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非甾体抗炎药(NSAIDs)对关节软骨外植体和软骨细胞单层培养物中蛋白聚糖合成影响的比较。

Comparison of the effects of non-steroidal anti-inflammatory drugs (NSAIDs) on proteoglycan synthesis by articular cartilage explant and chondrocyte monolayer cultures.

作者信息

Collier S, Ghosh P

机构信息

Raymond Purves Research Laboratories, (University of Sydney), Royal North Shore Hospital of Sydney, St Leonards, N.S.W., Australia.

出版信息

Biochem Pharmacol. 1991 May 1;41(9):1375-84. doi: 10.1016/0006-2952(91)90111-h.

Abstract

Experiments were conducted to study proteoglycan biosynthesis by rabbit articular chondrocytes cultured in the presence of NSAIDs and 35SO4(2-) for up to 8 days. Both articular cartilage explants and confluent chondrocyte monolayer culture models were used. Medium was changed every 2 days and the [35SO4]proteoglycans which had accumulated in the medium and the extracellular matrix during the culture intervals were assayed separately. In long-term experiments, drugs were removed on day 8, and proteoglycan production during a 10-12 day culture interval also was assayed. The drugs studied were diclofenac, indomethacin, ketoprofen, piroxicam and tiaprofenic acid, at concentrations of 0, 0.1, 1, 10, 50 and 100 micrograms/mL. Whereas proteoglycan production by cell cultures was maximal early in the culture period, explants produced more proteoglycans as time progressed. The highest concentrations of all of the drugs, especially diclofenac and indomethacin, inhibited proteoglycan secretion by both cell and explant cultures. However, after removal of the drugs from the cultures, suppressed proteoglycan production reversed to levels equivalent to, or higher than controls in the cell cultures, but largely persisted in explant cultures. About 70-80% of proteoglycans produced by explants were retained in the matrix, whereas about 80-90% of proteoglycans produced by cell cultures were secreted into the medium. Where drugs inhibited proteoglycan production, the levels were reduced by approximately the same proportions in both extracellular matrix and culture medium fractions. Of the NSAIDs examined only ketoprofen demonstrated a stimulatory effect on PG synthesis in explant cultures at a physiological concentration (0.1 microgram/mL).

摘要

进行了实验,以研究在非甾体抗炎药(NSAIDs)和35SO4(2-)存在的情况下培养长达8天的兔关节软骨细胞的蛋白聚糖生物合成。使用了关节软骨外植体和汇合的软骨细胞单层培养模型。每2天更换一次培养基,并分别测定培养期间在培养基和细胞外基质中积累的[35SO4]蛋白聚糖。在长期实验中,在第8天去除药物,并测定10 - 12天培养期间的蛋白聚糖产量。所研究的药物为双氯芬酸、吲哚美辛、酮洛芬、吡罗昔康和噻洛芬酸,浓度分别为0、0.1、1、10、50和100微克/毫升。细胞培养物产生的蛋白聚糖在培养期早期产量最高,而随着时间推移外植体产生的蛋白聚糖更多。所有药物的最高浓度,尤其是双氯芬酸和吲哚美辛,抑制了细胞和外植体培养物中蛋白聚糖的分泌。然而,从培养物中去除药物后,细胞培养物中受抑制的蛋白聚糖产量恢复到与对照相当或更高的水平,但在外植体培养物中大部分仍然持续受到抑制。外植体产生的蛋白聚糖约70 - 80%保留在基质中,而细胞培养物产生的蛋白聚糖约80 - 90%分泌到培养基中。当药物抑制蛋白聚糖产生时,细胞外基质和培养基部分中的水平降低的比例大致相同。在所检测的NSAIDs中,只有酮洛芬在生理浓度(0.1微克/毫升)下对外植体培养物中的蛋白聚糖合成表现出刺激作用。

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