Liang Xi, Zhang Zhe, Lv Youyou, Lu Haiyan, Liu Tongjie, Yi Huaxi, Zhao Maozhen, Zhang Lanwei, Gong Pimin
College of Food Science and Engineering, Ocean University of China, Qingdao 266003, China.
Foods. 2021 Oct 6;10(10):2374. doi: 10.3390/foods10102374.
There has been an increasing number of studies on the interaction between active substances and probiotics to improve disease. Both krill oil (KO) and probiotics have the effect of improving atherosclerotic cardiovascular disease, but the combined effect has not been explored. Therefore, the purpose of this study was to explore the improvement effect of KO combined with probiotics on atherosclerosis. The atherosclerotic plaque area of ApoE mice was detected after the intervention of KO, subsp. F1-7 ( F1-7), and KO combined with F1-7. The results showed that F1-7, KO, and KO combined with F1-7 could significantly reduce the area of atherosclerotic plaque and improve the levels of serum lipids and inflammatory factors. They could regulate the farnesoid X receptor (FXR)/cholesterol 7-alpha hydroxylase (CYP7A1) pathway to reduce lipid accumulation. The intervention groups could also improve the inflammatory response by downregulating the Toll-like receptor 4 (TLR4)/myeloid differentiation factor 88 (MyD88) pathway. The anti-inflammatory effect of the interaction group was significantly better than that of KO. It proved that F1-7 might play a synergistic effect in the improvement of inflammation by KO to the alleviation of atherosclerosis.
为改善疾病,关于活性物质与益生菌之间相互作用的研究越来越多。磷虾油(KO)和益生菌都有改善动脉粥样硬化性心血管疾病的作用,但二者的联合作用尚未得到探索。因此,本研究的目的是探讨KO与益生菌联合应用对动脉粥样硬化的改善作用。在分别给予KO、 亚种F1-7(F1-7)以及KO与F1-7联合干预后,检测载脂蛋白E(ApoE)小鼠的动脉粥样硬化斑块面积。结果显示,F1-7、KO以及KO与F1-7联合应用均可显著减小动脉粥样硬化斑块面积,改善血脂和炎症因子水平。它们可调节法尼醇X受体(FXR)/胆固醇7α-羟化酶(CYP7A1)通路以减少脂质蓄积。干预组还可通过下调Toll样受体4(TLR4)/髓样分化因子88(MyD88)通路来改善炎症反应。联合作用组的抗炎效果显著优于KO。这证明F1-7在KO改善炎症从而减轻动脉粥样硬化的过程中可能起到协同作用。