Martin James A, McCabe Daniel, Walter Morgan, Buckwalter Joseph A, McKinley Todd O
Orthopaedic Cell and Molecular Biology Laboratory, Department of Orthopaedics and Rehabilitation, The University of Iowa, 1182 ML, Iowa City, IA 52242, USA.
J Bone Joint Surg Am. 2009 Aug;91(8):1890-7. doi: 10.2106/JBJS.H.00545.
Chondrocyte death has been linked to injury-induced oxidative damage, suggesting that antioxidants could substantially improve viability. However, since reactive oxygen species play roles in normal physiology, there are concerns that antioxidants may have deleterious side effects. To address these issues, we studied the effects of N-acetylcysteine, a potent free radical scavenger, on chondrocyte viability and cartilage proteoglycan content in an in vitro cartilage injury model. We hypothesized that treatment with N-acetylcysteine soon after an impact injury would have significant chondrocyte-sparing effects and would prevent injury-induced proteoglycan losses.
Bovine osteochondral explants were subjected to a single impact load with use of a drop-tower device. Chondrocyte viability was measured at multiple time points post-impact with use of fluorescent probes and confocal microscopy. Forty-eight hours after impact, the effects on viability of immediate post-impact treatment with N-acetylcysteine were compared with the effects of the caspase inhibitor N-CBZ-Val-Ala-Asp(O-Me) fluoromethyl ketone and those of the cell-membrane-stabilizing surfactant poloxamer 188. The effect of N-acetylcysteine on proteoglycan content was determined at seven and fourteen days post-impact.
Chondrocyte viability declined sharply within an hour and reached a steady state within six to twelve hours after impact. Immediate treatment with N-acetylcysteine doubled the number of viable chondrocytes assayed forty-eight hours after impact, and this effect was significantly greater than that of N-CBZ-Val-Ala-Asp(O-Me) fluoromethyl ketone. Even when N-acetylcysteine treatment was delayed for up to four hours after injury, it still had significant positive effects on cell viability at forty-eight hours. Moreover, N-acetylcysteine treatment significantly improved proteoglycan content at the impact sites at both seven and fourteen days after injury.
Treatment with N-acetylcysteine soon after a blunt impact injury can reduce chondrocyte death and proteoglycan loss measured seven to fourteen days after injury.
软骨细胞死亡与损伤诱导的氧化损伤有关,这表明抗氧化剂可能会显著提高细胞活力。然而,由于活性氧在正常生理过程中发挥作用,人们担心抗氧化剂可能会产生有害的副作用。为了解决这些问题,我们在体外软骨损伤模型中研究了强效自由基清除剂N - 乙酰半胱氨酸对软骨细胞活力和软骨蛋白聚糖含量的影响。我们假设在撞击损伤后不久用N - 乙酰半胱氨酸进行治疗会对软骨细胞产生显著的保护作用,并能防止损伤诱导的蛋白聚糖损失。
使用落塔装置对牛骨软骨外植体施加单次撞击负荷。使用荧光探针和共聚焦显微镜在撞击后的多个时间点测量软骨细胞活力。撞击后48小时,将撞击后立即用N - 乙酰半胱氨酸治疗对活力的影响与半胱天冬酶抑制剂N - CBZ - Val - Ala - Asp(O - Me)氟甲基酮以及细胞膜稳定表面活性剂泊洛沙姆188的影响进行比较。在撞击后7天和14天测定N - 乙酰半胱氨酸对蛋白聚糖含量的影响。
软骨细胞活力在1小时内急剧下降,并在撞击后6至12小时内达到稳定状态。撞击后立即用N - 乙酰半胱氨酸治疗使撞击后48小时检测到的存活软骨细胞数量增加了一倍,且这种效果显著大于N - CBZ - Val - Ala - Asp(O - Me)氟甲基酮。即使在损伤后延迟长达4小时进行N - 乙酰半胱氨酸治疗,在48小时时对细胞活力仍有显著的积极影响。此外,N - 乙酰半胱氨酸治疗在损伤后7天和14天均显著改善了撞击部位的蛋白聚糖含量。
钝性撞击损伤后不久用N - 乙酰半胱氨酸进行治疗可以减少损伤后7至14天测量的软骨细胞死亡和蛋白聚糖损失。