Skeletal Effects of a Prolonged Oral Metformin Treatment in Adult Wistar Rats.

Nahuel E Wanionok, María S Molinuevo, Juan M Fernández, Besada Lucas, Ana M Cortizo, Evelyn J Castillo, Jessica M Jiron, Sedlinsky Claudia, Schurman Leon, José I Aguirre, Antonio D McCarthy
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Abstract

Introduction: We previously showed that a 3-week oral metformin (MET) treatment enhances the osteogenic potential of bone marrow stromal cells (BMSCs) and improves several bone histomorphometric parameters in Wistar rats with metabolic syndrome (MetS). However, the skeletal effects of extended periods of MET need to be completely elucidated. Hence, in this study, the impact of a prolonged (3-month) MET treatment was investigated on bone architecture, histomorphometric and biomechanics variables, and osteogenic potential of BMSCs in Wistar rats with or without MetS.

Materials and methods: Young male Wistar rats (n=36) were randomized into four groups (n=9) that received either 20% fructose (F), MET (MET), F plus MET treatments (FMET), or drinking water alone (Veh). Rats were euthanized, blood was collected, and bones were dissected and processed for peripheral quantitative computed tomography (pQCT) analysis, static and dynamic histomorphometry, and bone biomechanics. In addition, BMSCs were isolated to determine their osteogenic potential.

Results: MET affected trabecular and cortical bone, altering bone architecture and biomechanics. Furthermore, MET increased the pro-resorptive profile of BMSCs. In addition, fructose-induced MetS practically did not affect the the structural or mechanical variables of the skeleton.

Conclusion: A 3-month treatment with MET (with or without MetS) affects bone architecture and biomechanical variables in Wistar rats.

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成年 Wistar 大鼠长期口服二甲双胍对骨骼的影响
简介:我们以前的研究表明,在患有代谢综合征(MetS)的Wistar大鼠中,口服三周二甲双胍(MET)可增强骨髓基质细胞(BMSCs)的成骨潜能,并改善骨骼组织形态学的一些参数。然而,长期服用 MET 对骨骼的影响仍未完全阐明。因此,我们研究了长期(3 个月)MET 处理对有或没有 MetS 的 Wistar 大鼠骨结构、组织形态计量学和生物力学变量以及 BMSCs 成骨潜能的影响。材料和方法:36 只年轻雄性 Wistar 大鼠被随机分为四组(n=9),分别接受 20% 果糖(F)、MET(MET)、F 加 MET 处理(FMET)或单独饮用水(Veh)。对大鼠实施安乐死,收集血液,解剖并处理骨骼,进行 pQCT 分析、静态和动态组织形态测量以及骨生物力学分析。此外,还分离了 BMSCs,以确定其成骨细胞的潜力:结果:MET影响了骨小梁和皮质骨,改变了骨结构和生物力学。此外,MET 增加了 BMSCs 的促骨吸收特性。此外,果糖诱导的 MetS 实际上并不影响骨骼的结构或机械变量:结论:为期 3 个月的 MET 治疗(无论是否存在 MetS)都会影响 Wistar 大鼠的骨骼结构和生物力学变量。
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