scholarly journals Persistent degenerative changes in the intervertebral disc after burst fracture in an in vitro model mimicking physiological post-traumatic conditions

2014 ◽  
Vol 24 (9) ◽  
pp. 1901-1908 ◽  
Author(s):  
Stefan Dudli ◽  
Daniel Haschtmann ◽  
Stephen John Ferguson
1995 ◽  
Vol 77-B (6) ◽  
pp. 967-970 ◽  
Author(s):  
W Thomas Rde ◽  
JJ Batten ◽  
S Want ◽  
ID McCarthy ◽  
M Brown ◽  
...  

2006 ◽  
Vol 5 (3) ◽  
pp. 243-250 ◽  
Author(s):  
Richard M. Hall ◽  
Robert J. Oakland ◽  
Ruth K. Wilcox ◽  
David C. Barton

Object The purpose of the study was to develop an in vitro model of the bone fragment and spinal cord interactions that occur during a burst fracture and further the understanding of how the velocity of the bone fragment and the status of the posterior longitudinal ligament (PLL) affect the deformation of the cord. Methods An in vitro model was developed such that high-speed video and pressure measurements recorded the impact of a simulated bone fragment on sections of explanted bovine spinal cord. The model simulated the PLL and the posterior elements. The status of the PLL had a significant effect on both the maximum occlusion of the spinal cord and the time for occlusion to occur. Raising the fragment velocity led to an overall increase in the spinal cord deformation. Interestingly the dura mater appeared to have little or no effect on the extent of occlusion. Conclusions These findings may indicate the importance of the dura’s interaction with the cerebrospinal fluid in protecting the cord during this type of impact.


2008 ◽  
Vol 41 ◽  
pp. S258
Author(s):  
Daniel Haschtmann ◽  
Jivko V. Stoyanov ◽  
Philippe Gédet ◽  
Stephen J. Ferguson

2010 ◽  
Vol 10 (9) ◽  
pp. S138
Author(s):  
Chitra Dahia ◽  
Eric Mahoney ◽  
Eric Wall ◽  
Christopher Wylie

Spine ◽  
2005 ◽  
Vol 30 (18) ◽  
pp. E534-E539 ◽  
Author(s):  
Albert J. van der Veen ◽  
Margriet Mullender ◽  
Theo H. Smit ◽  
Idsart Kingma ◽  
Jaap H. van Dieën

Author(s):  
Hoda Keshmiri Neghab ◽  
Mohammad Hasan Soheilifar ◽  
Gholamreza Esmaeeli Djavid

Abstract. Wound healing consists of a series of highly orderly overlapping processes characterized by hemostasis, inflammation, proliferation, and remodeling. Prolongation or interruption in each phase can lead to delayed wound healing or a non-healing chronic wound. Vitamin A is a crucial nutrient that is most beneficial for the health of the skin. The present study was undertaken to determine the effect of vitamin A on regeneration, angiogenesis, and inflammation characteristics in an in vitro model system during wound healing. For this purpose, mouse skin normal fibroblast (L929), human umbilical vein endothelial cell (HUVEC), and monocyte/macrophage-like cell line (RAW 264.7) were considered to evaluate proliferation, angiogenesis, and anti-inflammatory responses, respectively. Vitamin A (0.1–5 μM) increased cellular proliferation of L929 and HUVEC (p < 0.05). Similarly, it stimulated angiogenesis by promoting endothelial cell migration up to approximately 4 fold and interestingly tube formation up to 8.5 fold (p < 0.01). Furthermore, vitamin A treatment was shown to decrease the level of nitric oxide production in a dose-dependent effect (p < 0.05), exhibiting the anti-inflammatory property of vitamin A in accelerating wound healing. These results may reveal the therapeutic potential of vitamin A in diabetic wound healing by stimulating regeneration, angiogenesis, and anti-inflammation responses.


2011 ◽  
Vol 71 (05) ◽  
Author(s):  
M Salama ◽  
K Winkler ◽  
KF Murach ◽  
S Hofer ◽  
L Wildt ◽  
...  

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