4.6 Article

Influence of nonenzymatic glycation on biomechanical properties of cortical bone

期刊

BONE
卷 28, 期 2, 页码 195-201

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/S8756-3282(00)00434-8

关键词

nonenzymatic glycation; cortical bone; mechanical properties; collagen; cross-link

资金

  1. NIAMS NIH HHS [AR-40776, AR-41210, R01 AR041210] Funding Source: Medline

向作者/读者索取更多资源

In this study, the influence of nonenzymatic glycation (NEG) on the mechanical properties of bone and bone collagen were investigated. Bovine cortical bone specimens were incubated in ribose to cause collagen cross-links in vitro, and nondestructive mechanical testing was used to determine tensile and compressive elastic modulus as a function of incubation time. Mechanical properties associated with yield, postyield, and final fracture of bone were determined at the end of the incubation period. The stiffness of the collagen network was measured using stress relaxation tests of demineralized bone cylinders extracted periodically throughout the incubation period, It was found that accumulation of nonenzymatic glycation end-products in cortical bone caused stiffening of the type I collagen network in bone (r(2) = 0.92; p < 0.001) but did not significantly affect the overall stiffness of the mineralized bone (p = 0.98). The ribosylated group had significantly more NEG products and higher yield stress and strain than the control group (p < 0.05). Postyield properties including postyield strain and strain energy were lower in the ribosylated group but were not significantly different from the control group (p = 0.24). Compared with the control group, the ribosylated group was characterized by significantly higher secant modulus and lower damage fraction (p < 0.05). Taken together, the results of this study suggest that collagen in bone is susceptible to the same NEG-mediated changes as collagen in other connective tissues and that an increased stiffness of the collagen network in bone due to NEG may explain some of the age-related increase in skeletal fragility and fracture risk. (Bone 28:195-201; 2001) (C) 2001 by Elsevier Science Inc. All rights reserved.

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