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甲状旁腺激素(PTH)合成代谢作用在去卵巢大鼠松质骨中的时间表达。

Temporal expression of the anabolic action of PTH in cancellous bone of ovariectomized rats.

作者信息

Meng X W, Liang X G, Birchman R, Wu D D, Dempster D W, Lindsay R, Shen V

机构信息

Regional Bone Center, Helen Hayes Hospital, W. Haverstraw, New York, USA.

出版信息

J Bone Miner Res. 1996 Apr;11(4):421-9. doi: 10.1002/jbmr.5650110402.

Abstract

When administered intermittently, parathyroid hormone (PTH) is a potent anabolic agent in both human and animal bone. To improve our understanding of this anabolic effect, we have examined the time course of PTH action in an established animal model of estrogen deficiency-induced bone loss: the ovariectomized rat. Animals were ovariectomized (Ovx) and allowed to lose bone for 6 weeks. A dose of 20 micrograms/kg/d of rat PTH (1-34) was administered s.c., 6 days each week for periods of 1, 2, 3, 4, 6 and 8 weeks. Animals were sacrificed for evaluation of skeletal histomorphometry of the proximal tibia and mechanical strength of the cancellous bone in the marrow cavity of the distal femur. Cancellous bone volume (Cn-BV/TV) increased gradually over 8 weeks of treatment (16.8 +/- 1.6 to 24.1 +/- 2.7%) as did the bone formation rate (0.308 +/- 0.054 to 1.659 +/- 0.293 microns3/micron2/d), as determined by an increase in both total mineralization surface (15.5 +/- 2.1 to 42.7 +/- 5.0%) and mineral apposition rate (1.88 +/- 0.20 to 3.55 +/- 0.39 microns/d). The largest increments in these variables reflecting bone formation occurred over the first week of treatment. This bone formation was accompanied by an increase in trabecular thickness (Tb.Th) (55.3 +/- 3.4 to 80.5 +/- 5.0 microns) without a corresponding increment in trabecular number (Tb.N) (3.65 +/- 0.17 to 3.55 +/- 0.26). Extensive tetracycline labels were visualized on the surface of trabecular rod-like and plate-like structures. A small transient, though not statistically significant, increase occurred in both eroded surface and urinary pyridinoline concentration immediately after the onset of PTH administration. Osteocalcin showed a small decrement in the first two weeks after PTH administration, but the levels were elevated when compared with the Ovx control in later weeks. Mechanical strength of the cancellous bone also increased significantly with PTH treatment (20.5 +/- 2.4 to 46.1 +/- 10.0 Newtons). Our results showed that: 1) intermittent PTH treatment of Ovx rats elicited an immediate increase of bone formation activity by the existing osteoblasts, 2) the increase of Cn-BV/TV after PTH administration resulted primarily from an increase in Tb.Th, and 3) improved mechanical strength after PTH treatment can be achieved by increases in Tb.Th without an increase in Tb.N.

摘要

间歇性给予甲状旁腺激素(PTH)时,其在人类和动物骨骼中都是一种有效的促合成代谢因子。为了更好地理解这种促合成代谢作用,我们在雌激素缺乏诱导的骨质流失的既定动物模型——去卵巢大鼠中,研究了PTH作用的时间进程。将动物去卵巢(Ovx),使其骨质流失6周。以20微克/千克/天的剂量皮下注射大鼠PTH(1 - 34),每周6天,持续1、2、3、4、6和8周。处死动物,以评估近端胫骨的骨骼组织形态计量学和远端股骨骨髓腔松质骨的机械强度。在8周的治疗过程中,松质骨体积(Cn - BV/TV)逐渐增加(从16.8±1.6%增至24.1±2.7%),骨形成率也如此(从0.308±0.054增至1.659±0.293立方微米/平方微米/天),这是由总矿化表面(从15.5±2.1%增至42.7±5.0%)和矿化沉积率(从1.88±0.20增至3.55±0.39微米/天)的增加所决定的。反映骨形成的这些变量的最大增幅出现在治疗的第一周。这种骨形成伴随着小梁厚度(Tb.Th)的增加(从55.3±3.4微米增至80.5±5.0微米),而小梁数量(Tb.N)没有相应增加(从3.65±0.17降至3.55±0.26)。在小梁棒状和板状结构表面可见广泛的四环素标记。在开始给予PTH后,侵蚀表面和尿吡啶啉浓度立即出现小的短暂增加,尽管无统计学意义。骨钙素在给予PTH后的前两周略有下降,但在随后几周与Ovx对照组相比水平升高。PTH治疗后松质骨的机械强度也显著增加(从20.5±2.4牛顿增至46.1±10.0牛顿)。我们的结果表明:1)对Ovx大鼠进行间歇性PTH治疗可使现存成骨细胞的骨形成活性立即增加;2)给予PTH后Cn - BV/TV的增加主要源于Tb.Th的增加;3)PTH治疗后机械强度的改善可通过Tb.Th的增加而实现,而Tb.N不增加。

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