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大型动物模型中可重复的长期椎间盘退变

Reproducible long-term disc degeneration in a large animal model.

作者信息

Hoogendoorn Roel J W, Helder Marco N, Kroeze Robert Jan, Bank Ruud A, Smit Theo H, Wuisman Paul I J M

机构信息

Department of Orthopaedic Surgery, VU University Medical Center, VUmc, Amsterdam.

出版信息

Spine (Phila Pa 1976). 2008 Apr 20;33(9):949-54. doi: 10.1097/BRS.0b013e31816c90f0.

Abstract

STUDY DESIGN

Twelve goats were chemically degenerated and the development of the degenerative signs was followed for 26 weeks to evaluate the progression of the induced degeneration. The results were also compared with a previous study to determine the reproducibility.

OBJECTIVES

The purpose of this study was determine whether this Chondroitinase ABC (CABC) induced goat model is reproducible and to study the development of the degeneration in time up to 26 weeks.

SUMMARY OF BACKGROUND DATA

Injecting CABC into goat intervertebral discs results in mild disc degeneration after 12 weeks. Spontaneous recovery or leveling off of the degeneration has been reported before and is relevant when the goat model is used in regeneration studies. Reproducibility of the induced degeneration is relevant as well.

METHODS

Twelve goats were used in this study. The development of degeneration was studied after the injection of 0.25 U/mL CABC intradiscally. The development of degenerative signs was studied after 18 (n = 6) and 26 (n = 6) weeks by means of radiograph, magnetic resonance imaging, macroscopic analysis, and histology and biochemical evaluation. The induced degeneration was compared with the results from a previous study, in which degeneration was induced similarly and analysis was performed after 12 weeks.

RESULTS

The severity of the degenerative signs was mild and was consequently present in all parameters analyzed. When compared with the results after 12 weeks, the degeneration was similar in the present study. Spontaneous recovery was not observed up to 26 weeks.

CONCLUSION

The injection with CABC in the intervertebral disc reproducibly results in mild disc degeneration in the goat. These findings corroborate the goat model as a suitable large animal model to evaluate mild disc degeneration and potential new therapies.

摘要

研究设计

对12只山羊进行化学性退变,并观察退变体征的发展情况达26周,以评估诱导退变的进展。还将结果与之前的一项研究进行比较,以确定其可重复性。

目的

本研究的目的是确定这种软骨素酶ABC(CABC)诱导的山羊模型是否具有可重复性,并研究长达26周的退变发展情况。

背景数据总结

向山羊椎间盘内注射CABC,12周后会导致轻度椎间盘退变。此前已有自发恢复或退变趋于平稳的报道,这在将山羊模型用于再生研究时具有相关性。诱导退变的可重复性也很重要。

方法

本研究使用了12只山羊。椎间盘内注射0.25 U/mL CABC后,研究退变的发展情况。在18周(n = 6)和26周(n = 6)后,通过X线摄影、磁共振成像、宏观分析、组织学和生化评估来研究退变体征的发展。将诱导退变的结果与之前一项研究的结果进行比较,在之前的研究中,采用类似方法诱导退变,并在12周后进行分析。

结果

退变体征的严重程度较轻,因此在所有分析参数中均有体现。与12周后的结果相比,本研究中的退变情况相似。直至26周均未观察到自发恢复。

结论

向椎间盘内注射CABC可在山羊中可重复性地导致轻度椎间盘退变。这些发现证实了山羊模型是评估轻度椎间盘退变和潜在新疗法的合适大型动物模型。

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