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骆驼奶可改善酒精性肝损伤小鼠模型中的炎症机制。

Camel milk ameliorates inflammatory mechanisms in an alcohol-induced liver injury mouse model.

机构信息

Key Laboratory of Dairy Biotechnology and Bioengineering, Ministry of Education, College of Food Science and Engineering, Inner Mongolia Agricultural University, Hohhot, 010018, Inner Mongolia, China.

Camel Research Institute of Inner Mongolia, Alashan, 737300, Inner Mongolia, China.

出版信息

Sci Rep. 2021 Nov 24;11(1):22811. doi: 10.1038/s41598-021-02357-1.

Abstract

Camel milk (CM) is considered to protect the liver in the practice of traditional medicine in nomadic areas. The purpose of the present study was to investigate the effects of CM on the hepatic biochemical and multiple omics alterations induced by chronic alcoholic liver disease (ALD). An intragastric gavage mice Lieber DeCarli + Gao binge model (NIAAA model) was employed to investigate the inflammatory mechanism of camel milk on the liver tissue of mice. A gut microbiota of the feces of mice and transcriptomic and proteomic analyses of the liver of mice were performed. Analysis of serum and liver biochemical indexes revealed that camel milk not only prevents alcohol-induced colonic dysfunction and lipid accumulation, but also regulates oxidative stress and inflammatory cytokine production to protect against chronic ALD in mouse. The gut microbial community of mice treated with camel milk was more similar to the untreated control group than to the model group, indicating that the intake of camel milk pre- and post-alcohol gavage effectively prevents and alleviates the intestinal microbial disorder caused by chronic alcoholism in mice. Furthermore, the results of the transcriptomic and proteomic analyses of the liver tissue showed that camel milk can improve alcoholic liver injury in mice by regulating inflammatory factors and immune system disruptions. This study provides insights into the molecular mechanism by which camel milk can be developed as a potential functional food with no side effects and against liver injury.

摘要

骆驼奶(CM)在游牧地区的传统医学实践中被认为具有保护肝脏的作用。本研究的目的是研究骆驼奶对慢性酒精性肝病(ALD)引起的肝生化和多种组学改变的影响。采用灌胃小鼠 Lieber DeCarli+Gao binge 模型(NIAAA 模型)研究骆驼奶对小鼠肝组织的炎症机制。对小鼠粪便中的肠道微生物群和小鼠肝的转录组和蛋白质组进行了分析。血清和肝生化指标分析表明,骆驼奶不仅可以预防酒精引起的结肠功能障碍和脂质积累,还可以调节氧化应激和炎症细胞因子的产生,从而预防小鼠慢性 ALD。用骆驼奶处理的小鼠肠道微生物群与未处理的对照组更相似,而与模型组差异较大,这表明在酒精灌胃前后摄入骆驼奶可以有效预防和缓解慢性酒精引起的小鼠肠道微生物失调。此外,肝组织的转录组和蛋白质组分析结果表明,骆驼奶可以通过调节炎症因子和免疫系统紊乱来改善小鼠的酒精性肝损伤。本研究为开发具有无副作用和抗肝损伤作用的潜在功能性食品提供了分子机制的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d047/8613211/c830c029ff3b/41598_2021_2357_Fig1_HTML.jpg

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