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建立灵长类动物早期腰椎间盘退变模型的微创诱导方法。

Minimally invasive induction of an early lumbar disc degeneration model in rhesus monkeys.

机构信息

Department of Spinal Surgery, Affiliated Hospital of Medical College, Qingdao University, Qingdao, Shandong, China.

出版信息

Spine (Phila Pa 1976). 2013 May 1;38(10):E579-86. doi: 10.1097/BRS.0b013e31828b695b.

Abstract

STUDY DESIGN

Animal experimental study.

OBJECTIVE

To establish an early and reproducible intervertebral disc (IVD) degeneration model to provide a basis for studying IVD degeneration.

SUMMARY OF BACKGROUND DATA

The pathophysiology and pathogenesis of IVD degeneration, a common condition that causes low back pain, are not clearly understood. An experimental animal model of human IVD degeneration is needed.

METHODS

A total of 91 IVDs were grouped as follows: group 1, percutaneous puncture using a 20-gauge needle; group 2, percutaneous puncture using a 15-gauge needle; and group 3, nonpuncture. The pre- and postpunctured IVDs were examined and graded. Hematoxylin and eosin, Masson trichrome, safranin O staining methods, and immunohistochemistry for type II collagen were performed.

RESULTS

In group 1, the magnetic resonance imaging (MRI) signal intensity was grade I for all IVDs before puncture, and at the different time points after puncture. In group 2, the MRI signal intensity was grade III in the 4th week and grade IV in the 8th week after puncture. In group 3, the MRI signal intensity was grade I at all time points. In groups 1 and 2, a marked reduction in nucleus pulposus cells was observed in the 12th week. Fissures in the annulus fibrosus were observed in the 8th week. Decreased proteoglycans in the model discs was noted in the 8th and 12th week, and collagen II significantly decreased in the 12th week after puncture (P < 0.05). In group 2, the number of cells and fissures in the IVDs were decreased, with decreased proteoglycan and collagen II content in the 8th week. No changes were found in group 3.

CONCLUSION

Slowly progressive and mild disc degeneration can be induced by puncture using 20-gauge needles through the IVDs, which might be suitable for investigating novel therapies for disc degeneration/pain.

LEVEL OF EVIDENCE

摘要

研究设计

动物实验研究。

目的

建立一种早期且可重复的椎间盘(IVD)退变模型,为研究 IVD 退变提供基础。

背景资料概要

导致腰痛的常见疾病——IVD 退变的病理生理学和发病机制尚不清楚。需要建立一种人类 IVD 退变的实验动物模型。

方法

共 91 个 IVD 分组如下:1 组,经皮 20 号针穿刺;2 组,经皮 15 号针穿刺;3 组,非穿刺。穿刺前后对 IVD 进行检查和分级。行苏木精-伊红、Masson 三色、番红 O 染色及 II 型胶原免疫组化染色。

结果

1 组中所有 IVD 在穿刺前 MRI 信号强度均为 I 级,穿刺后不同时间点均为 I 级。2 组中,第 4 周 MRI 信号强度为 III 级,第 8 周为 IV 级。3 组中所有时间点 MRI 信号强度均为 I 级。1 组和 2 组在第 12 周时可见明显的髓核细胞减少,第 8 周时可见纤维环裂隙。第 8 周和第 12 周模型椎间盘内蛋白聚糖减少,胶原 II 明显减少(P < 0.05)。2 组中 IVD 细胞和裂隙减少,第 8 周时蛋白聚糖和胶原 II 含量减少,3 组无变化。

结论

经皮 20 号针穿刺 IVD 可导致缓慢进展的轻度椎间盘退变,可能适合研究治疗椎间盘退变/疼痛的新方法。

证据等级

2 级。

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