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从肠道菌群改变探讨青砖茶对非酒精性脂肪肝的预防作用

  • 周婷婷 ,
  • 陈桂婷 ,
  • 曹楠 ,
  • 何建刚 ,
  • 何功威 ,
  • 肖长义 ,
  • 李世刚
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  • 1.三峡大学医学院,湖北宜昌 443002;
    2.湖北长盛川青砖茶研究所,湖北宜昌 443000
周婷婷,女,硕士,主要从事中药有效性与安全性评价方面的研究。

收稿日期: 2021-02-05

  修回日期: 2021-04-23

  网络出版日期: 2021-10-12

基金资助

湖北省区域创新发展科技专项(2020BGC015)、宜昌市科技研究与开发项目(A21-1-075)、三峡大学学位论文培优基金资助项目(2020SSPY112)

Preventive Effect of Green Brick Tea on Non-alcoholic Fatty Liver Disease via Gut Microbiota Changes

  • ZHOU Tingting ,
  • CHEN Guiting ,
  • CAO Nan ,
  • HE Jiangang ,
  • HE Gongwei ,
  • XIAO Changyi ,
  • LI Shigang
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  • 1. Medical College of China Three Gorges University, Yichang 443002, China;
    2. Changshengchuan Green-brick Tea Research Institute of Hubei Province, Yichang 443000, China

Received date: 2021-02-05

  Revised date: 2021-04-23

  Online published: 2021-10-12

摘要

通过肠道菌群改变研究青砖茶(GBT)对小鼠非酒精性脂肪肝(NAFLD)的预防作用。C57BL/6小鼠随机分为5组,即正常对照组(NC),模型对照组(MC),阳性药物对照组(PC)以及青砖茶低剂量组(LD)、高剂量组(HD),高脂饲料喂养小鼠建立NAFLD模型,同时预防性给予低、高剂量青砖茶水提取物和阳性药物血脂康,分别测定小鼠的体重、食物利用率、肝重、肝指数、TC、LDL-C/HDL-C及ALT含量,HE染色和油红O染色观察肝组织病理切片,ELISA检测肝组织IL-1β、IL-18含量变化,16 S rDNA V3-V4区高通量测序分析肠道菌群变化,Spearman相关性分析方法分析菌群与NAFLD表型的相关性。与模型组比较,青砖茶组小鼠体重、食物利用率、肝重、肝指数、血清TC、LDL-C/HDL-C、ALT、肝组织TC、IL-1β、IL-18含量均有显著性降低,肝脏病变程度有所改善;肠道菌群分析及相关性分析显示Bacteroides物种丰度降低,且与NAFLD表型呈正相关,LactobacillusAlloprevotellaSaccharibacteria_genera_incertae_sedis物种丰度增加,且与NAFLD表型呈负相关,与NAFLD表型相关性最强的菌群为BacteroidesLactobacillus。青砖茶对NAFLD具有一定的预防作用,其作用可能与影响肠道菌群的改变有关。

本文引用格式

周婷婷 , 陈桂婷 , 曹楠 , 何建刚 , 何功威 , 肖长义 , 李世刚 . 从肠道菌群改变探讨青砖茶对非酒精性脂肪肝的预防作用[J]. 茶叶科学, 2021 , 41(5) : 669 -680 . DOI: 10.13305/j.cnki.jts.20210914.001

Abstract

The preventive effect of green brick tea (GBT) on the mouse non-alcoholic fatty liver disease (NAFLD) model was studied by affecting changes in gut microbiota. C57BL/6 mice were randomly divided into 5 groups, including normal control group (NC), model control group (MC), positive drug control group (PC), low-dose group (LD) and high-dose group (HD) of GBT. A NAFLD model was established by feeding mice with high-fat diet, and supplemented with low and high doses of GBT water extract and positive drug (Xuezhikang) respectively. The body weight, food utilization efficiency, liver weight, liver index, TC, LDL-C/HDL-C and ALT contents of mice were determined. Liver tissue pathological sections were observed by HE staining and Oil Red O staining. ELISA method was used to detect changes of IL-1β and IL-18 in liver tissue. The changes of gut microbiota were analyzed by high-throughput sequencing in 16 S rDNA V3-V4 region, and Spearman's correlation analysis method was used to analyze the correlation between gut microbiota and NAFLD phenotype. Compared with the model control group, the body weight, food utilization efficiency, liver weight, liver index, serum TC, LDL-C/HDL-C, ALT, liver tissue TC, IL-1β, and IL-18 contents of mice in the GBT group were significantly reduced, and the degree of liver disease was improved. Gut microbiota analysis and correlation analysis show that the species abundance of Bacteroides decreased, and it was positively correlated with the NAFLD phenotype. The species abundance of Lactobacillus, Alloprevotella, and Saccharibacteria_genera_incertae_sedis increased, and they were negatively correlated with the NAFLD phenotype. Bacteroides and Lactobacillus had the strongest correlation with NAFLD phenotype. Green brick tea has a certain preventive effect on NAFLD, and its effect may be related to the changes in gut microbiota.

