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羟基酪醇通过调节仔猪模型中的胆汁酸代谢缓解肠道氧化应激。

Hydroxytyrosol Alleviates Intestinal Oxidative Stress by Regulating Bile Acid Metabolism in a Piglet Model.

机构信息

State Key Laboratory of Animal Nutrition and Feeding, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

出版信息

Int J Mol Sci. 2024 May 21;25(11):5590. doi: 10.3390/ijms25115590.

DOI:10.3390/ijms25115590
PMID:38891778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11171822/
Abstract

Infants and young animals often suffer from intestinal damage caused by oxidative stress, which may adversely affect their overall health. Hydroxytyrosol, a plant polyphenol, has shown potential in decreasing intestinal oxidative stress, but its application and mechanism of action in infants and young animals are still inadequately documented. This study selected piglets as a model to investigate the alleviating effects of hydroxytyrosol on intestinal oxidative stress induced by diquat and its potential mechanism. Hydroxytyrosol improved intestinal morphology, characterized by higher villus height and villus height/crypt depth. Meanwhile, hydroxytyrosol led to higher expression of Occludin, MUC2, Nrf2, and its downstream genes, and lower expression of cytokines IL-1β, IL-6, and TNF-α. Both oxidative stress and hydroxytyrosol resulted in a higher abundance of , and a lower abundance of and , without a significant effect on short-chain fatty acids levels. Oxidative stress also led to disorders in bile acid (BA) metabolism, such as the lower levels of primary BAs, hyocholic acid, hyodeoxycholic acid, and tauroursodeoxycholic acid, which were partially restored by hydroxytyrosol. Correlation analysis revealed a positive correlation between these BA levels and the expression of Nrf2 and its downstream genes. Collectively, hydroxytyrosol may reduce oxidative stress-induced intestinal damage by regulating BA metabolism.

摘要

婴儿和幼小动物常因氧化应激而遭受肠道损伤,这可能会对其整体健康产生不利影响。羟基酪醇是一种植物多酚,已显示出降低肠道氧化应激的潜力,但它在婴儿和幼小动物中的应用及其作用机制仍未得到充分记录。本研究选择仔猪作为模型,研究羟基酪醇对百草枯诱导的肠道氧化应激的缓解作用及其潜在机制。羟基酪醇改善了肠道形态,表现为更高的绒毛高度和绒毛高度/隐窝深度。同时,羟基酪醇导致 Occludin、MUC2、Nrf2 及其下游基因的表达增加,而细胞因子 IL-1β、IL-6 和 TNF-α的表达降低。氧化应激和羟基酪醇都会导致 增加, 和 减少,但对短链脂肪酸水平没有显著影响。氧化应激还导致胆汁酸(BA)代谢紊乱,如初级 BAs、胆酸、甘胆酸和牛磺熊脱氧胆酸水平降低,羟基酪醇部分恢复了这些水平。相关性分析显示,这些 BA 水平与 Nrf2 及其下游基因的表达呈正相关。综上所述,羟基酪醇可能通过调节 BA 代谢来减轻氧化应激诱导的肠道损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38bd/11171822/5e0a5f4d0e11/ijms-25-05590-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38bd/11171822/0e41d966d3d7/ijms-25-05590-g001.jpg
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