药物对新型软骨破裂体外模型的影响。

M el-Ghazaly, P Braquet, A Moore, D A Willoughby
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引用次数: 0

摘要

本研究采用了一种新的体外模型来研究软骨损伤。将多形核中性粒细胞(PMNs)与肉豆酸酯佛波酯(PMA)分层在2微米的牛鼻软骨低温切片上。孵育后,固定切片,染色,用微密度法测定糖胺聚糖(GAG)含量。PMNs引起部分GAG缺失,当PMNs被PMA激活时,这种缺失大大增强。然后加入各种药物,分别是乙酰水杨酸、吲哚美辛、布洛芬、吡罗昔康、地塞米松、d -青霉胺、氯喹和BN50548。所测试的药物对软骨基质没有直接影响,也没有影响未刺激PMNs处理的部分的GAG损失。然而,一种新型蛋白酶抑制剂BN50548对PMA刺激的PMNs造成的GAG损失具有剂量反应保护作用。该模型在筛选具有软骨保护活性的新型抗蛋白酶方面可能具有一定的价值。
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Drug effects on a novel in vitro model of cartilage breakdown.

A new in vitro model for studying cartilage breakdown has been utilised in this work. Polymorphonuclear neutrophils (PMNs) with phorbol myristate acetate (PMA) were layered onto 2 microns cryostat sections of bovine nasal cartilage. After incubation, the sections were fixed, stained, and the amount of glycosaminoglycan (GAG) contents measured by microdensitometry. PMNs caused GAG loss from sections and this was greatly enhanced when the PMNs were activated by PMA. Various pharmacological agents were then added to the system, namely acetyl salicylic acid, indomethacin, ibuprofen, piroxicam, dexamethasone, D-penicillamine, chloroquine and BN50548. The drugs tested had no direct effect on cartilage matrix, nor did they affect GAG loss from sections treated with non-stimulated PMNs. However, BN50548, a novel protease inhibitor, afforded a dose response protection of cartilage section from GAG loss by PMA stimulated PMNs. This model may prove to be of value in screening novel antiproteases with chondroprotective activity.

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