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应变停止促进植入兔胫骨的微动室内的骨形成。

Cessation of strain facilitates bone formation in the micromotion chamber implanted in the rabbit tibia.

作者信息

Goodman S B, Song Y, Doshi A, Aspenberg P

机构信息

Division of Orthopaedic Surgery, Stanford University Medical Center, CA 94305-5326.

出版信息

Biomaterials. 1994 Sep;15(11):889-93. doi: 10.1016/0142-9612(94)90112-0.

Abstract

Short, daily periods of externally-applied strain have been shown previously to affect the differentiation of mesenchymal tissue. In this study, we examine the effects of discontinuing a strain protocol known to produce primarily fibrous tissue rather than bone in the micromotion chamber (MC). Five MCs were inserted into the proximal tibial metaphysis of mature male New Zealand white rabbits. The MC has a 1 x 1 x 5 mm pore for tissue ingrowth. After osseointegration of the fixed outer cylinder of the chamber, the inner movable core was manipulated for 40 cycles per day delivered at a rate of 1 Hertz ('40'). This provided motion at the interface between the cylinder and the core. The tissue in the pore was harvested after 3 wks. The MCs were then manipulated at 40 cycles per day for 3 wks and then the manipulations were discontinued for 3 additional wks ('40 + 0'); the contents of the chamber were harvested after 6 wks. Finally, the chambers were left without manipulation ('0') and harvested after 3 wks. Histological sections from unmoved chambers ('0') contained extensive trabecular bone, embedded in a fibrovascular stroma. The '40' specimens were composed primarily of longitudinally orientated fibrous tissue. The '40 + 0' specimens were similar histologically to the '0' specimens. The amount of bone ingrowth expressed as a percentage of the area of the section averaged 37 +/- 6 (mean +/- standard error of the mean) for the '0' specimens, 20 +/- 2 for the '40' specimens and 37 +/- 7 for the '40 + 0' specimens.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

此前研究表明,每日短时间的外部施加应变会影响间充质组织的分化。在本研究中,我们检测了在微动室(MC)中停止一种已知主要产生纤维组织而非骨组织的应变方案所产生的影响。将五个微动室植入成年雄性新西兰白兔的胫骨近端干骺端。微动室有一个1×1×5毫米的孔隙以供组织向内生长。在微动室外固定圆柱体骨整合后,每天以1赫兹的频率操作内部可移动核心40个周期(“40”)。这在圆柱体和核心之间的界面处产生了运动。3周后收集孔隙内的组织。然后将微动室每天操作40个周期,持续3周,然后停止操作3周(“40 + 0”);6周后收集微动室内的内容物。最后,让微动室不进行操作(“0”),3周后收集。未移动的微动室(“0”)的组织学切片包含大量小梁骨,嵌入纤维血管基质中。“40”组标本主要由纵向排列的纤维组织组成。“40 + 0”组标本在组织学上与“0”组标本相似。以切片面积百分比表示的骨向内生长量,“0”组标本平均为37±6(平均值±平均标准误差),“40”组标本为20±2,“40 + 0”组标本为37±7。(摘要截断于250字)

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