Hyperbaric oxygen potentiates platelet-rich plasma composition and accelerates bone healing

IF 5.9 1区 医学 Q1 ORTHOPEDICS Journal of Orthopaedic Translation Pub Date : 2025-03-01 Epub Date: 2025-01-19 DOI:10.1016/j.jot.2024.10.016
Wen-Shuo Chang , Chien-Cheng Huang , Tzu-Hao Chen , Ssu-Han Chao , Cheng-Hsien Lin , Ching-Ping Chang , Chi-Sheng Chien
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Abstract

Objective

This study aimed to investigate whether platelet-rich plasma (PRP) obtained from the blood of rats preconditioned with hyperbaric oxygen (HBOP) would enhance the biological activity of PRP and accelerate the healing process of femur fractures in a rat model.

Design

PRP was derived from blood samples of healthy rats subjected to either hyperbaric oxygen (hPRP) or normobaric air (nPRP). A closed femur fracture model was established in male Wistar rats, with treatments of hPRP or nPRP administered around the fracture site immediately post-fracture and on days 7, 14, 21, and 28. Growth factor concentrations in hPRP and nPRP were biochemically quantified. Bone healing was assessed weekly by X-ray, while histological and immunofluorescence analyses evaluated inflammatory status, osteoprotegerin (OPG), receptor activator of nuclear factor kappa-B ligand (RANKL) expression, and the presence of osteoblasts, osteoclasts, and osteocytes during healing. The effects of hPRP and nPRP on MC3T3-E1 preosteoblast migration and proliferation were also tested in vitro.

Results

hPRP showed significantly higher concentrations of growth factors such as activin-A, brain-derived neurotrophic factor, nerve growth factor, Flt-3 Ligand, granulocyte-macrophage colony-stimulating factor, hepatocyte growth factor, and platelet-derived growth factor, compared to nPRP. In vitro, hPRP demonstrated more significant effects on preosteoblast migration and proliferation. In vivo, hPRP treatment resulted in enhanced bone healing, higher OPG levels in osteoblasts and osteoclasts, and an elevated OPG/RANKL ratio compared to nPRP.

Conclusions

HBOP enhances the biological activity of PRP and accelerates bone healing in a closed femur fracture model in rats. This study highlights the regenerative potential of PRP when preconditioned with hyperbaric oxygen for use in bone fracture therapy.

Significance statement

PRP is widely used in treating bone defects and fractures, but its enhancement through HBOP remains underexplored. Our findings demonstrate that HBOP potentiates the biological activity of PRP, offering promising therapeutic potential for bone fracture healing.

The translational potential of this article

Enriching growth factors in PRP through HBOP could significantly improve tissue regeneration, especially in bone healing. The potential of hPRP in clinical applications is highly promising, particularly in orthopaedic surgery, trauma care, sports medicine, and managing bone healing in compromised patients.

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高压氧增强富血小板血浆成分,加速骨愈合。
目的:探讨高压氧(HBOP)预处理大鼠血液中富血小板血浆(PRP)是否能增强PRP的生物活性,加速大鼠股骨骨折模型的愈合过程。设计:PRP来源于健康大鼠接受高压氧(hPRP)或常压空气(nPRP)的血液样本。建立雄性Wistar大鼠闭合性股骨骨折模型,骨折后立即及第7、14、21、28天在骨折部位周围给予hPRP或nPRP治疗。对hPRP和nPRP中的生长因子浓度进行生化定量。每周通过x射线评估骨愈合情况,同时通过组织学和免疫荧光分析评估炎症状态、骨保护素(OPG)、核因子κ b配体受体激活剂(RANKL)表达以及愈合过程中成骨细胞、破骨细胞和骨细胞的存在。体外实验还检测了hPRP和nPRP对MC3T3-E1成骨前细胞迁移和增殖的影响。结果:hPRP中激活素- a、脑源性神经营养因子、神经生长因子、Flt-3配体、粒细胞-巨噬细胞集落刺激因子、肝细胞生长因子、血小板源性生长因子等生长因子浓度显著高于nPRP。在体外,hPRP对成骨前细胞迁移和增殖的影响更为显著。在体内,与nPRP相比,hPRP治疗导致骨愈合增强,成骨细胞和破骨细胞中OPG水平升高,OPG/RANKL比值升高。结论:HBOP能增强PRP的生物活性,促进闭合性股骨骨折模型大鼠骨愈合。这项研究强调了PRP在高压氧预处理后用于骨折治疗的再生潜力。意义说明:PRP广泛应用于骨缺损和骨折的治疗,但通过HBOP增强PRP的应用尚不充分。我们的研究结果表明,HBOP增强了PRP的生物活性,为骨折愈合提供了有希望的治疗潜力。本文的转化潜力:通过HBOP富集PRP中的生长因子可以显著促进组织再生,尤其是骨愈合。hPRP在临床应用中的潜力是非常有希望的,特别是在骨科手术、创伤护理、运动医学和管理受损患者的骨愈合方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Orthopaedic Translation
Journal of Orthopaedic Translation Medicine-Orthopedics and Sports Medicine
CiteScore
11.80
自引率
13.60%
发文量
91
审稿时长
29 days
期刊介绍: The Journal of Orthopaedic Translation (JOT) is the official peer-reviewed, open access journal of the Chinese Speaking Orthopaedic Society (CSOS) and the International Chinese Musculoskeletal Research Society (ICMRS). It is published quarterly, in January, April, July and October, by Elsevier.
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