Assessment of the early impact of different doses of radiotherapy on bone structure in mice using Micro-CT Scanning and biomechanical testing

Author:

Jia Cheng1,Yang Hui1,Xin Yue1,Li Changqin1,Yao Qianqian1,Liu Qi1,Hu Bei1,Yuan Xiaoqing1,Qin Jian1

Affiliation:

1. The Second Affiliated Hospital of Shandong First Medical University

Abstract

Abstract Objective: To establish a mice model of systemic bone injury induced by different doses of radiation, and evaluate the effects of different radiation doses on bone microstructure and biomechanical properties. Methods and materials: Forty female healthy C57BL/6J mice were randomly divided into 5 groups (N = 8 in each group): the control group (0 Gy) received no irradiation, the other four groups received single dose whole body irradiation of 1 Gy, 3 Gy, 6 Gy, 9 Gy, respectively. One week after irradiation, bilateral femurs and L5 lumbar vertebrae were dissected completely for micro-Computed Tomography (micro-CT) scanning, biological modulus detection and histomorphological observation. One-way design analysis of variance was used for comparison of measurement data among groups, and two-by-two comparisons between groups were performed using the Dunnet Test. Results: Compared with the control group ,the differences of the bone microstructure indexes in low-dose group (1 Gy), including BV/TV, Tb.N, Tb.Th, Tb.Sp, Tb.Pf , Conn.D and Ct.Th, were not statistically significant (P>0.05), but the elastic modulus decreased significantly (P<0.05). In high-dose groups (3 Gy, 6 Gy, 9 Gy) , BV/TV, Tb. N, Conn.D decreased significantly (P<0.05) , Tb. Sp and Tb.Pf increased significantly (P<0.05) and elastic modulus decreased significantly (P<0.05). Conclusion: Low-dose (1 Gy) radiotherapy had little effect on bone microstructure, but significant effect on bone biomechanical properties; while higher dose radiotherapy had both significant effect on bone microstructure and biomechanical properties, which leaded to the destruction of bone microstructure and the decrease of bone strength.

Publisher

Research Square Platform LLC

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