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中国精品科技期刊2020
邵仕娟,王浩,史雯馨,等. 基于代谢组学探究葛根素对慢性酒精性肝损伤小鼠的保护作用[J]. 华体会体育,2024,45(16):25−35. doi: 10.13386/j.issn1002-0306.2023120219.
引用本文: 邵仕娟,王浩,史雯馨,等. 基于代谢组学探究葛根素对慢性酒精性肝损伤小鼠的保护作用[J]. 华体会体育,2024,45(16):25−35. doi: 10.13386/j.issn1002-0306.2023120219.
SHAO Shijuan, WANG Hao, SHI Wenxin, et al. Protective Effect of Puerarin on Chronic Alcoholic Liver Injury in Mice Based on Metabolomics[J]. Science and Technology of Food Industry, 2024, 45(16): 25−35. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023120219.
Citation: SHAO Shijuan, WANG Hao, SHI Wenxin, et al. Protective Effect of Puerarin on Chronic Alcoholic Liver Injury in Mice Based on Metabolomics[J]. Science and Technology of Food Industry, 2024, 45(16): 25−35. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023120219.

基于代谢组学探究葛根素对慢性酒精性肝损伤小鼠的保护作用

Protective Effect of Puerarin on Chronic Alcoholic Liver Injury in Mice Based on Metabolomics

  • 摘要: 目的:采用非靶向代谢组学技术对慢性酒精性肝损伤(alcoholic liver disease,ALD)小鼠的血清和肝脏中的代谢产物进行分析,以鉴定筛选出与酒精性肝损伤相关的差异代谢物,并构建其代谢通路,从而探究葛根素保护酒精性肝损伤小鼠的作用机制。方法:连续8周灌胃52°白酒建立慢性酒精性肝损伤小鼠模型;采用肝功能生化指标、病理组织切片评价葛根素对ALD小鼠的保护作用;采用超高效液相色谱-四级杆飞行时间质谱法(UPLC-Q-TOF-MS)代谢组学技术对小鼠肝脏及血清代谢物进行分析;采用多元统计分析对数据进行处理,以第一主成分的变量重要性投影(VIP)>1且t检验P<0.05为条件筛选出差异代谢物;运用KEGG数据库对差异代谢物进行代谢通路分析。结果:葛根素可以显著降低酒精性肝损伤小鼠的ALT和AST水平(P<0.05或P<0.01),病理切片结果显示葛根素能够改善ALD小鼠肝脏炎症细胞浸润。经多元统计分析,在血清代谢组中发现模型组和空白组之间存在11个差异代谢物,在葛根素干预下,11种差异代谢物水平趋于空白组,主要涉及氨基酸的合成与代谢、谷胱甘肽代谢、卟啉和叶绿素代谢等代谢途径;在肝脏代谢组发现模型组和空白组之间存在32个差异代谢物,在葛根素干预下,31种差异代谢物水平趋于空白组,主要涉及氨基酸合成与代谢、初级胆汁酸的生物合成、嘌呤代谢、磷脂酰肌醇信号系统、类固醇激素代谢等代谢途径。结论:葛根素具有保护酒精性肝损伤小鼠的作用,其作用机制可能通过调节血清及肝脏代谢物紊乱发挥作用,为今后解酒保健食品的开发提供了有价值的参考。

     

    Abstract: Objective: The Non-targeted metabolomics technology was used to analyze the metabolites in the serum and liver of mice with chronic alcoholic liver injury (ALD), to identify and screen out the differential metabolites related to alcoholic liver injury and construct its metabolic pathway, and to explore the protective mechanism of puerarin against alcoholic liver injury in mice. Methods: The mouse model of chronic alcoholic liver injury was established by intragastric administration of 52 liquor for 8 weeks. Meanwhile, the protective effects of puerarin on ALD mice were evaluated using biochemical indexes of liver function and pathological tissue sections. Ultra performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) metabonomics technique was used to analyze the metabolites of mouse liver and serum. Multivariate statistics were used to process the data, and the variable importance projection (VIP) of the first principal component was >1 and the t-test P<0.05 was used to screen out the differential metabolites. Metabolic pathways of differential metabolites using KEGG database. Results: Puerarin could significantly improve ALT and AST levels in alcohol-induced liver injury mice (P<0.05 or P<0.01). Furthermore, the pathological section results indicated that puerarin could improve liver inflammatory cell infiltration in ALD mice. Through multivariate statistics, 11 metabolites were found in serum metabolites between the model group and the blank group. Under puerarin intervention, the levels of 11 metabolites tended to blank group, mainly related to amino acid synthesis and metabolism, glutathione metabolism, porphyrin metabolism and chlorophyll metabolism. There were 32 different metabolites between the model group and blank group in liver metabonomics, and the levels of 31 different metabolites tended to blank group under puerarin intervention, which mainly involved the amino acid synthesis and metabolism, biosynthesis of primary bile acids, purine metabolism, phosphatidylinositol signalling system, steroid metabolism and other metabolic pathways. Conclusion: Puerarin has a protective effect on alcoholic liver injury in mice, and its mechanism may be through regulating the disorder of serum and liver metabolites, which provides a valuable reference for anti-alcoholism health food in the future.

     

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