First Propaedeutic Department of Surgery, Hippocration General Hospital, School of Medicine, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Department of Clinical Nutrition, Hippocration General Hospital, 11527 Athens, Greece.
Int J Mol Sci. 2023 May 28;24(11):9399. doi: 10.3390/ijms24119399.
Cyanidin-3-O-glucoside (C3G), the most widely distributed anthocyanin (ACN) in edible fruits, has been proposed for several bioactivities, including anti-inflammatory, neuro-protective, antimicrobial, anti-viral, anti-thrombotic and epigenetic actions. However, habitual intake of ACNs and C3G may vary widely among populations, regions, and seasons, among individuals with different education and financial status. The main point of C3G absorption occurs in the small and large bowel. Therefore, it has been supposed that the treating properties of C3G might affect inflammatory bowel diseases (IBD), such as ulcerative colitis (UC) and Crohn's disease (CD). IBDs develop through complex inflammatory pathways and sometimes may be resistant to conventional treatment strategies. C3G presents antioxidative, anti-inflammatory, cytoprotective, and antimicrobial effects useful for IBD management. In particular, different studies have demonstrated that C3G inhibits NF-κB pathway activation. In addition, C3G activates the Nrf2 pathway. On the other hand, it modulates the expression of antioxidant enzymes and cytoprotective proteins, such as NAD(P)H, superoxide dismutase, heme-oxygenase (HO-1), thioredoxin, quinone reductase-oxide 1 (NQO1), catalase, glutathione S-transferase and glutathione peroxidase. Interferon I and II pathways are downregulated by C3G inhibiting interferon-mediating inflammatory cascades. Moreover, C3G reduces reactive species and pro-inflammatory cytokines, such as C reactive protein, interferon-γ, tumor necrosis factor-α, interleukin (IL)-5, IL-9, IL-10, IL-12p70, and IL-17A in UC and CD patients. Finally, C3G modulates gut microbiota by inducing an increase in beneficial gut bacteria and increasing microbial abundances, thus mitigating dysbiosis. Thus, C3G presents activities that may have potential therapeutic and protective actions against IBD. Still, in the future, clinical trials should be designed to investigate the bioavailability of C3G in IBD patients and the proper therapeutic doses through different sources, aiming to the standardization of the exact clinical outcome and efficacy of C3G.
矢车菊素-3-O-葡萄糖苷(C3G)是食用水果中分布最广泛的花色苷(ACN),具有多种生物活性,包括抗炎、神经保护、抗菌、抗病毒、抗血栓和表观遗传作用。然而,ACN 和 C3G 的习惯性摄入在人群、地区和季节之间,以及在教育和经济地位不同的个体之间可能存在很大差异。C3G 的主要吸收部位发生在小肠和大肠。因此,人们推测 C3G 的治疗特性可能会影响炎症性肠病(IBD),如溃疡性结肠炎(UC)和克罗恩病(CD)。IBD 通过复杂的炎症途径发展,有时可能对传统治疗策略产生抗性。C3G 具有抗氧化、抗炎、细胞保护和抗菌作用,可用于 IBD 管理。特别是,不同的研究表明 C3G 抑制 NF-κB 途径的激活。此外,C3G 还激活 Nrf2 途径。另一方面,它调节抗氧化酶和细胞保护蛋白的表达,如 NAD(P)H、超氧化物歧化酶、血红素加氧酶(HO-1)、硫氧还蛋白、醌还原酶-氧化物 1(NQO1)、过氧化氢酶、谷胱甘肽 S-转移酶和谷胱甘肽过氧化物酶。C3G 通过抑制干扰素介导的炎症级联反应,下调干扰素 I 和 II 途径。此外,C3G 减少活性物质和促炎细胞因子,如 C 反应蛋白、干扰素-γ、肿瘤坏死因子-α、白细胞介素(IL)-5、IL-9、IL-10、IL-12p70 和 IL-17A 在 UC 和 CD 患者中。最后,C3G 通过诱导有益肠道细菌的增加和微生物丰度的增加来调节肠道微生物群,从而减轻失调。因此,C3G 具有针对 IBD 的潜在治疗和保护作用。尽管如此,未来仍应设计临床试验,以研究 C3G 在 IBD 患者中的生物利用度和通过不同来源的适当治疗剂量,旨在使 C3G 的精确临床结果和疗效标准化。
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