Department of Clinical Pharmacy, Jordan University of Science and Technology, Irbid, Jordan.
Department of Clinical Pharmacy, Jordan University of Science and Technology, Irbid, Jordan.
Life Sci. 2019 Jun 15;227:1-7. doi: 10.1016/j.lfs.2019.04.028. Epub 2019 Apr 15.
The current study aims to evaluate the possible protective effect of omega-3 fatty acids on memory impairment induced by sleep-deprivation in rats.
Animals were chronically sleep deprived using the modified multiple platform model (8 h/day for 8 weeks). Omega-3 fatty acids were administered as fish oil via oral gavage at a daily dose of 100 mg omega-3 PUFA/100 g BWT. The spatial learning and memory were evaluated using the radial arm water maze (RAWM). Additionally, the following oxidative stress biomarkers were measured in the hippocampus: glutathione (GSH), oxidized glutathione (GSSG), GSH/GSSG, glutathione peroxidase (GPx), catalase, superoxide dismutase (SOD), and thiobarbituric acid reactive substance (TBARS).
Animals in the SD group committed significantly more errors in both short- and long- term memory tests of the RAWM compared to other groups. On the other hand, animals that were sleep deprived and treated with omega-3 fatty acids committed similar number of errors compared to the control group. This indicates that SD impaired both short- and long- term memories, and that chronic omega-3 fatty acids administration prevented these effects. Omega-3 fatty acids also prevented the decreases in hippocampal GPx, catalase and GSH/GSSG ratio and normalized the increases in GSSG levels, which were impaired by SD model. No changes were observed on hippocampal TBARS levels, or activity of SOD among experimental groups.
In conclusion, a protective effect of omega-3 fatty acids administration has been observed against chronic SD-induced memory impairment probably via improving hippocampus antioxidant effects.
本研究旨在评估ω-3 脂肪酸对睡眠剥夺诱导的大鼠记忆障碍的可能保护作用。
采用改良的多平台模型(每天 8 小时,持续 8 周)对动物进行慢性睡眠剥夺。ω-3 脂肪酸通过口服灌胃以 100mg ω-3PUFA/100gBWt 的日剂量给予鱼油。使用放射臂水迷宫(RAWM)评估空间学习和记忆。此外,还测量了海马中的以下氧化应激生物标志物:谷胱甘肽(GSH)、氧化型谷胱甘肽(GSSG)、GSH/GSSG、谷胱甘肽过氧化物酶(GPx)、过氧化氢酶、超氧化物歧化酶(SOD)和硫代巴比妥酸反应物质(TBARS)。
与其他组相比,SD 组动物在 RAWM 的短期和长期记忆测试中犯的错误明显更多。另一方面,与对照组相比,接受 ω-3 脂肪酸睡眠剥夺和治疗的动物犯的错误数量相似。这表明 SD 损害了短期和长期记忆,而慢性 ω-3 脂肪酸给药可预防这些影响。ω-3 脂肪酸还可防止海马 GPx、过氧化氢酶和 GSH/GSSG 比值降低,并使因 SD 模型而受损的 GSSG 水平升高正常化。各组间海马 TBARS 水平或 SOD 活性均无变化。
总之,ω-3 脂肪酸给药对慢性 SD 诱导的记忆障碍具有保护作用,可能是通过改善海马抗氧化作用。