Dallaudiere Benjamin, Zurlinden Olivier, Perozziello Anne, Deschamps Lydia, Larbi Ahmed, Louedec Liliane, Pesquer Lionel, Benayoun Yohan, Silvestre Alain, Serfaty Jean Michel
Centre d'Imagerie Ostéo-articulaire, Clinique du Sport de Bordeaux-Mérignac Département d'Imagerie Musculo-squeletrique, Centre Hospitalier Universitaire Pellegrin Bordeaux, France.
Département d'Imagerie Musculo-squeletrique, Centre Hospitalier Universitaire Bichat, Paris, France.
Muscles Ligaments Tendons J. 2014 Nov 17;4(3):351-6. eCollection 2014 Jul.
the aim of our study was to assess the potential of combined intratendinous injection of an anti-angiogenic drug: bevacizumab (AA) and Platelet Rich Plasma (PRP) to treat tendinopathy in a murine model of patellar and Achilles tendinopathy, and to evaluate its local toxicity.
twenty rats (80 patellar and Achilles tendons) were used for the study. We induced tendinosis (T+) in 80 tendons (patellar=40 and Achilles=40) by injecting under ultrasonography (US) guidance Collagenase 1® (day 0 = D0). Clinical examination was performed at D3, immediately followed by either PRP and AA (AAPRPT+, n=40) or PRP (PRPT+ n=40, control) US-guided intratendinous injection. Follow-up at D6, D18 and D25 using clinical, US and histology, and comparison between the 2 groups were performed. To study AA+PRP toxicity, we looked for necrosis or rupture on the 40 AAPRPT+.
all AAPRPT+ showed better joint mobilization compared to PRPT+ at D6 (p=0.03), D18 (p=0.04) and D25 (p=0.02). Similar results were found regarding US and histology, with smaller collagen fiber diameters (D6, p≤0.017, D25, p≤0.015), less disorganization and fewer neovessels (D25, p=0.004) in AAPRPT+ compared to PRPT+. No AA+PRP local toxicity was discovered in histology assessment.
our study suggests that combined injection of AA and PRP in tendinosis accelerates and improves tendon's healing compared PRP used alone, with no local toxicity.
我们研究的目的是评估在小鼠髌腱和跟腱病模型中联合腱鞘内注射抗血管生成药物贝伐单抗(AA)和富血小板血浆(PRP)治疗肌腱病的潜力,并评估其局部毒性。
本研究使用了20只大鼠(80条髌腱和跟腱)。我们通过在超声(US)引导下注射胶原酶1®(第0天 = D0),在80条肌腱(髌腱 = 40条,跟腱 = 40条)中诱导肌腱病(T+)。在D3进行临床检查,随后立即进行US引导下的腱鞘内注射PRP和AA(AAPRPT+,n = 40)或PRP(PRPT+,n = 40,对照组)。在D6、D18和D25进行随访,采用临床、US和组织学检查,并对两组进行比较。为了研究AA + PRP的毒性,我们在40只AAPRPT+中观察坏死或破裂情况。
与PRPT+相比,所有AAPRPT+在D6(p = 0.03)、D18(p = 0.04)和D25(p = 0.02)时关节活动度均更好。在US和组织学方面也发现了类似结果,与PRPT+相比,AAPRPT+的胶原纤维直径更小(D6,p≤0.017,D25,p≤0.015),结构紊乱更少,新生血管更少(D25,p = 0.004)。在组织学评估中未发现AA + PRP的局部毒性。
我们的研究表明,与单独使用PRP相比,在肌腱病中联合注射AA和PRP可加速并改善肌腱愈合,且无局部毒性。