@article {10146,
	title = {Unremodeled endochondral bone is a major architectural component of the cortical bone of the rat (Rattus norvegicus)},
	journal = {JOURNAL OF STRUCTURAL BIOLOGY},
	volume = {183},
	number = {2},
	year = {2013},
	pages = {132-140},
	abstract = {The laboratory rat is one of the most frequently-used animal models for studying bone biology and skeletal diseases. Here we show that a substantial portion of the cortical bone of mature rats is primary endochondral bone, consisting of a disorganized arrangement of mineralized collagen fibers. We characterize the structure and mechanical properties of the cortical bone of the rat. We show that the cortical bone consists of two architecturally distinct regions. One region, consisting of well-organized circumferential lamellae (CLB), is located in the endosteal and/or the periosteal regions while another, disorganized region, is located in the more central region of the cortex. Unexpectedly, we found that the disorganized region contains many islands of highly mineralized cartilage.\&nbsp;Micro tomography showed different structural and compositional properties of the two primary structural elements; the CLB region has lower mineral density, lower porosity, larger but fewer blood vessels and fewer lacunae. However, no difference was found in the average lacunar volume. Additionally the mean indentation modulus of the CLB region was lower than that of the disorganized region. The islands of calcified cartilage were found to be extremely stiff, with an indentation modulus of 33.4 +/- 3.5 GPa.\&nbsp;We conclude that though the cortical bone of rats is in part lamellar, its architecture is markedly different from that of the cortical bone of humans, a fact that must be borne in mind when using the rat as a model animal for studies of human bone biology and disease. (c) 2013 Elsevier Inc. All rights reserved.},
	url = {http://www.sciencedirect.com/science/article/pii/S104784771300110X},
	author = {Shipov, A. and Zaslansky, P. and Riesemeier, H. and Segev, G. and Atkins, A. and Shahar, R.}
}
