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叶黄素可预防慢性酒精摄入大鼠的肝损伤和肠屏障功能障碍。

Lutein Prevents Liver Injury and Intestinal Barrier Dysfunction in Rats Subjected to Chronic Alcohol Intake.

机构信息

Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao 266071, China.

Department of Nutrition and Food Hygiene, School of Public Health, Soochow University, Suzhou 215127, China.

出版信息

Nutrients. 2023 Feb 28;15(5):1229. doi: 10.3390/nu15051229.

Abstract

Chronic alcohol intake can affect both liver and intestinal barrier function. The goal of this investigation was to evaluate the function and mechanism of lutein administration on the chronic ethanol-induced liver and intestinal barrier damage in rats. During the 14-week experimental cycle, seventy rats were randomly divided into seven groups, with 10 rats in each group: a normal control group (Co), a control group of lutein interventions (24 mg/kg/day), an ethanol model group (Et, 8-12 mL/kg/day of 56% (v/v) ethanol), three intervention groups with lutein (12, 24 and 48 mg/kg/day) and a positive control group (DG). The results showed that liver index, ALT, AST and TG levels were increased, and SOD and GSH-Px levels were reduced in the Et group. Furthermore, alcohol intake over a long time increased the level of pro-inflammatory cytokines TNF-α and IL-1β, disrupted the intestinal barrier, and stimulated the release of LPS, causing further liver injury. In contrast, lutein interventions prevented alcohol-induced alterations in liver tissue, oxidative stress and inflammation. In addition, the protein expression of Claudin-1 and Occludin in ileal tissues was upregulated by lutein intervention. In conclusion, lutein can improve chronic alcoholic liver injury and intestinal barrier dysfunction in rats.

摘要

慢性酒精摄入会影响肝脏和肠道屏障功能。本研究旨在评估叶黄素对大鼠慢性乙醇诱导的肝和肠道屏障损伤的功能和机制。在 14 周的实验周期中,70 只大鼠被随机分为 7 组,每组 10 只:正常对照组(Co)、叶黄素干预对照组(24mg/kg/天)、乙醇模型组(Et,8-12mL/kg/天的 56%(v/v)乙醇)、叶黄素干预组(12、24 和 48mg/kg/天)和阳性对照组(DG)。结果表明,Et 组的肝指数、ALT、AST 和 TG 水平升高,SOD 和 GSH-Px 水平降低。此外,长期饮酒会增加促炎细胞因子 TNF-α和 IL-1β的水平,破坏肠道屏障,并刺激 LPS 的释放,导致进一步的肝损伤。相比之下,叶黄素干预可预防酒精引起的肝组织、氧化应激和炎症改变。此外,叶黄素干预可上调回肠组织中 Claudin-1 和 Occludin 的蛋白表达。综上所述,叶黄素可改善大鼠慢性酒精性肝损伤和肠道屏障功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b8/10005241/5df6fdbbda4f/nutrients-15-01229-g001.jpg

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