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Influence of Prednisolone and Alendronate on the de novo Mineralization of Zebrafish Caudal Fin

机译:泼尼松龙与alynethate对斑马鱼尾鳍De Novo矿化的影响

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Dysregulated balance between bone resorption and formation mediates the onset and progression of osteoporosis. The administration of prednisolone is known to induce osteoporosis, whereas alendronate is commonly used to reverse the process. However, the assessment of the effects of such medicines on the nanostructure of bone remodeling and mechanical properties remains a major technical challenge. The aim of this study was to apply various analytical approaches to evaluate the compositional, morphological, and mechanical properties of regenerative zebrafish caudal fin bony rays affected by prednisolone and alendronate. Adult wild‐type AB strain zebrafish were first exposed to 125μM of prednisolone for 14?days to develop glucocorticoid‐induced osteoporosis. Fish fins were then amputated and let to regenerate for 21?days in tank water containing 30μM of alendronate or no alendronate. The lepidotrichia in the proximal and distal regions were evaluated separately using confocal microscope, scanning electron microscope, electron‐dispersive spectroscopy, Raman spectroscopy, atomic force microscopy, and a triboindenter. As expected, prednisolone led to significant osteoporotic phenotypes. A decrease of Ca/P ratio was observed in the osteoporotic subjects (1.46?±?0.04) as compared to the controls (1.74?±?0.10). Subsequent treatment of alendronate overmineralized the bony rays during regeneration. Enhanced phosphate deposition was detected in the proximal part with alendronate treatment. Moreover, prednisolone attenuated the reduced elastic modulus and hardness levels (5.60?±?5.04?GPa and 0.12?±?0.17?GPa, respectively), whereas alendronate recovered them to the pre‐amputation condition (8.68?±?8.74?GPa and 0.34?±?0.47?GPa, respectively). As an emerging model of osteoporosis, regrowth of zebrafish caudal fin was shown to be a reliable assay system to investigate the various effects of medicines in the de novo mineralization process. ? 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
机译:骨吸收和地层之间的失调平衡介导骨质疏松症的发病和进展。已知泼尼松龙的给药诱导骨质疏松症,而阿仑膦酸盐通常用于逆转该过程。然而,评估这种药物对骨重塑和机械性能纳米结构的影响仍然是主要的技术挑战。本研究的目的是应用各种分析方法,以评估受泼尼松龙和醛酸酯影响的再生斑马鱼尾鳍骨磁射线的组成,形态和力学性能。成人野生型AB菌株斑马鱼首先暴露于125μm的泼尼松龙14.天,以发展糖皮质激素诱导的骨质疏松症。然后截肢鱼鳍片并使其在含有30μm的醛酸盐或不醛酸的水箱中再生21天。使用共聚焦显微镜,扫描电子显微镜,电子色散光谱,拉曼光谱,原子力显微镜和摩擦丁基,分别评估近端区域中的LepidoTriChia。正如预期的那样,泼尼松龙导致了显着的骨质疏松表型。与对照相比,在骨质疏松受试者中观察到骨质疏松受试者(1.46?±0.04)的降低(1.74?±0.10)。随后治疗反常膦酸盐在再生期间的骨射线过度。在近端部分中检测到增强的磷酸盐沉积,用醛膦酸盐处理检测。此外,泼尼松龙分别减弱了降低的弹性模量和硬度水平(5.60?±5.04?GPA和0.12? 0.34?±0.47?GPA)。作为骨质疏松症的新出现模型,斑马鱼尾鳍的再生被证明是一种可靠的测定系统,以研究药物在德诺矿化过程中的各种影响。还2020作者。 JBMR Plus由Wiley Moustiongs LLC发布代表美国骨骼和矿物学研究。

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