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抗氧化添加剂可减少关节软骨在暴露于冷冻保护剂时产生的活性氧物质。

Antioxidant additives reduce reactive oxygen species production in articular cartilage during exposure to cryoprotective agents.

机构信息

Department of Surgery, University of Alberta, Edmonton, AB, Canada.

Department of Surgery, University of Alberta, Edmonton, AB, Canada; Department of Orthopedic Surgery, First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.

出版信息

Cryobiology. 2020 Oct;96:114-121. doi: 10.1016/j.cryobiol.2020.07.008. Epub 2020 Aug 8.

Abstract

High concentrations of cryoprotective agents (CPA) are required during articular cartilage cryopreservation but these CPAs can be toxic to chondrocytes. Reactive oxygen species have been linked to cell death due to oxidative stress. Addition of antioxidants has shown beneficial effects on chondrocyte survival and functions after cryopreservation. The objectives of this study were to investigate (1) oxidative stress experienced by chondrocytes and (2) the effect of antioxidants on cellular reactive oxygen species production during articular cartilage exposure to high concentrations of CPAs. Porcine cartilage dowels were exposed to a multi-CPA solution supplemented with either 0.1 mg/mL chondroitin sulfate or 2000 μM ascorbic acid, at 4 °C for 180 min (N = 7). Reactive oxygen species production was measured with 5 μM dihydroethidium, a fluorescent probe that targets reactive oxygen species. The cell viability was quantified with a dual cell membrane integrity stain containing 6.25 μM Syto 13 + 9 μM propidium iodide using confocal microscopy. Supplementation of CPA solutions with chondroitin sulfate or ascorbic acid resulted in significantly lower dihydroethidium counts (p < 0.01), and a lower decrease in the percentage of viable cells (p < 0.01) compared to the CPA-treated group without additives. These results indicated that reactive oxygen species production is induced when articular cartilage is exposed to high CPA concentrations, and correlated with the amount of dead cells. Both chondroitin sulfate and ascorbic acid treatments significantly reduced reactive oxygen species production and improved chondrocyte viability when articular cartilage was exposed to high concentrations of CPAs.

摘要

高浓度的冷冻保护剂(CPA)在关节软骨冷冻保存过程中是必需的,但这些 CPA 对软骨细胞可能有毒性。活性氧与氧化应激引起的细胞死亡有关。抗氧化剂的添加已显示出对冷冻保存后软骨细胞存活和功能的有益影响。本研究的目的是研究(1)软骨细胞经历的氧化应激,以及(2)抗氧化剂对关节软骨暴露于高浓度 CPAs 时细胞活性氧产生的影响。将猪软骨栓子暴露于补充有 0.1mg/ml 硫酸软骨素或 2000μM 抗坏血酸的多-CPA 溶液中,在 4°C 下孵育 180 分钟(N=7)。使用 5μM 二氢乙啶(一种靶向活性氧的荧光探针)测量活性氧的产生。使用含有 6.25μM Syto 13 和 9μM 碘化丙啶的双重细胞膜完整性染料通过共聚焦显微镜定量细胞活力。与不含添加剂的 CPA 处理组相比,CPA 溶液中添加硫酸软骨素或抗坏血酸可导致二氢乙啶计数明显降低(p<0.01),活细胞百分比降低(p<0.01)。这些结果表明,当关节软骨暴露于高浓度的 CPA 时,会诱导活性氧的产生,并且与死亡细胞的数量相关。当关节软骨暴露于高浓度的 CPAs 时,硫酸软骨素和抗坏血酸处理均显著降低活性氧的产生并提高软骨细胞活力。

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