Diabetic Rats Induced Using a High-Fat Diet and Low-Dose Streptozotocin Treatment Exhibit Gut Microbiota Dysbiosis and Osteoporotic Bone Pathologies

被引:4
|
作者
Huang, Kuo-Chin [1 ,2 ]
Chuang, Po-Yao [1 ,2 ]
Yang, Tien-Yu [1 ,2 ]
Tsai, Yao-Hung [1 ,2 ]
Li, Yen-Yao [1 ,2 ]
Chang, Shun-Fu [3 ]
机构
[1] Chang Gung Univ Coll Med, Sch Med, Taoyuan City 33302, Taiwan
[2] Chiayi Chang Gung Mem Hosp, Dept Orthoped Surg, Chiayi City 61363, Taiwan
[3] Chang Gung Mem Hosp, Dept Med Res & Dev, Chiayi City 61363, Taiwan
关键词
gut microbiota; diabetic bone disease; firmicutes/bacteroidetes ratio; osteoporosis; type 2 diabetes mellitus; TYPE-2; INSULIN; MODELS; RESISTANCE; OBESITY; INDEX; LINKS;
D O I
10.3390/nu16081220
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Type 2 diabetes mellitus (T2DM) presents a challenge for individuals today, affecting their health and life quality. Besides its known complications, T2DM has been found to contribute to bone/mineral abnormalities, thereby increasing the vulnerability to bone fragility/fractures. However, there is still a need for appropriate diagnostic approaches and targeted medications to address T2DM-associated bone diseases. This study aims to investigate the relationship between changes in gut microbiota, T2DM, and osteoporosis. To explore this, a T2DM rat model was induced by combining a high-fat diet and low-dose streptozotocin treatment. Our findings reveal that T2DM rats have lower bone mass and reduced levels of bone turnover markers compared to control rats. We also observe significant alterations in gut microbiota in T2DM rats, characterized by a higher relative abundance of Firmicutes (F) and Proteobacteria (P), but a lower relative abundance of Bacteroidetes (B) at the phylum level. Further analysis indicates a correlation between the F/B ratio and bone turnover levels, as well as between the B/P ratio and HbA1c levels. Additionally, at the genus level, we observe an inverse correlation in the relative abundance of Lachnospiraceae. These findings show promise for the development of new strategies to diagnose and treat T2DM-associated bone diseases.
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页数:18
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