的 BDNF 水平增加。
这些数据表明,EE 是一种非侵入性治疗方法,可使新生儿脑膜炎引起的记忆缺陷得到恢复。