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转化生长因子-β1对宿主组织照射后临界尺寸骨缺损骨再生的影响。

Effect of transforming growth factor-beta1 on bone regeneration in critical-sized bone defects after irradiation of host tissues.

作者信息

Ehrhart Nicole P, Hong Liu, Morgan Abby L, Eurell JoAnn A, Jamison Russell D

机构信息

Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO 80523-1601, USA.

出版信息

Am J Vet Res. 2005 Jun;66(6):1039-45. doi: 10.2460/ajvr.2005.66.1039.

Abstract

OBJECTIVE

To determine whether sustained release of transforming growth factor (TGF)-beta1 from a gelatin hydrogel would enhance bone regeneration in critical-sized long-bone defects and overcome inhibitory effects of preoperative irradiation.

ANIMALS

24 adult New Zealand White rabbits.

PROCEDURE

Rabbits were allocated to 2 groups. Twelve rabbits received localized megavoltage radiation to the right ulna by use of a cobalt 60 teletherapy unit, and 12 rabbits received no irradiation. Then, a 1.5-cm defect was aseptically created in the right ulna of each rabbit. Gelatin hydrogel that contained 5 microg of adsorbed recombinant-human (rh)TGF-beta1 was placed in the defect of 12 rabbits (6 irradiated and 6 nonirradiated), and the other 12 rabbits received hydrogel without rhTGF-beta1. Rabbits were euthanatized 10 weeks after surgery. New bone formation within the defect was analyzed by use of nondecalcified histomorphometric methods. A 1-way ANOVA was used to compare differences among groups.

RESULTS

New bone formation within the defect was significantly greater in TGF-beta1-treated rabbits than in rabbits treated with hydrogel carrier alone. Local delivery of rhTGF-beta1 via a hydrogel carrier in irradiated defects resulted in amounts of bone formation similar to those for nonirradiated defects treated by use of rhTGF-beta1.

CONCLUSIONS AND CLINICAL RELEVANCE

Local delivery of TGF-beta1 by use of a hydrogel carrier appears to have therapeutic potential for enhancing bone formation in animals after radiation treatments.

IMPACT FOR HUMAN MEDICINE

This technique may be of value for treating human patients at risk for delayed bone healing because of prior radiation therapy.

摘要

目的

确定明胶水凝胶持续释放转化生长因子(TGF)-β1是否能增强临界尺寸长骨缺损的骨再生,并克服术前放疗的抑制作用。

动物

24只成年新西兰白兔。

步骤

将兔子分为2组。12只兔子使用钴60远距离治疗装置对右侧尺骨进行局部兆伏级放疗,12只兔子未接受放疗。然后,在每只兔子的右侧尺骨无菌制造一个1.5厘米的缺损。将含有5微克吸附重组人(rh)TGF-β1的明胶水凝胶置于12只兔子(6只接受放疗,6只未接受放疗)的缺损处,另外12只兔子接受不含rhTGF-β1的水凝胶。术后10周对兔子实施安乐死。使用未脱钙组织形态计量学方法分析缺损内的新骨形成情况。采用单因素方差分析比较组间差异。

结果

与仅用水凝胶载体治疗的兔子相比,TGF-β1治疗的兔子缺损内新骨形成明显更多。在接受放疗的缺损处通过水凝胶载体局部递送rhTGF-β1,其骨形成量与未接受放疗但使用rhTGF-β1治疗的缺损处相似。

结论及临床意义

使用水凝胶载体局部递送TGF-β1似乎对放疗后动物增强骨形成具有治疗潜力。

对人类医学的影响

该技术对于治疗因先前放疗而有骨愈合延迟风险的人类患者可能具有价值。

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