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人源与大鼠富血小板纤维蛋白在胶原膜上的比较:大鼠颅骨缺损模型矿化的初步研究

Human versus Rat PRF on Collagen Membranes: A Pilot Study of Mineralization in Rat Calvaria Defect Model.

作者信息

Apaza Alccayhuaman Karol Ali, Heimel Patrick, Tangl Stefan, Lettner Stefan, Kampleitner Carina, Panahipour Layla, Kuchler Ulrike, Gruber Reinhard

机构信息

Department of Oral Biology, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria.

Karl Donath Laboratory for Hard Tissue and Biomaterial Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria.

出版信息

Bioengineering (Basel). 2024 Apr 23;11(5):414. doi: 10.3390/bioengineering11050414.

Abstract

Platelet-rich fibrin, the coagulated plasma fraction of blood, is commonly used to support natural healing in clinical applications. The rat calvaria defect is a standardized model to study bone regeneration. It remains, however, unclear if the rat calvaria defect is appropriate to investigate the impact of human PRF (Platelet-Rich Fibrin) on bone regeneration. To this end, we soaked Bio-Gide collagen membranes in human or rat liquid concentrated PRF before placing them onto 5 mm calvarial defects in Sprague Dawley rats. Three weeks later, histology and micro-computed tomography (μCT) were performed. We observed that the collagen membranes soaked with rat PRF show the characteristic features of new bone and areas of mineralized collagen matrix, indicated by a median mineralized volume of 1.5 mm (range: 0.9; 5.3 mm). Histology revealed new bone growing underneath the membrane and hybrid bone where collagen fibers are embedded in the new bone. Moreover, areas of passive mineralization were observed. The collagen membranes soaked with human PRF, however, were devoid of histological features of new bone formation in the center of the defect; only occasionally, new bone formed at the defect margins. Human PRF (h-PRF) caused a median bone volume of 0.9 mm (range: 0.3-3.3 mm), which was significantly lower than what was observed with rat PRF (r-PRF), with a BV median of 1.2 mm (range: 0.3-5.9 mm). Our findings indicate that the rat calvaria defect model is suitable for assessing the effects of rat PRF on bone formation, but caution is warranted when extrapolating conclusions regarding the efficacy of human PRF.

摘要

富含血小板纤维蛋白是血液的凝固血浆部分,在临床应用中常用于支持自然愈合。大鼠颅骨缺损是研究骨再生的标准化模型。然而,大鼠颅骨缺损是否适合研究人富含血小板纤维蛋白(PRF)对骨再生的影响仍不清楚。为此,我们将Bio-Gide胶原膜浸泡在人或大鼠浓缩液态PRF中,然后将其放置在Sprague Dawley大鼠的5毫米颅骨缺损上。三周后,进行组织学和显微计算机断层扫描(μCT)。我们观察到,浸泡有大鼠PRF的胶原膜显示出新骨和矿化胶原基质区域的特征,矿化体积中位数为1.5毫米(范围:0.9;5.3毫米)。组织学显示膜下有新骨生长,以及胶原纤维嵌入新骨的混合骨。此外,还观察到被动矿化区域。然而,浸泡有人PRF的胶原膜在缺损中心没有新骨形成的组织学特征;仅偶尔在缺损边缘形成新骨。人PRF(h-PRF)导致的骨体积中位数为0.9毫米(范围:0.3 - 3.3毫米),明显低于大鼠PRF(r-PRF)观察到的结果,r-PRF的骨体积中位数为1.2毫米(范围:0.3 - 5.9毫米)。我们的研究结果表明,大鼠颅骨缺损模型适用于评估大鼠PRF对骨形成的影响,但在推断关于人PRF疗效的结论时需谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adda/11117948/69582a3c9538/bioengineering-11-00414-g001.jpg

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