山竹果皮提取物通过激活NRF2/HO-1、恢复肠道屏障完整性和调节肠道微生物群减轻diquat诱导的肝脏氧化应激。

IF 6.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Weichen Huang, Yujie Lv, Chenhao Zou, Chaoyue Ge, Shenao Zhan, Xinyu Shen, Lianchi Wu, Xiaoxu Wang, Hongmeng Yuan, Gang Lin, Dongyou Yu, Bing Liu
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引用次数: 0

摘要

家禽生产使鸟类暴露于各种环境和生理应激源,这些应激源会破坏氧化还原平衡,损害肠-肝轴功能,损害健康和生产力。本研究旨在探讨山竹果皮提取物(MPE)对蛋鸡diquat诱导氧化应激模型的肝脏保护和抗氧化作用。选取270只海兰白蛋鸡,随机分为对照组(CON)、双夸特挑战组(DQ)和MEP干预双夸特挑战组(MQ) 3组,每组6个重复,每个重复15只鸡。结果表明,添加MPE可有效减轻diquat引起的肝脏氧化损伤,表现为ALT和AST活性升高,脂质代谢改善,肝纤维化减少。从机制上讲,MPE激活了NRF2/HO-1抗氧化途径,从而增强了肝脏抵抗ros损伤的能力,减少了肝组织中脂滴的积累。MPE补充剂通过上调紧密连接蛋白(Occludin-1和ZO-1)的表达,增强MUC-2的表达,从而减少肠道微生物来源的LPS从肠道转移,从而恢复肠屏障的完整性。此外,MPE还通过丰富有益菌属(如乳杆菌和瘤胃球菌),同时抑制潜在有害菌群(如拟杆菌和UCG-010)的生长,来调节肠道微生物群的组成。从MPE处理的供体到暴露于diquat的受体的粪便微生物群移植(FMT)再现了这些有益效果,进一步强调了肠道微生物群调节在介导MPE系统保护作用中的作用。综上所述,这些研究结果表明,MPE通过抗氧化活性、保护肠道屏障功能和调节肠道微生物群来减轻dq诱导的肝损伤和氧化应激,这将MPE定位为通过调节肠道微生物群和肠-肝轴来减轻氧化应激相关肝损伤的一种有前景的天然策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mangosteen Pericarp Extract Mitigates Diquat-Induced Hepatic Oxidative Stress by NRF2/HO-1 Activation, Intestinal Barrier Integrity Restoration, and Gut Microbiota Modulation.

Poultry production exposes birds to diverse environmental and physiological stressors that disrupt redox balance, impair gut-liver axis function, and undermine health and productivity. This study investigated the hepatoprotective and antioxidative effects of mangosteen pericarp extract (MPE) in an experimental model of diquat-induced oxidative stress in laying hens. A total of 270 Hy-Line White laying hens were randomly assigned to three groups: control group (CON), diquat-challenged group (DQ), and MEP intervention with diquat-challenged group (MQ), with six replicates of 15 birds each. The results showed that MPE supplementation effectively mitigated the hepatic oxidative damage caused by diquat, as evidenced by the increased ALT and AST activity, improved lipid metabolism, and reduced hepatic fibrosis. Mechanistically, MPE activated the NRF2/HO-1 antioxidant pathway, thus enhancing the liver's ability to counteract ROS-induced damage and reducing lipid droplet accumulation in liver tissue. MPE supplementation restored intestinal barrier integrity by upregulating tight junction protein expression (Occludin-1 and ZO-1), enhancing MUC-2 expression, and thereby decreasing gut microbiota-derived LPS transferring from the intestine. Additionally, MPE also modulated gut microbiota composition by enriching beneficial bacterial genera such as Lactobacillus and Ruminococcus while suppressing the growth of potentially harmful taxa (e.g., Bacteroidales and UCG-010). Fecal microbiota transplantation (FMT) from MPE-treated donors into diquat-exposed recipients reproduced these beneficial effects, further highlighting the role of gut microbiota modulation in mediating MPE's systemic protective actions. Together, these findings demonstrated that MPE alleviated DQ-induced liver injury and oxidative stress through a combination of antioxidant activity, protection of intestinal barrier function, and modulation of gut microbiota, positioning MPE as a promising natural strategy for mitigating oxidative stress-related liver damage by regulating the gut microbiota and gut-liver axis in poultry.

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来源期刊
Antioxidants
Antioxidants Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
10.60
自引率
11.40%
发文量
2123
审稿时长
16.3 days
期刊介绍: Antioxidants (ISSN 2076-3921), provides an advanced forum for studies related to the science and technology of antioxidants. It publishes research papers, reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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