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首页> 外文期刊>Mechanisms of Ageing and Development >Impairment of the ABCA1 and SR-BI-mediated cholesterol efflux pathways and HDL anti-inflammatory activity in Alzheimer's disease
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Impairment of the ABCA1 and SR-BI-mediated cholesterol efflux pathways and HDL anti-inflammatory activity in Alzheimer's disease

机译:阿尔茨海默氏病中ABCA1和SR-BI介导的胆固醇外排途径和HDL抗炎活性受损

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The aim of our study was to investigate the effect of Alzheimer's disease (AD) on the cholesterol efflux capacity and anti-inflammatory activity of HDL. HDL and apoA-I were isolated from 20 healthy subjects and from 39 AD patients. Our results showed that serum- and HDL-mediated cholesterol efflux is significantly impaired in AD patients. This impairment of serum and HDL cholesterol efflux capacity was significantly inversely correlated to the AD severity as evaluated by MMSE scores. Results obtained from SR-BI-enriched Fu5AH and ABCA1-enriched J774 cells revealed that AD impaired the interaction of HDL and apoA-I with both the ABCA1 transporter and SR-BI receptor. Purified apoA-I from AD patients also failed to remove free excess cholesterol from ABCA1-enriched J774 macrophages. Interestingly, the decrease in plasma α-tocopherol content and the increase in MDA formation and HDL relative electrophoretic mobility indicated that AD patients had higher levels of oxidative stress. The anti-inflammatory activity of HDL was also significantly lower in AD patients as measured by the level of ICAM-1 expression. In conclusion, our study provides evidence for the first time that the functionality of HDL is impaired in AD and that this alteration might be caused by AD-associated oxidative stress and inflammation.
机译:我们研究的目的是研究阿尔茨海默氏病(AD)对HDL的胆固醇外排能力和抗炎活性的影响。从20名健康受试者和39名AD患者中分离出HDL和apoA-I。我们的结果表明,AD患者的血清和HDL介导的胆固醇外排显着受损。血清和HDL胆固醇外排能力的这种损害与MMSE评分评估的AD严重程度呈显着负相关。从富含SR-BI的Fu5AH和富含ABCA1的J774细胞获得的结果表明,AD损害了HDL和apoA-I与ABCA1转运蛋白和SR-BI受体的相互作用。来自AD患者的纯化的apoA-I也不能从富含ABCA1的J774巨噬细胞中除去游离的过量胆固醇。有趣的是,血浆α-生育酚含量的减少以及MDA形成和HDL相对电泳迁移率的增加表明,AD患者的氧化应激水平更高。通过ICAM-1表达水平的测定,HDL的抗炎活性在AD患者中也显着降低。总之,我们的研究首次证明了HDL的功能在AD中受损,并且这种改变可能是由AD相关的氧化应激和炎症引起的。

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