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持续输注糖皮质激素对大鼠骨代谢的影响。

Effects of continuous glucocorticoid infusion on bone metabolism in the rat.

作者信息

King C S, Weir E C, Gundberg C W, Fox J, Insogna K L

机构信息

Section of Comparative Medicine, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

出版信息

Calcif Tissue Int. 1996 Sep;59(3):184-91. doi: 10.1007/s002239900107.

Abstract

The effects of continuous administration of supraphysiologic doses of dexamethasone (DEX) on bone metabolism were examined in rats. Adult, male, Sprague Dawley rats were infused with DEX at a constant rate of 16.25 microg/day for 19 days. Despite soft tissue catabolism, DEX treatment led to a significant increase in bone volume in all experiments. This was accompanied by a significant gain in femoral weight and calcium content. These findings were also observed in DEX-treated parathyroidectomized animals indicating that intact parathyroid function was not required for this effect. DEX treatment did not affect mean levels of serum calcium or phosphorus but led to significant declines in circulating levels of PTH and 1,25(OH)2D and in the urinary calcium/creatinine ratio. This latter finding was also observed in PTX animals in which 1,25(OH)2D levels did not change. Serum concentrations of osteocalcin and tartrate-resistant acid phosphatase both declined in a time-dependent manner with DEX treatment suggesting a slowing of bone turnover with the net effect favoring formation. However, histomorphometric findings were variable. Two of three experiments demonstrated a decrease in cellular parameters of formation and resorption and in one experiment, these indices increased. Mineralized surface increased with DEX treatment. We conclude that, in marked contrast to the findings in man and certain other species, DEX treatment increases bone mass in rats. This may in part relate to a relatively greater suppression of resorption vis à vis formation.

摘要

研究了持续给予超生理剂量地塞米松(DEX)对大鼠骨代谢的影响。成年雄性Sprague Dawley大鼠以16.25微克/天的恒定速率输注DEX,持续19天。尽管存在软组织分解代谢,但在所有实验中,DEX治疗均导致骨量显著增加。这伴随着股骨重量和钙含量的显著增加。在接受DEX治疗的甲状旁腺切除动物中也观察到了这些结果,表明这种效应不需要完整的甲状旁腺功能。DEX治疗不影响血清钙或磷的平均水平,但导致循环中甲状旁腺激素(PTH)和1,25(OH)2D水平以及尿钙/肌酐比值显著下降。在1,25(OH)2D水平未改变的甲状旁腺切除动物中也观察到了后一结果。随着DEX治疗,骨钙素和抗酒石酸酸性磷酸酶的血清浓度均呈时间依赖性下降,提示骨转换减慢,净效应有利于骨形成。然而,组织形态计量学结果存在差异。三个实验中有两个显示成骨和吸收的细胞参数降低,而在一个实验中,这些指标增加。DEX治疗使矿化表面增加。我们得出结论,与人类和某些其他物种的研究结果形成显著对比的是,DEX治疗可增加大鼠的骨量。这可能部分与相对于骨形成而言对骨吸收的抑制作用相对更大有关。

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