[椎间盘内注射高渗生理盐水、酚甘油和锇酸治疗腰椎间盘突出症:一项实验研究]。

Nihon Seikeigeka Gakkai zasshi Pub Date : 1995-10-01
M Shioda
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引用次数: 0

摘要

未标记:本研究旨在探讨高渗盐水(HS)、甘油酚(PHG)和锇酸(OSA)在椎间盘内治疗中的可能临床应用。材料与方法:将不同浓度的HS、10% PHG和4% OSA分别注射于60只日本大白兔的腰椎间盘。此外,这些物质被直接放置在48只豚鼠的脊髓硬脑膜上。定期处死动物,光镜下进行组织学检查。结果:HS致髓核细胞局部坏死呈浓度相关。一些圆盘的高度降低了。随着时间的推移,所有椎间盘通常恢复正常的组织结构。10% PHG组髓核细胞坏死面积较HS组大,但再生或修复反应较HS组弱。经4% OSA治疗的椎间盘检查显示髓核和纤维内环发生严重改变,导致椎间盘间隙狭窄。注射OSA后的修复组织为纤维软骨组织。在给药后,周围组织包括神经组织未见组织学改变。讨论:凝乳蛋白酶是临床化学核溶解最常用的物质。凝乳蛋白的主要临床并发症是过敏反应。目前的物质已在其他临床应用中使用,没有过敏反应的报告。在本报告中,HS被证明具有降低椎间盘内压力的潜力,而不会诱导瘢痕组织或显著的椎间盘功能丧失。PHG和OSA对椎间盘组织造成相当大但有限的组织学损害,但对神经组织没有影响。这些数据提示HS、PHG和OSA可能作为椎间盘内治疗的药物具有临床应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Intradiscal injection of hypertonic saline, phenol-glycerin and osmic acid for the treatment of lumbar disc herniation: an experimental study].

Unlabelled: The present study was designed to investigate the possible clinical application of hypertonic saline (HS), phenol in glycerin (PHG) and osmic acid (OSA) for intradiscal therapy.

Materials & methods: HS in several concentrations, 10% PHG and 4% OSA were separately injected into the lumbar intervertebral discs of 60 Japanese white rabbits. Additionally, these substances were placed directly on the dura of the spinal cord of 48 guinea pigs. The animals were sacrificed periodically and were submitted to histological examination using light microscopy.

Results: HS caused localized necrosis of the nucleus pulposus cells in a concentration-related fashion. Some discs decreased their height. With time, all the discs generally regained their normal histology. Following administration of 10% PHG, the area of necrosis of the nucleus pulposus cells was more extensive than that by HS, but the regenerative or reparative reaction was not so brisk. Examination of the discs treated with 4% OSA demonstrated severe changes in the nucleus pulposus and the inner annulus fibrosus with resultant disc-space narrowing. The reparative tissue seen after injection of OSA was fibrocartilage in nature. No histological change was seen in the surrounding tissue including the neural tissue following administration of any of the substances.

Discussion: Chymopapain is the substance most frequently used for clinical chemonucleolysis. The major clinical complication with chymopapain has been anaphylaxis. The present substances have been used in other clinical applications without reports of anaphylaxis. In this report, HS was shown to hold the potential for reducing intradiscal pressure without induction of scar tissue or significant loss of disc function. PHG and OSA caused considerable but circumscribed histological damage to the disc tissue, but had no such effect on the neural tissues. These data suggested that HS, PHG and OSA may have clinical applications as agents in intradiscal therapy.

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