Literature DB >> 16519891

Use of the rat forelimb compression model to create discrete levels of bone damage in vivo.

Brian A Uthgenannt1, Matthew J Silva.   

Abstract

Skeletal responses to damage are significant for understanding the etiology of stress fractures and possibly osteoporotic fractures. We refined the rat forelimb-loading model to produce a range of sub-fracture damage levels during in vivo cyclic loading. A total of 98 right forelimbs of anesthetized, male, 5-month old Fischer rats were loaded cyclically (2 Hz) in axial compression. Rats were killed immediately after loading. In the first experiment, forelimbs were loaded to fracture, which occurred after an increase in peak displacement of 2.0+/-0.2 mm, independent of peak force or cycle number. In the next experiment, we loaded forelimbs at a constant peak force until the peak displacement increased by 0.6-1.8 mm (30-90% of fracture displacement). Mechanical properties of the loaded (right) and contralateral control (left) ulnae were determined ex vivo using three-point bending, and cracks were analyzed using micro-computed tomography. Results demonstrated a dose-response between increased forelimb displacement and increased ulnar damage, with four discrete damage levels. "Low" damage was produced by cyclic loading to 30% of fracture displacement, with no visible cracks and a 10% strength loss. "Mild" damage was produced by loading to 45% of fracture displacement, with variable linear cracks and 20% strength loss. "Moderate" damage was produced by loading to 60-75% of fracture displacement, with consistent linear cracks and 40% strength loss. "High" damage was produced by loading to 85-90% of fracture displacement, with branching cracks and 60% strength loss. This loading model will be useful for examining biological responses to a range of sub-fracture damage levels in future experiments.

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Year:  2006        PMID: 16519891     DOI: 10.1016/j.jbiomech.2006.01.005

Source DB:  PubMed          Journal:  J Biomech        ISSN: 0021-9290            Impact factor:   2.712


  22 in total

1.  In vivo static creep loading of the rat forelimb reduces ulnar structural properties at time-zero and induces damage-dependent woven bone formation.

Authors:  Jennifer A Lynch; Matthew J Silva
Journal:  Bone       Date:  2008-01-26       Impact factor: 4.398

2.  Nitric oxide-mediated vasodilation increases blood flow during the early stages of stress fracture healing.

Authors:  Ryan E Tomlinson; Kooresh I Shoghi; Matthew J Silva
Journal:  J Appl Physiol (1985)       Date:  2013-12-19

3.  Healing of non-displaced fractures produced by fatigue loading of the mouse ulna.

Authors:  Mario D Martinez; Gregory J Schmid; Jennifer A McKenzie; David M Ornitz; Matthew J Silva
Journal:  Bone       Date:  2010-03-06       Impact factor: 4.398

4.  Development of an in vivo bone fatigue damage model using axial compression of the rabbit forelimb.

Authors:  Evan G Buettmann; Matthew J Silva
Journal:  J Biomech       Date:  2016-08-25       Impact factor: 2.712

5.  Load/strain distribution between ulna and radius in the mouse forearm compression loading model.

Authors:  Yunkai Lu; Ganesh Thiagarajan; Daniel P Nicolella; Mark L Johnson
Journal:  Med Eng Phys       Date:  2011-09-07       Impact factor: 2.242

6.  Comparing histological, vascular and molecular responses associated with woven and lamellar bone formation induced by mechanical loading in the rat ulna.

Authors:  Jennifer A McKenzie; Matthew J Silva
Journal:  Bone       Date:  2010-09-22       Impact factor: 4.398

7.  Skeletal self-repair: stress fracture healing by rapid formation and densification of woven bone.

Authors:  Brian A Uthgenannt; Michael H Kramer; Joyce A Hwu; Brigitte Wopenka; Matthew J Silva
Journal:  J Bone Miner Res       Date:  2007-10       Impact factor: 6.741

8.  Stress fracture healing: fatigue loading of the rat ulna induces upregulation in expression of osteogenic and angiogenic genes that mimic the intramembranous portion of fracture repair.

Authors:  Gregory R Wohl; Dwight A Towler; Matthew J Silva
Journal:  Bone       Date:  2008-10-07       Impact factor: 4.398

9.  Angiogenesis is required for stress fracture healing in rats.

Authors:  Ryan E Tomlinson; Jennifer A McKenzie; Anne H Schmieder; Gregory R Wohl; Gregory M Lanza; Matthew J Silva
Journal:  Bone       Date:  2012-10-05       Impact factor: 4.398

10.  Damaging fatigue loading stimulates increases in periosteal vascularity at sites of bone formation in the rat ulna.

Authors:  Hironori Matsuzaki; Gregory R Wohl; Deborah V Novack; Jennifer A Lynch; Matthew J Silva
Journal:  Calcif Tissue Int       Date:  2007-06-06       Impact factor: 4.333

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