Department of Therapeutic Chemistry, National Research Centre, 33 El-Bohouth St., Dokki, Cairo, 12622, Egypt.
Neurochem Res. 2020 May;45(5):1142-1155. doi: 10.1007/s11064-020-02996-2. Epub 2020 Mar 2.
Alzheimer's disease (AD) is the most common form of dementia that progressively disrupts neurocognitive function, which has neither cure nor effective treatment. Hypercholesterolemia might be involved in brain alterations that could evolve into AD. The present study aims to evaluate the potential of omega-3, Co-enzyme Q10 (Co-Q10), as well as their combination in ameliorating hypercholesterolemia-initiated AD-like disease. We adapted a hypercholesterolemic (HC) rat model, a model of oxidative stress-mediated neurodegeneration, to study AD-like pathology. Hypercholesterolemia resulted in increased lipid peroxidation coupled with declined nitric oxide production, reduced glutathione levels, and decreased antioxidant activities of glutathione-s-transferase (GST) and glutathione peroxidase (GSH-Px) in the brain. Moreover, hypercholesterolemia resulted in decreased acetylcholine (ACh) levels and increased acetylcholine-esterase (AChE) activity, along with an increment of tumor necrosis factor and amyloid-β 42. Behaviorally, HC-rats demonstrated depressive-like behavior and declined memory. Treatment of HC-rats with omega-3 and Co-Q10 (alone or in combination) alleviated the brain oxidative stress and inflammation, regulated cholinergic functioning, and enhanced the functional outcome. These findings were verified by the histopathological investigation of brain tissues. This neuroprotective potential of omega-3 and Co-Q10 was achieved through anti-oxidative, anti-inflammatory, anti-amyloidogenic, pro-cholinergic, and memory-enhancing activities against HC-induced AD-like disease; suggesting that they may be useful as prophylactic and therapeutic agents against the neurotoxic effects of hypercholesterolemia.
阿尔茨海默病(AD)是最常见的痴呆症形式,它会逐渐破坏神经认知功能,目前既没有治愈方法,也没有有效的治疗方法。高胆固醇血症可能与导致 AD 的大脑改变有关。本研究旨在评估ω-3、辅酶 Q10(Co-Q10)及其组合在改善由高胆固醇血症引起的 AD 样疾病中的潜力。我们适应了高胆固醇血症(HC)大鼠模型,这是一种氧化应激介导的神经退行性变模型,用于研究 AD 样病理学。高胆固醇血症导致脂质过氧化增加,同时一氧化氮生成减少,谷胱甘肽水平降低,以及大脑中的谷胱甘肽-s-转移酶(GST)和谷胱甘肽过氧化物酶(GSH-Px)的抗氧化活性降低。此外,高胆固醇血症导致乙酰胆碱(ACh)水平降低和乙酰胆碱酯酶(AChE)活性增加,同时肿瘤坏死因子和淀粉样β 42 增加。行为上,HC 大鼠表现出抑郁样行为和记忆减退。用 ω-3 和 Co-Q10(单独或联合)治疗 HC 大鼠可减轻大脑氧化应激和炎症,调节胆碱能功能,并改善功能结果。这些发现通过对脑组织的组织病理学研究得到了验证。ω-3 和 Co-Q10 的这种神经保护潜力是通过抗氧化、抗炎、抗淀粉样变性、促胆碱能和增强记忆作用实现的,这些作用可对抗由 HC 引起的 AD 样疾病;表明它们可能作为预防和治疗高胆固醇血症神经毒性作用的有用药物。