Li Qian, Li Konghui, Hu Tenggen, Liu Fan, Liao Sentai, Zou Yuxiao
Guangdong Academy of Agricultural Sciences, Sericultural & Agri-Food Research Institute/Key Laboratory of Functional Foods, Ministry of Agriculture and Rural Affairs/Guangdong Key Laboratory of Agricultural Products Processing, Guangzhou 510610, China.
J Agric Food Chem. 2021 Apr 28;69(16):4720-4731. doi: 10.1021/acs.jafc.1c00487. Epub 2021 Mar 24.
In this study, we evaluated the protective effect and molecular mechanism of a dominant phenanthrene, (6,7-dihydroxy-2,4-dimethoxyphenanthrene, CYP4), from Chinese yam peels on intestinal epithelial integrity. Three doses of Chinese yam phenolic extract (CYPE) and Chinese yam phenanthrene 4 (CYP4) were administered to BALB/c mice for 7 days before dextran sulfate sodium (DSS) treatment, with berberine hydrochloride as a positive control (PC). Results showed that both disease activity indexes (DAIs), histological damage score (HDS) and survival rate in DSS mice, were improved with preintervention of CYPE and CYP4, which exhibited better efficiency than PC. Further studies showed that administration of CYP4 downregulated the oxidative stress-associated factors, MPO and NO, and improved tight junction protein occludin. Besides, the CYP4 treatment substantially downregulated the caspase-3 expression and the apoptosis rate of intestinal epithelial cells. In addition, the CYP4 treatment ameliorated the production of inflammatory cytokines including TNF-α, IFN-γ, IL-10, and IL-23 in the colon. Furthermore, the protein expression of ERK1/2, NF-κB p65, pNF-κB, and COX-2 was suppressed in CYE4 groups as compared with that in model control (MC). These findings suggested that CHP4 could effectively inhibit the activation of NF-κB/COX-2 in an experimental UC model in vivo. It was demonstrated for the first time that CYPE and CYP4 protected intestinal mucosa from damage and prevented DSS-induced colitis in mice. CYP4 was one of the active principles obligatory for the biological effect of Chinese yam in protecting intestinal health. These findings indicated that CYP4 might be a promising and useful approach for treatment of UC in humans.
在本研究中,我们评估了来自山药皮的一种主要菲类化合物(6,7 - 二羟基 - 2,4 - 二甲氧基菲,CYP4)对肠上皮完整性的保护作用及其分子机制。在给予葡聚糖硫酸钠(DSS)处理前7天,对BALB/c小鼠施用三种剂量的山药酚提取物(CYPE)和山药菲4(CYP4),以盐酸小檗碱作为阳性对照(PC)。结果显示,CYPE和CYP4预处理可改善DSS小鼠的疾病活动指数(DAIs)、组织学损伤评分(HDS)和存活率,其效果优于PC。进一步研究表明,施用CYP4可下调氧化应激相关因子MPO和NO,并改善紧密连接蛋白occludin。此外,CYP4处理显著下调caspase - 3表达和肠上皮细胞凋亡率。另外,CYP4处理改善了结肠中包括TNF - α、IFN - γ、IL - 10和IL - 23在内的炎性细胞因子的产生。此外,与模型对照(MC)组相比,CYE4组中ERK1/2、NF - κB p65、pNF - κB和COX - 2的蛋白表达受到抑制。这些发现表明,CHP4可在体内实验性UC模型中有效抑制NF - κB/COX - 2的激活。首次证明CYPE和CYP4可保护肠黏膜免受损伤并预防DSS诱导的小鼠结肠炎。CYP4是山药保护肠道健康生物学效应所必需的活性成分之一。这些发现表明,CYP4可能是治疗人类UC的一种有前景且有用的方法。