Zhang Anja Z, Ficklscherer Andreas, Gülecyüz Mehmet F, Paulus Alexander C, Niethammer Thomas R, Jansson Volkmar, Müller Peter E
Department of Orthopaedic Surgery, Physical Medicine and Rehabilitation, University Hospital of Munich, Munich, Germany.
Orthopaedie Oberland, Bavaria, Germany.
Arthroscopy. 2017 Apr;33(4):840-848. doi: 10.1016/j.arthro.2016.10.026. Epub 2017 Jan 12.
To analyze the ability of ropivacaine, bupivacaine, and triamcinolone to induce apoptosis and necrosis in fibroblasts, tenocytes, and human mesenchymal stem cells.
Human dermal fibroblasts, adipose-derived human mesenchymal stem cells (hMSCs), and tenocytes gained from the rotator cuff tendon were seeded with a cell density of 0.5 × 10/cm. One specimen of ropivacaine, bupivacaine, and triamcinolone was tested separately on the cells with separate concentrations of 0.5%, 0.25%, and 0.125% for each specimen. The negative control received no agent, only a change of medium. The incubation period for each agent was 30 minutes. After a change of medium and 1 hour, 24 hours, and 7 days of incubation, 10 cells were harvested and analyzed via fluorescence-activated cell sorting with double-staining with annexin V and propidium iodide. Statistical analysis to determine significant difference (P < .05) between the groups with SPSS statistics 23 through one-way analysis of variance with a univariate general linear model was performed.
Bupivacaine showed necrosis-inducing effects on fibroblasts and tenocytes, with the necrotic effect peaking at 0.5% and 0.25%. Ropivacaine and triamcinolone caused no significant necrosis. Compared with fibroblasts and tenocytes, hMSCs did not show significant necrotic or apoptotic effects after exposure to bupivacaine. Overall, no significant differences in apoptosis were detected between different cell lines, varying concentrations, or time measurements.
Bupivacaine 0.5% and 0.25% have the most necrosis-inducing effects on fibroblasts and tenocytes. Ropivacaine caused less necrosis than bupivaine. Compared with fibroblasts and tenocytes, hMSCs were not affected by necrosis using any of the tested agents. A significant apoptosis-inducing effect could not be detected for the different cell lines.
Possible cell toxicity raises questions of concern for intra-articular injections using local anesthetics and corticosteroids. The present study demonstrates the necrotic and apoptotic effects of ropivacaine, bupivacaine, and triamcinolone and may give recommendations for intra-articular use of local anesthetics and corticosteroids.
分析罗哌卡因、布比卡因和曲安奈德诱导成纤维细胞、肌腱细胞和人间充质干细胞凋亡及坏死的能力。
将人皮肤成纤维细胞、脂肪来源的人间充质干细胞(hMSCs)和从肩袖肌腱获取的肌腱细胞以0.5×10⁶/平方厘米的细胞密度接种。罗哌卡因、布比卡因和曲安奈德的一个样本分别用0.5%、0.25%和0.125%的不同浓度对细胞进行测试。阴性对照不给予任何药物,仅更换培养基。每种药物的孵育期为30分钟。更换培养基后,经过1小时、24小时和7天的孵育,收集10⁶个细胞,通过通过细胞并通过用膜联蛋白V和碘化丙啶进行双重染色的荧光激活细胞分选进行分析。使用SPSS统计学软件23,通过单因素一般线性模型的单因素方差分析进行统计分析以确定组间的显著差异(P < 0.05)。
布比卡因对成纤维细胞和肌腱细胞显示出坏死诱导作用,坏死效应在0.5%和0.25%时达到峰值。罗哌卡因和曲安奈德未引起显著坏死。与成纤维细胞和肌腱细胞相比,hMSCs在暴露于布比卡因后未显示出显著的坏死或凋亡效应。总体而言,在不同细胞系、不同浓度或不同时间测量之间未检测到凋亡的显著差异。
0.5%和0.25%的布比卡因对成纤维细胞和肌腱细胞具有最强的坏死诱导作用。罗哌卡因引起的坏死比布比卡因少。与成纤维细胞和肌腱细胞相比,hMSCs使用任何一种测试药物均未受到坏死影响。未检测到不同细胞系有显著的凋亡诱导作用。
可能的细胞毒性引发了对使用局部麻醉药和皮质类固醇进行关节内注射的担忧。本研究证明了罗哌卡因、布比卡因和曲安奈德的坏死和凋亡效应,并可能为局部麻醉药和皮质类固醇的关节内使用提供建议。