Wheeler D L, Vander Griend R A, Wronski T J, Miller G J, Keith E E, Graves J E
Division of Orthopaedics, Oregon Health Sciences University, School of Medicine, Portland, USA.
Bone. 1995 Feb;16(2):215-21. doi: 10.1016/8756-3282(94)00032-u.
Both clinical and laboratory studies have shown that the chemotherapy drug, Methotrexate (MTX), has adverse short-term effects on bone. There are no studies that demonstrate the long-term response of bone to MTX. The purpose of this study was to determine the short- and long-term effects of MTX on bone volume, turnover, mineralization and strength. Three-month-old Sprague-Dawley rats were randomly assigned to a control (CTL) or MTX group and were given either daily MTX or saline injections for two separate 5-day courses (5 on/9 off/5 on). Fluorochrome compounds were injected prior to killing to label actively mineralizing bone surfaces. One CTL and MTX group were killed at 30, 80 and 170 days after treatment. Both femurs and tibiae were harvested for cancellous and cortical bone histomorphometry and biomechanical testing (torsion). Standard cancellous and cortical histomorphometric parameters were measured from undecalcified, methyl-methacrylate-embedded sections from the right proximal tibia and tibial and femoral diaphyses. The contralateral femur and tibia were torsionally loaded to failure and standard mechanical parameters were measured. All bone responses were statistically analyzed using a two-way ANOVA followed by Duncan's multiple comparison procedure (significance: p = 0.05). Cancellous bone volume was significantly lower in the MTX-treated group at 80 and 170 days. Cancellous mineralizing surface and longitudinal bone growth were significantly depressed at all time points yet mineral apposition rate was only depressed at the 170-day point. Cancellous osteoclast surface was increased at all time points for the MTX-treated animals.(ABSTRACT TRUNCATED AT 250 WORDS)
临床和实验室研究均表明,化疗药物甲氨蝶呤(MTX)对骨骼有短期不良影响。目前尚无研究证明骨骼对MTX的长期反应。本研究的目的是确定MTX对骨体积、骨转换、矿化和强度的短期和长期影响。将3个月大的Sprague-Dawley大鼠随机分为对照组(CTL)或MTX组,分别接受每日MTX或生理盐水注射,共两个独立的5天疗程(5天用药/9天停药/5天用药)。在处死前注射荧光染料化合物以标记活跃矿化的骨表面。在治疗后30、80和170天处死一组CTL和MTX组动物。采集双侧股骨和胫骨用于松质骨和皮质骨组织形态计量学分析及生物力学测试(扭转试验)。从右侧近端胫骨以及胫骨和股骨干的未脱钙、甲基丙烯酸甲酯包埋切片中测量标准的松质骨和皮质骨组织形态计量学参数。对另一侧股骨和胫骨进行扭转加载直至破坏,并测量标准力学参数。所有骨反应均采用双向方差分析,随后进行邓肯多重比较程序进行统计学分析(显著性:p = 0.05)。在80天和170天时,MTX治疗组的松质骨体积显著降低。在所有时间点,松质骨矿化表面和纵向骨生长均显著降低,但骨矿化沉积率仅在170天时降低。MTX治疗动物在所有时间点的松质骨破骨细胞表面均增加。(摘要截断于250字)