Faculty of Food Science and Nutrition, Universiti Malaysia Sabah, Kota Kinabalu 88400, Sabah, Malaysia.
Natural Medicines and Products Research Laboratory, Institute of Bioscience, Universiti Putra Malaysia (UPM), Serdang 43400, Selangor, Malaysia.
Molecules. 2022 Jul 31;27(15):4907. doi: 10.3390/molecules27154907.
The oxidative stress resulting from the production of reactive oxygen species plays a vital role in inflammatory processes and is associated with neurodegenerative changes. In view of the ability of germinated brown rice (GBR) to improve learning and memory, this present study aimed to investigate the mechanistic basis of GBR's neuroprotection in a high-fat diet (HFD)-induced oxidative changes in adult Sprague-Dawley rats. Ferulate-rich GBR ethyl acetate extract (GBR-EA; 100 mg/kg and 200 mg/kg body weight) was supplemented orally for the last 3 months of 6 months HFD feeding during the study. GBR-EA supplementation was found to improve lipid profile and serum antioxidant status, when compared to the HFD group. Elevated mRNA expressions of SOD1, SOD2, SOD3, Catalase, and GPX were demonstrated in the frontal cortex and hippocampus of GBR-EA treated animals. The pro-inflammatory changes induced by HFD in the hippocampus were attenuated by GBR-EA through the downregulation of CRP and TNF- α and upregulation of PPAR-γ. GBR also reduced the hippocampal mRNA expression and enzyme level of acetylcholinesterase. In conclusion, this study proposed the possible transcriptomic regulation of antioxidant and inflammation in neurodegenerative processes resulting from high cholesterol consumption, with an emphasis on GBR's potential to ameliorate such changes.
活性氧物种产生导致的氧化应激在炎症过程中起着至关重要的作用,并且与神经退行性变化有关。鉴于发芽糙米(GBR)改善学习和记忆的能力,本研究旨在探讨 GBR 在高脂肪饮食(HFD)诱导的成年 Sprague-Dawley 大鼠氧化变化中的神经保护作用的机制基础。富阿魏酸的 GBR 乙酸乙酯提取物(GBR-EA;100mg/kg 和 200mg/kg 体重)在研究期间最后 3 个月的 HFD 喂养期间口服补充。与 HFD 组相比,GBR-EA 补充可改善脂质谱和血清抗氧化状态。在 GBR-EA 处理动物的额叶皮层和海马体中,SOD1、SOD2、SOD3、Catalase 和 GPX 的 mRNA 表达升高。GBR-EA 通过下调 CRP 和 TNF-α和上调 PPAR-γ,减轻了 HFD 在海马体中引起的促炎变化。GBR 还降低了海马体中乙酰胆碱酯酶的 mRNA 表达和酶水平。总之,本研究提出了高胆固醇摄入导致的神经退行性过程中抗氧化和炎症的可能转录组调节,重点是 GBR 改善这种变化的潜力。