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拟钙剂NPS R - 568诱导的血浆甲状旁腺激素水平每日短暂下降,减缓了去卵巢大鼠的骨质流失速率,但并未增加其骨量。

Daily transient decreases in plasma parathyroid hormone levels induced by the calcimimetic NPS R-568 slows the rate of bone loss but does not increase bone mass in ovariectomized rats.

作者信息

Miller M A, Fox J

机构信息

NPS Pharmaceuticals, Inc., Salt Lake City, UT, USA.

出版信息

Bone. 2000 Oct;27(4):511-9. doi: 10.1016/s8756-3282(00)00350-1.

Abstract

Daily parathyroid hormone (PTH) injections that transiently increase plasma PTH levels within the physiological range increase bone mass in osteopenic, ovariectomized (ovx) rats. This study tested the hypothesis that repeated transient decreases in plasma PTH levels from normal, induced by the daily oral administration of the calcimimetic NPS R-568, would induce an anabolic effect in bone of ovx rats with established osteopenia and/or prevent the rapid bone loss that occurs following ovx. In the reversal study, NPS R-568 was administered orally (10 or 100 micromol/kg) for 30 days to 14-month-old retired breeder rats that were ovx 5 months earlier. NPS R-568 treatment did not increase bone formation rate (BFR) or cancellous bone area (B.Ar) in the proximal tibial metaphysis, or bone mineral density (BMD), at any femoral site. In the prevention study, 3-month-old virgin rats were ovx and given NPS R-568 for the following 28 days. The 10 micromol/kg dose prevented the increase in osteoclast number and 42% of the loss of B.Ar, without affecting the elevated osteoblast populations or BFR. Surprisingly, the 100 micromol/kg dose had fewer protective effects, despite preventing the increase in BFR in both cancellous and cortical bone. Detailed analysis of cancellous bone showed that tendency for a dose-related protection of true cancellous bone occurred, but, while the 10 micromol/kg dose prevented 88% of the loss of calcified cartilage seen in control ovx rats, the 100 micromol/kg dose increased that loss by a further 31%. The mechanism underlying these disparate effects of NPS R-568 on calcified cartilage accumulation in the tibial metaphysis is unclear, but may be related to the different effects that the two doses have on plasma Ca(2+) levels. In conclusion, transient increases in PTH levels above basal, and not simple oscillations in hormone levels below normal, appear necessary for the anabolic properties of endogenous PTH to be manifested in the bones of osteopenic ovx rats.

摘要

每日注射甲状旁腺激素(PTH),使血浆PTH水平在生理范围内短暂升高,可增加骨质减少的去卵巢(ovx)大鼠的骨量。本研究检验了以下假设:每日口服钙敏感受体激动剂NPS R - 568,使血浆PTH水平从正常水平反复短暂降低,会在已发生骨质减少的ovx大鼠骨骼中产生合成代谢效应,和/或预防ovx后发生的快速骨质流失。在逆转研究中,将NPS R - 568以10或100微摩尔/千克的剂量口服给药30天,给予5个月前已去卵巢的14月龄退役繁殖大鼠。NPS R - 568治疗在任何股骨部位均未增加胫骨近端干骺端的骨形成率(BFR)、松质骨面积(B.Ar)或骨矿物质密度(BMD)。在预防研究中,对3月龄处女大鼠进行去卵巢手术,并在接下来的28天给予NPS R - 568。10微摩尔/千克的剂量可预防破骨细胞数量增加以及42%的B.Ar丢失,且不影响升高的成骨细胞数量或BFR。令人惊讶的是,100微摩尔/千克的剂量尽管可预防松质骨和皮质骨中BFR的增加,但其保护作用却较少。对松质骨的详细分析表明,确实存在与剂量相关的对真正松质骨的保护趋势,但虽然10微摩尔/千克的剂量可预防对照ovx大鼠中88%的钙化软骨丢失,100微摩尔/千克的剂量却使该丢失进一步增加了31%。NPS R - 568对胫骨近端干骺端钙化软骨积累产生这些不同影响的潜在机制尚不清楚,但可能与两种剂量对血浆Ca(2+)水平的不同影响有关。总之,对于骨质减少的ovx大鼠骨骼中内源性PTH的合成代谢特性的显现而言,PTH水平高于基础水平的短暂升高似乎是必要的,而非激素水平低于正常水平的简单波动。

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