Dong Yao, Gai Zhonghui, Han Mei, Xu Jiaqi, Zou Kang
Germline Stem Cells and Microenvironment Lab, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, 210095, China.
Stem Cell Research and Translation Center, Nanjing Agricultural University, Nanjing, 210095, China.
Probiotics Antimicrob Proteins. 2024 Jun 3. doi: 10.1007/s12602-024-10293-5.
Gut microbiota dysbiosis and consequent impairment of gut barrier function, culminating in elevated levels of uremic toxins, are prevalent in chronic kidney disease (CKD) patients. These toxins, notably indoxyl sulphate (IS), indole-3-acetic acid (IAA), and trimethylamine oxide (TMAO), are implicated in a spectrum of CKD-related complications, including cardiovascular disease, bone and mineral disorders, and inflammation. The specific impacts of various probiotics on these CKD manifestations remain unexplored. This study delved into the potential of dietary probiotic interventions, particularly Bifidobacterium longum subsp. longum BL21, to modulate gut microbiota and mitigate metabolic disorders in a CKD rat model. Over a six-week period, we administered a dietary regimen of BL21 and conducted comprehensive analyses, including serum uremic toxin quantification and 16S rRNA gene sequencing, to systematically profile gut microbial alterations at the phylogenetic level. Our findings reveal that BL21 intervention significantly ameliorated CKD-induced disruptions in gut microbial populations, enhancing both microbial richness and the relative abundance of key taxa. Importantly, BL21 appeared to exert its beneficial effects by modulating the abundance of crucial species such as Barnesiella and Helicobacter. Functionally, the intervention markedly normalized serum levels of IS, IAA, and TMAO, while potentially attenuating p-cresol sulphate (PCS) and p-cresol glucuronide (PCG) concentrations. Consequently, BL21 demonstrated efficacy in regulating gut microbiota and curtailing the accumulation of uremic toxins. Our results advocate for the utilization of BL21 as a dietary intervention to diminish serum uremic toxins and re-establish gut microbiota equilibrium at the phylogenetic level, underscoring the promise of probiotic strategies in the management of CKD.
肠道微生物群失调以及随之而来的肠道屏障功能受损,最终导致尿毒症毒素水平升高,在慢性肾脏病(CKD)患者中普遍存在。这些毒素,特别是硫酸吲哚酚(IS)、吲哚 - 3 - 乙酸(IAA)和氧化三甲胺(TMAO),与一系列CKD相关并发症有关,包括心血管疾病、骨与矿物质紊乱以及炎症。各种益生菌对这些CKD表现的具体影响仍未得到探索。本研究深入探讨了膳食益生菌干预措施,特别是长双歧杆菌亚种长双歧杆菌BL21,在CKD大鼠模型中调节肠道微生物群和减轻代谢紊乱的潜力。在六周的时间里,我们给予了BL21饮食方案,并进行了全面分析,包括血清尿毒症毒素定量和16S rRNA基因测序,以系统地描绘系统发育水平上的肠道微生物变化。我们的研究结果表明,BL21干预显著改善了CKD引起的肠道微生物种群破坏,提高了微生物丰富度和关键分类群的相对丰度。重要的是,BL21似乎通过调节诸如Barnesiella和Helicobacter等关键物种的丰度发挥其有益作用。在功能上,该干预显著使IS、IAA和TMAO的血清水平正常化,同时可能降低硫酸对甲酚(PCS)和对甲酚葡萄糖醛酸苷(PCG)的浓度。因此,BL21在调节肠道微生物群和减少尿毒症毒素积累方面显示出功效。我们的结果主张将BL21用作膳食干预措施,以降低血清尿毒症毒素并在系统发育水平上重建肠道微生物群平衡,强调了益生菌策略在CKD管理中的前景。