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鞣花酸可改善百草枯诱导的肝损伤,其机制与改善肠道微生物特征有关。

Ellagic acid ameliorates paraquat-induced liver injury associated with improved gut microbial profile.

机构信息

National Engineering Laboratory for Pollution Control and Waste Utilization in Livestock and Poultry Production, Key Laboratory of Agro-ecological Processes in Subtropical Region, Laboratory of Animal Nutritional Physiology and Metabolic Process, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha, 410125, Hunan, China; College of Animal Science and Technology, Hunan Agricultural University, Changsha, 410000, Hunan, China; University of Chinese Academy of Sciences, Beijing, 100008, China.

College of Animal Science and Technology, Hunan Agricultural University, Changsha, 410000, Hunan, China.

出版信息

Environ Pollut. 2022 Jan 15;293:118572. doi: 10.1016/j.envpol.2021.118572. Epub 2021 Nov 24.

Abstract

Paraquat, a widely used herbicide, causes environmental pollution, and liver injury in humans and animals. As a natural compound in fruits, ellagic acid (EA) shows anti-inflammatory and antioxidant effects. This study examines the beneficial effects of dietary EA against the paraquat-induced hepatic injury and further explores the underlying molecular mechanisms using a piglet model. Post-weaning piglets are fed basal diet supplemented with 50 mg/kg, 100 mg/kg, or 200 mg/kg EA for 3 weeks. At week 2, hepatic injury is induced by 4 mg/kg paraquat followed by 7 days recovery. EA supplementation significantly mitigates paraquat-induced hepatic fibrosis, steatosis, and high apoptotic rate. In agreement, EA supplementation reduces serum pro-inflammatory levels, ameliorates inflammatory cells infiltration into hepatic tissue, which are associated with suppressed NF-κB signaling during paraquat exposure. In addition, EA supplementation significantly improves activities of antioxidative enzymes which were correlated with activated Nrf2/Keap 1 signaling during paraquat exposure. Furthermore, EA supplementation restores cecal microbial community during paraquat exposure. The protective effect of EA is strongly linked with increased relative abundance of Lactobacillus reuteri and Lactobacillus amylovorus. Taken together, EA supplementation effectively reduced the occurrence of hepatic oxidative damage and inflammation induced by paraquat through modulating cecal microbial communities, which provides a novel nutritional therapeutic strategy for hepatic injury.

摘要

百草枯是一种广泛使用的除草剂,会对人类和动物造成环境污染和肝损伤。鞣花酸(EA)作为一种天然存在于水果中的化合物,具有抗炎和抗氧化作用。本研究使用仔猪模型探讨了膳食 EA 对百草枯诱导的肝损伤的有益作用,并进一步探讨了其潜在的分子机制。断奶后的仔猪喂食基础日粮,并补充 50mg/kg、100mg/kg 或 200mg/kg 的 EA,持续 3 周。在第 2 周,用 4mg/kg 的百草枯诱导肝损伤,然后进行 7 天的恢复。EA 补充显著减轻了百草枯诱导的肝纤维化、脂肪变性和高凋亡率。同样,EA 补充降低了血清促炎水平,改善了炎症细胞浸润到肝组织的情况,这与 NF-κB 信号在百草枯暴露期间受到抑制有关。此外,EA 补充显著提高了抗氧化酶的活性,这与 Nrf2/Keap1 信号在百草枯暴露期间被激活有关。此外,EA 补充在百草枯暴露期间恢复了盲肠微生物群落。EA 的保护作用与罗伊氏乳杆菌和淀粉乳杆菌相对丰度的增加密切相关。总之,EA 补充通过调节盲肠微生物群落,有效减少了百草枯引起的肝氧化损伤和炎症的发生,为肝损伤提供了一种新的营养治疗策略。

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