Globus R K, Bikle D D, Morey-Holton E
Endocrinology. 1986 Feb;118(2):733-42. doi: 10.1210/endo-118-2-733.
A model of weightlessness in which the hindlimbs of rats are elevated by their tails at a 40 degrees angle to unload the hindlimbs while maintaining normal weight bearing on the forelimbs has been used to simulate certain conditions of space flight. When we used this model in growing rats, we found that growth in bone weight ceased by 1 week in the hindlimbs and lumbar vertebrae, whereas growth in bone weight in the forelimbs and cervical vertebrae remained unaffected. Within 2 weeks, however, the accretion of bone weight in the hindlimbs and lumbar vertebrae returned to normal despite continued skeletal unloading. Since bone weight in the growing rat is primarily determined by bone formation (bone resorption is modest), we investigated the effects of selective skeletal unloading on bone formation during 2 weeks of hindlimb elevation using radioisotope incorporation (with 45Ca and [3H]proline) and histomorphometry (with tetracycline labeling). The studies using radioisotope incorporation showed that bone formation was inhibited by the fifth day of skeletal unloading. By the 10th to 12th day, bone formation had returned toward normal. In comparison with cortical bone, cancellous bone (lumbar vertebrae and proximal tibiae) incorporated more 45Ca and [3H]proline (indicating greater metabolic activity) and had a greater absolute response to skeletal unloading. The results of these studies were confirmed by histomorphometric measurements of bone formation using triple tetracycline labeling. We conclude that this model of simulated weightlessness results in an initial inhibition of bone formation in the unloaded bones. This temporary cessation of bone formation is followed by a cessation in the accretion of bone weight, which then resumes at a normal rate by 14 days despite continued skeletal unloading. We believe that this cycle of inhibition and resumption of bone formation has profound implications for understanding bone dynamics during space flight, immobilization, or bed rest and offers an opportunity to study the hormonal and mechanical factors that regulate bone formation.
一种失重模型,即通过将大鼠的后肢以40度角用尾巴吊起,以使后肢卸载,同时前肢保持正常负重,已被用于模拟太空飞行的某些条件。当我们在生长中的大鼠中使用这个模型时,我们发现后肢和腰椎的骨重量增长在1周内停止,而前肢和颈椎的骨重量增长未受影响。然而,在2周内,尽管骨骼持续卸载,后肢和腰椎的骨重量增加恢复正常。由于生长中大鼠的骨重量主要由骨形成决定(骨吸收程度适中),我们使用放射性同位素掺入法(用45Ca和[3H]脯氨酸)和组织形态计量学(用四环素标记)研究了后肢抬高2周期间选择性骨骼卸载对骨形成的影响。使用放射性同位素掺入法的研究表明,骨骼卸载第5天时骨形成受到抑制。到第10至12天,骨形成已恢复至正常。与皮质骨相比,松质骨(腰椎和胫骨近端)掺入了更多的45Ca和[3H]脯氨酸(表明代谢活性更高),并且对骨骼卸载的绝对反应更大。这些研究结果通过使用三联四环素标记的骨形成组织形态计量学测量得到了证实。我们得出结论,这种模拟失重模型会导致卸载骨骼中骨形成的初始抑制。这种骨形成的暂时停止随后是骨重量增加的停止,然后尽管骨骼持续卸载,到14天时骨重量增加又以正常速率恢复。我们认为,这种骨形成抑制和恢复的循环对于理解太空飞行、固定或卧床休息期间的骨动力学具有深远意义,并为研究调节骨形成的激素和机械因素提供了一个机会。