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Synoviocytes, not chondrocytes, release free radicals after cycles of anoxia/re-oxygenation

机译:在缺氧/再充氧循环后,滑膜细胞而非软骨细胞释放自由基

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摘要

By oxymetry and electron paramagnetic resonance (EPR), we investigated the effects of repeated anoxia/re-oxygenation (A/R) periods on the respiration and production of free radicals by synoviocytes (rabbit HIG-82 cell line and primary equine synoviocytes) and equine articular chondrocytes. Three periods of 20 min anoxia followed by re-oxygenation were applied to 10(7)cells; O(2) consumption was measured before anoxia and after each re-oxygenation. After the last A/R, cellular free radical formation was investigated by EPR spectroscopy with spin trapping technique (n=3 for each cell line). Both types of synoviocytes showed a high O(2) consumption, which was slowered after anoxia. By EPR with the spin trap POBN, we proved a free radical formation. Results were similar for equine and rabbit synoviocytes. For chondrocytes, we observed a low O(2) consumption, unchanged by anoxia, and no free radical production. These observations suggest an oxidant activity of synoviocytes, potentially important for the onset of osteoarthritis.
机译:通过血氧测定法和电子顺磁共振(EPR),我们研究了反复缺氧/复氧(A / R)周期对滑膜细胞(兔HIG-82细胞系和初级马滑膜细胞)呼吸和自由基产生的影响,以及马关节软骨细胞。将三个20分钟的缺氧然后再充氧的时间应用于10(7)个电池。 O(2)消耗量在缺氧之前和每次重新充氧后进行测量。在最后一次A / R之后,通过EPR光谱和自旋捕获技术研究了细胞自由基的形成(每个细胞系n = 3)。两种类型的滑膜细胞均显示高O(2)消耗量,缺氧后速度减慢。通过EPR和自旋阱POBN,我们证明了自由基的形成。马和兔滑膜细胞的结果相似。对于软骨细胞,我们观察到低的O(2)消耗,由缺氧状态不变,并且没有自由基产生。这些观察结果表明滑膜细胞的氧化活性,对于骨关节炎的发作潜在重要。

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