Ferulic Acid Inhibits Arsenic-Induced Colon Injury by Improving Intestinal Barrier Function

IF 4.4 3区 医学 Q2 ENVIRONMENTAL SCIENCES
Shumin Wang, Yan Hong, Yuxiu Li, Zhenfen Zhang, Jing Han, Zhe Yang, Yanping Yang, Zhaolei Ma, Qi Wang
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Abstract

The prolonged exposure to arsenic results in intestinal barrier dysfunction, which is strongly concerned with detrimental processes such as oxidative stress and the inflammatory response. Ferulic acid (FA), as a phenolic acid, possesses the capability to mitigate arsenic-induced liver damage and cardiotoxic effects dependent on inhibition of oxidative stress and inflammatory responses. FA can mitigate testicular tissue damage and alveolar epithelial dysfunction, the mechanism of which may rely on nuclear factor erythroid 2-related factor 2/heme oxygenase 1 (Nrf2/HO-1) activation and nuclear factor-kappa B (NF-κB) pathway blocking. Based on the antioxidant and anti-inflammatory properties of FA, we speculated that FA might have the potential to inhibit arsenic-induced intestinal damage. To confirm this scientific hypothesis, mice exposed to sodium arsenite were treated with FA to observe colonic histopathology and TJ protein levels, and oxidative stress and TJ protein levels in Caco-2 cells exposed to sodium arsenite were assessed after FA intervention. In addition, molecular levels of NF-κB and Nrf2/HO-1 pathway in colon and Caco-2 cells were also detected. As shown in our data, FA inhibited arsenic-induced colon injury, which was reflected in the improvement of mucosal integrity, the decrease of down-regulated expression of tight junction (TJ) proteins (Claudin-1, Occludin, and ZO-1) and the inhibition of oxidative stress. Similarly, treatment with FA attenuated the inhibitory effect of arsenic on TJ protein expression in Caco-2 cells. In addition to suppressing the activation of NF-κB pathway, FA retrieved the activation of Nrf2/HO-1 pathway in colon and intestinal epithelial cells induced by arsenic. In summary, our findings propose that FA has the potential to mitigate arsenic-induced intestinal damage by preserving the integrity of intestinal epithelial TJs and suppressing oxidative stress. These results lay the groundwork for the potential use of FA in treating colon injuries caused by arsenic.

阿魏酸通过改善肠道屏障功能抑制砷诱发的结肠损伤
长期接触砷会导致肠道屏障功能失调,这与氧化应激和炎症反应等有害过程密切相关。阿魏酸(FA)作为一种酚酸,具有减轻砷引起的肝损伤和心脏毒性效应的能力,这取决于对氧化应激和炎症反应的抑制。FA能减轻睾丸组织损伤和肺泡上皮功能障碍,其机制可能依赖于核因子红细胞2相关因子2/血红素氧合酶1(Nrf2/HO-1)激活和核因子卡巴B(NF-κB)通路阻断。基于 FA 的抗氧化和抗炎特性,我们推测 FA 可能具有抑制砷引起的肠道损伤的潜力。为了证实这一科学假设,我们用 FA 治疗暴露于亚砷酸钠的小鼠,观察结肠组织病理学和 TJ 蛋白水平,并评估 FA 干预后暴露于亚砷酸钠的 Caco-2 细胞的氧化应激和 TJ 蛋白水平。此外,还检测了结肠和 Caco-2 细胞中 NF-κB 和 Nrf2/HO-1 通路的分子水平。如我们的数据所示,FA 可抑制砷诱导的结肠损伤,这体现在改善粘膜完整性、减少下调的紧密连接(TJ)蛋白(Claudin-1、Occludin 和 ZO-1)的表达以及抑制氧化应激。同样,用 FA 处理可减轻砷对 Caco-2 细胞中 TJ 蛋白表达的抑制作用。除了抑制 NF-κB 通路的激活外,FA 还能恢复砷诱导的结肠和肠上皮细胞中 Nrf2/HO-1 通路的激活。总之,我们的研究结果表明,FA 有可能通过保护肠上皮 TJ 的完整性和抑制氧化应激来减轻砷诱导的肠道损伤。这些结果为 FA 治疗砷引起的结肠损伤奠定了基础。
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来源期刊
Environmental Toxicology
Environmental Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
8.90%
发文量
261
审稿时长
4.5 months
期刊介绍: The journal publishes in the areas of toxicity and toxicology of environmental pollutants in air, dust, sediment, soil and water, and natural toxins in the environment.Of particular interest are: Toxic or biologically disruptive impacts of anthropogenic chemicals such as pharmaceuticals, industrial organics, agricultural chemicals, and by-products such as chlorinated compounds from water disinfection and waste incineration; Natural toxins and their impacts; Biotransformation and metabolism of toxigenic compounds, food chains for toxin accumulation or biodegradation; Assays of toxicity, endocrine disruption, mutagenicity, carcinogenicity, ecosystem impact and health hazard; Environmental and public health risk assessment, environmental guidelines, environmental policy for toxicants.
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