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Gut microbiota trigger host liver immune responses that affect drug-metabolising enzymes.

作者信息

Rao Jiaoyu, Qiu Peng, Zhang Yonggang, Wang Xiaokang

机构信息

Department of Pharmacy, Shenzhen Longhua District Central Hospital, Shenzhen, China.

Clinical Laboratory Department, Shenzhen Longhua District Central Hospital, Shenzhen, China.

出版信息

Front Immunol. 2024 Dec 11;15:1511229. doi: 10.3389/fimmu.2024.1511229. eCollection 2024.


DOI:10.3389/fimmu.2024.1511229
PMID:39720713
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11668346/
Abstract

There is increasing evidence that the intestinal microbiota plays an integral role in disease pathogenesis and treatment. Specifically, the intestinal microbiota significantly influences the pharmacokinetics and pharmacodynamics of orally administered drugs through direct involvement in drug metabolism and, consequently, drug bioavailability. However, the gut microbiota also exerts immunoregulatory effects on the liver-the organ primarily responsible for drug metabolism-thereby indirectly impacting the body's capacity to metabolise and process drugs. Individual differences in this pathway substantially contribute to the variability in clinical drug treatment outcomes observed between patients. This review examines the impact of liver immune responses, as triggered by the intestinal microbiota, on the activity of drug-metabolising enzymes and discusses the implications for precision medicine.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9895/11668346/95db9222a0eb/fimmu-15-1511229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9895/11668346/030c0423f2ca/fimmu-15-1511229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9895/11668346/95db9222a0eb/fimmu-15-1511229-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9895/11668346/030c0423f2ca/fimmu-15-1511229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9895/11668346/95db9222a0eb/fimmu-15-1511229-g002.jpg

相似文献

[1]
Gut microbiota trigger host liver immune responses that affect drug-metabolising enzymes.

Front Immunol. 2024-12-11

[2]
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[3]
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[4]
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[5]
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[7]
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[8]
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引用本文的文献

[1]
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[2]
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Front Immunol. 2025-7-31

[3]
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[4]
1-methylnicotinamide modulates IL-10 secretion and voriconazole metabolism.

Front Immunol. 2025-2-13

本文引用的文献

[1]
Spatial single-cell profiling and neighbourhood analysis reveal the determinants of immune architecture connected to checkpoint inhibitor therapy outcome in hepatocellular carcinoma.

Gut. 2025-2-6

[2]
Schisanhenol ameliorates non-alcoholic fatty liver disease inhibiting miR-802 activation of AMPK-mediated modulation of hepatic lipid metabolism.

Acta Pharm Sin B. 2024-9

[3]
Corynoline alleviates hepatic ischemia-reperfusion injury by inhibiting NLRP3 inflammasome activation through enhancing Nrf2/HO-1 signaling.

Inflamm Res. 2024-12

[4]
Specific Bacterial Co-abundance Groups Are Associated With Inflammatory Status in Patients With Ulcerative Colitis.

J Crohns Colitis. 2025-1-11

[5]
Functional and epigenetic changes in monocytes from adults immunized with an AS01-adjuvanted vaccine.

Sci Transl Med. 2024-7-31

[6]
Washed microbiota transplantation promotes homing of group 3 innate lymphoid cells to the liver via the CXCL16/CXCR6 axis: a potential treatment for metabolic-associated fatty liver disease.

Gut Microbes. 2024

[7]
Inflammasomes in chronic liver disease: Hepatic injury, fibrosis progression and systemic inflammation.

J Hepatol. 2024-11

[8]
Epigenomic partitioning of a polygenic risk score for asthma reveals distinct genetically driven disease pathways.

Eur Respir J. 2024-8

[9]
Circadian time-dependent effects of experimental colitis on theophylline disposition and toxicity.

Br J Pharmacol. 2024-10

[10]
The human gut microbiome and aging.

Gut Microbes. 2024

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