Ferrari Daniela, Speciale Antonio, Cristani Mariateresa, Fratantonio Deborah, Molonia Maria Sofia, Ranaldi Giulia, Saija Antonella, Cimino Francesco
Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Italy.
Council for Agricultural Research and Economics, Food and Nutrition Research Centre, (CREA - NUT), Rome, Italy.
Toxicol Lett. 2016 Dec 15;264:51-58. doi: 10.1016/j.toxlet.2016.10.014. Epub 2016 Oct 25.
Chronic intestinal inflammatory disorders, such as Inflammatory Bowel Diseases (IBDs), are characterized by excessive release of proinflammatory mediators, intestinal barrier dysfunction and excessive activation of NF-kB cascade. Previous studies shown that TNF-α plays a central role in intestinal inflammation of IBDs and supported beneficial effects of flavonoids against chronic inflammatory diseases. In this study, we employed an in vitro model of acute intestinal inflammation using intestinal Caco-2 cells exposed to TNF-α. The protective effects of cyanidin-3-glucoside (C3G), an anthocyanin widely distributed in mediterranean diet, were then evaluated. Caco-2 cells exposure to TNF-α activated NF-kB proinflammatory pathway and induced IL6 and COX-2 expression. Cells pretreatment for 24h with C3G (20-40μM) prevented TNF-α-induced changes, and improved intracellular redox status. Our results demonstrated that C3G, also without any kind of stimulus, increased the translocation of the transcription factor Nrf2 into the nucleus so activating antioxidant and detoxifying genes. In conclusion, C3G exhibited protective effects through the inhibition of NF-kB signalling in Caco-2 cells and these beneficial effects appear to be due to its ability to activate cellular protective responses modulated by Nrf2. These data suggest that anthocyanins could contribute, as complementary or preventive approaches, to the management of chronic inflammatory diseases.
慢性肠道炎症性疾病,如炎症性肠病(IBDs),其特征在于促炎介质的过度释放、肠道屏障功能障碍以及NF-κB级联的过度激活。先前的研究表明,TNF-α在IBDs的肠道炎症中起核心作用,并支持类黄酮对慢性炎症性疾病的有益作用。在本研究中,我们使用暴露于TNF-α的肠道Caco-2细胞建立了急性肠道炎症的体外模型。然后评估了矢车菊素-3-葡萄糖苷(C3G)的保护作用,C3G是一种广泛分布于地中海饮食中的花青素。Caco-2细胞暴露于TNF-α会激活NF-κB促炎途径并诱导IL6和COX-2表达。用C3G(20-40μM)对细胞进行24小时预处理可预防TNF-α诱导的变化,并改善细胞内氧化还原状态。我们的结果表明,C3G在没有任何刺激的情况下,也会增加转录因子Nrf2向细胞核的转位,从而激活抗氧化和解毒基因。总之,C3G通过抑制Caco-2细胞中的NF-κB信号传导表现出保护作用,这些有益作用似乎归因于其激活由Nrf2调节的细胞保护反应的能力。这些数据表明,花青素可以作为补充或预防方法,对慢性炎症性疾病的管理做出贡献。
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