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胰岛素样生长因子-I在未成熟软骨修复反应中的作用。

Role of insulin like growth factor-I in repair response in immature cartilage.

作者信息

Tuncel Mehmet, Halici Mehmet, Canoz Ozlem, Yildirim Turk Cemil, Oner Mithat, Ozturk Figen, Kabak Sevki

机构信息

Orthopaedics and Traumatology Department, Medical Faculty, Erciyes University, Kayseri 38039, Turkey.

出版信息

Knee. 2005 Apr;12(2):113-9. doi: 10.1016/j.knee.2004.04.003.

Abstract

OBJECTIVE

The purpose of this study was to investigate the effects of exogenous local Insulin like growth factor-I (IGF-I) on the repair of full-thickness articular cartilage defects in immature rabbits.

DESIGN

Thirty-six skeletally immature New Zealand rabbits between 6 and 8 weeks old were used. A single defect, 3.5-mm-wide by 4-mm-deep full-thickness articular cartilage defect in the medial femoral condyle, was created. The defect was either filled with a collagen sponge or with a collagen sponge impregnated with 5 mug of recombinant IGF-I. The animals were sacrificed at 4, 8 or 12 weeks, and the repair tissue was examined macroscopically and histologically. Repair tissue was also examined immunohistochemically for the presence of type-I collagen, type-II collagen and PCNA at all weeks.

RESULTS

Newly formed tissue in all of the defects in the IGF-I group had the gross, histological and histochemical appearance of a smooth, intact hyaline articular cartilage. The average total scores on the histological grading scale were significantly better (p<0.05) for the defects treated with recombinant IGF-I at all time points. Immunostaining with an antibody against type-II collagen showed the diffuse presence of the repair cartilage in the IGF-I treated defects. The control groups demonstrated minimum staining with type-II collagen antibody.

CONCLUSIONS

These findings suggest that repair of full-thickness immature cartilage defects can be enhanced by recombinant IGF-I.

摘要

目的

本研究旨在探讨外源性局部胰岛素样生长因子-I(IGF-I)对未成熟兔全层关节软骨缺损修复的影响。

设计

选用36只6至8周龄骨骼未成熟的新西兰兔。在内侧股骨髁制造一个单一缺损,为宽3.5毫米、深4毫米的全层关节软骨缺损。缺损处要么填充胶原海绵,要么填充浸渍有5微克重组IGF-I的胶原海绵。在4周、8周或12周处死动物,并对修复组织进行大体和组织学检查。在所有时间点,还对修复组织进行免疫组织化学检查,以检测I型胶原、II型胶原和增殖细胞核抗原(PCNA)的存在情况。

结果

IGF-I组所有缺损处新形成的组织在大体、组织学和组织化学上均呈现出光滑、完整的透明关节软骨外观。在所有时间点,用重组IGF-I治疗的缺损在组织学分级量表上的平均总分明显更好(p<0.05)。用抗II型胶原抗体进行免疫染色显示,在IGF-I治疗的缺损处有弥漫性的修复软骨存在。对照组用II型胶原抗体染色最少。

结论

这些发现表明重组IGF-I可增强未成熟全层软骨缺损的修复。

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