骨量形成的理论模型研究

Nirmalendu Hui, B. Chattopadhyay
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引用次数: 0

摘要

人类骨量的形成是为了了解潜在的动力学,以非侵入性途径治疗骨折和骨不连。成骨细胞、破骨细胞和骨细胞是形成新骨或骨物质的重要生物细胞,其中许多激素、蛋白质和矿物质具有不可缺少的支持作用。假设上述三个细胞的种群为变量,我们构建了一个理论模型,该模型表示为一组时间微分方程。这些方程模拟了骨物质生成的动态过程。在我们的模型中,高值的骨细胞和中等水平的成骨细胞和破骨细胞,均处于渐近尺度,意味着新骨物质的产生。对该模型进行了分析和数值研究。重点介绍了一些重要的结果,并作出了相应的预测,为今后的实验检验提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on Bone-mass Formation within a Theoretical Model
Bone-mass formation in human is looked at to understand the underlying dynamics with an eye on healing of bone-fracture and non-unions in non-invasive pathways. Three biological cells osteoblasts, osteoclasts and osteocytes are important players in creating new bone or osseous matter in which quite a few hormones, proteins and minerals have indispensable supportive role. Assuming populations of the three mentioned cells as variables, we frame a theoretical model which is represented as a set of time differential equations. These equations imitate the dynamic process of bone matter creation. High value of osteocytes with moderate level values of osteoblast and osteoclast, all at asymptotic scale, imply creation of new bone-matter in our model. The model is studied both analytically and numerically. Some important results are highlighted and relevant predictions are made which could be put to future experimental test.
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