Bartra Clara, Yuan Yi, Vuraić Kristijan, Valdés-Quiroz Haydeé, Garcia-Baucells Pau, Slevin Mark, Pastorello Ylenia, Suñol Cristina, Sanfeliu Coral
Institut d'Investigacions Biomèdiques de Barcelona (IIBB), CSIC, 08036 Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi i Sunyer (DIBAPS), 08036 Barcelona, Spain.
Antioxidants (Basel). 2024 Jan 31;13(2):177. doi: 10.3390/antiox13020177.
Resveratrol is a natural phenolic compound with known benefits against neurodegeneration. We analyzed in vitro the protective mechanisms of resveratrol against the proinflammatory monomeric C-reactive protein (mCRP). mCRP increases the risk of AD after stroke and we previously demonstrated that intracerebral mCRP induces AD-like dementia in mice. Here, we used BV2 microglia treated with mCRP for 24 h in the presence or absence of resveratrol. Cells and conditioned media were collected for analysis. Lipopolysaccharide (LPS) has also been implicated in AD progression and so LPS was used as a resveratrol-sensitive reference agent. mCRP at the concentration of 50 µg/mL activated the nitric oxide pathway and the NLRP3 inflammasome pathway. Furthermore, mCRP induced cyclooxygenase-2 and the release of proinflammatory cytokines. Resveratrol effectively inhibited these changes and increased the expression of the antioxidant enzyme genes and . As central mechanisms of defense, resveratrol activated the hub genes and and inhibited the nuclear translocation of the signal transducer NF-ĸB. Proinflammatory changes induced by mCRP in primary mixed glial cultures were also protected by resveratrol. This work provides a mechanistic insight into the protective benefits of resveratrol in preventing the risk of AD induced by proinflammatory agents.
白藜芦醇是一种天然酚类化合物,已知对神经退行性变有保护作用。我们在体外分析了白藜芦醇对促炎单体C反应蛋白(mCRP)的保护机制。mCRP会增加中风后患阿尔茨海默病(AD)的风险,我们之前证明脑内mCRP会在小鼠中诱发类似AD的痴呆症。在此,我们使用在有或无白藜芦醇的情况下用mCRP处理24小时的BV2小胶质细胞。收集细胞和条件培养基进行分析。脂多糖(LPS)也与AD进展有关,因此LPS被用作白藜芦醇敏感的参照剂。浓度为50µg/mL的mCRP激活了一氧化氮途径和NLRP3炎性小体途径。此外,mCRP诱导了环氧化酶-2和促炎细胞因子的释放。白藜芦醇有效抑制了这些变化,并增加了抗氧化酶基因和的表达。作为主要的防御机制,白藜芦醇激活了关键基因和,并抑制了信号转导子NF-κB的核转位。白藜芦醇也保护了原代混合神经胶质细胞培养物中由mCRP诱导的促炎变化。这项工作为白藜芦醇在预防由促炎剂诱发的AD风险中的保护作用提供了机制性见解。