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Molecular Response of Rabbit Menisci to Surgically Induced Hemarthrosis and a Single Intra‐Articular Dexamethasone Treatment

机译:兔肿瘤的分子响应到手术诱导的腹水和单个关节内塞米松治疗

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ABSTRACT Anterior cruciate ligament reconstructive surgery can restore biomechanical stability, however, such surgery cannot reliably prevent the onset of posttraumatic osteoarthritis. The aim of this study was to elucidate the molecular response that occurs within the menisci following a surgical injury that allows bleeding into the joint space, and then to investigate the effect of dexamethasone (DEX) on this molecular response. Cell viability studies following acute controlled exposure to blood and blood plus DEX were also conducted. Fortyeight New Zealand white rabbits were randomly allocated into control, sham, surgical, and surgical + DEX groups (each groupn = 6). Animals were sacrificed at 48 h and 9 weeks, and menisci were harvested. The messenger RNA (mRNA) expression levels for key inflammatory, and degradative proteins, as well as mRNA levels for autophagy pathway molecules were quantified, and statistically significant changes were described. Meniscal cell viability was calculated by incubating groups of medial and lateral menisci in autologous blood, or autologous blood plus DEX for 48 h (each groupn = 4; total of eight medial and eight lateral menisci), and then conducting a histological live/dead assay. Results indicated a significant reduction in only medial meniscal cell viability when the tissue was exposed to blood in combination with DEX. A single administration of DEX following surgery significantly suppresses the elevated molecular expression for key inflammatory and degradative markers within menisci at 48 h and 9 weeks postsurgery. In vitro, autologous blood did not affect cell viability, but addition of DEX uniquely impacted the medial menisci. ?2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:20432052, 2019
机译:摘要前令人毛骨悚然的重建手术可以恢复生物力学稳定性,然而,这种手术不能可靠地防止错误骨关节炎的发作。本研究的目的是阐明在手术损伤后允许出血到关节空间的细胞膜内发生的分子响应,然后研究地塞米松(DEX)对该分子反应的影响。还进行了急性受控暴露后的细胞活力研究。 40年代新西兰白兔被随机分配给控制,假,手术和外科+ DEX组(每组= 6)。在48小时和9周处处死动物,并收获半月核。量化致炎症和降解蛋白的信使RNA(mRNA)表达水平以及用于自噬途径分子的mRNA水平,并描述了统计学上显着的变化。通过在自体血液中的内侧和横向肿瘤组中孵育的组和横向肿瘤组或48小时的自体血液加曲线(每组= 4;总共八个内侧和八个侧半月形)来计算半月核细胞活力。然后进行组织学活/死导。结果表明,当组织与DEX组合将组织暴露于血液时,只有内侧半月板的活力显着降低。手术后的单一施用DEX显着抑制了48小时和9周后肿瘤内的关键炎症和降解标志物的升高的分子表达。体外,自体血液不影响细胞活力,但添加DEX唯一影响内侧肿瘤。 ?2019年骨科研究会。由Wiley Hearyicals,Inc.J orthop Res 37:20432052,2019

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