Morphologic and morphometric evaluation of experimental acute crush injuries of the sciatic nerve of rats

被引:59
作者
Cantalejo Nagima Mazzer, Patricia Yume [1 ,2 ]
Barbieri, Claudio Henrique [1 ,2 ]
Mazzer, Nilton [1 ,2 ]
Sassoli Fazan, Valeria Paula [1 ,2 ]
机构
[1] Univ Sao Paulo, Ribeirao Preto Sch Med, Dept Biomech Med & Rehabil Locomotor Apparatus, Lab Microsurg, BR-14049900 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Ribeirao Preto Sch Med, Dept Surg & Anat, Lab Neural Microanat, BR-14049900 Ribeirao Preto, SP, Brazil
关键词
sciatic nerve of rats; crush injury; mechanical load; morphometric parameters; axonotmesis;
D O I
10.1016/j.jneumeth.2008.06.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In order to qualify and quantify nerve fiber lesion following an acute crush injury, a morphologic and morphometric study was carried out in 25 Wistar rats divided into live groups of five animals each according to the crushing load applied, i.e., 500,1000, 5000, 10 000, and 15 000 g. The injury was produced under general anesthesia on a 5 mm-long intermediate segment of the right sciatic nerve for 10 min using a dead-weight machine. The animals were killed with an excessive dose of anesthetics 72 h later and submitted to perfusion with a fixing solution through the abdominal aorta immediately after death. Both the right and left sciatic nerves were removed and prepared for histologic and morphometric examinations: 5 mu m-thick sections stained with 1% Toluidine blue were examined under a light microscope equipped with a video camera linked to a computer loaded with a graphic program (KS 400). The morphometric studies included measuring total number of fibers, fiber density, fiber diameter, myelin fiber area, axon diameter, axon area and G ratio. The results showed that damage to the nerve fibers began to appear as early as with the 500g load and was similar in all groups despite the load applied, increasing with the 10000 and 15000g loads, although the external supporting tissues and small diameter fibers were preserved. The predominant type of lesion produced was axonotmesis. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:249 / 258
页数:10
相关论文
共 19 条
[1]   FUNCTIONAL-EVALUATION OF COMPLETE SCIATIC, PERONEAL, AND POSTERIOR TIBIAL NERVE LESIONS IN THE RAT [J].
BAIN, JR ;
MACKINNON, SE ;
HUNTER, DA .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1989, 83 (01) :129-136
[2]   NERVE CRUSH INJURIES - A MODEL FOR AXONOTMESIS [J].
BRIDGE, PM ;
BALL, DJ ;
MACKINNON, SE ;
NAKAO, Y ;
BRANDT, K ;
HUNTER, DA ;
HERTL, C .
EXPERIMENTAL NEUROLOGY, 1994, 127 (02) :284-290
[3]  
CARLTON J M, 1986, Surgical Forum (Chicago), V37, P611
[4]   THE INFLUENCE OF MAGNITUDE AND DURATION OF CRUSH LOAD ON FUNCTIONAL RECOVERY OF THE PERIPHERAL-NERVE [J].
CHEN, LE ;
SEABER, AV ;
URBANIAK, JR .
JOURNAL OF RECONSTRUCTIVE MICROSURGERY, 1993, 9 (04) :299-306
[5]   THE FUNCTIONAL RECOVERY OF PERIPHERAL-NERVES FOLLOWING DEFINED ACUTE CRUSH INJURIES [J].
CHEN, LE ;
SEABER, AV ;
GLISSON, RR ;
DAVIES, H ;
MURRELL, GAC ;
ANTHONY, DC ;
URBANIAK, JR .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1992, 10 (05) :657-664
[6]   CONDUCTION VELOCITY OF REGENERATED PERIPHERAL NERVE FIBRES [J].
CRAGG, BG ;
THOMAS, PK .
JOURNAL OF PHYSIOLOGY-LONDON, 1964, 171 (01) :164-&
[7]   RAT SCIATIC FUNCTIONAL INDEX DATA MANAGEMENT-SYSTEM WITH DIGITIZED INPUT [J].
DEMEDINACELI, L ;
DERENZO, E ;
WYATT, RJ .
COMPUTERS AND BIOMEDICAL RESEARCH, 1984, 17 (02) :185-192
[8]   AN INDEX OF THE FUNCTIONAL-CONDITION OF RAT SCIATIC-NERVE BASED ON MEASUREMENTS MADE FROM WALKING TRACKS [J].
DEMEDINACELI, L ;
FREED, WJ ;
WYATT, RJ .
EXPERIMENTAL NEUROLOGY, 1982, 77 (03) :634-643
[9]   Methods to evaluate functional nerve recovery in adult rats: walking track analysis, video analysis and the withdrawal reflex [J].
Dijkstra, JR ;
Meek, MF ;
Robinson, PH ;
Gramsbergen, A .
JOURNAL OF NEUROSCIENCE METHODS, 2000, 96 (02) :89-96
[10]   Analysis of gene expression following sciatic nerve crush and spinal cord hemisection in the mouse by microarray expression profiling [J].
Fan, M ;
Mi, RF ;
Yew, DT ;
Chan, WY .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2001, 21 (05) :497-508