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罗伊氏乳杆菌预防抗生素后骨丢失通过减少肠道菌群失调和防止屏障破坏。

Probiotic Lactobacillus reuteri Prevents Postantibiotic Bone Loss by Reducing Intestinal Dysbiosis and Preventing Barrier Disruption.

机构信息

Department of Physiology, Michigan State University, East Lansing, MI, USA.

Comparative Medicine and Integrative Biology Program, Michigan State University, East Lansing, MI, USA.

出版信息

J Bone Miner Res. 2019 Apr;34(4):681-698. doi: 10.1002/jbmr.3635. Epub 2019 Jan 28.

Abstract

Antibiotic treatment, commonly prescribed for bacterial infections, depletes and subsequently causes long-term alterations in intestinal microbiota composition. Knowing the importance of the microbiome in the regulation of bone density, we investigated the effect of postantibiotic treatment on gut and bone health. Intestinal microbiome repopulation at 4-weeks postantibiotic treatment resulted in an increase in the Firmicutes:Bacteroidetes ratio, increased intestinal permeability, and notably reduced femoral trabecular bone volume (approximately 30%, p < 0.01). Treatment with a mucus supplement (a high-molecular-weight polymer, MDY-1001 [MDY]) prevented the postantibiotic-induced barrier break as well as bone loss, indicating a mechanistic link between increased intestinal permeability and bone loss. A link between the microbiome composition and bone density was demonstrated by supplementing the mice with probiotic bacteria. Specifically, Lactobacillus reuteri, but not Lactobacillus rhamnosus GG or nonpathogenic Escherichia coli, reduced the postantibiotic elevation of the Firmicutes:Bacteroidetes ratio and prevented femoral and vertebral trabecular bone loss. Consistent with causing bone loss, postantibiotic-induced dysbiosis decreased osteoblast and increased osteoclast activities, changes that were prevented by both L. reuteri and MDY. These data underscore the importance of microbial dysbiosis in the regulation of intestinal permeability and bone health, as well as identify L. reuteri and MDY as novel therapies for preventing these adverse effects. © 2018 American Society for Bone and Mineral Research.

摘要

抗生素治疗常用于治疗细菌感染,但会消耗肠道微生物群落的组成,并随后导致长期的改变。鉴于微生物组在调节骨密度方面的重要性,我们研究了抗生素治疗后对肠道和骨骼健康的影响。抗生素治疗 4 周后肠道微生物群落的再定植导致厚壁菌门与拟杆菌门的比例增加、肠道通透性增加,并且显著降低了股骨小梁骨体积(约 30%,p < 0.01)。用黏液补充剂(一种高分子聚合物,MDY-1001[MDY])治疗可预防抗生素治疗引起的屏障破坏和骨丢失,这表明肠道通透性增加和骨丢失之间存在机制联系。通过用益生菌补充小鼠,证明了微生物群落组成与骨密度之间存在联系。具体而言,鼠李糖乳杆菌,但不是罗伊氏乳杆菌 GG 或非致病性大肠杆菌,可降低抗生素治疗后厚壁菌门与拟杆菌门比例的升高,并防止股骨和椎骨小梁骨丢失。与引起骨丢失一致,抗生素治疗引起的菌群失调降低了成骨细胞的活性并增加了破骨细胞的活性,这一变化可被 L. reuteri 和 MDY 预防。这些数据强调了微生物失调在调节肠道通透性和骨骼健康方面的重要性,并确定了 L. reuteri 和 MDY 是预防这些不良反应的新型治疗方法。

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