参考文献

[1] Mantovani A, Dalbeni A.Treatments for NAFLD: state of art[J]. Int J Mol Sci, 2021, 22(5): 2350. doi: 10.3390/ijms22052350.
[2] Huang D Q, El-Serag H B, Loomba R. Global epidemiology of NAFLD-related HCC: trends, predictions, risk factors and prevention[J]. Nat Rev Gastroenterol Hepatol, 2021, 18(4): 223-238.
[3] Day C P, James O F.Steatohepatitis: a tale of two "hits"?[J]. Gastroenterology, 1998, 114(4): 842-845.
[4] Buzzetti E, Pinzani M, Tsochatzis E A.The multiple-hit pathogenesis of non-alcoholic fatty liver disease (NAFLD)[J]. Metabolism, 2016, 65: 1038-1048.
[5] Borrelli A, Bonelli P, Tuccillo F M, et al.Role of gut microbiota and oxidative stress in the progression of non-alcoholic fatty liver disease to hepatocarcinoma: current and innovative therapeutic approaches[J]. Redox Biol, 2018, 15: 467-479.
[6] Tripathi A, Debelius J, Brenner D A, et al.The gut-liver axis and the intersection with the microbiome[J]. Nat Rev Gastroenterol Hepatol, 2018, 15(7): 397-411.
[7] 卢素芳, 郑鹏程, 刘盼盼, 等. 青砖茶研究进展[J]. 茶叶学报, 2018, 59(3): 162-167.
Lu S F, Zheng P C, Liu P P, et al.Research progress on Qingzhuan tea[J]. Acta Tea Sinica, 2018, 59(3): 162-167.
[8] 张伟. 青砖茶对实验大鼠的减肥和调节血脂作用及其机制研究[D]. 武汉: 华中农业大学, 2009.
Zhang W.Studies on anti-obesity, blood lipid regulation effects and mechanisms of dark brick tea on rats [D]. Wuhan: Huazhong Agricultural University, 2009.
[9] 何建刚, 李世刚, 肖长义, 等. 青砖茶的抗氧化作用研究[J]. 农技服务, 2016, 33(3): 94-95.
He J G, Li S G, Xiao C Y, et al.Research on antioxidant effect of Qingzhuan tea[J]. Agricultural Technology Service, 2016, 33(3): 94-95.
[10] 陈玉琼, 张伟, 倪德江, 等. 湖北青砖茶辅助降血脂作用及其抗氧化效果[J]. 茶叶科学, 2010, 30(2): 124-128.
Chen Y Q, Zhang W, Ni D J, et al.Study on the hypolipidemic effect and antioxidative activity of Hubei Qingzhuan tea[J]. Journal of Tea Science, 2010, 30(2): 124-128.
[11] 刘云涛, 何建刚, 肖长义, 等. 湖北长盛川青砖茶对2型糖尿病合并血脂异常患者胰岛素抵抗、血脂的影响[J]. 中国老年学杂志, 2019, 39(6): 1317-1320.
Liu Y T, He J G, Xiao C Y, et al.Effects of Hubei Changshengchuan green brick tea on insulin resistance and blood lipid in type 2 diabetes patients with dyslipidemia[J]. Chinese Journal of Gerontology, 2019, 39(6): 1317-1320.
[12] 王蝶, 黄建安, 叶小燕, 等. 茯砖茶减肥作用研究[J]. 茶叶科学, 2012, 32(1): 81-86.
Wang D, Huang J A, Ye X Y, et al.The anti-obesity effects of Fuzhuan brick tea on high-fat-diet induced obesity in rats[J]. Journal of Tea Science, 2012, 32(1): 81-86.
[13] 赵伟, 孙国志. 不同种实验动物间用药量换算[J]. 畜牧兽医科技信息, 2010(5): 52-53.
Zhao W, Sun G Z.Conversion of dosage between different kinds of experimental animals[J]. Chinese Journal of Animal Husbandry and Veterinary Medicine, 2010(5): 52-53.
[14] 余婕, 闫梦真, 陈桂婷, 等. 青砖茶水提物对HepG2细胞脂肪变性的干预作用[J]. 三峡大学学报(自然科学版), 2020, 42(2): 107-112.
Yu J, Yan M Z, Chen G T, et al.Intervention effect of water extract of green brick tea on steatosis of HepG2 cells[J]. Journal of China Three Gorges University (Natural Sciences), 2020, 42(2): 107-112.
[15] Pierantonelli I, Svegliati-Baroni G.Nonalcoholic fatty liver disease: basic pathogenetic mechanisms in the progression from NAFLD to NASH[J]. Transplantation, 2019, 103(1): e1-e13.
[16] Safari Z, Gérard P.The links between the gut microbiome and non-alcoholic fatty liver disease (NAFLD)[J]. Cell Mol Life Sci, 2019, 76(8): 1541-1558.
[17] Fan Y, Pedersen O.Gut microbiota in human metabolic health and disease[J]. Nat Rev Microbiol, 2021, 19(1): 55-71.
[18] Suk K T, Kim D J.Gut microbiota: novel therapeutic target for nonalcoholic fatty liver disease[J]. Expert Rev Gastroenterol Hepatol, 2019, 13(3): 193-204.
[19] Milosevic I, Vujovic A, Barac A, et al.Gut-liver axis, gut microbiota, and its modulation in the management of liver diseases: a review of the literature[J]. Int J Mol Sci, 2019, 20(2): 395. doi: 10.3390/ijms20020395.
[20] Zhu L, Baker S S, Gill C, et al.Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: a connection between endogenous alcohol and NASH[J]. Hepatology, 2013, 57(2): 601-609.
[21] Lee N Y, Shin M J, Youn G S, et al.Lactobacillus attenuates progression of nonalcoholic fatty liver disease by lowering cholesterol and steatosis[J]. Clin Mol Hepatol, 2021, 27(1): 110-124.
[22] Bashiardes S, Shapiro H, Rozin S, et al.Non-alcoholic fatty liver and the gut microbiota[J]. Mol Metab, 2016, 5(9): 782-794.
[23] Kolodziejczyk A A, Zheng D, Shibolet O, et al.The role of the microbiome in NAFLD and NASH[J]. EMBO Mol Med, 2019, 11(2): e9302. doi: 10.15252/emmm.201809302.
[24] Leung C, Rivera L, Furness J B, et al.The role of the gut microbiota in NAFLD[J]. Nat Rev Gastroenterol Hepatol, 2016, 13(7): 412-425.
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