Load/strain distribution between ulna and radius in the mouse forearm compression loading model
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Updated: May 29, 2026

Mouse Lumbar Vertebra Uniaxial Compression Testing with Embedding of the Loading Surface
Published on: December 1, 2023
Yunkai Lu1, Ganesh Thiagarajan, Daniel P Nicolella
1Department of Civil and Mechanical Engineering, University of Missouri-Kansas City, Kansas City, MO 64110, United States.
Abstract:
Finite element analysis (FEA) of the mouse forearm compression loading model is used to relate strain distributions with downstream changes in bone formation and responses of bone cells. The objective of this study was to develop two FEA models - the first one with the traditional ulna only and the second one in which both the ulna and radius are included, in order to examine the effect of the inclusion of the radius on the strain distributions in the ulna. The entire mouse forearm was scanned using microCT and images were converted into FEA tetrahedral meshes using a suite of software programs. The performance of both linear and quadratic tetrahedral elements and coarse and fine meshes were studied. A load of 2N was applied to the ulna/radius model and a 1.3N load (based on previous investigations of load sharing between the ulna and radius in rats) was applied to the ulna only model for subsequent simulations. The results showed differences in the cross sectional strain distributions and magnitude within the ulna for the combined ulna/radius model versus the ulna only model. The maximal strain in the combined model occurred about 4mm toward the distal end from the ulna mid-shaft in both models. Results from the FEA model simulations were also compared to experimentally determined strain values. We conclude that inclusion of the radius in FE models to predict strains during in vivo forearm loading increases the magnitude of the estimated ulna strains compared to those predicted from a model of the ulna alone but the distribution was similar. This has important ramifications for future studies to understand strain thresholds needed to activate bone cell responses to mechanical loading.
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