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拟钙剂NPS R-568可预防重度继发性甲状旁腺功能亢进大鼠的甲状旁腺增生。

Calcimimetic NPS R-568 prevents parathyroid hyperplasia in rats with severe secondary hyperparathyroidism.

作者信息

Wada M, Nagano N, Furuya Y, Chin J, Nemeth E F, Fox J

机构信息

Pharmaceutical Development Laboratory, Kirin Brewery Co; Ltd, Gunma, Japan.

出版信息

Kidney Int. 2000 Jan;57(1):50-8. doi: 10.1046/j.1523-1755.2000.00837.x.

Abstract

UNLABELLED

Calcimimetic NPS R-568 prevents parathyroid hyperplasia in rats with severe secondary hyperparathyroidism.

BACKGROUND

Secondary hyperparathyroidism (secondary HPT) in chronic renal insufficiency (CRI) is characterized by multiglandular hyperplasia.

METHODS

In this study, we investigated the effects of the calcimimetic NPS R-568 on the parathyroid gland in rats with CRI induced by ligation of the renal arteries and severe secondary HPT induced by dietary phosphorus loading. Six days after surgery, high-phosphorus diet feeding was started, and NPS R-568 was administered to the rats for 56 days either by daily gavage (30 or 100 micromol/kg) or by continuous subcutaneous infusion (20 micromol/kg. day).

RESULTS

After 54 days, serum PTH levels in vehicle-treated CRI rats were 1019 vs. 104 pg/mL in sham-operated controls. Infusion of NPS R-568 maintained serum PTH at levels comparable with those of sham-operated controls, whereas daily gavage also prevented much of the increase in CRI controls and decreased PTH levels intermittently in a dose-dependent fashion. Parathyroid gland enlargement was caused predominantly by hyperplasia. Total cell number per kg body wt was 3.5-fold higher in vehicle-treated CRI rats than in sham-operated controls. Both infusion and high-dose gavage of NPS R-568 completely prevented the increase in parathyroid cell number.

CONCLUSION

These results demonstrate that the calcimimetic compound NPS R-568 can prevent both the increase in serum PTH levels and parathyroid hyperplasia in rats with CRI and severe secondary HPT. Moreover, these changes occurred despite decreases in serum 1, 25(OH)2D3 and increases in serum phosphate, suggesting a dominant role for the calcium receptor in regulating parathyroid cell proliferation.

摘要

未标记

拟钙剂NPS R-568可预防重度继发性甲状旁腺功能亢进大鼠的甲状旁腺增生。

背景

慢性肾功能不全(CRI)中的继发性甲状旁腺功能亢进(继发性HPT)的特征是多腺体增生。

方法

在本研究中,我们研究了拟钙剂NPS R-568对肾动脉结扎诱导的CRI大鼠以及饮食磷负荷诱导的重度继发性HPT大鼠甲状旁腺的影响。手术后6天,开始高磷饮食喂养,通过每日灌胃(30或100微摩尔/千克)或连续皮下输注(20微摩尔/千克·天)给大鼠施用NPS R-568,持续56天。

结果

54天后,未处理的CRI大鼠血清甲状旁腺激素(PTH)水平为1019 pg/mL,而假手术对照组为104 pg/mL。输注NPS R-568可使血清PTH维持在与假手术对照组相当的水平,而每日灌胃也可在很大程度上阻止CRI对照组中的升高,并以剂量依赖方式间歇性降低PTH水平。甲状旁腺肿大主要由增生引起。未处理的CRI大鼠每千克体重的总细胞细胞总数比假手术对照组高3.5倍。NPS R-568的输注和高剂量灌胃均完全阻止了甲状旁腺细胞数量的增加。

结论

这些结果表明拟钙剂化合物NPS R-568可预防CRI和重度继发性HPT大鼠血清PTH水平升高和甲状旁腺增生。此外,尽管血清1,25(OH)2D3降低和血清磷酸盐升高,但这些变化仍然发生,提示钙受体在调节甲状旁腺细胞增殖中起主导作用。

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