Elizabeth C Welsch, Matthew R Barron, Katelyn M Storage, Alexis B Kazen, Fatima A Aboulalazm, John R Kirby, Tammy L Kindel
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SG significantly increased the BA pool and decreased liver transcription of slc10a1 (<i>P</i> = 0.04) and cyp8b1 (<i>P</i> = 0.03). Random forest analysis identified several features with significantly increased relative abundance in SG compared with sham mice, including <i>Lactobacillus</i>. Examination of metabolic profiles with metagenomic analysis revealed a BA salt hydrolase produced by the <i>Ligilactobacillus</i> species. FMT of SG stool to surgically naïve mice significantly decreased the BA pool compared with sham FMT (<i>P</i> = 0.034). Unlike SG surgery, we found no effect of SG or sham FMT on bile acid-related enzymes in the liver after 14 wk of treatment. Overall, we propose that the metabolic benefits of SG surgery are related to decreased liver transcription of cyp8b1 and slc10a1 with subsequent increases in the systemic and enterohepatic BA pool, including lithocholic acid. 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引用次数: 0
摘要
由于肝脏、胆囊酸(BA)池和肠道微生物群之间的复杂关系,了解袖式胃切除术(SG)如何实现代谢改善是具有挑战性的。我们假设SG改变了肠道微生物群,从而增加了BA池,从而提高了代谢效率。方法我们将SG或假小鼠的粪便物质转移(FMT)到具有完整微生物组的surgically-naïve小鼠。我们通过16s和宏基因组分析评估了手术和FMT对BA相关肝酶、BA浓度和肠道微生物组组成的影响。结果与假手术相比,SG明显扭转了体重增加,分别为5±2 g和10±3 g (p= 0.004)。SG显著增加了BA库,降低了slc10a1 (p=0.04)和cyp8b1 (p=0.03)的肝脏转录。随机森林分析发现,与假小鼠相比,SG中有几个特征的相对丰度显著增加,包括乳酸杆菌。代谢谱的宏基因组分析显示,一种BA盐水解酶是由Ligilactobacillus产生的。与假FMT相比,SG粪便FMT给surgically-naïve小鼠显著降低BA池(p=0.034)。与SG手术不同,我们发现SG或假FMT在治疗14周后对肝脏中胆汁酸相关酶没有影响。综上所述,我们认为SG手术的代谢益处与肝脏cyp8b1和slc10a1转录的降低以及随后包括LCA在内的全身和肠肝BA池的增加有关。肠道微生物群适应BA池的改变,并随之增加乳酸菌和胆盐水解酶的产量。
Gut microbiome and bile acid changes after male rodent sleeve gastrectomy: what comes first?
Understanding how a sleeve gastrectomy (SG) achieves metabolic improvement is challenging due to the complex relationship between the liver, bile acid (BA) pool, and gut microbiome. We hypothesized that SG alters the gut microbiome, which then increases the BA pool, leading to metabolic efficacy. We performed fecal material transfer (FMT) from SG or sham mice to surgically naïve mice with an intact microbiome. We evaluated the effect of surgery and FMT on BA-related liver enzymes, BA concentrations, and gut microbiome composition via 16S and metagenomic analysis. SG significantly deflected weight gain compared with sham surgery, 5 ± 2 g versus 10 ± 3 g, respectively (P = 0.004). SG significantly increased the BA pool and decreased liver transcription of slc10a1 (P = 0.04) and cyp8b1 (P = 0.03). Random forest analysis identified several features with significantly increased relative abundance in SG compared with sham mice, including Lactobacillus. Examination of metabolic profiles with metagenomic analysis revealed a BA salt hydrolase produced by the Ligilactobacillus species. FMT of SG stool to surgically naïve mice significantly decreased the BA pool compared with sham FMT (P = 0.034). Unlike SG surgery, we found no effect of SG or sham FMT on bile acid-related enzymes in the liver after 14 wk of treatment. Overall, we propose that the metabolic benefits of SG surgery are related to decreased liver transcription of cyp8b1 and slc10a1 with subsequent increases in the systemic and enterohepatic BA pool, including lithocholic acid. The gut microbiome adapts to the altered BA pool with associated increases in Ligilactobacillus and bile salt hydrolase production.NEW & NOTEWORTHY We propose that the metabolic benefits of sleeve gastrectomy are initiated by decreased liver transcription of cyp8b1 and slc10a1. A notable downstream effect includes changes in systemic bile acid composition and circulation, including increased LCA. An altered gut microbiome after surgery includes increases in Ligilactobacillus that was shown to express a bile salt hydrolase, which could be a contributor to the post-sleeve gastrectomy gut microbiome changes.
期刊介绍:
The American Journal of Physiology-Regulatory, Integrative and Comparative Physiology publishes original investigations that illuminate normal or abnormal regulation and integration of physiological mechanisms at all levels of biological organization, ranging from molecules to humans, including clinical investigations. Major areas of emphasis include regulation in genetically modified animals; model organisms; development and tissue plasticity; neurohumoral control of circulation and hypertension; local control of circulation; cardiac and renal integration; thirst and volume, electrolyte homeostasis; glucose homeostasis and energy balance; appetite and obesity; inflammation and cytokines; integrative physiology of pregnancy-parturition-lactation; and thermoregulation and adaptations to exercise and environmental stress.