Irritable bowel syndrome: A microbiome-gut-brain axis disorder?

被引:293
作者
Kennedy, Paul J. [1 ]
Cryan, John F. [2 ]
Dinan, Timothy G. [1 ]
Clarke, Gerard [1 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Dept Psychiat, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Dept Anat & Neurosci, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
Irritable bowel syndrome; Microbiome; Anxiety; Tryptophan; Abdominal pain; Gastrointestinal motility; Cognition; ANXIETY-LIKE BEHAVIOR; CHAIN FATTY-ACIDS; ANTIBIOTIC-ASSOCIATED DIARRHEA; BIFIDOBACTERIUM-INFANTIS; 35624; MATERNAL IMMUNE ACTIVATION; INTESTINAL MICROBIOTA; FECAL MICROBIOTA; VISCERAL HYPERSENSITIVITY; GASTROINTESTINAL MICROBIOTA; TRYPTOPHAN DEGRADATION;
D O I
10.3748/wjg.v20.i39.14105
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Irritable bowel syndrome (IBS) is an extremely prevalent but poorly understood gastrointestinal disorder. Consequently, there are no clear diagnostic markers to help diagnose the disorder and treatment options are limited to management of the symptoms. The concept of a dysregulated gut-brain axis has been adopted as a suitable model for the disorder. The gut microbiome may play an important role in the onset and exacerbation of symptoms in the disorder and has been extensively studied in this context. Although a causal role cannot yet be inferred from the clinical studies which have attempted to characterise the gut microbiota in IBS, they do confirm alterations in both community stability and diversity. Moreover, it has been reliably demonstrated that manipulation of the microbiota can influence the key symptoms, including abdominal pain and bowel habit, and other prominent features of IBS. A variety of strategies have been taken to study these interactions, including probiotics, antibiotics, faecal transplantations and the use of germ-free animals. There are clear mechanisms through which the microbiota can produce these effects, both humoral and neural. Taken together, these findings firmly establish the microbiota as a critical node in the gut-brain axis and one which is amenable to therapeutic interventions. (C) 2014 Baishideng Publishing Group Inc. All rights reserved.
引用
收藏
页码:14105 / 14125
页数:21
相关论文
共 250 条
[1]
Selective processing of gastrointestinal symptom-related stimuli in irritable bowel syndrome [J].
Afzal, Muhammad ;
Potokar, John P. ;
Probert, Christopher S. J. ;
Munafo, Marcus R. .
PSYCHOSOMATIC MEDICINE, 2006, 68 (05) :758-761
[2]
Altered Cognitive Function of Prefrontal Cortex During Error Feedback in Patients With Irritable Bowel Syndrome, Based on fMRI and Dynamic Causal Modeling [J].
Aizawa, Emiko ;
Sato, Yasuhiro ;
Kochiyama, Takanori ;
Saito, Naohiro ;
Izumiyama, Masahiro ;
Morishita, Joe ;
Kanazawa, Motoyori ;
Shima, Keisetsu ;
Mushiake, Hajime ;
Hongo, Michio ;
Fukudo, Shin .
GASTROENTEROLOGY, 2012, 143 (05) :1188-1198
[3]
Biological and psychological markers of stress in humans: Focus on the Trier Social Stress Test [J].
Allen, Andrew P. ;
Kennedy, Paul J. ;
Cryan, John F. ;
Dinan, Timothy G. ;
Clarke, Gerard .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2014, 38 :94-124
[4]
Gut Microbial Products Regulate Murine Gastrointestinal Motility via Toll-Like Receptor 4 Signaling [J].
Anitha, Mallappa ;
Vijay-Kumar, Matam ;
Sitaraman, Shanthi V. ;
Gewirtz, Andrew T. ;
Srinivasan, Shanthi .
GASTROENTEROLOGY, 2012, 143 (04) :1006-+
[5]
Minocycline produced antidepressant-like effects on the learned helplessness rats with alterations in levels of monoamine in the amygdala and no changes in BDNF levels in the hippocampus at baseline [J].
Arakawa, Shiho ;
Shirayama, Yukihiko ;
Fujita, Yuko ;
Ishima, Tamaki ;
Horio, Mao ;
Muneoka, Katsumasa ;
Iyo, Masaomi ;
Hashimoto, Kenji .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2012, 100 (03) :601-606
[6]
Cognitive function in people with chronic illness: Inflammatory bowel disease and Irritable Bowel Syndrome [J].
Attree, EA ;
Dancey, CP ;
Keeling, D ;
Wilson, C .
APPLIED NEUROPSYCHOLOGY, 2003, 10 (02) :96-104
[7]
Defining a Healthy Human Gut Microbiome: Current Concepts, Future Directions, and Clinical Applications [J].
Backhed, Fredrik ;
Fraser, Claire M. ;
Ringel, Yehuda ;
Sanders, Mary Ellen ;
Sartor, R. Balfour ;
Sherman, Philip M. ;
Versalovic, James ;
Young, Vincent ;
Finlay, B. Brett .
CELL HOST & MICROBE, 2012, 12 (05) :611-622
[8]
Linkage of gut microbiome with cognition in hepatic encephalopathy [J].
Bajaj, Jasmohan S. ;
Ridlon, Jason M. ;
Hylemon, Phillip B. ;
Thacker, Leroy R. ;
Heuman, Douglas M. ;
Smith, Sean ;
Sikaroodi, Masoumeh ;
Gillevet, Patrick M. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2012, 302 (01) :G168-G175
[9]
Functional gastrointestinal disorders and mast cells: implications for therapy [J].
Barbara, G ;
Stanghellini, V ;
De Giorgio, R ;
Corinaldesi, R .
NEUROGASTROENTEROLOGY AND MOTILITY, 2006, 18 (01) :6-17
[10]
γ-Aminobutyric acid production by culturable bacteria from the human intestine [J].
Barrett, E. ;
Ross, R. P. ;
O'Toole, P. W. ;
Fitzgerald, G. F. ;
Stanton, C. .
JOURNAL OF APPLIED MICROBIOLOGY, 2012, 113 (02) :411-417