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香柠檬果汁提取物通过MAPK和AP-1途径减轻β-淀粉样蛋白诱导的THP-1细胞促炎激活。

Citrus bergamia Juice Extract Attenuates β-Amyloid-Induced Pro-Inflammatory Activation of THP-1 Cells Through MAPK and AP-1 Pathways.

作者信息

Currò Monica, Risitano Roberto, Ferlazzo Nadia, Cirmi Santa, Gangemi Chiara, Caccamo Daniela, Ientile Riccardo, Navarra Michele

机构信息

Department of Biomedical Sciences and Morphological and Functional Images, University of Messina, Messina, I-98100, Italy.

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, I-98168, Italy.

出版信息

Sci Rep. 2016 Feb 8;6:20809. doi: 10.1038/srep20809.

Abstract

Flavonoids have been shown to be effective in protecting against age-related cognitive and motor decline in both in vitro and in vivo models. Recently, a flavonoid-rich extract of Citrus bergamia juice (BJe) has been shown to display anti-oxidant and anti-inflammatory properties against LPS-induced activation of human THP-1 monocytes. In the light of these observations, we wondered whether BJe may be beneficial against neuroinflammatory processes, such as those observed in Alzheimer's disease. To this aim we used THP-1 monocytes to investigate the mechanisms underlying the beneficial potential of BJe against amyloid-beta1-42 (Aβ1-42) -mediated inflammation. Exposure of THP-1 cells to Aβ1-42 significantly induced the expression and secretion of IL-6 and IL-1β in THP-1 cells and increased the phosphorylation of ERK 1/2 as well as p46 and p54 members of JNK family. Moreover, Aβ1-42 raises AP-1 DNA binding activity in THP-1-treated cells. Interestingly, all these effects were reduced in the presence of BJe. Our data indicate that BJe may effectively counteract the pro-inflammatory activation of monocytes/microglial cells exposed to amyloid fibrils, suggesting a promising role as a natural drug against neuroinflammatory processes.

摘要

在体外和体内模型中,黄酮类化合物已被证明能有效预防与年龄相关的认知和运动功能衰退。最近,一项研究表明,富含黄酮类化合物的香柠檬果汁提取物(BJe)对脂多糖诱导的人THP-1单核细胞激活具有抗氧化和抗炎特性。鉴于这些观察结果,我们想知道BJe是否对神经炎症过程有益,比如在阿尔茨海默病中观察到的那些过程。为了实现这一目标,我们使用THP-1单核细胞来研究BJe对β淀粉样蛋白1-42(Aβ1-42)介导的炎症有益作用的潜在机制。将THP-1细胞暴露于Aβ1-42可显著诱导THP-1细胞中IL-6和IL-1β的表达和分泌,并增加ERK 1/2以及JNK家族的p46和p54成员的磷酸化。此外,Aβ1-42提高了经THP-1处理的细胞中AP-1的DNA结合活性。有趣的是,在存在BJe的情况下,所有这些效应都有所降低。我们的数据表明,BJe可能有效地对抗暴露于淀粉样纤维的单核细胞/小胶质细胞的促炎激活,这表明其作为一种抗神经炎症过程的天然药物具有广阔前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6d9/4745106/b3210c7f4198/srep20809-f1.jpg

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