HISTOPATHOLOGIC AND MORPHOMETRIC STUDY OF SPINAL-CORD LESION IN A CHRONIC CORD COMPRESSION MODEL USING BONE MORPHOGENETIC PROTEIN IN RABBITS

被引:28
作者
SAITO, H
MIMATSU, K
SATO, K
HASHIZUME, Y
机构
[1] Department of Orthopaedic Surgery, Nagoya University School of Medicine, Nagoya
[2] Department of Pathology, Nagoya University Hospital, Nagoya
关键词
SPINAL CORD COMPRESSION; MYELOPATHY; EXPERIMENTAL MODEL; CORD COMPRESSION RATIO; HISTOPATHOLOGY; WHITE MATTER;
D O I
10.1097/00007632-199211000-00017
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Chronic compressive myelopathy was induced in domestic rabbits by implanting bone morphogenetic protein on the ligamentum flavum of the lumbar spine, and the resulting spinal cord lesion was studied histopathologically. In addition, morphometry of myelinated nerve fibers of the white matter in the pathologic specimens was performed to elucidate the mechanisms of cord injury. No loss of white matter nerve fibers was seen when the cord compression ratio (sagittal diameter/transverse diameter) was > 45%, although 6 months later myelin thinning was present throughout the white matter. When the cord compression ratio was less-than-or-equal-to 45%, loss of fibers, particularly of large fibers, was seen in the superficial layer of the white matter, with the nerve fibers remaining after 6 months showing decreased diameters. No motor paresis was evident in any animal. These histologic changes represent the early pathologic condition induced by chronic cord compression.
引用
收藏
页码:1368 / 1374
页数:7
相关论文
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  • [1] Aguayo A., Nair C.P.V., Midgley R., Experimental progressive compression neuropathy in the rabbit, Arch Neurol, 24, pp. 358-364, (1971)
  • [2] Anderson M.H., Fullerton P.M., Gilliatt R.W., Hern J.E.C., Changes in the forearm associated with median nerve compression at the wrist in the guinea-pig, J Neurol Neurosurg Psychiatry, 33, pp. 70-79, (1970)
  • [3] Blight A.R., Cellular morphology of chronic spinal cord injury in the cat: Analysis of myelinated axons by line-sampling, Neuroscience, 10, pp. 521-543, (1983)
  • [4] Eidelberg E., Straehley D., Erspamer R., Watkins C.J., Rela-tionship between residual hindlimb-assisted locomotion and surviving axons after incomplete spinal cord injuries, Exp Neurol, 56, pp. 312-322, (1977)
  • [5] Fujiwara K., Yonenobu K., Ono K., Et al., Morphometry of the cervical spinal cord and its relation to pathology in cases with compression myelopathy, Spine, 13, pp. 1212-1216, (1988)
  • [6] Hanamura H., Iwata H., Urist M.R., Et al., Solubilization and purification of bone morphogenetic protein (BMP) from Dunn osteosarcoma, Clin Orthop, 153, pp. 232-240, (1980)
  • [7] Hashizume Y., Iijima S., Yanagi T., Et al., Pathology of spinal cord lesions caused by ossification of the posterior longitudinal ligament, Acta Neuropathol, 63, pp. 123-130, (1984)
  • [8] Hashizume Y., Asai J., Mizuno J., Et al., Pathology of spinal cord lesions caused by ossification of the posterior longitudinal ligament (In Japanese), Spine and Spinal Cord, 2, pp. 641-646, (1989)
  • [9] Hoff J., Nishimura M., Lagger R., Et al., The role of ischemia in the pathogenesis of cervical spondylotic myelopathy: A review and new microangiographic evidence, Spine, 2, pp. 100-108, (1977)
  • [10] Hoshino Y., Goshima T., Hongo T., Sasaki N., Progression of the spinal cord lesion in chronic experimental compression model (In Japanese), Japanese Ministry of Welfare Study Group Report on Spinal Ossification, pp. 16-20, (1991)