Pu-erh Tea Restored Circadian Rhythm Disruption by Regulating Tryptophan Metabolism

被引:37
作者
Hu, Shanshan [1 ]
Luo, Liyong [1 ]
Bian, Xintong [2 ]
Liu, Rui Hai [3 ]
Zhao, Sibo [1 ]
Chen, Yu [1 ]
Sun, Kang [1 ]
Jiang, Jielin [4 ]
Liu, Zhonghua [5 ]
Zeng, Liang [6 ,7 ]
机构
[1] Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
[2] Chongqing Med Univ, Key Lab Clin Lab Diagnost, Minist Educ, Coll Lab Med, Chongqing 400016, Peoples R China
[3] Cornell Univ, Dept Food Sci, Ithaca, NY 14850 USA
[4] Menghai Tea Factory, TAETEA Grp, Shanghai 666200, Yunnan, Peoples R China
[5] Hunan Agr Univ, Minist Educ Tea Sci, Key Lab, Changsha 410128, Peoples R China
[6] Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
[7] Chongqing Southwest Univ, Chongqing Key Lab Special Food Cobuilt Sichuan &, Chongqing 400715, Peoples R China
关键词
circadian rhythm disruption; Pu-erh tea; gut-liver-brain axis; gut microbiota; tryptophan metabolism; GUT MICROBIOTA; RECEPTOR; MODULATION; DEPRESSION; ACID;
D O I
10.1021/acs.jafc.2c01883
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Pu-erh tea is a healthy beverage rich in phytochemicals, and its effect on the risk of inducing circadian rhythm disorders (CRD) is unclear. In this study, healthy mice were given water or 0.25% (w/v) Pu-erh tea for 7 weeks, followed by a 40 day disruption of the light/dark cycle. CRD caused dysregulation of neurotransmitter secretion and clock gene oscillations, intestinal inflammation, and disruption of intestinal microbes and metabolites. Pu-erh tea boosted the indole and 5-hydroxytryptamine pathways of tryptophan metabolism via the gut-liver-brain axis. Furthermore, its metabolites (e.g., IAA, Indole, 5-HT) enhanced hepatic glycolipid metabolism and down-regulated intestinal oxidative stress by improving the brain hormone release. Tryptophan metabolites and bile acids also promoted liver lipid metabolism and inhibited intestinal inflammation (MyD88/NF-Kappa B) via the enterohepatic circulation. Collectively, 0.25% (w/v) Pu-erh tea has the potential to prevent CRD by promoting indole and 5-HT pathways of tryptophan metabolism and signaling interactions in the gut-liver-brain axis.
引用
收藏
页码:5610 / 5623
页数:14
相关论文
共 80 条
[1]   Ten-year trend in sleeping pills use in Switzerland: the CoLaus study [J].
Abolhassani, Nazanin ;
Haba-Rubio, Jose ;
Heinzer, Raphael ;
Vollenweider, Peter ;
Marques-Vidal, Pedro .
SLEEP MEDICINE, 2019, 64 :56-61
[2]   Gut Microbiota Regulation of Tryptophan Metabolism in Health and Disease [J].
Agus, Allison ;
Planchais, Julien ;
Sokol, Harry .
CELL HOST & MICROBE, 2018, 23 (06) :716-724
[3]   Transient receptor potential channels and energy homeostasis [J].
Ahern, Gerard P. .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2013, 24 (11) :554-560
[4]   The circadian phase of antenatal glucocorticoid treatment affects the risk of behavioral disorders [J].
Astiz, Mariana ;
Heyde, Isabel ;
Fortmann, Mats Ingmar ;
Bossung, Verena ;
Roll, Claudia ;
Stein, Anja ;
Gruettner, Berthold ;
Goepel, Wolfgang ;
Haertel, Christoph ;
Obleser, Jonas ;
Oster, Henrik .
NATURE COMMUNICATIONS, 2020, 11 (01)
[5]   METTL3 Regulates Liver Homeostasis, Hepatocyte Ploidy, and Circadian Rhythm-Controlled Gene Expression in Mice [J].
Barajas, Juan M. ;
Lin, Cho-Hao ;
Sun, Hui-Lung ;
Alencastro, Frances ;
Zhu, Allen C. ;
Aljuhani, Mona ;
Navari, Ladan ;
Yilmaz, Selen A. ;
Yu, Lianbo ;
Corps, Kara ;
He, Chuan ;
Duncan, Andrew W. ;
Ghoshal, Kalpana .
AMERICAN JOURNAL OF PATHOLOGY, 2022, 192 (01) :56-71
[6]   Sex Differences in Hippocampal Memory and Kynurenic Acid Formation Following Acute Sleep Deprivation in Rats [J].
Baratta, Annalisa M. ;
Buck, Silas A. ;
Buchla, Austin D. ;
Fabian, Carly B. ;
Chen, Shuo ;
Mong, Jessica A. ;
Pocivavsek, Ana .
SCIENTIFIC REPORTS, 2018, 8
[7]   A role for inflammatory metabolites as modulators of the glutamate N-methyl-D-aspartate receptor in depression and suicidality [J].
Bay-Richter, Cecilie ;
Linderholm, Klas R. ;
Lim, Chai K. ;
Samuelsson, Martin ;
Traskman-Bendz, Lil ;
Guillemin, Gilles J. ;
Erhardt, Sophie ;
Brundin, Lena .
BRAIN BEHAVIOR AND IMMUNITY, 2015, 43 :110-117
[8]   Gut microbiota impact on the peripheral immune response in non-alcoholic fatty liver disease related hepatocellular carcinoma [J].
Behary, Jason ;
Amorim, Nadia ;
Jiang, Xiao-Tao ;
Raposo, Anita ;
Gong, Lan ;
McGovern, Emily ;
Ibrahim, Ragy ;
Chu, Francis ;
Stephens, Carlie ;
Jebeili, Hazem ;
Fragomeli, Vincenzo ;
Koay, Yen Chin ;
Jackson, Miriam ;
O'Sullivan, John ;
Weltman, Martin ;
McCaughan, Geoffrey ;
El-Omar, Emad ;
Zekry, Amany .
NATURE COMMUNICATIONS, 2021, 12 (01)
[9]   IL-17 and IL-17-producing cells and liver diseases, with focus on autoimmune liver diseases [J].
Beringer, Audrey ;
Miossec, Pierre .
AUTOIMMUNITY REVIEWS, 2018, 17 (12) :1176-1185
[10]   The microbiota coordinates diurnal rhythms in innate immunity with the circadian clock [J].
Brooks, John F. ;
Behrendt, Cassie L. ;
Ruhn, Kelly A. ;
Lee, Syann ;
Raj, Prithvi ;
Takahashi, Joseph S. ;
Hooper, Lora, V .
CELL, 2021, 184 (16) :4154-+