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富含血管生成因子的富血小板血浆增强了异种移植物周围的体内骨形成。

Angiogenic factor-enriched platelet-rich plasma enhances in vivo bone formation around alloplastic graft material.

机构信息

Department of Oral & Maxillofacial Surgery, College of Medicine, Chungnam National University, Daejeon, Korea.

出版信息

J Adv Prosthodont. 2010 Mar;2(1):7-13. doi: 10.4047/jap.2010.2.1.7. Epub 2010 Mar 31.

Abstract

PURPOSE

Although most researchers agree that platelet-rich plasma (PRP) is a good source of autogenous growth factors, its effect on bone regeneration is still controversial. The purpose of this study was to evaluate whether increasing angiogenic factors in the human PRP to enhance new bone formation through rapid angiogenesis.

MATERIAL AND METHODS

In vitro, the human platelets were activated with application of shear stress, 20 µg/ml collagen, 2 mM CaCl(2) and 10U thrombin/1 × 10(9) platelets. Level of vascular endothelial growth factor (VEGF) and platelet microparticle (PMP) in the activated platelets were checked. In the animal study, human angiogenic factors-enriched PRP was tested in 28 athymic rat's cranial critical bone defects with β-TCP. Angiogenesis and osteogenesis were evaluated by laser Doppler perfusion imaging, histology, dual energy X-ray densinometry, and micro-computed tomography.

RESULTS

In vitro, this human angiogenic factors-enriched PRP resulted in better cellular proliferation and osteogenic differentiation. In vivo, increasing angiogenic potential of the PRP showed significantly higher blood perfusion around the defect and enhanced new bone formation around acellular bone graft material.

CONCLUSION

Angiogenic factor-enriched PRP leads to faster and more extensive new bone formation in the critical size bone defect. The results implicate that rapid angiogenesis in the initial healing period by PRP could be supposed as a way to overcome short term effect of the rapid angiogenesis.

摘要

目的

虽然大多数研究人员都认为富血小板血浆(PRP)是自体生长因子的良好来源,但它对骨再生的作用仍存在争议。本研究旨在评估通过快速血管生成增加人 PRP 中的血管生成因子是否能增强新骨形成。

材料和方法

在体外,通过应用切应力、20μg/ml 胶原蛋白、2mM CaCl2 和 10U 凝血酶/1×109血小板来激活人血小板。检查激活血小板中的血管内皮生长因子(VEGF)和血小板微粒(PMP)的水平。在动物研究中,用人血管生成因子富集的 PRP 在 28 只无胸腺大鼠颅骨临界骨缺损中用β-TCP 进行了测试。通过激光多普勒灌注成像、组织学、双能 X 射线密度计和微计算机断层扫描评估血管生成和成骨作用。

结果

在体外,这种富含人血管生成因子的 PRP 导致更好的细胞增殖和成骨分化。在体内,增加 PRP 的血管生成潜能显示出缺陷周围的血液灌注明显增加,并增强了无细胞骨移植物周围的新骨形成。

结论

富含血管生成因子的 PRP 可导致临界大小骨缺损中更快、更广泛的新骨形成。结果表明,PRP 在初始愈合期的快速血管生成可以被认为是克服快速血管生成短期效应的一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a35e/2984511/640c5d25f2ef/jap-2-7-g001.jpg

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