Ivey J L, Wright D R, Tashjian A H
J Clin Invest. 1976 Dec;58(6):1327-38. doi: 10.1172/JCI108588.
The ionophores A23187 and X-537A were used as probes to investigate the possible role of calcium uptake by bone as a mediator for the stimulation of bone resorption induced by parathyroid hormone (PTH) and other agents in cultured mouse calvaria. The ionophores alone at concentrations from 1 nM to 20 muM did not stimulate bone resorption, nor did they potentiate bone resorption stimulated by submaximal concentrations of PTH after either brief (15-60 min) or extended (1-3 day) exposure to the ionophores. Unexpectedly, we found that the ionophores inhibit in a dose-dependent manner bone resorption stimulated by PTH and a wide variety of other compounds (prostaglandin E2, 1alpha-hydroxycholecalciferol, 3-isobutyl-1-methyl-xanthine, and phorbol myristate acetate). This inhibition was not due to irreversible damage to the bones by the ionophores, because the inhibition was reversible even after 24 h of treatment. Inhibition of bone resorption by the ionophores was observed in media of both high and low calcium concentration, indicating that the inhibition was not due to a critical extracellular calcium concentration. Inhibition by the ionophores differs qualitatively in several ways from that produced by calcitonin, a natural inhibitor of bone resorption. Furthermore, A23187 at 1.0 mug/ml had no effect on the accumulation of cyclic AMP in the medium of either control, PTH- or calcitonin treated calvaria. We conclude that the ionophores A23187 or X537A do not stimulate bone resorption nor potentiate the effects of stimulators of bone resorption; instead they are inhibitors of bone resorption stimulated by a wide variety of compounds.
离子载体A23187和X-537A被用作探针,以研究骨对钙的摄取作为甲状旁腺激素(PTH)和其他试剂在培养的小鼠颅骨中诱导骨吸收刺激的介质的可能作用。单独的离子载体在1 nM至20 μM的浓度下不会刺激骨吸收,在短暂(15 - 60分钟)或延长(1 - 3天)暴露于离子载体后,它们也不会增强由亚最大浓度的PTH刺激的骨吸收。出乎意料的是,我们发现离子载体以剂量依赖性方式抑制由PTH和多种其他化合物(前列腺素E2、1α-羟基胆钙化醇、3-异丁基-1-甲基黄嘌呤和佛波醇肉豆蔻酸酯)刺激的骨吸收。这种抑制不是由于离子载体对骨骼的不可逆损伤,因为即使在处理24小时后抑制也是可逆的。在高钙浓度和低钙浓度的培养基中均观察到离子载体对骨吸收的抑制,表明该抑制不是由于临界细胞外钙浓度所致。离子载体的抑制在几个方面与降钙素(一种天然的骨吸收抑制剂)产生的抑制在性质上有所不同。此外,1.0 μg/ml的A23187对对照、PTH或降钙素处理的颅骨培养基中环状AMP的积累没有影响。我们得出结论,离子载体A23187或X537A不会刺激骨吸收,也不会增强骨吸收刺激剂的作用;相反,它们是多种化合物刺激的骨吸收的抑制剂。