Department of Nutrition, University of California, Davis, CA, 95618, USA.
Cleveland Clinic, Cleveland, OH, 44194, USA.
Redox Biol. 2024 Sep;75:103275. doi: 10.1016/j.redox.2024.103275. Epub 2024 Jul 20.
Diet is of major importance in modulating intestinal inflammation, as the gastrointestinal tract is directly exposed to high concentrations of dietary components. Procyanidins are flavan-3-ol oligomers abundant in fruits and vegetables. Although with limited or no intestinal absorption, they can have GI health benefits which can promote overall health. We previously observed that epicatechin gallate (ECG) and epigallocatechin gallate (EGCG) dimers inhibit in vitro colorectal cancer cell proliferation and invasiveness. Inflammation-mediated intestinal barrier permeabilization can result in a chronic inflammatory condition and promote colorectal cancer onset/progression. Thus, this study investigated the structure-dependent capacity of ECG, EGCG and (-)-epicatechin (EC) dimers to inhibit tumor necrosis factor alpha (TNFα)-induced inflammation, oxidative stress, and loss of barrier integrity in Caco-2 cells differentiated into an intestinal epithelial cell monolayer. Cells were incubated with TNFα (10 ng/ml), in the absence/presence of ECG, EGCG and EC dimers. The three dimers inhibited TNFα-mediated Caco-2 cell monolayer permeabilization, modulating events involved in the loss of barrier function and inflammation, i.e. decreased tight junction protein levels; increased matrix metalloproteinases expression and activity; increased NADPH oxidase expression and oxidant production; activation of the NF-κB and ERK1/2 pathways and downstream events leading to tight junction opening. For some of these mechanisms, the galloylated ECG and EGCG dimers had stronger protective potency than the non-galloylated EC dimer. These differences could be due to differential membrane interactions as pointed out by molecular dynamics simulation of procyanidin dimers-cell membrane interactions and/or by differential interactions with NOX1. Results show that dimeric procyanidins, although poorly absorbed, can promote health by alleviating intestinal inflammation, oxidative stress and barrier permeabilization.
饮食在调节肠道炎症方面非常重要,因为胃肠道直接暴露于高浓度的膳食成分中。原花青素是一种在水果和蔬菜中含量丰富的黄烷-3-醇低聚物。尽管原花青素的肠道吸收率有限或几乎没有,但它们可能对胃肠道健康有益,从而促进整体健康。我们之前观察到表儿茶素没食子酸酯(ECG)和表没食子儿茶素没食子酸酯(EGCG)二聚体抑制体外结直肠癌细胞的增殖和侵袭性。炎症介导的肠道屏障通透性会导致慢性炎症状态,并促进结直肠癌的发生/进展。因此,本研究调查了 ECG、EGCG 和(-)-表儿茶素(EC)二聚体抑制肿瘤坏死因子-α(TNFα)诱导的炎症、氧化应激和分化为肠上皮细胞单层的 Caco-2 细胞屏障完整性丧失的结构依赖性能力。用 TNFα(10ng/ml)孵育细胞,在不存在/存在 ECG、EGCG 和 EC 二聚体的情况下孵育。这三种二聚体抑制 TNFα介导的 Caco-2 细胞单层通透性,调节屏障功能丧失和炎症相关的事件,即下调紧密连接蛋白水平;增加基质金属蛋白酶表达和活性;增加 NADPH 氧化酶表达和氧化产物产生;激活 NF-κB 和 ERK1/2 通路及下游导致紧密连接开放的事件。对于其中一些机制,与非没食子酸酯 EC 二聚体相比,没食子酸酯化的 ECG 和 EGCG 二聚体具有更强的保护作用。这些差异可能是由于膜相互作用的差异,如原花青素二聚体-细胞膜相互作用的分子动力学模拟或与 NOX1 的不同相互作用所指出的。结果表明,尽管二聚体原花青素吸收率低,但通过缓解肠道炎症、氧化应激和屏障通透性,仍可促进健康。