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人甲状旁腺激素(1-34)间歇性和持续性给药对大鼠骨骼影响的比较

Comparison of the effects of intermittent and continuous administration of human parathyroid hormone(1-34) on rat bone.

作者信息

Uzawa T, Hori M, Ejiri S, Ozawa H

机构信息

Laboratory for Life Science Research, Asahi Chemical Industry Co., Ltd., Shizuoka-ken, Japan.

出版信息

Bone. 1995 Apr;16(4):477-84. doi: 10.1016/8756-3282(95)90194-9.

Abstract

We compared the effects of synthetic human parathyroid hormone (1-34) (hPTH[1-34]) on rat bones when administered by intermittent injection and by continuous infusion for 4 weeks. Continuous infusion of hPTH(1-34) caused a dose-dependent decrease in the dry weight of the femur and a hyperparathyroidism-like condition in the high-dose group (214 ng/kg/h). In this group, although bone morphology was quite abnormal, the metaphyseal trabecular bone volume increased, whereas the epiphyseal trabecular bone volume tended to decrease, enhancing both bone resorption and formation. The diaphyseal cortical bone of the tibia became markedly porous, and this appeared to be the main cause of the decrease in total bone weight. Conversely, the dry weight of the femur increased in a dose-dependent manner in the intermittent-injection groups. Neither porosity of the cortical bone nor abnormal morphology of the trabecular bone was observed. The volume of the metaphyseal trabecular bone increased while retaining its normal morphology. The epiphyseal trabecular bone formation obviously increased without increase in the number of osteoclasts. In other words, it was postulated that the total weight of bone increased because intermittent injection of hPTH(1-34) increased the trabecular bone volume without loss of the cortical bone volume. These results show that either mode of treatment with hPTH(1-34) continuously accelerated bone formation, whereas the continuous infusion was essential for persistently and markedly enhanced acceleration of bone resorption. It appears that the increase in bone volume with intermittent injection of hPTH(1-34) resulted from the prominent manifestation of its bone-formative action rather than from its bone-resorptive action.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们比较了合成人甲状旁腺激素(1-34)(hPTH[1-34])通过间歇性注射和持续输注给药4周对大鼠骨骼的影响。持续输注hPTH(1-34)导致股骨干重呈剂量依赖性下降,高剂量组(214 ng/kg/h)出现类似甲状旁腺功能亢进的状态。在该组中,尽管骨形态非常异常,但干骺端小梁骨体积增加,而骨骺端小梁骨体积有下降趋势,同时骨吸收和形成均增强。胫骨骨干皮质骨变得明显多孔,这似乎是总骨重量下降的主要原因。相反,间歇性注射组的股骨干重呈剂量依赖性增加。未观察到皮质骨孔隙率或小梁骨形态异常。干骺端小梁骨体积增加,同时保持其正常形态。骨骺端小梁骨形成明显增加,而破骨细胞数量未增加。换句话说,据推测骨总重量增加是因为间歇性注射hPTH(1-34)增加了小梁骨体积而未损失皮质骨体积。这些结果表明,hPTH(1-34)的任何一种治疗方式都持续加速了骨形成,而持续输注对于持续且显著增强骨吸收的加速是必不可少的。似乎间歇性注射hPTH(1-34)导致的骨体积增加是其骨形成作用而非骨吸收作用显著表现的结果。(摘要截断于250字)

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