Abstract | BACKGROUND: Historically, the beneficial effects of the nonsystemic oral agent rifaximin on various gastrointestinal (GI) disorders have been attributed to direct antibiotic activity on gut microbiota. However, data are accumulating to suggest that other nonantibacterial effects may be involved in rifaximin efficacy. AIM: METHODS: RESULTS: Gut microbiota dysbiosis and proinflammatory activities are thought to significantly contribute to disease pathophysiology of these conditions. Rifaximin may resolve gut microbiota dysbiosis by promoting GI colonisation of beneficial bacterial species without drastic alterations in overall diversity. Rifaximin-induced changes in the production and metabolism of bacteria-produced agents (e.g. deoxycholic acid, lipopolysaccharides) also may help preserve normal gut microbiota. Rifaximin may suppress local and systemic inflammatory processes by preserving epithelial function (e.g. limiting bacterial translocation), modulating bacterial virulence and reducing proinflammatory cytokine production. CONCLUSION: The commonality of pathological mechanisms underlying multiple GI diseases and the ability of rifaximin to modulate the gut microenvironment (i.e. gut microenvironment modulator) may explain its diverse efficacy profile.
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Authors | H L DuPont |
Journal | Alimentary pharmacology & therapeutics
(Aliment Pharmacol Ther)
Vol. 43 Suppl 1
Pg. 1-2
(Jan 2016)
ISSN: 1365-2036 [Electronic] England |
PMID | 26618920
(Publication Type: Introductory Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2015 John Wiley & Sons Ltd. |
Chemical References |
- Anti-Bacterial Agents
- Gastrointestinal Agents
- Rifamycins
- Rifaximin
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Topics |
- Anti-Bacterial Agents
(therapeutic use)
- Diarrhea
(drug therapy)
- Gastrointestinal Agents
(pharmacology, therapeutic use)
- Gastrointestinal Diseases
(drug therapy, physiopathology)
- Gastrointestinal Microbiome
- Hepatic Encephalopathy
(drug therapy)
- Humans
- Inflammatory Bowel Diseases
(drug therapy)
- Irritable Bowel Syndrome
(drug therapy)
- Rifamycins
(pharmacology, therapeutic use)
- Rifaximin
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