Department of Pharmacology and Therapeutics, Health Science Center, State University of Maringá, Maringá 87020-900, Paraná, Brazil.
Physiol Behav. 2013 Jul 2;119:61-71. doi: 10.1016/j.physbeh.2013.06.001. Epub 2013 Jun 11.
We previously reported that long-term treatment with fish oil (FO) facilitates memory recovery after transient, global cerebral ischemia (TGCI), despite the presence of severe hippocampal damage. The present study tested whether this antiamnesic effect resulted from an action of FO on behavioral performance itself, or whether it resulted from an anti-ischemic action. Different treatment regimens were used that were distinguished from each other by their initiation or duration with regard to the onset of TGCI and memory assessment. Naive rats were trained in an eight-arm radial maze, subjected to TGCI (4-VO model, 15 min), and tested for memory performance up to 6 weeks after TGCI. Fish oil (docosahexaenoic acid, 300 mg/kg/day) was given orally according to one of the following regimens: regimen 1 (from 3 days prior to ischemia until 4 weeks post-ischemia), regimen 2 (from 3 days prior to ischemia until 1 week post-ischemia), and regimen 3 (from week 2 to week 5 post-ischemia). When administered according to regimens 1 and 2, FO abolished amnesia completely. This effect persisted for at least 5 weeks after discontinuing the treatment. Such an effect did not occur, however, in the group treated according to regimen 3. Hippocampal and cortical damage was not alleviated by FO. The present results demonstrate that FO-mediated memory recovery (or preservation) following TGCI is a reproducible, robust, and long-lasting effect. Moreover, such an effect was found with a relatively short period of treatment, provided it covered the first days prior to and after ischemia. This suggests that FO prevented amnesia by changing some acute, ischemia/reperfusion-triggered process and not by stimulating memory performance on its own.
我们之前报道过,长期服用鱼油(FO)可促进短暂全脑缺血(TGCI)后的记忆恢复,尽管海马损伤严重。本研究测试了这种抗遗忘作用是源自 FO 对行为表现本身的作用,还是源自抗缺血作用。使用了不同的治疗方案,这些方案在 TGCI 发作和记忆评估方面的起始或持续时间上有所不同。未处理的大鼠在八臂放射迷宫中接受训练,然后进行 TGCI(4-VO 模型,15 分钟),并在 TGCI 后 6 周内测试记忆表现。鱼油(二十二碳六烯酸,300mg/kg/天)根据以下方案之一口服给药:方案 1(从缺血前 3 天到缺血后 4 周),方案 2(从缺血前 3 天到缺血后 1 周),以及方案 3(从缺血后第 2 周到第 5 周)。按照方案 1 和 2 给药时,FO 完全消除了遗忘。这种效果至少在停止治疗后持续 5 周。然而,按照方案 3 治疗的组中并未出现这种效果。FO 并未减轻海马和皮质损伤。本研究结果表明,FO 介导的 TGCI 后记忆恢复(或保存)是一种可重现、稳健且持久的效应。此外,在较短的治疗期间(只要覆盖缺血前后的最初几天)就发现了这种效应。这表明 FO 通过改变一些急性缺血/再灌注触发的过程而不是通过自身刺激记忆表现来预防遗忘。