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鱼油对慢性乙醇诱导的肝损伤大鼠脑损伤的保护作用:涉及NRF2通路和氧化应激

Protective Effects of Fish Oil Against Brain Impairment in Rats with Chronic Ethanol-Induced Liver Damage Involving the NRF2 Pathway and Oxidative Stress.

作者信息

Xiao Qian, Chen Yi-Hsiu, Fu Lu-Chi, Nurrahma Herlin Ajeng, Lai Jing-Huei, Shirakawa Hitoshi, Yang Suh-Ching

机构信息

School of Nutrition and Health Sciences, Taipei Medical University, Taipei 11031, Taiwan.

Core Laboratory of Neuroscience, Office of R&D, Taipei Medical University, Taipei 11031, Taiwan.

出版信息

Antioxidants (Basel). 2025 Jun 10;14(6):704. doi: 10.3390/antiox14060704.

Abstract

Fish oil's neuroprotective effects in ethanol-induced liver injury was investigated through the factor 2 (NRF2)/Kelch-like ECH-associated protein 1 (KEAP1) pathway. Male Wistar rats received a control liquid diet (C) or an ethanol diet (E), with 25% or 57% of fat replaced by fish oil (CF25, CF57, EF25, EF57) for 8 weeks. Compared to the C group, the E group exhibited brain damage, including impaired performance of Y maze and novel object recognition test, increased glial fibrillary acidic protein (GFAP)-positive astrocytes, and ionized calcium-binding adapter molecule 1 (Iba-1)-positive microglia. In the prefrontal cortex, glutathione (GSH) and phosphorylated (p)-NRF2 decreased, catalase activity increased, and mRNA declined; hippocampal NRF2 and were also downregulated. However, compared to the E group, the EF25 and EF57 groups exhibited restored spatial and memory functions, reduced GFAP and Iba-1 expressions, potentiated β-amyloid (Aβ) clearance, and escalated catalase activity. Furthermore, increases in p-NRF2 and elevated hippocampal mRNA expressions in the prefrontal cortex were observed in the EF25 and EF57 groups. In conclusion, fish oil ameliorated deficits in spatial and memory functions, and enhanced Aβ1-42 clearance in the prefrontal cortex and hippocampus of rats with chronic ethanol-induced liver damage by activating the NRF2/KEAP1 pathway.

摘要

通过因子2(NRF2)/ Kelch样ECH相关蛋白1(KEAP1)途径研究了鱼油对乙醇诱导的肝损伤的神经保护作用。雄性Wistar大鼠接受对照液体饮食(C)或乙醇饮食(E),其中25%或57%的脂肪被鱼油替代(CF25、CF57、EF25、EF57),持续8周。与C组相比,E组表现出脑损伤,包括Y迷宫和新物体识别测试的表现受损、胶质纤维酸性蛋白(GFAP)阳性星形胶质细胞增加以及离子钙结合衔接分子1(Iba-1)阳性小胶质细胞增加。在额叶皮质中,谷胱甘肽(GSH)和磷酸化(p)-NRF2减少,过氧化氢酶活性增加,且mRNA下降;海马体中的NRF2也下调。然而,与E组相比,EF25和EF57组表现出空间和记忆功能恢复、GFAP和Iba-1表达减少、β-淀粉样蛋白(Aβ)清除增强以及过氧化氢酶活性升高。此外,在EF25和EF57组中观察到额叶皮质中p-NRF2增加以及海马体mRNA表达升高。总之,鱼油通过激活NRF2/KEAP1途径改善了慢性乙醇诱导的肝损伤大鼠额叶皮质和海马体的空间和记忆功能缺陷,并增强了Aβ1-42清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf7/12189729/cae07f2a2ee4/antioxidants-14-00704-g0A1.jpg

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