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Effects of Short-Term Administration of Hydrocortisone, Prednisolone and Dexamethasone on Bone Metabolism in Rats

机译:短期施用氢化可的松,泼尼松龙和地塞米松对大鼠骨代谢的影响

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摘要

Prolonged administration of glucocorticoid (GC) causes a serious osteoporosis. GCs with different anti-inflammatory potency, so hydrocortisone (20 mg/kg), prednisolone (5 mg/kg), and dexamethasone (0.8 mg/kg) were administered daily to rats for two weeks, and we compared and examined effects of each GC on bone metabolism in this study. As the results, significant decreases in serum osteocalcin levels (bone formation marker) and serum tartrate-resistant acid phosphatase-5b levels (bone resorption marker) and a significant decrease in the bone mineral density (BMD) of the femoral metaphysis were observed in the dexamethasone administered group. However, there is no significant change on the serum biochemical markers and BMD levels after administration of hydrocortisone or prednisolone. As the results of bone histomorphometric analysis, both osteoid volume per bone volume (OV/BV) and osteoblast number per bone surface (N.Ob/BS) which represents bone formation parameters, and eroded surface per bone surface (ES/BS) and osteoclast number per bone surface (N.Oc/BS) which represents bone resorption parameters were significantly decreased by administration of dexamethasone. These results suggest that GCs with a high anti-inflammatory potency, such as dexamethasone, have a great influence on the bone metabolism and cause a change in BMD even in a short-term administration.
机译:长时间施用糖皮质激素(GC)导致严重的骨质疏松症。具有不同抗炎效力的GCS,因此氢化可松(20mg / kg),泼尼松龙(5mg / kg)和地塞米松(0.8mg / kg)每天向大鼠施用两周,我们比较和检查各自的效果本研究中骨代谢的GC。结果,在血清骨钙素水平(骨形成标志物)和血清尿酸尿酸磷酸酶-5b水平(骨吸收标志物)中的显着降低以及股骨复合的骨密度(BMD)的显着降低地塞米松施用组。然而,在施用氢化胞松子或泼尼松龙后,血清生物化学标记和BMD水平没有显着变化。作为骨组织形态分析的结果,每骨体积(OV / BV)的骨质体积(OV / BV)和骨表(N.OB / BS)的成骨细胞数(N.OB / BS)表示骨形成参数,并且每骨表面的侵蚀表面(ES / BS)和代表骨吸收参数的骨表面(N.OC / BS)的骨壳数量通过施用地塞米松显着降低。这些结果表明,具有高抗炎效力的GCS,如地塞米松,对骨代谢产生很大影响,即使在短期给药中也会导致BMD的变化。

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