Chronic intrathecal infusions after spinal cord injury cause scarring and compression

被引:87
作者
Jones, LL
Tuszynski, MH
机构
[1] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[2] Vet Affairs Med Ctr, San Diego, CA 92161 USA
关键词
Evans Blue; microglia; IBA1; tissue damage; fibroglial scar; gliosis; delivery;
D O I
10.1002/jemt.1144
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Intrathecal infusions are used in a number of rodent studies to deliver substances to the injured spinal cord. Whereas this method has been successful in certain paradigms, two potential limitations of this model have not been extensively reported: (1) scar formation at the catheter tip, which can lead to infusion failure, and (2) damage to the spinal cord caused by the catheter itself. Thus, the purpose of the present study was threefold: (1) to determine intrathecal infusion efficiency over 14 days following spinal cord injury; (2) to examine possible secondary damage caused by intrathecal tubing; and (3) to explore whether alternative protocols that avoid such damage are effective. Adult Fischer 344 rats were subjected to spinal cord lesions at T7, followed by placement of an intrathecal catheter attached to an Alzet minipump. Seven or 14 days following injury and catheter placement, tube patency was evaluated by diffusion of Evans Blue dye from the minipump. Results indicate that infusion was efficient 7 days following injury but was markedly reduced after 14 days. Further, histology and immunocytochemistry 14 days after injury demonstrated compression damage to the cord where the tubing rested. Alternative protocols, including intrathecal infusions through metal cannulae, or "drip" infusions directly over the lesion, did not improve delivery. These data suggest that results from rodent studies using infusion from catheters placed adjacent to lesion sites may be attributable to acute or subacute effects of the delivered substance. Future rodent studies using intrathecal infusions should include rigorous evaluation of infusion efficiency and possible secondary tissue damage. Microsc. Res. Tech. 54: 317-324, 2001. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:317 / 324
页数:8
相关论文
共 34 条
[1]   Intrathecal anti-IL-6 antibody and IgG attenuates peripheral nerve injury-induced mechanical allodynia in the rat: possible immune modulation in neuropathic pain [J].
Arruda, JL ;
Sweitzer, SA ;
Rutkowski, MD ;
DeLeo, JA .
BRAIN RESEARCH, 2000, 879 (1-2) :216-225
[2]   The peripheral benzodiazepine binding site in the brain in multiple sclerosis -: Quantitative in vivo imaging of microglia as a measure of disease activity [J].
Banati, RB ;
Newcombe, J ;
Gunn, RN ;
Cagnin, A ;
Turkheimer, F ;
Heppner, F ;
Price, G ;
Wegner, F ;
Giovannoni, G ;
Miller, DH ;
Perkin, GD ;
Smith, T ;
Hewson, AK ;
Bydder, G ;
Kreutzberg, GW ;
Jones, T ;
Cuzner, ML ;
Myers, R .
BRAIN, 2000, 123 :2321-2337
[3]   Evidence-based review of the literature on intrathecal delivery of pain medication [J].
Bennett, G ;
Serafini, M ;
Burchiel, K ;
Buchser, E ;
Classen, A ;
Deer, T ;
Du Pen, S ;
Ferrante, FM ;
Hassenbusch, SJ ;
Lou, L ;
Maeyaert, J ;
Penn, R ;
Portenoy, RK ;
Rauck, R ;
Willis, KD ;
Yaksh, T .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2000, 20 (02) :S12-S36
[4]   Systemically administered interleukin-10 reduces tumor necrosis factor-alpha production and significantly improves functional recovery following traumatic spinal cord injury in rats [J].
Bethea, JR ;
Nagashima, H ;
Acosta, MC ;
Briceno, C ;
Gomez, F ;
Marcillo, AE ;
Loor, K ;
Green, J ;
Dietrich, WD .
JOURNAL OF NEUROTRAUMA, 1999, 16 (10) :851-863
[5]  
Blesch A, 1998, PROG BRAIN RES, V117, P473
[6]   Continuous intrathecal fluid infusions elevate nerve growth factor levels and prevent functional deficits after spinal cord ischemia [J].
Bowes, M ;
Tuszynski, MH ;
Conner, J ;
Zivin, JA .
BRAIN RESEARCH, 2000, 883 (02) :178-183
[7]   NT-3 promotes growth of lesioned adult rat sensory axons ascending in the dorsal columns of the spinal cord [J].
Bradbury, EJ ;
Khemani, S ;
King, VR ;
Priestley, JV ;
McMahon, SB .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (11) :3873-3883
[8]   Spinal cord injury and anti-NGF treatment results in changes in CGRP density and distribution in the dorsal horn in the rat [J].
Christensen, MD ;
Hulsebosch, CE .
EXPERIMENTAL NEUROLOGY, 1997, 147 (02) :463-475
[9]   Chronic central pain after spinal cord injury [J].
Christensen, MD ;
Hulsebosch, CE .
JOURNAL OF NEUROTRAUMA, 1997, 14 (08) :517-537
[10]   The glial scar and central nervous system repair [J].
Fawcett, JW ;
Asher, RA .
BRAIN RESEARCH BULLETIN, 1999, 49 (06) :377-391