Yamaguchi M, Ehara Y
Laboratory of Metabolism and Endocrinology, Graduate School of Nutritional Sciences, University of Shizuoka, Japan.
Calcif Tissue Int. 1995 Sep;57(3):218-23. doi: 10.1007/BF00310262.
Whether the decrease of zinc content in the femoral-metaphyseal tissues of rats with skeletal unloading is involved in the alteration of bone metabolism was investigated. Skeletal unloading was designed using the model of hindlimb suspension in rats. Animals were fed for 4 days with the unloading. The metaphyseal zinc content were significantly decreased by the unloading. Zinc accumulation in the metaphyseal tissues by a single oral administration of zinc sulfate (20 mg Zn/100 g body weight) was partially depressed by the unloading, although serum zinc concentration was higher than that in normal rats, suggesting an impaired movement of zinc from serum into bone tissues by the unloading. Skeletal unloading caused a significant decrease of alkaline phosphatase activity and deoxyribonucleic acid (DNA) content in the metaphyseal tissues. These decreases were completely restored by addition of zinc sulfate (10(-4) M) or beta-alanyl-L-histidinato zinc (AHZ; 10(-5) M) in a culture medium with the metaphyseal tissues in vitro. The effects of zinc compounds were abolished by the presence of cycloheximide (10(-8) M), suggesting that the zinc effect is based on a newly synthesized protein. Dipicolinate (10(-4) and 10(-5) M), a potent zinc-chelating agent, caused an appreciable decrease of zinc content and alkaline phosphatase activity in the metaphyseal tissues. This decrease was restored by zinc supplement. The present results suggest that the skeletal unloading-induced decrease of zinc content in the femoral-metaphyseal tissues plays a role in the deterioration of bone metabolism in the unloaded rats.
研究了骨骼卸载大鼠股骨干骺端组织中锌含量的降低是否与骨代谢改变有关。采用大鼠后肢悬吊模型设计骨骼卸载。动物在卸载状态下喂养4天。卸载导致干骺端锌含量显著降低。尽管血清锌浓度高于正常大鼠,但单次口服硫酸锌(20mg锌/100g体重)后干骺端组织中的锌积累被卸载部分抑制,这表明卸载会损害锌从血清向骨组织的转运。骨骼卸载导致干骺端组织中碱性磷酸酶活性和脱氧核糖核酸(DNA)含量显著降低。在体外将硫酸锌(10^(-4)M)或β-丙氨酰-L-组氨酸锌(AHZ;10^(-5)M)添加到含有干骺端组织的培养基中,这些降低完全恢复。环己酰亚胺(10^(-8)M)的存在消除了锌化合物的作用,表明锌的作用基于新合成的蛋白质。强力锌螯合剂吡啶二羧酸(10^(-4)和10^(-5)M)导致干骺端组织中锌含量和碱性磷酸酶活性明显降低。补充锌可恢复这种降低。目前的结果表明,骨骼卸载诱导的股骨干骺端组织中锌含量的降低在卸载大鼠骨代谢恶化中起作用。