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淫羊藿素和磷酸化淫羊藿素对脂多糖诱导的肠上皮细胞损伤的保护作用。

The protective effect of icariin and phosphorylated icariin against LPS-induced intestinal epithelial cells injury.

机构信息

College of Animal Science and Technology, Southwest University, Chongqing, China.

College of Pharmaceutical Sciences, Southwest University, Chongqing, China.

出版信息

Biomed Pharmacother. 2019 Oct;118:109246. doi: 10.1016/j.biopha.2019.109246. Epub 2019 Aug 3.

Abstract

Icariin (ICA) and phosphorylated icariin (pICA) have excellent antiviral and antioxidant effects. However, whether ICA and pICA cause anti-LPS-induced intestinal damage remains unclear. In this study, we used Caco-2 cells as a model to investigate the protective effects of ICA and pICA on human colonic epithelial cells and explore their potential mechanisms. Our results indicated that ICA and pICA increased cell viability and decreased lactate dehydrogenase activity in Caco-2 cells. ICA and pICA also attenuated LPS-induced changes in intestinal epithelial cell permeability and reduced the levels of oxidative stress indicators, such as reactive oxygen species, malondialdehyde, and hydrogen peroxide, in Caco-2 cells. Antioxidant indicators, such as superoxide dismutase, glutathione peroxidase, catalase and total antioxidant capacity, were increased, while the levels of IL-1β, IL-6, IL-8 and TNF-α were reduced in the ICA and pICA groups. Furthermore, ICA and pICA decreased the gene abundance and enzyme activities of caspase-3, -8, -9 and -10 in Caco-2 cells. Our data suggest that ICA and pICA effectively attenuated LPS-induced changes in the oxidative stress, inflammation, apoptosis and intestinal permeability of intestinal epithelial cells. These findings provide new insight for treating LPS-induced intestinal injury.

摘要

淫羊藿苷(ICA)和磷酸化淫羊藿苷(pICA)具有优异的抗病毒和抗氧化作用。然而,ICA 和 pICA 是否会引起 LPS 诱导的肠道损伤尚不清楚。在这项研究中,我们使用 Caco-2 细胞作为模型,研究了 ICA 和 pICA 对人结肠上皮细胞的保护作用,并探讨了它们的潜在机制。结果表明,ICA 和 pICA 增加了 Caco-2 细胞的活力并降低了乳酸脱氢酶的活性。ICA 和 pICA 还减轻了 LPS 诱导的肠上皮细胞通透性的变化,并降低了 Caco-2 细胞中氧化应激指标(如活性氧、丙二醛和过氧化氢)的水平。抗氧化指标(如超氧化物歧化酶、谷胱甘肽过氧化物酶、过氧化氢酶和总抗氧化能力)增加,而 ICA 和 pICA 组中白细胞介素-1β、白细胞介素-6、白细胞介素-8 和肿瘤坏死因子-α的水平降低。此外,ICA 和 pICA 降低了 Caco-2 细胞中 caspase-3、-8、-9 和 -10 的基因丰度和酶活性。我们的数据表明,ICA 和 pICA 可有效减轻 LPS 诱导的肠上皮细胞氧化应激、炎症、凋亡和通透性变化。这些发现为治疗 LPS 诱导的肠道损伤提供了新的思路。

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