Opioid-induced gut microbial disruption and bile dysregulation leads to gut barrier compromise and sustained systemic inflammation

被引:227
作者
Banerjee, S. [1 ]
Sindberg, G. [2 ]
Wang, F. [2 ]
Meng, J. [1 ]
Sharma, U. [1 ]
Zhang, L. [3 ]
Dauer, P. [3 ]
Chen, C. [4 ]
Dalluge, J. [5 ]
Johnson, T. [2 ]
Roy, S. [1 ,3 ]
机构
[1] Univ Minnesota, Dept Surg & Pharmacol, Div Infect Inflammat & Vasc Biol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Vet Med, Minneapolis, MN USA
[3] Univ Minnesota, Dept Pharmacol, 3-249 Millard Hall, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Dept Food Sci & Nutr, Minneapolis, MN 55455 USA
[5] Univ Minnesota, Dept Chem, 207 Pleasant St SE, Minneapolis, MN 55455 USA
关键词
FECAL MICROBIOTA; MORPHINE; SEPSIS; HOST; TRANSPLANTATION; MODULATION; MUCOSAL; EXACERBATION; COINFECTION; DYSFUNCTION;
D O I
10.1038/mi.2016.9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Morphine and its pharmacological derivatives are the most prescribed analgesics for moderate to severe pain management. However, chronic use of morphine reduces pathogen clearance and induces bacterial translocation across the gut barrier. The enteric microbiome has been shown to have a critical role in the preservation of the mucosal barrier function and metabolic homeostasis. Here, we show for the first time, using bacterial 16s rDNA sequencing, that chronic morphine treatment significantly alters the gut microbial composition and induces preferential expansion of Gram-positive pathogenic and reduction in bile-deconjugating bacterial strains. A significant reduction in both primary and secondary bile acid levels was seen in the gut, but not in the liver with morphine treatment. Morphine-induced microbial dysbiosis and gut barrier disruption was rescued by transplanting placebo-treated microbiota into morphine-treated animals, indicating that microbiome modulation could be exploited as a therapeutic strategy for patients using morphine for pain management.
引用
收藏
页码:1418 / 1428
页数:11
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