糖基化肉桂醛衍生物的合成及其对小鼠结肠炎和痛风模型的抗炎作用。

IF 7.5
Wei-Ting Wong, Lan-Hui Li, Hsiao-Wen Chiu, Po-Yu Chiang, Hsueh-Chen Lu, Chun-Hsien Wu, Chen-Lung Ho, Lee-Chiang Lo, Kuo-Feng Hua
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引用次数: 0

摘要

肉桂醛是一种具有多种生物活性的天然化合物,由于其潜在的细胞毒性,在生物医学上的应用受到限制。在本研究中,我们通过改变糖段及其在芳香环上的附着位置,合成了一系列新的糖基化肉桂醛衍生物。细胞毒性和抗炎活性的初步筛选表明,这些结构修饰严重影响生物活性。在这些衍生物中,化合物1a在肉桂醛苯基环的对位上含有β- d -半乳糖基,显示出最有希望的治疗潜力。相反,用β- d -葡萄糖基(1b)或α- d -甘露糖基(1c)残基取代β- d -半乳糖基导致抗炎活性丧失。同样,将β- d -半乳糖基移至元(1d)或邻位(1e)也会消除活性,这突出了糖的同一性及其位置附着在决定功能中的重要性。随后的机制研究集中在化合物1a及其对NOD-, LRR-和pyrin结构域蛋白3 (NLRP3)炎症小体的影响,炎症小体是炎症疾病的中心介质。化合物1a通过减少巨噬细胞线粒体损伤和破坏炎性小体复合物组装,有效抑制NLRP3炎性小体激活。此外,1a促进sirt1介导的自噬,这有助于额外抑制炎性体的激活。值得注意的是,1a不仅抑制了巨噬细胞中的NLRP3炎性体,还抑制了NLRC4炎性体。在体内,口服1a主要通过抑制NLRP3炎性小体,显著减轻小鼠葡聚糖硫酸钠(DSS)诱导的结肠炎和尿酸钠(MSU)诱导的腹膜炎。总的来说,这些发现确定了化合物1a是治疗炎性小体驱动的炎症性疾病的有希望的先导化合物,并强调了肉桂醛的合理糖基化修饰的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and anti-inflammatory properties of glycosylated cinnamaldehyde derivatives in mice models of colitis and gout.

Cinnamaldehyde, a natural compound with diverse biological activities, has limited biomedical application due to its potential cytotoxicity. In this study, we synthesized a series of novel glycosylated cinnamaldehyde derivatives by varying both the sugar moiety and its attachment position on the aromatic ring. Preliminary screening for cytotoxicity and anti-inflammatory activity revealed that these structural modifications critically influenced bioactivity. Among the derivatives, compound 1a, bearing a β-D-galactosyl group at the para-position of the cinnamaldehyde phenyl ring, exhibited the most promising therapeutic potential. In contrast, replacing the β-D-galactosyl group with β-D-glucosyl (1b) or α-D-mannosyl (1c) residues resulted in loss of anti-inflammatory activity. Similarly, shifting the β-D-galactosyl group to the meta (1d) or ortho (1e) positions also abolished activity, highlighting the importance of both sugar identity and its positional attachment in determining function. Subsequent mechanistic studies focused on compound 1a and its effect on the NOD-, LRR- and pyrin domain-containing protein 3 (NLRP3) inflammasome, a central mediator in inflammatory disorders. Compound 1a effectively suppressed NLRP3 inflammasome activation by reducing mitochondrial damage and disrupting inflammasome complex assembly in macrophages. Furthermore, 1a promoted Sirt1-mediated autophagy, which contributed to additional inhibition of inflammasome activation. Notably, 1a inhibited not only the NLRP3 inflammasome but also the NLRC4 inflammasome in macrophages. In vivo, oral administration of 1a significantly alleviated both dextran sulfate sodium (DSS)-induced colitis and monosodium urate (MSU)-induced peritonitis in mice, primarily through NLRP3 inflammasome suppression. Collectively, these findings identify compound 1a as a promising lead compound for the treatment of inflammasome-driven inflammatory diseases and underscore the therapeutic potential of rational glycosylation-based modification of cinnamaldehyde.

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