Aged Ripe Pu-erh Tea Reduced Oxidative Stress-Mediated Inflammation in Dextran Sulfate Sodium-Induced Colitis Mice by Regulating Intestinal Microbes

被引:86
作者
Hu, Shanshan [1 ]
Li, Shi [2 ]
Liu, Yan [1 ]
Sun, Kang [1 ]
Luo, Liyong [1 ]
Zeng, Liang [1 ]
机构
[1] Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
[2] Hunan Agr Univ, Key Lab Tea Sci, Minist Educ, Changsha 410128, Hunan, Peoples R China
关键词
aged ripe pu-erh tea; oxidative stress-mediated inflammation; intestinal microbes; intestinal immune barrier; FMT; DSS-INDUCED COLITIS; NF-KAPPA-B; GUT MICROBIOTA; CHEMICAL-CONSTITUENTS; GREEN TEA; IN-VITRO; HIGH-FAT; ANTIOXIDANT; POLYSACCHARIDES; EXTRACT;
D O I
10.1021/acs.jafc.1c04032
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Ripened pu-erh tea has the biological activity of antioxidation and anti-inflammation, which inhibits the related parameters of colitis. However, the role of storage-induced changes in bioactive ingredients of ripened pu-erh tea in colitis remains unclear. In this study, 3.5% dextran sulfate sodium-induced colitis mice were treated with 10 mg/kg bw/day extracts, aged 14 years (P2006) and unaged (P2020) ripened pu-erh tea, respectively, for 1 week. We found that ripened pu-erh tea, especially P2006, inhibited the intestinal oxidative stress-mediated inflammation pathway (TLR4/MyD88/ROS/p38MAPK/NF-kappa B p65), upregulated the expression of intestinal tight junction proteins (Mucin-2, ZO-1, occludin), promoted M2 polarization of macrophages, and in turn, improved the intestinal immune barrier, which stemmed from the reshaping of intestinal microbiota (e.g., increased Lachnospiraceae_NK4A136_group and Akkermansia levels). Our results speculate that drinking aged ripe pu-erh tea (10 mg/kg bw/day in mice, a human equivalent dose of 7 g/60 kg bw/day) has a practical effect on alleviating and preventing the development of intestinal inflammation.
引用
收藏
页码:10592 / 10605
页数:14
相关论文
共 66 条
[1]   Deconstructing Mechanisms of Diet-Microbiome-Immune Interactions [J].
Alexander, Margaret ;
Turnbaugh, Peter J. .
IMMUNITY, 2020, 53 (02) :264-276
[2]   Optimizing the extraction of bioactive compounds from pu-erh tea (Camellia sinensis var. assamica) and evaluation of antioxidant, cytotoxic, antimicrobial, antihemolytic, and inhibition of α-amylase and α-glucosidase activities [J].
Armstrong, Lorene ;
Vieira do Carmo, Mariana Araujo ;
Wu, You ;
Esmerino, Luis Antonio ;
Azevedo, Luciana ;
Zhang, Liang ;
Granato, Daniel .
FOOD RESEARCH INTERNATIONAL, 2020, 137
[3]  
Asakura H., 2018, POLYPHENOLS PREVENTI, P279, DOI 10.1016/B978-0-12-813008-7.00023-0.
[4]   NADPH oxidases and ROS signaling in the gastrointestinal tract [J].
Aviello, Gabriella ;
Knaus, Ulla G. .
MUCOSAL IMMUNOLOGY, 2018, 11 (04) :1011-1023
[5]   Probiotics Efficacy on Oxidative Stress Values in Inflammatory Bowel Disease: A Randomized Double-Blinded Placebo-Controlled Pilot Study [J].
Ballini, Andrea ;
Santacroce, Luigi ;
Cantore, Stefania ;
Bottalico, Lucrezia ;
Dipalma, Gianna ;
Topi, Skender ;
Saini, Rajiv ;
De Vito, Danila ;
Inchingolo, Francesco .
ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS, 2019, 19 (03) :373-381
[6]   NF-κB, Nrf2, and HO-1 interplay in redox-regulated VCAM-1 expression [J].
Banning, A ;
Brigelius-Flohé, R .
ANTIOXIDANTS & REDOX SIGNALING, 2005, 7 (7-8) :889-899
[7]   Green tea: A possibility in the therapeutic approach of inflammatory bowel diseases? Green tea and inflammatory bowel diseases [J].
Barbalho, Sandra Maria ;
Bosso, Henrique ;
Salzedas-Pescinini, Leticia M. ;
Goulart, Ricardo de Alvares .
COMPLEMENTARY THERAPIES IN MEDICINE, 2019, 43 :148-153
[8]   Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2 [J].
Bolyen, Evan ;
Rideout, Jai Ram ;
Dillon, Matthew R. ;
Bokulich, NicholasA. ;
Abnet, Christian C. ;
Al-Ghalith, Gabriel A. ;
Alexander, Harriet ;
Alm, Eric J. ;
Arumugam, Manimozhiyan ;
Asnicar, Francesco ;
Bai, Yang ;
Bisanz, Jordan E. ;
Bittinger, Kyle ;
Brejnrod, Asker ;
Brislawn, Colin J. ;
Brown, C. Titus ;
Callahan, Benjamin J. ;
Caraballo-Rodriguez, Andres Mauricio ;
Chase, John ;
Cope, Emily K. ;
Da Silva, Ricardo ;
Diener, Christian ;
Dorrestein, Pieter C. ;
Douglas, Gavin M. ;
Durall, Daniel M. ;
Duvallet, Claire ;
Edwardson, Christian F. ;
Ernst, Madeleine ;
Estaki, Mehrbod ;
Fouquier, Jennifer ;
Gauglitz, Julia M. ;
Gibbons, Sean M. ;
Gibson, Deanna L. ;
Gonzalez, Antonio ;
Gorlick, Kestrel ;
Guo, Jiarong ;
Hillmann, Benjamin ;
Holmes, Susan ;
Holste, Hannes ;
Huttenhower, Curtis ;
Huttley, Gavin A. ;
Janssen, Stefan ;
Jarmusch, Alan K. ;
Jiang, Lingjing ;
Kaehler, Benjamin D. ;
Bin Kang, Kyo ;
Keefe, Christopher R. ;
Keim, Paul ;
Kelley, Scott T. ;
Knights, Dan .
NATURE BIOTECHNOLOGY, 2019, 37 (08) :852-857
[9]  
Callahan BJ, 2016, NAT METHODS, V13, P581, DOI [10.1038/NMETH.3869, 10.1038/nmeth.3869]
[10]   Epithelial-Derived Reactive Oxygen Species Enable AppBCX-Mediated Aerobic Respiration of Escherichia coli during Intestinal Inflammation [J].
Chanin, Rachael B. ;
Winter, Maria G. ;
Spiga, Luisella ;
Hughes, Elizabeth R. ;
Zhu, Wenhan ;
Taylor, Savannah J. ;
Arenales, Alexandre ;
Gillis, Caroline C. ;
Buettner, Lisa ;
Jimenez, Angel G. ;
Smoot, Madeline P. ;
Santos, Renato L. ;
Winter, Sebastian E. .
CELL HOST & MICROBE, 2020, 28 (06) :780-+