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甲基强的松龙和机械负荷对犬关节软骨外植体培养的影响。

Effect of methylprednisolone and mechanical loading on canine articular cartilage in explant culture.

作者信息

Farquhar T, Todhunter R J, Fubini S L, Burton-Wurster N, Lust G

机构信息

Department of Mechanical Engineering, University of Maryland Baltimore County 21228, USA.

出版信息

Osteoarthritis Cartilage. 1996 Mar;4(1):55-62. doi: 10.1016/s1063-4584(96)80007-0.

Abstract

The objective of this study was to assess the effect of mechanical load on articular cartilage after in vitro corticosteroid exposure. Canine humeral cartilage was equilibrated for 4 days in defined medium with a serum substitute, then exposed to methylprednisolone sodium succinate for 20 h at 0, 0.01 or 1.0 mg/ml. After a drug-free recovery period, the explants were subjected to 0, 1 or 10 mega pascals (MPa) for 1 out every 5 s for 20 min, then incubated with [35S]-sulfate and [3H]-leucine for 4 h to measure proteoglycan and protein synthesis, respectively. When the loading occurred 22 h after drug exposure, proteoglycan synthesis was inhibited and protein synthesis, was unaffected by the drug. Both were stimulated by load, relative to controls. When the loading was delayed until 142 h after drug exposure, there was no biosynthetic response to load whether or not the explant had been exposed to the drug. Proteoglycan and protein synthesis 142 h after 0 or 0.01 mg/ml were unchanged or slightly higher than at 22 h, in explants which did not receive load. In contrast, biosynthesis were strongly inhibited 142 h after 1.0 mg/ml, and there was a 40% loss of proteoglycan content, relative to 22 h controls. If explants receiving 1.0 mg/ml also received heavy (10 MPa) loads 142 h later, there was a 17% reduction in total dry content suggesting severe matrix damage. These in vitro results suggest that articular load can help maintain normal cartilage metabolism after corticosteroid exposure, but also suggest that heavy loading after a sub-clinical dose can cause a marked loss of matrix solids.

摘要

本研究的目的是评估体外皮质类固醇暴露后机械负荷对关节软骨的影响。将犬肱骨软骨在含有血清替代品的特定培养基中平衡4天,然后分别在0、0.01或1.0mg/ml的甲泼尼龙琥珀酸钠中暴露20小时。在无药物恢复期后,将外植体每5秒承受0、1或10兆帕斯卡(MPa)的压力,持续20分钟,然后分别与[35S] - 硫酸盐和[3H] - 亮氨酸孵育4小时,以测量蛋白聚糖和蛋白质合成。当在药物暴露后22小时施加负荷时,蛋白聚糖合成受到抑制,而蛋白质合成不受药物影响。相对于对照组,两者均受到负荷刺激。当负荷延迟至药物暴露后142小时时,无论外植体是否暴露于药物,均未出现对负荷的生物合成反应。在未接受负荷的外植体中,0或0.01mg/ml处理142小时后的蛋白聚糖和蛋白质合成与22小时时相比无变化或略有升高。相比之下,1.0mg/ml处理142小时后生物合成受到强烈抑制,相对于22小时对照组,蛋白聚糖含量损失40%。如果接受1.0mg/ml处理的外植体在142小时后也接受重负荷(10MPa),则总干重减少17%,表明基质严重受损。这些体外实验结果表明,关节负荷有助于维持皮质类固醇暴露后软骨的正常代谢,但也表明亚临床剂量后重负荷可导致基质固体显著损失。

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