Adedigba Pelumi, Ice John A, Alake Sanmi E, Hatter Bethany, Islam Proapa, Ford Versypt Ashlee N, Knotts Trina A, Ritchey Jerry, Lucas Edralin A, Smith Brenda J
Indiana Center for Musculoskeletal Health, Indiana School of Medicine, Indianapolis, IN 46202, USA.
Nutritional Sciences Department, Oklahoma State University, Stillwater, OK 74078, USA.
Nutrients. 2025 Aug 30;17(17):2829. doi: 10.3390/nu17172829.
Fructooligosaccharides (FOS) and dried tart cherry (TC) are examples of simple and complex (i.e., within a food matrix) prebiotics that have demonstrated promising osteoprotective activity. In this study, we examined how dietary supplementation with TC or FOS shapes the gut-bone axis to promote bone accrual in young adult mice, and the role of the gut microbiota in mediating these responses. Studies were performed using 10-wk-old female C57BL/6 mice (n = 10-12/group) fed a control diet or control diet supplemented with 10% TC or FOS for 10 wks alone or in combination with an antibiotic/anti-fungal cocktail to suppress the gut microbiota. The bone phenotype was characterized by dual-energy X-ray absorptiometry, micro-computed tomography and static and dynamic bone histomorphometry. The gut-microbiota was profiled and short chain fatty acids (SCFA) were assessed based on 16S rRNA profiling and gas chromatographic techniques, respectively. FOS and TC enhanced bone structure, with FOS yielding more pronounced benefits across cortical and trabecular compartments. These skeletal improvements with FOS occurred in the absence of systemic changes in bone turnover markers but were accompanied by increases in local bone formation, osteoblast and osteocyte numbers, and bone mineralization in the femur. Both diets altered gut microbiota composition and increased fecal concentrations of the most abundant SCFAs (i.e., acetate, propionate and butyrate), but the response was greater with FOS. Suppression of the gut microbiota and fecal SCFAs with the antibiotic/anti-fungal cocktail inhibited the effects of FOS and TC on cortical bone, but induced unexpected improvements in the trabecular bone. These findings demonstrate differential effects of simple and complex prebiotics on the gut-bone axis in young adult female mice and support a role for SCFA in the cortical bone response, but not in the trabecular bone response with this model of gut microbiota suppression.
低聚果糖(FOS)和干酸樱桃(TC)是简单型和复合型(即在食物基质中)益生元的例子,它们已显示出有前景的骨保护活性。在本研究中,我们研究了用TC或FOS进行膳食补充如何塑造肠-骨轴以促进年轻成年小鼠的骨积累,以及肠道微生物群在介导这些反应中的作用。研究使用10周龄雌性C57BL/6小鼠(每组n = 10 - 12只),给其喂食对照饮食或补充了10% TC或FOS的对照饮食,单独或与抗生素/抗真菌混合物联合使用10周以抑制肠道微生物群。通过双能X线吸收法、显微计算机断层扫描以及静态和动态骨组织形态计量学来表征骨表型。分别基于16S rRNA分析和气相色谱技术对肠道微生物群进行分析并评估短链脂肪酸(SCFA)。FOS和TC增强了骨结构,FOS在皮质骨和小梁骨区域产生了更显著的益处。FOS带来的这些骨骼改善在骨转换标志物无全身变化的情况下出现,但伴随着股骨局部骨形成、成骨细胞和骨细胞数量增加以及骨矿化。两种饮食都改变了肠道微生物群组成并增加了粪便中最丰富的SCFA(即乙酸盐、丙酸盐和丁酸盐)的浓度,但FOS的反应更大。用抗生素/抗真菌混合物抑制肠道微生物群和粪便SCFA可抑制FOS和TC对皮质骨的作用,但却意外地改善了小梁骨。这些发现证明了简单型和复合型益生元对年轻成年雌性小鼠肠-骨轴的不同影响,并支持SCFA在皮质骨反应中的作用,但在这种肠道微生物群抑制模型的小梁骨反应中则不然。