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性腺抑制对女性甲状旁腺激素及1,25-二羟维生素D分泌调节的影响

Effects of gonadal suppression on the regulation of parathyroid hormone and 1,25-dihydroxyvitamin D secretion in women.

作者信息

Finkelstein J S, Schoenfeld D A

机构信息

Department of Medicine, Massachusetts General Hospital, Boston 02114, USA.

出版信息

J Clin Endocrinol Metab. 1999 Jun;84(6):2151-6. doi: 10.1210/jcem.84.6.5758.

Abstract

Although a causal association between estrogen deficiency and bone loss has been established for many years, the mechanism by which estrogen deficiency leads to bone loss is unclear. Estrogen deficiency could induce bone loss either by a direct effect on bone cells to modify the production of bone-resorbing cytokines or by altering the production or response to calcium regulatory hormones such as PTH and 1,25-dihydroxyvitamin D. To assess the effects of ovarian hormones on calcium regulatory hormones, we evaluated the ability of calcium to suppress PTH secretion and the ability of PTH to increase serum 1,25-dihydroxyvitamin D and whole blood ionic calcium levels in women before and after GnRH analog-induced ovarian suppression. Sixteen women with endometriosis underwent i.v. infusion of calcium (1.1 mg calcium gluconate/cc in 5% dextrose) at a rate of 4 cc/kg x h (n = 7) or human PTH-(1-34) (Parathar) at a dose of 0.55 U/kg x h (n = 9) before and after 6 months of suppression of ovarian function with the GnRH analog nafarelin acetate (200 microg, intranasally, twice daily). Initial infusions were performed between days 6-10 of the menstrual cycle. Serum PTH and whole blood ionic calcium levels were measured at -20, -10, and 0 min and then every 10 min for 2 h during i.v. calcium infusions. Whole blood ionic calcium and 1,25-dihydroxyvitamin D levels were measured every 6 h for 24 h during i.v. human PTH-(1-34) infusions. Serum estradiol levels were markedly suppressed by nafarelin therapy in both groups of women. The relationship between whole blood ionic calcium and serum PTH levels was similar before and during nafarelin-induced ovarian suppression. The net change and rate of rise in serum 1,25-dihydroxyvitamin D levels in response to PTH infusion were similar before and during nafarelin therapy. Peak whole blood ionic calcium and incremental increases in ionic calcium in response to PTH were similar before and during nafarelin therapy. Our data suggest that ovarian suppression does not alter the regulation of PTH secretion in response to calcium, the ability of PTH to stimulate 1,25-dihydroxyvitamin D formation, or the skeletal sensitivity to PTH. These findings suggest that alterations in calcium regulatory hormones by estrogen deficiency are unlikely to play a major role in the pathogenesis of estrogen deficiency bone loss.

摘要

尽管雌激素缺乏与骨质流失之间的因果关系已被确立多年,但雌激素缺乏导致骨质流失的机制尚不清楚。雌激素缺乏可能通过直接作用于骨细胞以改变骨吸收细胞因子的产生,或通过改变对钙调节激素(如甲状旁腺激素和1,25 - 二羟维生素D)的产生或反应来诱导骨质流失。为了评估卵巢激素对钙调节激素的影响,我们在促性腺激素释放激素(GnRH)类似物诱导卵巢抑制前后,评估了女性体内钙抑制甲状旁腺激素分泌的能力以及甲状旁腺激素增加血清1,25 - 二羟维生素D和全血离子钙水平的能力。16名患有子宫内膜异位症的女性在使用GnRH类似物醋酸那法瑞林(200μg,经鼻,每日两次)抑制卵巢功能6个月前后,分别以4cc/kg×h的速率静脉输注钙(5%葡萄糖中含1.1mg葡萄糖酸钙/cc,n = 7)或0.55U/kg×h的剂量静脉输注人甲状旁腺激素 - (1 - 34)(特立帕肽)(n = 9)。初始输注在月经周期的第6 - 10天进行。在静脉输注钙期间,于 - 20、 - 10和0分钟时测量血清甲状旁腺激素和全血离子钙水平,然后每10分钟测量一次,共测量2小时。在静脉输注人甲状旁腺激素 - (1 - 34)期间,每6小时测量一次全血离子钙和1,25 - 二羟维生素D水平,共测量24小时。两组女性中,那法瑞林治疗均显著抑制了血清雌二醇水平。在那法瑞林诱导的卵巢抑制之前和期间,全血离子钙与血清甲状旁腺激素水平之间的关系相似。在那法瑞林治疗之前和期间,对甲状旁腺激素输注反应的血清1,25 - 二羟维生素D水平的净变化和上升速率相似。在那法瑞林治疗之前和期间,对甲状旁腺激素反应的全血离子钙峰值和离子钙的增量增加相似。我们的数据表明,卵巢抑制不会改变对钙反应的甲状旁腺激素分泌调节、甲状旁腺激素刺激1,25 - 二羟维生素D形成的能力或骨骼对甲状旁腺激素的敏感性。这些发现表明,雌激素缺乏引起的钙调节激素改变不太可能在雌激素缺乏性骨质流失的发病机制中起主要作用。

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