Energy metabolism and the intestinal barrier: implications for understanding and managing intestinal diseases

被引:1
作者
Chen, Shuai [1 ]
Shen, Caifei [2 ]
Zeng, Xiaorui [1 ]
Sun, Luqiang [1 ]
Luo, Fangli [1 ]
Wan, Renhong [1 ]
Zhang, Yupeng [1 ]
Chen, Xinyun [1 ]
Hou, Yujun [1 ]
Wang, Wen [1 ]
Zheng, Qianhua [1 ]
Li, Ying [1 ]
机构
[1] Chengdu Univ Tradit Chinese Med, Acupuncture & Tuina Coll, Chengdu, Sichuan, Peoples R China
[2] Hosp Chengdu Univ Tradit Chinese Med, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
energy metabolism; intestinal barrier; SCFAs; cross-talk; intestinal diseases; OXIDATIVE STRESS; GUT MICROBIOTA; BUTYRATE; CELL; COLON; MECHANISMS; INTEGRITY; DISRUPTS; COLITIS; OBESITY;
D O I
10.3389/fmicb.2025.1515364
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The interplay between energy metabolism and the gut barrier is crucial for maintaining intestinal physiological homeostasis. Energy metabolism and the intestinal barrier perform distinct yet complementary roles that uphold intestinal ecological equilibrium. Disruptions in energy metabolism can compromise the integrity of the intestinal barrier; for example, inactivation of the AMPK pathway may lead to reduced expression of proteins associated with tight junctions. Conversely, impairment of the intestinal barrier can result in metabolic dysregulation, such as alterations in the gut microbiota that impede the production of short-chain fatty acids (SCFAs), which are essential substrates for energy metabolism. This disruption can affect energy production and modify the gut's hypoxic environment. Imbalances in these systems have been associated with the onset of various intestinal diseases. Research indicates that dietary interventions, such as a low FODMAP diet, can enhance the colonization of probiotics and improve the fermentation metabolism of SCFAs. Pharmacological strategies to elevate SCFA levels can activate the AMPK pathway and rectify abnormalities in energy metabolism. This review provides a comprehensive summary of recent advancements in elucidating the interactions between energy metabolism and the intestinal barrier.
引用
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页数:12
相关论文
共 113 条
[1]   Vitamin D and lactoferrin attenuate stress-induced colitis in Wistar rats via enhancing AMPK expression with inhibiting mTOR-STAT3 signaling and modulating autophagy [J].
Abdelmalak, Marian F. L. ;
Abdelrahim, Dina S. S. ;
Michael, Tari M. A. George ;
Abdel-Maksoud, Omnia M. M. ;
Labib, Jolly M. W. .
CELL BIOCHEMISTRY AND FUNCTION, 2023, 41 (02) :211-222
[2]   An insight into gut microbiota and its functionalities [J].
Adak, Atanu ;
Khan, Mojibur R. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2019, 76 (03) :473-493
[3]   Microbial dysbiosis-induced obesity: role of gut microbiota in homoeostasis of energy metabolism [J].
Amabebe, Emmanuel ;
Robert, Faith O. ;
Agbalalah, Tarimoboere ;
Orubu, Ebiowei S. F. .
BRITISH JOURNAL OF NUTRITION, 2020, 123 (10) :1127-1137
[4]   "Driver-passenger" bacteria and their metabolites in the pathogenesis of colorectal cancer [J].
Avril, Marion ;
DePaolo, R. William .
GUT MICROBES, 2021, 13 (01)
[5]   Mitochondria, the gut microbiome and ROS [J].
Ballard, J. William O. ;
Towarnicki, Samuel G. .
CELLULAR SIGNALLING, 2020, 75
[6]  
Bastard JP, 2006, EUR CYTOKINE NETW, V17, P4
[7]   Linking E-cadherin mechanotransduction to cell metabolism through force-mediated activation of AMPK [J].
Bays, Jennifer L. ;
Campbell, Hannah K. ;
Heidema, Christy ;
Sebbagh, Michael ;
DeMali, Kris A. .
NATURE CELL BIOLOGY, 2017, 19 (06) :724-+
[8]   Mitochondrial function controls intestinal epithelial stemness and proliferation [J].
Berger, Emanuel ;
Rath, Eva ;
Yuan, Detian ;
Waldschmitt, Nadine ;
Khaloian, Sevana ;
Allgaeuer, Michael ;
Staszewski, Ori ;
Lobner, Elena M. ;
Schoettl, Theresa ;
Giesbertz, Pieter ;
Coleman, Olivia I. ;
Prinz, Marco ;
Weber, Achim ;
Gerhard, Markus ;
Klingenspor, Martin ;
Janssen, Klaus-Peter ;
Heikenwalder, Mathias ;
Haller, Dirk .
NATURE COMMUNICATIONS, 2016, 7
[9]   Intestinal Epithelium-Specific MyD88 Signaling Impacts Host Susceptibility to Infectious Colitis by Promoting Protective Goblet Cell and Antimicrobial Responses [J].
Bhinder, Ganive ;
Stahl, Martin ;
Sham, Ho Pan ;
Crowley, Shauna M. ;
Morampudi, Vijay ;
Dalwadi, Udit ;
Ma, Caixia ;
Jacobson, Kevan ;
Vallance, Bruce A. .
INFECTION AND IMMUNITY, 2014, 82 (09) :3753-3763
[10]   Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion [J].
Byndloss, Mariana X. ;
Olsan, Erin E. ;
Rivera-Chavez, Fabian ;
Tiffany, Connor R. ;
Cevallos, Stephanie A. ;
Lokken, Kristen L. ;
Torres, Teresa P. ;
Byndloss, Austin J. ;
Faber, Franziska ;
Gao, Yandong ;
Litvak, Yael ;
Lopez, Christopher A. ;
Xu, Gege ;
Napoli, Eleonora ;
Giulivi, Cecilia ;
Tsolis, Renee M. ;
Revzin, Alexander ;
Lebrilla, Carlito B. ;
Baumler, Andreas J. .
SCIENCE, 2017, 357 (6351) :570-+