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Icariin prevents bone loss by inhibiting bone resorption and stabilizing bone biological apatite in a hindlimb suspension rodent model

机译:鹰嘴豆素通过抑制后肢悬浮啮齿动物模型中的骨吸收并稳定骨生物磷灰石来防止骨质流失

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摘要

Bone loss induced by microgravity is a substantial barrier to humans in long-term spaceflight. Recent studies have revealed that icariin (ICA) can attenuate osteoporosis in postmenopausal women and ovariectomized rats. However, whether ICA can protect against microgravity-induced bone loss remains unknown. In this study, the effects of ICA on a hindlimb suspension rodent model were investigated. Two-month-old female Wistar rats were hindlimb suspended and treated with ICA (25 mg·kg−1·d−1, i.g.) or a vehicle for 4 weeks (n = 6). The bone mass density of the hindlimbs was analyzed using dual-energy X-ray absorptiometry and micro-CT. mRNA expression of osteogenic genes in the tibia and the content of bone metabolism markers in serum were measured using qRT-PCR and ELISA, respectively. The bone mineral phase was analyzed using X-ray diffraction and atomic spectrometry. The results showed that ICA treatment significantly rescued the hindlimb suspension-induced reduction in bone mineral density, trabecular number and thickness, as well as the increases in trabecular separation and the structure model index. In addition, ICA treatment recovered the decreased bone-related gene expression, including alkaline phosphatase (ALP), bone glaprotein (BGP), and osteoprotegerin/receptor activator of the NF-κB ligand ratio (OPG/RANKL), in the tibia and the decreased bone resorption marker TRACP-5b levels in serum caused by simulated microgravity. Notably, ICA treatment restored the instability of bone biological apatite and the metabolic disorder of bone mineral elicited by simulated microgravity. These results demonstrate that ICA treatment plays osteoprotective roles in bone loss induced by simulated microgravity by inhibiting bone resorption and stabilizing bone biological apatite.
机译:微重力引起的骨质流失是人类长期太空飞行的主要障碍。最近的研究表明,icariin(ICA)可以减轻绝经后妇女和去卵巢大鼠的骨质疏松症。但是,ICA是否可以防止微重力引起的骨质流失尚不清楚。在这项研究中,研究了ICA对后肢悬浮啮齿动物模型的影响。将两个月大的Wistar雌性大鼠后肢悬吊,并用ICA(25 mg·kg -1 ·d -1 ,ig)或载体治疗4周( n = 6)。使用双能X射线吸收法和micro-CT分析后肢的骨密度。使用qRT-PCR和ELISA分别测量胫骨中成骨基因的mRNA表达和血清中骨代谢标志物的含量。骨矿相使用X射线衍射和原子光谱分析。结果表明,ICA治疗显着地挽救了后肢悬吊引起的骨矿物质密度,小梁数量和厚度的减少,以及小梁分离和结构模型指数的增加。此外,ICA治疗可恢复胫骨和胫骨中与骨相关的基因表达降低,包括碱性磷酸酶(ALP),骨蛋白(BGP)和NF-κB配体比例的骨保护素/受体激活剂(OPG / RANKL)。模拟微重力导致血清中骨吸收标志物TRACP-5b水平降低。值得注意的是,ICA治疗可恢复骨骼生物磷灰石的不稳定性和模拟微重力引起的骨骼矿物质代谢紊乱。这些结果表明,ICA治疗通过抑制骨吸收和稳定骨生物磷灰石,在模拟微重力诱导的骨丢失中发挥骨保护作用。

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