Department of Veterinary Preclinical Sciences, Faculty of Veterinary Medicine, Universiti Putra Malaysia, Selangor, Malaysia.
Department of Veterinary Physiology, Faculty of Veterinary Medicine, Universitas Brawijaya, East Java, Indonesia.
Pharm Biol. 2024 Dec;62(1):447-455. doi: 10.1080/13880209.2024.2351933. Epub 2024 May 16.
Menhaden fish oil (FO) is widely recognized for inhibiting neuroinflammatory responses and preserving brain function. Nevertheless, the mechanisms of FO influencing brain cognitive function in diabetic states remain unclear.
This study examines the potential role of FO in suppressing LPS-induced neuroinflammation and cognitive impairment in diabetic animals (DA).
Thirty male Wistar rats were divided into 5 groups: i) DA received LPS induction (DA-LPS); ii) DA received LPS induction and 1 g/kg FO (DA-LPS-1FO); iii) DA received LPS induction and 3 g/kg FO (DA-LPS-3FO); iv) animals received normal saline and 3 g/kg FO (NS-3FO) and v) control animals received normal saline (CTRL). Y-maze test was used to measure cognitive performance, while brain samples were collected for inflammatory markers and morphological analysis.
DA received LPS induction, and 1 or 3 g/kg FO significantly inhibited hyperglycaemia and brain inflammation, as evidenced by lowered levels of pro-inflammatory mediators. Additionally, both DA-LPS-1FO and DA-LPS-3FO groups exhibited a notable reduction in neuronal damage and glial cell migration compared to the other groups. These results were correlated with the increasing number of entries and time spent in the novel arm of the Y-maze test.
This study indicates that supplementation of menhaden FO inhibits the LPS signaling pathway and protects against neuroinflammation, consequently maintaining cognitive performance in diabetic animals. Thus, the current study suggested that fish oil may be effective as a supporting therapy option for diabetes to avoid diabetes-cognitive impairment.
鲱鱼油(FO)被广泛认为可抑制神经炎症反应并保护大脑功能。然而,FO 影响糖尿病状态下大脑认知功能的机制仍不清楚。
本研究旨在探讨 FO 抑制糖尿病动物(DA)中 LPS 诱导的神经炎症和认知障碍的潜在作用。
30 只雄性 Wistar 大鼠分为 5 组:i)DA 接受 LPS 诱导(DA-LPS);ii)DA 接受 LPS 诱导和 1g/kg FO(DA-LPS-1FO);iii)DA 接受 LPS 诱导和 3g/kg FO(DA-LPS-3FO);iv)给予生理盐水和 3g/kg FO(NS-3FO)的动物;v)给予生理盐水的对照组(CTRL)。Y 迷宫测试用于测量认知表现,同时收集脑样本用于炎症标志物和形态分析。
DA 接受 LPS 诱导和 1 或 3g/kg FO 显著抑制高血糖和脑炎症,表现为促炎介质水平降低。此外,与其他组相比,DA-LPS-1FO 和 DA-LPS-3FO 组的神经元损伤和神经胶质细胞迁移明显减少。这些结果与 Y 迷宫测试中进入新臂的次数和时间的增加相关。
本研究表明,鲱鱼油补充剂可抑制 LPS 信号通路并防止神经炎症,从而维持糖尿病动物的认知表现。因此,本研究表明,鱼油可能是治疗糖尿病以避免糖尿病认知障碍的有效辅助治疗选择。