首页> 外文期刊>Cancer biology & therapy >Natural dietary compound naringin prevents azoxymethane/dextran sodium sulfate-induced chronic colorectal inflammation and carcinogenesis in mice
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Natural dietary compound naringin prevents azoxymethane/dextran sodium sulfate-induced chronic colorectal inflammation and carcinogenesis in mice

机译:天然饮食化合物柚皮素可防止偶氮甲烷/葡聚糖硫酸钠诱导的慢性结直肠炎症和小鼠致癌作用

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摘要

Naringin, a natural occurring flavonoid compound, enriches in citrus fruits. We aimed to evaluate the inhibitory effect of naringin on colitis and chronic inflammation-driven carcinogenesis. Male C57BL/6 mice were exposed to AOM/DSS to induce colorectal inflammation and carcinogenesis. Naringin by oral administration prevented AOM/DSS-induced ulcerative colitis and carcinogenesis without significant side effects. Naringin attenuated the severity of colitis and colorectal adenomas through inhibiting myeloid-derived suppressor cells (MDSCs), pro-inflammatory mediators GM-CSF/M-CSF, IL-6 and TNF-α and the NF-κB/IL-6/STAT3 cascades in colorectal tissues. Naringin-treated mice exhibited normalized structures of colorectal tissues. Electron microscopy analysis showed the suppression of robust endoplasmic reticulum (ER) stress-induced autophagy. Naringin inhibited the secretion of the ER-spanning transmembrane proteins, such as GRP78 ATF6, IREIα and activated PERK phosphorylated elF-2α and complex of autophagosomes ATG3, ATG5, ATG7, ATG12, ATG16 and ATG16L1 in the colorectal mucosal cells. Conclusion: Naringin prevented colitis and colorectal carcinogenesis through suppressing robust ER stress-induced autophagy in colorectal mucosal cells. Naringin could develop a promising therapeutic agent for the prevention of ulcerative colitis and colorectal tumor.
机译:Naringin,一种天然的类黄酮化合物,丰富柑橘类水果。我们的旨在评估柚皮蛋白对结肠炎和慢性炎症驱动的致癌作用的抑制作用。将雄性C57BL / 6小鼠暴露于AOM / DSS以诱导结直肠炎症和致癌作用。口服给药的柚皮蛋白预防AOM / DSS诱导的溃疡性结肠炎和致癌作用,而无明显副作用。 Naringin通过抑制骨髓衍生的抑制细胞(MDSC),促炎介质GM-CSF / M-CSF,IL-6和TNF-α和NF-κB/ IL-6 / Stat3,衰减结肠炎和结肠直肠腺瘤的严重程度结肠直肠组织中的瀑布。 Naringin治疗的小鼠表现出结直肠组织的标准化结构。电子显微镜分析显示抑制强大的内质网(ER)应激诱导的自噬。 Naringin抑制了ER跨越跨膜蛋白的分泌,例如GRP78 ATF6,IREIα和活化的PERK磷酸化的ELF-2α,其自噬蛋白ATG3,ATG5,ATG7,ATG12,ATG16和ATG16L1中的综合体。结论:Naringin通过抑制结直肠粘膜细胞抑制鲁棒ER应激诱导的自噬导致结肠炎和结肠直肠癌。 Naringin可以制定有助于预防溃疡性结肠炎和结肠直肠肿瘤的有前途的治疗剂。

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