ligament model
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2018 ◽  
Vol 66 ◽  
pp. 175-179
Author(s):  
Jeff M. Barrett ◽  
Jack P. Callaghan
Keyword(s):  

2015 ◽  
Vol 118 (10) ◽  
pp. 1250-1257 ◽  
Author(s):  
Cassandra A. Lee ◽  
Ann Lee-Barthel ◽  
Louise Marquino ◽  
Natalie Sandoval ◽  
George R. Marcotte ◽  
...  

Women are more likely to suffer an anterior cruciate ligament (ACL) rupture than men, and the incidence of ACL rupture in women rises with increasing estrogen levels. We used an engineered ligament model to determine how an acute rise in estrogen decreases the mechanical properties of ligaments. Using fibroblasts isolated from human ACLs from male or female donors, we engineered ligaments and determined that ligaments made from female ACL cells had more collagen and were equal in strength to those made from male ACL cells. We then treated engineered ligaments for 14 days with low (5 pg/ml), medium (50 pg/ml), or high (500 pg/ml) estrogen, corresponding to the range of in vivo serum estrogen concentrations and found that collagen within the grafts increased without a commensurate increase in mechanical strength. Mimicking the menstrual cycle, with 12 days of low estrogen followed by 2 days of physiologically high estrogen, resulted in a decrease in engineered ligament mechanical function with no change in the amount of collagen in the graft. The decrease in mechanical stiffness corresponded with a 61.7 and 76.9% decrease in the activity of collagen cross-linker lysyl oxidase with 24 and 48 h of high estrogen, respectively. Similarly, grafts treated with the lysyl oxidase inhibitor β-aminoproprionitrile (BAPN) for 24 h showed a significant decrease in ligament mechanical strength [control (CON) = 1.58 ± 0.06 N; BAPN = 1.06 ± 0.13 N] and stiffness (CON = 7.7 ± 0.46 MPa; BAPN = 6.1 ± 0.71 MPa) without changing overall collagen levels (CON = 396 ± 11.5 μg; BAPN = 382 ± 11.6 μg). Together, these data suggest that the rise in estrogen during the follicular phase decreases lysyl oxidase activity in our engineered ligament model and if this occurs in vivo may decrease the stiffness of ligaments and contribute to the elevated rate of ACL rupture in women.


2014 ◽  
Vol 2 (5) ◽  
pp. 232596711453276 ◽  
Author(s):  
Matthew Posner ◽  
Brett Owens ◽  
Paul Johnson ◽  
Noreen Masciello ◽  
Kenneth Cameron ◽  
...  

2011 ◽  
Vol 13 (3) ◽  
pp. R98 ◽  
Author(s):  
Maxim Moreau ◽  
Pascale Rialland ◽  
Jean-Pierre Pelletier ◽  
Johanne Martel-Pelletier ◽  
Daniel Lajeunesse ◽  
...  

2008 ◽  
Vol 24 (3) ◽  
pp. 234-243 ◽  
Author(s):  
Luigi Bertozzi ◽  
Rita Stagni ◽  
Silvia Fantozzi ◽  
Angelo Cappello

The knowledge of how cruciate ligaments stabilize the knee joint could be very useful during the execution of daily living activities for the development of clinical procedures. The objective of this study was to evaluate a cruciate ligament model that could achieve this knowledge while avoiding any destructive measurements in living healthy subjects. Subject-specific geometries and kinematic data, acquired from a living subject, were the foundations of the devised model. Each cruciate ligament was modeled with 25 linear-elastic elements and their geometrical properties were subject specific. The anteroposterior drawer test was simulated, and the sensitivity to the reference length and the elastic modulus was performed. Laxity, anterior, and posterior stiffness were calculated and compared with the literature. The laxity was most sensitive to reference length but fitted the literature well considering the reference length estimated from the subject. Both stiffnesses were most sensitive to elastic modulus variations. At full extension, anterior stiffness overestimated the literature, but at 90° good comparisons with the literature were obtained. Posterior stiffness showed smaller overestimations. The devised model, when properly improved, could evaluate the role of the cruciate ligaments of a living subject during the execution of daily living activities.


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