Chang Je-Ken, Wang Gwo-Jaw, Tsai Shiu-Ting, Ho Mei-Ling
Department of Orthopaedics, School of Medicine, Orthopaedic Research Center, Kaohsiung Medical University Chug-Ho Memorial Hospital, Kaohsiung, Taiwan.
Connect Tissue Res. 2005;46(4-5):200-10. doi: 10.1080/03008200500344025.
Previous studies indicated that nonsteroidal anti-inflammatory drugs (NSAIDs) suppress bone repair, growth, and remodeling in vivo. Our previous in vitro study demonstrated that indomethacin and ketorolac inhibited osteoblast proliferation. In this study, we further investigated the influences of 4 NSAIDs on cell cycle kinetics, cytotoxicity, and cell death pattern in osteoblast cultures from rat fetal calvaria. Our results showed that NSAIDs significantly arrested cell cycle at the G(0)/G(1) phase and induced cytotoxicity and cell death of osteoblasts. Apoptosis was more pronounced than necrosis caused by NSAIDs. Among these NSAIDs, piroxicam showed the least effect to produce osteoblastic dysfunction. Moreover, we found that the cytotoxic and apoptotic effects of NSAIDs on osteoblasts might not be prostaglandin related. These results suggest that the NSAID effects on cell cycle arrest and cell death induction in osteoblasts may be one of the important mechanisms contributing to their suppressive effect on bone formation.
先前的研究表明,非甾体抗炎药(NSAIDs)在体内会抑制骨修复、生长和重塑。我们之前的体外研究表明,吲哚美辛和酮咯酸会抑制成骨细胞增殖。在本研究中,我们进一步研究了4种非甾体抗炎药对大鼠胎儿颅骨成骨细胞培养物中细胞周期动力学、细胞毒性和细胞死亡模式的影响。我们的结果表明,非甾体抗炎药会使细胞周期在G(0)/G(1)期显著停滞,并诱导成骨细胞的细胞毒性和细胞死亡。非甾体抗炎药引起的细胞凋亡比坏死更明显。在这些非甾体抗炎药中,吡罗昔康对产生成骨细胞功能障碍的影响最小。此外,我们发现非甾体抗炎药对成骨细胞的细胞毒性和凋亡作用可能与前列腺素无关。这些结果表明,非甾体抗炎药对成骨细胞的细胞周期停滞和细胞死亡诱导作用可能是其对骨形成产生抑制作用的重要机制之一。