SELECTIVE VULNERABILITY OF WHITE MATTER DURING SPINAL-CORD ISCHEMIA

被引:43
作者
FOLLIS, F
SCREMIN, OU
BLISARD, KS
SCREMIN, AME
PETT, SB
SCOTT, WJ
KESSLER, RM
WERNLY, JA
机构
[1] UNIV NEW MEXICO, DEPT NEUROL, ALBUQUERQUE, NM 87131 USA
[2] UNIV NEW MEXICO, DEPT ORTHOPED & REHABIL, ALBUQUERQUE, NM 87131 USA
[3] UNIV CINCINNATI, MED CTR, DEPT PATHOL & LAB MED, CINCINNATI, OH 45267 USA
关键词
WHITE MATTER; SPINAL CORD; ISCHEMIA; THORACIC AORTA; PARAPLEGIA;
D O I
10.1038/jcbfm.1993.20
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The long-term effects of spinal cord ischemia were studied in 21 rats by lesion scores (LS, n = 21), somatosensory evoked potentials (SEP, n = 16), electromyographic measurements (EMG, n = 12) and histology of the spinal cord (n = 21) 48.5 +/- 57.2 days after 10- to 12-min occlusion of the thoracic aorta and subclavian arteries. All the animals were initially paraplegic with a spastic presentation but seven recovered within 2 days (group A), demonstrating low LS (3.4 +/- 1.05) normal EMGs (n = 3) and unremarkable histology. The 14 paraplegic animals presented relevant findings of the lumbar cord consisting of white matter lesions only (group B, n = 7) or white and gray matter lesions (group C, n = 7). Group B animals showed severe deficit (LS = 11.8 +/- 2.93) without denervation on EMG (n = 5) or muscle atrophy on histology. Group C animals displayed equal impairment (LS = 14.4 +/- 0.71), denervation on EMG (n = 4), and muscle atrophy. Resting motor unit activity of groups B and C were significantly different from group A (p < 0.001), while LS of groups B and C did not differ (p = 0.083). These data underscore the nature and the extent of white matter lesions during spinal cord ischemia, a finding which has generally been eclipsed by emphasis on gray matter lesions in previous studies.
引用
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页码:170 / 178
页数:9
相关论文
共 14 条
[1]   NEUROPATHOLOGY OF EXPERIMENTAL SPINAL-CORD ISCHEMIA IN THE RABBIT [J].
DEGIROLAMI, U ;
ZIVIN, JA .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1982, 41 (02) :129-149
[2]   INTERNEURONES AND RIGIDITY OF SPINAL ORIGIN [J].
GELFAN, S ;
TARLOV, IM .
JOURNAL OF PHYSIOLOGY-LONDON, 1959, 146 (03) :594-&
[3]  
Haggqvist G., 1938, Zeitschrift fuer Mikroskopisch-Anatomische Forschung, V44, P169
[4]   THE EFFECT OF ACUTE HYPOXIA ON THE MOTOR CELLS OF THE SPINAL CORD [J].
KROGH, E .
ACTA PHYSIOLOGICA SCANDINAVICA, 1950, 20 (04) :263-+
[5]   INSULIN ADMINISTRATION PROTECTS FROM PARAPLEGIA IN THE RAT AORTIC OCCLUSION MODEL [J].
LEMAY, DR ;
LU, AC ;
ZELENOCK, GB ;
DALECY, LG .
JOURNAL OF SURGICAL RESEARCH, 1988, 44 (04) :352-358
[6]   PARAPLEGIA IN THE RAT INDUCED BY AORTIC CROSS-CLAMPING - MODEL CHARACTERIZATION AND GLUCOSE EXACERBATION OF NEUROLOGIC DEFICIT [J].
LEMAY, DR ;
NEAL, S ;
NEAL, S ;
ZELENOCK, GB ;
DALECY, LG .
JOURNAL OF VASCULAR SURGERY, 1987, 6 (04) :383-390
[7]  
REXED B, 1940, ACTA PSYCHIAT NEUROL, V15, P365
[8]  
STENONIS N, 1969, STENO GEOLOGICAL PAP, P89
[9]   ROLE OF EXTRACELLULAR CALCIUM IN ANOXIC INJURY OF MAMMALIAN CENTRAL WHITE MATTER [J].
STYS, PK ;
RANSOM, BR ;
WAXMAN, SG ;
DAVIS, PK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (11) :4212-4216
[10]   Effect of experimental temporary vascular occlusion on the spinal cord I. Correlation between structural and functional changes [J].
Tureen, LL .
ARCHIVES OF NEUROLOGY AND PSYCHIATRY, 1936, 35 (04) :789-807