Department of Internal Medicine, Section Pharmacology and Vascular Medicine, Erasmus University Medical Center, 3015 GE Rotterdam, The Netherlands.
Department of Neuroscience, Biomedical Research Institute, Faculty of Medicine and Life Sciences, Hasselt University, B-3590 Hasselt, Belgium.
Nutrients. 2024 May 25;16(11):1614. doi: 10.3390/nu16111614.
We previously demonstrated that diet supplementation with seaweed () prevented AD-related pathology in a mouse model of Alzheimer's Disease (AD). Here, we tested a lipid extract of seaweed () and a supercritical fluid (SCF) extract of that is free of excess inorganic arsenic. Diet supplementation with extract prevented cognitive deterioration in APPswePS1ΔE9 mice. Similar trends were observed for the SCF extract. The cerebral amyloid-β plaque load remained unaffected. However, IHC analysis revealed that both extracts lowered glial markers in the brains of APPswePS1ΔE9 mice. While cerebellar cholesterol concentrations remained unaffected, both extracts increased desmosterol, an endogenous LXR agonist with anti-inflammatory properties. Both extracts increased cholesterol efflux, and particularly, extract decreased the production of pro-inflammatory cytokines in LPS-stimulated THP-1-derived macrophages. Additionally, our findings suggest a reduction of AD-associated phosphorylated tau and promotion of early oligodendrocyte differentiation by . RNA sequencing on the hippocampus of one-week-treated APPswePS1ΔE9 mice revealed effects of on, amongst others, acetylcholine and synaptogenesis signaling pathways. In conclusion, extracts of and show potential to reduce AD-related pathology in APPswePS1ΔE9 mice. Increasing desmosterol concentrations may contribute to these effects by dampening neuroinflammation.
我们之前的研究表明,海藻()的饮食补充可以预防阿尔茨海默病(AD)小鼠模型中的 AD 相关病理。在这里,我们测试了海藻()的脂质提取物和无过量无机砷的超临界流体(SCF)提取物。海藻提取物的饮食补充可预防 APPswePS1ΔE9 小鼠的认知能力下降。SCF 提取物也观察到了类似的趋势。大脑中的淀粉样β斑块负荷保持不变。然而,免疫组化分析显示,两种提取物均降低了 APPswePS1ΔE9 小鼠大脑中的神经胶质标志物。虽然小脑胆固醇浓度不受影响,但两种提取物均增加了内源性 LXR 激动剂具有抗炎特性的去甲固醇。两种提取物均增加了胆固醇外排,特别是,海藻提取物降低了 LPS 刺激的 THP-1 衍生巨噬细胞中促炎细胞因子的产生。此外,我们的研究结果表明,海藻提取物可减少 AD 相关的磷酸化 tau 并促进早期少突胶质细胞分化。对一周治疗的 APPswePS1ΔE9 小鼠海马的 RNA 测序显示,海藻提取物对乙酰胆碱和突触发生信号通路等产生影响。总之,海藻()和()的提取物具有降低 APPswePS1ΔE9 小鼠 AD 相关病理的潜力。增加去甲固醇浓度可能通过抑制神经炎症来促成这些作用。